US20160151476A1 - Combination neisserial compositions - Google Patents

Combination neisserial compositions Download PDF

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US20160151476A1
US20160151476A1 US15/015,041 US201615015041A US2016151476A1 US 20160151476 A1 US20160151476 A1 US 20160151476A1 US 201615015041 A US201615015041 A US 201615015041A US 2016151476 A1 US2016151476 A1 US 2016151476A1
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protein
composition
seq
meningitidis
animal
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Marzia Monica Giuliani
Mariagrazia Pizza
Rino Rappuoli
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GlaxoSmithKline Biologicals SA
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    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K39/00—Medicinal preparations containing antigens or antibodies
    • A61K39/02—Bacterial antigens
    • A61K39/095—Neisseria
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K38/00—Medicinal preparations containing peptides
    • A61K38/16—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
    • A61K38/164—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from bacteria
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K39/00—Medicinal preparations containing antigens or antibodies
    • A61K39/02—Bacterial antigens
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K39/00—Medicinal preparations containing antigens or antibodies
    • A61K39/39—Medicinal preparations containing antigens or antibodies characterised by the immunostimulating additives, e.g. chemical adjuvants
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A61P31/04—Antibacterial agents
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P37/00—Drugs for immunological or allergic disorders
    • A61P37/02—Immunomodulators
    • A61P37/04—Immunostimulants
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K14/00—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
    • C07K14/195—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from bacteria
    • C07K14/22—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from bacteria from Neisseriaceae (F)
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K39/00—Medicinal preparations containing antigens or antibodies
    • A61K2039/51—Medicinal preparations containing antigens or antibodies comprising whole cells, viruses or DNA/RNA
    • A61K2039/53—DNA (RNA) vaccination
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K39/00—Medicinal preparations containing antigens or antibodies
    • A61K2039/555—Medicinal preparations containing antigens or antibodies characterised by a specific combination antigen/adjuvant
    • A61K2039/55505—Inorganic adjuvants
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K39/00—Medicinal preparations containing antigens or antibodies
    • A61K2039/70—Multivalent vaccine
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K39/00—Medicinal preparations containing antigens or antibodies

Definitions

  • This invention relates to compositions comprising combinations of biological molecules from Neisseria bacteria, particularly N. meningitidis and N. gonorrhoeae.
  • Neisseria meningitidis and Neisseria gonorrhoeae are non-motile. Grain negative diplococci that are pathogenic in humans.
  • Serogroups of N. meningitidis Based on the organism's capsular polysaccharide, 12 serogroups of N. meningitidis have been identified. Group A is the pathogen most often implicated in epidemic disease in sub-Saharan Africa. Serogroups Band Care responsible for the vast majority of cases in the United States and in most developed countries. Serogroups W135 and Y are responsible for the rest of the cases in the United States and developed countries.
  • the meningococcal vaccine currently in use is a tetravalent polysaccharide vaccine composed of serogroups A, C, Y and W135. Meningococcus B remains a problem, however.
  • the polysaccharide approach cannot be used because the menB capsular polysaccharide is a polymer of ⁇ (2-8)-linked N-acetyl neuraminic acid that is also present in mammalian tissue.
  • One approach to a menB vaccine uses mixtures of outer membrane proteins (OMPs). To overcome the antigenic variability, multivalent vaccines containing up to nine different porins have been constructed [eg. Poolman J T (1992) Development of a meningococcal vaccine. Infect. Agents Dis. 4:13-28).
  • FIG. 4 coding DNA SEQ ID 4003 FIG. 4 protein SEQ ID 4004 FIG. 9 coding DNA SEQ ID 4005 FIG. 13 DNA SEQ ID 4006 FIG. 13 protein SEQ ID 4007 WO 96/29412 SEQ IDs 1-26 SEQ IDs 4008-4033 WO 95/03413 SEQ IDs 1-23 SEQ IDs 4034-4056 Tettelin et al. (2000) NMB0001-2160 (DNA) SEQ IDs 4057-6216 Science 287: 1809-15 NMB0001-2160 SEQ IDs 6217-8376 (encoded proteins)
  • compositions comprising a first biological molecule from a Neisseria bacterium and a second biological molecule from a Neisseria bacterium.
  • biological molecule includes proteins and nucleic acids.
  • compositions may also comprise further biological molecules, preferably also from Neisseria, that is to say the compositions may comprise two or more biological molecules (eg. 3, 4, 5, 6, 7, 8 etc.), at least two of which are from a Neisseria bacterium (eg. 3, 4, 5, 6, 7, 8 etc.).
  • Such compositions include those comprising (i) two or more different Neisserial proteins.
  • the first and second biological molecules are from different Neisseria species (eg. one is from N. meningitidis and one is from N. gonorrhoeae ), but they may be from the same species.
  • the biological molecules in the compositions may he from different serogroups or strains of the same species.
  • the first biological molecule is preferably selected from the group consisting of SEQ IDs 1-8376. More preferably, it is selected from the group consisting, of SEQ IDs 1-4002 and/or SEQ IDs 4057-8376. it is preferably a purified or isolated biological molecule.
  • the second biological molecule is preferably selected from the group consisting of SEQ IDs 1-8376. More preferably, it is selected from the group consisting of SEQ IDs 1-4002 and/or SEQ IDs 4057-8376. It is preferably a purified or isolated biological molecule.
  • first and second biological molecules may be a Neisserial biological molecule which is not specifically disclosed herein, and which may not have been identified, discovered, made available to the public or purified before this patent application was filed.
  • the invention provides a composition comprising one or more of the following pairs of first and second biological molecules (listed by SEQ ID):
  • the invention includes each of the 35074500 possible pairs of SEQ IDs 1-8376 (1&2, 1&3, 1&4, 1&5 . . . 1&8375, 1&8376, 2&3, 2&4, 2&5 . . . 2&8375, 2&8376, 3&4 . . . 1000&1001, 1000&1002 . . . 1000&8376 . . . 8374&8375, 8374&8376, 8373&8376) although, for reasons of space, these are not listed in full here.
  • SEQ IDs 1-8376 in the compositions of the invention may he supplemented or substituted with molecules comprising sequences homologous (ie. having sequence identity) to SEQ IDs 1-8376.
  • the degree of identity is preferably greater than 50% (eg. 65%, 80%, 90%, or more), and include mutants and allelic variants.
  • SEQ IDs 1-8376 in the compositions of the invention may be supplemented or substituted with molecules comprising fragments of SEQ IDs 1-8376.
  • Such fragments should comprise at least n consecutive monomers from the molecules and, depending on the particular sequence, n is either (i) 7 or more for protein molecules (eg. 8, 10, 12, 14, 16, 18, 20 or more), preferably such that the fragment comprises an epitope from the sequence, or (ii) 10 or more for nucleic acid molecules (eg 12, 14, 15, 18, 20, 25. 30, 35, 40 or more).
  • the mature form of the protein is preferably used.
  • the mature form of the NspA protein SEQ IDs 4008-4033: WO096/29412: FIG. 29 .
  • SEQ IDs 1-8376 in the compositions of the invention may be supplemented or substituted with an antibody that binds to the protein.
  • This antibody may be monoclonal or polyclonal.
  • SEQ IDs 1-8376 in the compositions of the invention may be supplemented or substituted with nucleic acid which can hybridise to the Neisserial nucleic acid, preferably under “high stringency” conditions (eg. 65° C. in a 0.1 ⁇ SSC. 0.5% SDS solution).
  • nucleic acid in the compositions can take various forms (eg. single stranded, double stranded, vectors, probes etc.).
  • nucleic acid includes DNA and RNA, and also their analogues, such as those containing modified backbones, and also peptide nucleic acids (PNA) etc.
  • the composition comprises molecules from different Neisseria species, such as one or more N. meningitidis molecule and one or more N. gonorrhoeae molecule.
  • the composition may comprise molecules from different serogroups and/or strains of the same species, such as strains A and B of N. meningitidis. Further embodiments comprise mixtures of one or more N. meningitidis molecules from different strains and also one or more N. gonorrhoeae molecules.
  • PCT/IB00/00642 includes a more detailed experimental analysis of conserved regions in these proteins. To ensure maximum cross-strain recognition and reactivity, regions of proteins that are conserved between different Neisserial species, serogroups and strains can he used in the compositions of the present invention.
  • the invention therefore provides proteins which comprise stretches of amino acid sequence that are shared across the majority of Neisseria. particularly N. meningitidis and N. gonorrhoeae.
  • the composition comprises a protein comprising a fragment of a Neisserial protein (preferably a protein from SEQ IDs 1-8376, or more preferably SEQ IDs 1-4002), wherein said fragment consists of n consecutive conserved amino acids.
  • u is 7 or more (eg. 8, 10, 12, 14, 16, 18, 20 or more).
  • the fragment preferably comprises an antigenic or immunogenic region of the Neisserial protein.
  • a “conserved” amino acid is one that is present in a particular Neisserial protein in at least x% of Neisseria (or, preferably, in at least of combined N. meningitidis and N. gonorrhoeae strains). The value of x may be 50% or more eg.
  • compositions according to the invention therefore include those comprising:
  • the invention also provides the compositions of the invention for use as medicaments (eg. as immunogenic compositions or vaccines) or as diagnostic reagents. It also provides the use of the compositions in the manufacture of: (i) a medicament for treating or preventing infection due to Neisserial bacteria: (ii) a diagnostic reagent for detecting the presence of Neisserial bacteria or of antibodies raised against Neisserial bacteria; and/or (iii) a reagent which can raise antibodies against Neisserial bacteria.
  • the invention also provides a method of treating a patient, comprising administering to the patient a therapeutically effective amount of a composition according to the invention.
  • the invention further provides a process for producing a composition according to the invention, comprising the step of bringing one or more of SEQ IDs 1-8376 into combination with one or more other of SEQ IDs 1-8376.
  • FIGS. 1A-1B shows SDS-PAGE results for the expression of ORFs 6, 7, 13, 65-1, 72, 73-1, 105-1, 137-1, 143-1 and 147-1.
  • the left-hand lanes show molecular weight markers (set M1).
  • FIGS. 2A-2C shows ( FIG. 2A ) SDS-PAGE results for ORF9 ( FIG. 2B ) the positions of the N. meningitidis immunoreactive band in a Western blot against a N. meningitidis outer membrane vesicle preparation ( FIG. 2C ) FACS analysis.
  • FIG. 3 shows SDS-PAGE results for the expression of ORFs 2-1, 5-1, 22-1, 132-1 and 4.
  • the left-hand lanes show molecular weight markers (set M1).
  • FIGS. 4 to 28 show a hydrophilicity plot (upper), antigenic index (middle), and AMPHI regions (lower) for ORFs 2, 5, 6, 7, 9, 13a, 15, 22, 23, 27, 28, 32, 65, 72, 73, 76, 79, 89, 105, 106-1, 132, 137, 138, 143 and 147.
  • FIGS. 29A-29C shows sequence variability of NspA from various strains of meningococeus B. These sequences may he used as alternatives to the NspA of WO 96/29412 (SEQ IDs 4008-4033).
  • FIGS. 30A-30B shows the binding of polyclonal anti-rNspA by indirect fluorescence flow cytometry to encapsulated and non-encapsulated menB strains.
  • FIGS. 31A-31E shows similar data for encapsulated strains 8047. CU385 & M986 ( FIGS. 31A-31B ) and non-encapsulated strains BZ232. MC58, NG3/88 & NGB 165 ( FIGS. 31C-E ).
  • FIG. 32 shows a model of NspA secondary structure.
  • FIGS. 33A-33I shows FACS analysis of non-encapsulated strain M7 ( FIG. 33A ) ethanol-treated (to disrupt the capsule) strains 2996, N44776, MC58, 1000, BZ232, BZ133, NG6/88, BZ198, NG3/88, 297-0, BZ147 and BZ169 ( FIGS. 33B-33I ).
  • FIGS. 34A-34C shows FACS analysis of M7 strain using a pentavalent mixture at 1:400 ( FIG. 34A ), 1:200 ( FIG. 34B ), & 1:100 ( FIG. 34C ) dilutions.
  • FIGS. 35A-35B show FACS for the individual antigens 287, 919, and 953 and combinations thereof.
  • ORFs 6, 7, 13, 65-1, 72, 73-1, 105-1, 137-1, 143-1 and 147-1 disclosed in WO99/24578 were expressed in E. coli and purified, as set out in the following table:
  • the ORF7-His fusion was used to immunise mice.
  • the sera were used in an ELLSA assay, essentially as described in WO99 24578, and gave possitive results.
  • Each of these ORFs can be combined with one or more of SEQ IDs 1-8376.
  • ORF9 disclosed in WO99/24578 was cloned in the pET vector and expressed in E. coli.
  • the purified ORF-His fusion protein was analysed by SDS-PAGE, as shown in FIG. 2A .
  • Mice were immunised with the purified ORF9-His and sera were used Western blot analysis ( FIG. 2B ).
  • FACS analysis FIG. 2C FACS analysis FIG. 2C ), and ELISA assay.
  • the protocols used were essentially the same as those set out in WO99/24578.
  • ORF9 is a surface-exposed protein
  • ORF9 is suitable for combining with one or more other of SEQ IDs 1-8376.
  • Each of these ORFs can be combined with one or more of SEQ IDs 1-8376.
  • ORF-4 is disclosed in WO99/24578 as containing a lipopeptide signal sequence (LPSS).
  • LPSS lipopeptide signal sequence
  • the amplified DNA fragment was cloned into the vector pET21b+ for expression as a C-terminus His-tagged fusion.
  • a log phase culture of E. coli containing pET21b+orf4-LPSS was induced with 1.0 mM IPTF for 3 h at 30° C. collected by centrifugation for 10 min at 8000 g, and resuspended in PBS.
  • the suspension was sonicated on ice and Triton X-114 added to a final concentration of 0.6% (v/v). The material was incubated on ice for 20 minutes then warmed to 37° C. until phase separation occurred (indicated by a high degree of cloudiness). After centrifugation for 10 min at 10,000 g at 20° C.
  • the upper aqueous phase was discarded, and the lower detergent phase collected without disrupting the bacterial pellet.
  • To the detergent phase was added 13 volumes of 20 mM Histidine, 2 mM EDTA, 30 mM NaCl (pH 5.8). This was centrifuged for 10 min at 4° C. and the supernatant combined batchwise at 4° C. for 30 min. with Q Sepharose Fast Flow resin (Pharmacia). The mixture was centrifuged, the supernatant retained and the resin washed with 20 mM Histidine, 2mM EDTA, 30 mM NaCl (pH 5.8). Triton X-100 0.3% (v/v) and eluted with 1 M NaCl in the same buffer.
  • Orf4 lipoprotein was found in the supernatant obtained after binding.
  • Final purification was accomplished by chromatography on Hi-TrapTM O (Pharmacia).
  • the binding-supernatant was adjusted to pH 7.0 by the addition of 0.1M HCl and applied to a Hi-TrapTM Q column equilibrated with 50 mM Tris-HCl (pH 7.0). 2 mM EDTA, 0.3% Triton X-100. 10 mM NaCl.
  • the column was washed with 5.0 ml of the equilibration buffer and a NaCl gradient from 10 mM to 1M was applied.
  • Two electrophoretically distinct forms of the protein eluted. One in the wash and the other in the NaCl gradient between 150 mM, and 300 mM NaCl.
  • the protein obtained in the wash was used for immunization of mice. This form of the protein probably represents the fully processed, lipidated molecule.
  • ORF4 is suitable for combining with one or more other of SEQ IDs 1-8376.
  • FIGS. 4 to 28 show, for each of these ORFs, a hydrophilicity plot (upper), an antigenic index plot (middle), and an AMPHI analysis (lower).
  • the AMPHI program has been used to predict T-cell epitopes [Gao et al. (1989) J. Immunol. 143:3007; Roberts et al. (1996) AIDS Res Hum Retrovir 12:593; Quakyi et al. (1992) Scand J Immunol suppl.11:9) and is available in the Protean package of DNASTAR. Inc. (1228 South Park Street. Madison, Wis. 53715 USA).
  • Each of these ORFs can be combined with one or more other of SEQ IDs 1-8376.
  • ORF4-L the lipidated protein—see example 4 above.
  • ORF37 WO99/24578, example 1.
  • ORF40 WO99/36544, example 1
  • 502 WO99/57280, pages 687-690
  • 8 WO99/57280, pages 165-167 was produced.
  • the ELISA titres against 13 test strains were as follows:
  • Proteins ORF1 e.g. example 77 of WO99/24578: see also WO99/55873
  • ‘287’ e.g. FIG. 21 of WO99/57280; also SEQ IDs 3103-3108 therein
  • ‘919’ e.g. WO99/57280 FIG. 23 and SEQ IDs 3069-3074 therein
  • the proteins were from the 2996 strain of MenB.
  • This mixture was also combined with a MenC polysaccharide conjugate antigen [e.g. Costantino el al. (1992) Vaccine 10:691-698]. OMVs were used as controls.
  • Titres were as follows:
  • Proteins 287, 919 and 953 are disclosed in WO99/57280. These proteins from N. meningitidis serogroup B strain 2996 were expressed and tested in a bactericidal assay against strain 2996, alone and in combinations. OMVs from 2996 were used as a positive control.
  • Antigen 287 919 953 Control Titre 8192 2048 128 65536 Combination 287 + 919 287 + 953 919 + 953 287 + 919 + 953 Titre 32000 8192 8192 8192
  • FIG. 35 shows FACS data for the individual antigens and for the four combinations.
  • Serogroup B strains MenA MenC Antigen 2996 BZ133 BZ232 MC58 NGH38 F6124 C11 287 8192 >4096 256 1024 2048 1024 2048 919 2048 — 1024 — — — 953 128 — — — — — — — 287 + 919 32000 >4096 512 512 1024 512 >2048 287 + 953 8192 >4096 1024 512 2048 2048 >2048 919 + 953 8192 — 8192 — — — — Trivalent 8192 >2048 256 — 1024 >2048 >2048 Control 65536 — 8192 2048 — 2048 32768
  • antigen mixtures are useful in conferring cross-strain activity.
  • titres for the individual antigens were as follows:
  • Serogroup B strains MenA MenC Antigen 2996 BZ133 BZ232 MC58 NGH38 F6124 C11 287 16000 2048 16 512 >2048 64 1024 919 16000 — 2048 — — — — 953 2048 — 16 — — — —
  • NspA protein is disclosed in WO96/29412, and is represented herein as SEQ IDs 4008-4033.
  • the academic literature disclosure of this protein [Martin et al. (1997) Exp. Med 185 1173-1183] reported the protein to be highly conserved between Neisseria strains (99% cross-reactivity of anti-NspA antibodies with 250 meningococcal A, B & C strains) and also efficient protection against deadly challenge with live bacteria. There have also been reports that NspA adsorbed on alum elicits serum meningococcal bactericidal antibody responses in rabbits and monkeys [Martin et al. (1998) Abstracts of 11 th International pathogenic Neisseria conference, page 198]. On the basis of these data, rNspA (recombinant NspA) is being developed as a vaccine for the prevention of meningococcal disease caused by all serogroups.
  • N. meningitidis strains tested in this example were isolated from patients residing in different countries over a period of more than 30 years (see table on page 72). These strains were selected to be representative of widely divergent ‘clonal’ groups, as defined by multilocus isoenzyme typing [Seiler et al. (1996) Mol. Microbiol. 19:841-856] and/or multilocus sequence typing [Maiden et al. (1998) PNAS USA 95:3140-45].
  • Strain M7 which is derived from strain NMB, contains a transposon insertion that blocks capsular polysaccharide biosynthesis [Stephens et al. (1991) Infect. Immun. 59:4097-4102], but all the other strains are encapsulated.
  • PCR primers were designed and the NspA gene from strain 8047 was amplified.
  • rNspA pSK+ plasmid
  • a plasmid pTrc.NspA.1 encoding a protein in which a portion of the signal sequence has been replaced with a poly-histidine tag was also used.
  • Both plasmids were expressed in E. coli strain BL21(DE3) and the proteins were purified.
  • rNspA is secreted, rather than being associated with the outer membrane.
  • the protein was partially purified from the culture medium by precipitation with 55% w/v ammonium sulphate, and had an apparent MW of 18.6 kDa, confirmed by Western Blot.
  • NspA The two forms of NspA (rNspA and denature His-tage NspA) were injected into 6-week old female CD-1 mice to raise antisera. The ability of these to bind to the surface of N. meningitidis strain B was determined using flow cytometric detection of indirect fluorescence assay [Granoff et at (1998) J. Immunol 160:5028-36]. The results for strains NMB and M7 (an acapsulated mutant of NMB) are shown in FIG. 30 .
  • anti-group B polysaccharide mAb SEAM-3 [Granoff et al] only binds to the encapsulated strain, whereas the positive anti-P1.2 (PorA) control mAb binds to both strains.
  • the antisera raised against rNspA is able to bind both strains.
  • Antisera against the His-tag NspA gave negative results, however. These antisera were also negative for strains 8047.
  • CU385 and M986 FIG. 31A ), but by Western Blot these antisera gave positive results.
  • FIG. 31A shows that murine antibodies raised against rNspA bind to the surface of strain 8047 (the strain from which the nspA gene was cloned) and strain CU385, but not to M986,
  • FIG. 31B shows similar negative results for strains BZ232, MC58, NG3/88 and N(31)165. In all of these negative cases, however, the anticapsular mAb control was positive.
  • the nspA genes from five of the six negative strains (BX232, NG3/88, NGP165. M136 & M986) and from three of the positive strains (8047, CU385 & NG6/88) were sequenced.
  • the sequence for the sixth negative strain (MC58) was already available from the complete genome sequence.
  • the nspA sequences for all ten strains were highly conserved, varying at most by 5 nucleotides from the prototype sequence of Martin et al.
  • the most variant protein had only 3 amino acid differences (see FIG. 29 ). With one exception, all of the amino acid variants involved the same respective residues in discrete segments of the protein. These include the signal peptide, which is not present in the mature protein, and two short segments in the 50 C-terminal residues. These differences do not explain the antisera results, as there are examples of identical variant sequences in strains that were positive and those that were negative (compare M136 & 8047; NGI'165 & NG6/88; MC58 & CU385).
  • NspA protein in the outer membranes of five strains 8047, CU385 & NG6/88—all positive for anti-rNspA; M986 & M136—both negative
  • Bacterial cell pellets were extracted with lauryl sarcosinate, and the insoluble outer membrane fractions were analysed.
  • An 18.6 kDa band was seen for all five strains, and this was cross-reactive with anti-His-tag-NspA by Western Blot. Thus strain differences in nspA expression also failed to explain the results.
  • anti-rNspA to bind to the bacterial cell surface could be influenced by the amount of polysaccharide capsule present.
  • the quantity of capsular polysaccharide produced by the 17 test strains was therefore assessed by inhibition ELISA.
  • Extracts of capsular polysaccharide were prepared based on a method described by Corn et al. [ J. Infect. Dis. (1993) 167:356-64]. Individual bacterial clones were grown to an OD 620 0.5-0.7 in 7 mL of Mueller-Hinton broth. Bacteria were collected by centrifugation at 5000 g for 15 min, washed in 0.6 mL of 10 mM Hepes, pH 8.0, and then resuspended in 0.6 mL of the same buffer containing 10 mM EDTA and incubated at 37° C. for 1 hr.
  • the cells were pelleted at 10,000 g for 1 minute and the relative amount of meningococcal B polysaccharide antigen released into the supernatant was determined by an inhibition ELISA, performed as described by Azmi et al. [ Infect. Immun. (1995) 63:1906-13].
  • the solid phase antigen in the ELISA was meningococcal B polysaccharide-ADH-biotin absorbed to avidin-coated microtiter plates [Granoff et al.].
  • the meningococcal B polysaccharide-reactive human paraprotein LIP [Azmi et al.] was used as the primary antibody (0.2 ⁇ g/ml).
  • the complement-dependent bactericidal activity of the anti-rNspA antisera were tested using an assay similar to that described by Mandrell et al. [ J. Infect. Dis. (1995) 172:1279-89].
  • the complement source was human serum from a healthy adult with no detectable anti-capsular antibody to group B polysaccharide and no intrinsic bactericidal activity against the test strain.
  • Serum bactericidal titres were defined as the serum dilution resulting in a 50% decrease in CFU/ml after 60 minutes incubation of bacteria in the reaction mixture, compared to the control CFU/ml at time zero.
  • bacteria incubated with a negative control antibody showed a 150-200% increase in CFU/ml during the 60 minutes of incubation.
  • the positive control antibody [anti-capsular IgG2a mAb SEAM 12, Granoff et al.] showed complement-mediated bactericidal activity against all 17 strains.
  • the six strains that were negative for anti-rNspA antisera binding by flow assay were resistant, showing no bactericidal or bacteriostatic effects.
  • test or control antibody positive control: anticapsular mAb; negative control: anti- E. coli .
  • blood specimens were obtained from the heart. Aliquots were plated onto chocolate agar, and CFU/ml was determined after overnight incubation at 37° C. in 5% CO 2 .
  • Anticapsular mAb 2 ⁇ g M986 0/6 ⁇ 1 ⁇ 1 Anti-rNspA 1:5 M986 6/6 44 a 45 Anti-rNspA 1:25 M986 6/6 93 a 95 Anti- E.coli 1:5 M986 6/6 98 a — control Anticapsular mAb 2 ⁇ g 8047 0/5 ⁇ 1 ⁇ 1 Anti-rNspA 1:5 8047 1/6 0.2 b 2 Anti-rNspA 1:25 8047 1/5 0.4 b 4 Anti- E.coli 1:5 8047 6/6 10 b — control a p > 0.5, compared to geometric mean CFU/ml of control rats b p ⁇ 0.001, compared to geometric mean CFU/ml of control rats
  • NspA does not seem to be effective in preventing meningococcal B infection.
  • Approximately one third of strains have decreased cell-surface expression of NspA epitopes when grown in vitro, are resistant to anti-NspA induced complement-mediated bacteriolysis, and are resistant to passive antiserum immunisation. These strains produce large amounts of capsular polysaccharide, and would thus be expected to have the greatest virulence.
  • the ability of a vaccine containing only NspA to confer broad protective immunity against meningococcal B thus has to be doubted.
  • compositions comprising NspA [SEC) IDs 4008-4033; FIG. 29 ] therefore advantageously comprise further antigens.
  • a preferred aspect of the invention is thus a combination of NspA protein with one or more further Neisserial antigens.
  • FIG. 32 A model of the secondary structure of NspA is shown in FIG. 32 , containing eight transmembrane ⁇ -strands and 4 surface-exposed connecting loops. This fits the pattern of alternating hydrophobic and hydrophilic amino acids in NspA, which is characteristic of many ⁇ -barrel porins [Weiss et al. (1990) FEBS Letts 267:268-272]
  • the grey shaded areas in the model indicate segments that are >40% identical and >70% similar to encoded amino acid sequences of opacity proteins (Opa) from N. meningitidis, N. gonorrhoeae, N. flavius, N sicca. and H. Influenzae identified in a BLAST search of the non-redundant GenBank CDS.
  • the alternating sequences are predicted amphiphilic ⁇ -strands; vertical segments correspond to transmembrane segments; the top of the figure corresponds to surface exposed segments, labelled as loops 1 to 4.
  • NspA the only significant homology between the deduced amino acid sequence of NspA and those of other proteins are weak homologies with the Neisseria opacity protein (Opa) family in two small segments ( ⁇ 20 amino acids) near the C-terminal end of the protein.
  • Opa Neisseria opacity protein
  • separate comparisons of the N- and C-termini of NspA with GenBank reveals a high degree of homology (>40% identity and >70% similarity) between NspA and Opa proteins from N. meningitidis, N. gonorrhoeae, N. flavius, N. sicca, and H. influenzae.
  • the Opa proteins are thought to he integral membrane proteins that have eight transmembrane segments and a ⁇ -barrel topology in the membrane similar to that of porin [Merker et al. (1997) Mol. Microbial. 23:281-293].
  • the presence of NspA in detergent-insoluble membrane preparations indicate that NspA is located in the outer membrane, which would be consistent with the Opa-like membrane topology shown in the model.
  • the segments of NspA that are most homologous to those of the Opa proteins are the putative transmembrane segments indicated in the shaded areas of FIG. 32 .
  • the opacity proteins of Neisseria can, under certain circumstances, elicit protective antibody.
  • problems with limited antibody accessibility of the opacity proteins in encapsulated bacteria, variability of amino acid sequences in exposed loop segments, and phase variation of protein expression during clinical infection have limited the ability of Opa to elicit protective antibody consistently [Maloniy et al, (1998) J. infect, Dis. 172:1279-89].
  • there appears to be little or no sequence variation in the surface exposed loops of NspA in FIG. 32 it was recently reported that a panel of anti- N.
  • meningitidis NspA monoclonal antibodies that reacted with all meningococcal strains tested reacted with only a limited number of N. gonorrhoeae strains, even though the respective amino acid sequences in the two species are 92% identical.
  • the respective NspA sequences of the meningococcal and gonococcal strains are compared ( FIG. 29 )
  • all of the respective amino acid differences result in changes in hydrophobicity or charge, and are located in the putative surface exposed connecting loops ( FIG. 32 ).
  • This finding suggests that the connecting loops in NspA, which are highly conserved in N. meningitidis, may be important epitopes for antibodies that bind to native NspA.
  • NspA are relatively small (10-14 amino acids) compared to, for example, the highly immunogenic external loops of PorA and O N (24 to 45 amino acids).
  • the shorter length of the loops may limit the accessibility of NspA surface epitopes for binding interactions with serum antibody, especially in the presence of abundant capsular polysaccharide.
  • the invention provides the fragments of NspA that are exposed on the cell-surface in FIG. 32 , namely SSSLGSAKG, NYKAPSTDFKLY, NRASVDLGGSDSFSQT and NYIGKVNTVKNVRSG, and also provides corresponding fragments from allelic variants of NspA.
  • the invention provides sub-sequences of these fragments, comprising 7 or more contiguous amino acids from the fragments.
  • the invention further provides proteins comprising these fragments. Nucleic acid encoding these fragments and proteins is also provided.
  • NspA fragments, proteins comprising the fragments, and nucleic acid may be used in the compositions of the invention, in particular as substitutes for full-length NspA.
  • these fragments, proteins and nucleic acids may be used as products in isolation, that is to say they need not exclusively be used in combination with other biological molecules.
  • Static refers to strains that were inhibited but not killed in the assay ( ⁇ 50% but ⁇ 100% survival at 60 mins).
  • e Titre defined as dilution of capsule extract giving 50% inhibition of antibody binding to meningococcal B polysaccharide antigen in an ELISA.

Abstract

Compositions comprising a first biological molecule from a Neisseria bacterium and a second biological molecule from a Neisseria bacterium. The term “biological molecule” includes proteins and nucleic acids. Preferred Neisseria species are N. meningitidis and N. gonorrhoeae.

Description

    CROSS REFERENCE TO RELATED APPLICATIONS
  • This application is a Continuation of U.S. patent application Ser. No. 14/284,326, filed May 21, 2014, which is a Continuation of U.S. patent application Ser. No. 13/921,087, filed Jun. 18, 2013, (now Abandoned), which is a Continuation of U.S. patent application Ser. No. 12/979,239, filed December 27, 2010, (now Abandoned), which is a Continuation of U.S. patent application Ser. No. 10/982,703, filed Nov. 5, 2004, (now U.S. Pat. No. 7,862,827), which is a Continuation of U.S. patent application Ser. No. 09/979,263, which claims an international filing date of May 19, 2000, (now Abandoned), which is the National Stage of International Patent Application of PCT/IB2000/000828, filed May 19, 2000, which claims the benefit of United Kingdom Patent Application No. 9911692.3, filed May 19, 1999, United Kingdom Patent Application No. 9919705.5, filed Aug. 19, 1999, and United Kingdom Patent Application No. 0005730.7, tiled Mar. 9, 2000, each of which is hereby incorporated by reference in its entirety.
    • SUBMISSION OF SEQUENCE LISTING AS ASCII TEXT FILE
  • The content of the following submission on ASCII text file is incorporated herein by reference in its entirety: a computer readable form (CRF) of the Sequence Listing (file name: 303822001.207SeqList.txt, date recorded: Feb. 2, 2016, size: 11,264 KB).
    • FIELD OF THE INVENTION
  • This invention relates to compositions comprising combinations of biological molecules from Neisseria bacteria, particularly N. meningitidis and N. gonorrhoeae.
    • BACKGROUND ART
  • Neisseria meningitidis and Neisseria gonorrhoeae are non-motile. Grain negative diplococci that are pathogenic in humans.
  • Based on the organism's capsular polysaccharide, 12 serogroups of N. meningitidis have been identified. Group A is the pathogen most often implicated in epidemic disease in sub-Saharan Africa. Serogroups Band Care responsible for the vast majority of cases in the United States and in most developed countries. Serogroups W135 and Y are responsible for the rest of the cases in the United States and developed countries.
  • The meningococcal vaccine currently in use is a tetravalent polysaccharide vaccine composed of serogroups A, C, Y and W135. Meningococcus B remains a problem, however. The polysaccharide approach cannot be used because the menB capsular polysaccharide is a polymer of α(2-8)-linked N-acetyl neuraminic acid that is also present in mammalian tissue. One approach to a menB vaccine uses mixtures of outer membrane proteins (OMPs). To overcome the antigenic variability, multivalent vaccines containing up to nine different porins have been constructed [eg. Poolman J T (1992) Development of a meningococcal vaccine. Infect. Agents Dis. 4:13-28). Additional proteins to be used in outer membrane vaccines have been the opa and opc proteins, but none of these approaches have been able to overcome the antigenic variability [eg. Ala' Aldeen & Boniello (1996) The meningococcal transferrin-binding proteins 1 and 2 are both surface exposed and generate bactericidal antibodies capable of killing homologous and heterologous strains. Vaccine 14(1):49-53].
  • Given the propensity for meningococcal disease during non-epidemic periods to be caused by multiple strains or strain variants [Russel et al. (1998) Abstracts of 11th International pathogenic Neisseria conference, page 281] together with frequent temporal shifts in the predominant strains in a community, it seems that a universal meningococcal B vaccine will require more than one antigenic species.
    • DESCRIPTION OF THE INVENTION
  • Neisserial protein and nucleotide sequences are disclosed in the following documents:
      • WO 99/24578
      • WO 99/36544
      • WO 99/57280
      • WO 97/28273
      • WO 96/29412
      • WO 95/03413
      • Tettelin et al. (2000) Science 287:1809-1815
  • For ease of reference, the sequences disclosed in these documents are referred to in the present application according to the following table:
  • Original sequence Sequence numbering
    Document numbering in this application
    WO 99/24578 SEQ IDs 1-892 SEQ IDs 1-892
    WO 99/36544 SEQ IDs 1-90 SEQ IDs 893-982
    WO 99/57280 SEQ IDs 1-3020 SEQ IDs 983-4002
    WO 97/28273 FIG. 4 coding DNA SEQ ID 4003
    FIG. 4 protein SEQ ID 4004
    FIG. 9 coding DNA SEQ ID 4005
    FIG. 13 DNA SEQ ID 4006
    FIG. 13 protein SEQ ID 4007
    WO 96/29412 SEQ IDs 1-26 SEQ IDs 4008-4033
    WO 95/03413 SEQ IDs 1-23 SEQ IDs 4034-4056
    Tettelin et al. (2000) NMB0001-2160 (DNA) SEQ IDs 4057-6216
    Science 287: 1809-15 NMB0001-2160 SEQ IDs 6217-8376
    (encoded proteins)
  • The present invention provides compositions comprising a first biological molecule from a Neisseria bacterium and a second biological molecule from a Neisseria bacterium. The term “biological molecule” includes proteins and nucleic acids.
  • The compositions may also comprise further biological molecules, preferably also from Neisseria, that is to say the compositions may comprise two or more biological molecules (eg. 3, 4, 5, 6, 7, 8 etc.), at least two of which are from a Neisseria bacterium (eg. 3, 4, 5, 6, 7, 8 etc.). Such compositions include those comprising (i) two or more different Neisserial proteins.
  • (ii) two or more different Neisserial nucleic acids, or mixtures of one or more Neisserial protein and one or more Neisserial nucleic acid.
  • In one preferred embodiment, the first and second biological molecules are from different Neisseria species (eg. one is from N. meningitidis and one is from N. gonorrhoeae), but they may be from the same species. The biological molecules in the compositions may he from different serogroups or strains of the same species.
  • The first biological molecule is preferably selected from the group consisting of SEQ IDs 1-8376. More preferably, it is selected from the group consisting, of SEQ IDs 1-4002 and/or SEQ IDs 4057-8376. it is preferably a purified or isolated biological molecule.
  • The second biological molecule is preferably selected from the group consisting of SEQ IDs 1-8376. More preferably, it is selected from the group consisting of SEQ IDs 1-4002 and/or SEQ IDs 4057-8376. It is preferably a purified or isolated biological molecule.
  • One or both of the first and second biological molecules may be a Neisserial biological molecule which is not specifically disclosed herein, and which may not have been identified, discovered, made available to the public or purified before this patent application was filed.
  • In particular, the invention provides a composition comprising one or more of the following pairs of first and second biological molecules (listed by SEQ ID):
  • First Second
    1 2-8376
    2 1 and 3-8376
    3 1-2 and 4-8376
    4 1-3 and 5-8376
    5 1-4 and 6-8376
    6 1-5 and 7-8376
    7 1-6 and 8-8376
    8 1-7 and 9-8376
    9 1-8 and 10-8376
    10 1-9 and 11-8376
    11 1-10 and 12-8376
    12 1-11 and 13-8376
    13 1-12 and 14-8376
    14 1-13 and 15-8376
    15 1-14 and 16-8376
    16 1-15 and 17-8376
    17 1-16 and 18-8376
    18 1-17 and 19-8376
    19 1-18 and 20-8376
    20 1-19 and 21-8376
    21 1-20 and 22-8376
    22 1-21 and 23-8376
    23 1-22 and 24-8376
    24 1-23 and 25-8376
    25 1-24 and 26-8376
    26 1-25 and 27-8376
    27 1-26 and 28-8376
    28 1-27 and 29-8376
    29 1-28 and 30-8376
    30 1-29 and 31-8376
    31 1-30 and 32-8376
    32 1-31 and 33-8376
    33 1-32 and 34-8376
    34 1-33 and 35-8376
    35 1-34 and 36-8376
    36 1-35 and 37-8376
    37 1-36 and 38-8376
    38 1-37 and 39-8376
    39 1-38 and 40-8376
    40 1-39 and 41-8376
    41 1-40 and 42-8376
    42 1-41 and 43-8376
    43 1-42 and 44-8376
    44 1-43 and 45-8376
    45 1-44 and 46-8376
    46 1-45 and 47-8376
    47 1-46 and 48-8376
    48 1-47 and 49-8376
    49 1-48 and 50-8376
    50 1-49 and 51-8376
    51 1-50 and 52-8376
    52 1-51 and 53-8376
    53 1-52 and 54-8376
    54 1-53 and 55-8376
    55 1-54 and 56-8376
    56 1-55 and 57-8376
    57 1-56 and 58-8376
    58 1-57 and 59-8376
    59 1-58 and 60-8376
    60 1-59 and 61-8376
    61 1-60 and 62-8376
    62 1-61 and 63-8376
    63 1-62 and 64-8376
    64 1-63 and 65-8376
    65 1-64 and 66-8376
    66 1-65 and 67-8376
    67 1-66 and 68-8376
    68 1-67 and 69-8376
    69 1-68 and 70-8376
    70 1-69 and 71-8376
    71 1-70 and 72-8376
    72 1-71 and 73-8376
    73 1-72 and 74-8376
    74 1-73 and 75-8376
    75 1-74 and 76-8376
    76 1-75 and 77-8376
    77 1-76 and 78-8376
    78 1-77 and 79-8376
    79 1-78 and 80-8376
    80 1-79 and 81-8376
    81 1-80 and 82-8376
    82 1-81 and 83-8376
    83 1-82 and 84-8376
    84 1-83 and 85-8376
    85 1-84 and 86-8376
    86 1-85 and 87-8376
    87 1-86 and 88-8376
    88 1-87 and 89-8376
    89 1-88 and 90-8376
    90 1-89 and 91-8376
    91 1-90 and 92-8376
    92 1-91 and 93-8376
    93 1-92 and 94-8376
    94 1-93 and 95-8376
    95 1-94 and 96-8376
    96 1-95 and 97-8376
    97 1-96 and 98-8376
    98 1-97 and 99-8376
    99 1-98 and 100-8376
    100 1-99 and 101-8376
    101 1-100 and 102-8376
    102 1-101 and 103-8376
    103 1-102 and 104-8376
    104 1-103 and 105-8376
    105 1-104 and 106-8376
    106 1-105 and 107-8376
    107 1-106 and 108-8376
    108 1-107 and 109-8376
    109 1-108 and 110-8376
    110 1-109 and 111-8376
    111 1-110 and 112-8376
    112 1-111 and 113-8376
    113 1-112 and 114-8376
    114 1-113 and 115-8376
    115 1-114 and 116-8376
    116 1-115 and 117-8376
    117 1-116 and 118-8376
    118 1-117 and 119-8376
    119 1-118 and 120-8376
    120 1-119 and 121-8376
    121 1-120 and 122-8376
    122 1-121 and 123-8376
    123 1-122 and 124-8376
    124 1-123 and 125-8376
    125 1-124 and 126-8376
    126 1-125 and 127-8376
    127 1-126 and 128-8376
    128 1-127 and 129-8376
    129 1-128 and 130-8376
    130 1-129 and 131-8376
    131 1-130 and 132-8376
    132 1-131 and 133-8376
    133 1-132 and 134-8376
    134 1-133 and 135-8376
    135 1-134 and 136-8376
    136 1-135 and 137-8376
    137 1-136 and 138-8376
    138 1-137 and 139-8376
    139 1-138 and 140-8376
    140 1-139 and 141-8376
    141 1-140 and 142-8376
    142 1-141 and 143-8376
    143 1-142 and 144-8376
    144 1-143 and 145-8376
    145 1-144 and 146-8376
    146 1-145 and 147-8376
    147 1-146 and 148-8376
    148 1-147 and 149-8376
    149 1-148 and 150-8376
    150 1-149 and 151-8376
    151 1-150 and 152-8376
    152 1-151 and 153-8376
    153 1-152 and 154-8376
    154 1-153 and 155-8376
    155 1-154 and 156-8376
    156 1-155 and 157-8376
    157 1-156 and 158-8376
    158 1-157 and 159-8376
    159 1-158 and 160-8376
    160 1-159 and 161-8376
    161 1-160 and 162-8376
    162 1-161 and 163-8376
    163 1-162 and 164-8376
    164 1-163 and 165-8376
    165 1-164 and 166-8376
    166 1-165 and 167-8376
    167 1-166 and 168-8376
    168 1-167 and 169-8376
    169 1-168 and 170-8376
    170 1-169 and 171-8376
    171 1-170 and 172-8376
    172 1-171 and 173-8376
    173 1-172 and 174-8376
    174 1-173 and 175-8376
    175 1-174 and 176-8376
    176 1-175 and 177-8376
    177 1-176 and 178-8376
    178 1-177 and 179-8376
    179 1-178 and 180-8376
    180 1-179 and 181-8376
    181 1-180 and 182-8376
    182 1-181 and 183-8376
    183 1-182 and 184-8376
    184 1-183 and 185-8376
    185 1-184 and 186-8376
    186 1-185 and 187-8376
    187 1-186 and 188-8376
    188 1-187 and 189-8376
    189 1-188 and 190-8376
    190 1-189 and 191-8376
    191 1-190 and 192-8376
    192 1-191 and 193-8376
    193 1-192 and 194-8376
    194 1-193 and 195-8376
    195 1-194 and 196-8376
    196 1-195 and 197-8376
    197 1-196 and 198-8376
    198 1-197 and 199-8376
    199 1-198 and 200-8376
    200 1-199 and 201-8376
    201 1-200 and 202-8376
    202 1-201 and 203-8376
    203 1-202 and 204-8376
    204 1-203 and 205-8376
    205 1-204 and 206-8376
    206 1-205 and 207-8376
    207 1-206 and 208-8376
    208 1-207 and 209-8376
    209 1-208 and 210-8376
    210 1-209 and 211-8376
    211 1-210 and 212-8376
    212 1-211 and 213-8376
    213 1-212 and 214-8376
    214 1-213 and 215-8376
    215 1-214 and 216-8376
    216 1-215 and 217-8376
    217 1-216 and 218-8376
    218 1-217 and 219-8376
    219 1-218 and 220-8376
    220 1-219 and 221-8376
    221 1-220 and 222-8376
    222 1-221 and 223-8376
    223 1-222 and 224-8376
    224 1-223 and 225-8376
    225 1-224 and 226-8376
    226 1-225 and 227-8376
    227 1-226 and 228-8376
    228 1-227 and 229-8376
    229 1-228 and 230-8376
    230 1-229 and 231-8376
    231 1-230 and 232-8376
    232 1-231 and 233-8376
    233 1-232 and 234-8376
    234 1-233 and 235-8376
    235 1-234 and 236-8376
    236 1-235 and 237-8376
    237 1-236 and 238-8376
    238 1-237 and 239-8376
    239 1-238 and 240-8376
    240 1-239 and 241-8376
    241 1-240 and 242-8376
    242 1-241 and 243-8376
    243 1-242 and 244-8376
    244 1-243 and 245-8376
    245 1-244 and 246-8376
    246 1-245 and 247-8376
    247 1-246 and 248-8376
    248 1-247 and 249-8376
    249 1-248 and 250-8376
    250 1-249 and 251-8376
    251 1-250 and 252-8376
    252 1-251 and 253-8376
    253 1-252 and 254-8376
    254 1-253 and 255-8376
    255 1-254 and 256-8376
    256 1-255 and 257-8376
    257 1-256 and 258-8376
    258 1-257 and 259-8376
    259 1-258 and 260-8376
    260 1-259 and 261-8376
    261 1-260 and 262-8376
    262 1-261 and 263-8376
    263 1-262 and 264-8376
    264 1-263 and 265-8376
    265 1-264 and 266-8376
    266 1-265 and 267-8376
    267 1-266 and 268-8376
    268 1-267 and 269-8376
    269 1-268 and 270-8376
    270 1-269 and 271-8376
    271 1-270 and 272-8376
    272 1-271 and 273-8376
    273 1-272 and 274-8376
    274 1-273 and 275-8376
    275 1-274 and 276-8376
    276 1-275 and 277-8376
    277 1-276 and 278-8376
    278 1-277 and 279-8376
    279 1-278 and 280-8376
    280 1-279 and 281-8376
    281 1-280 and 282-8376
    282 1-281 and 283-8376
    283 1-282 and 284-8376
    284 1-283 and 285-8376
    285 1-284 and 286-8376
    286 1-285 and 287-8376
    287 1-286 and 288-8376
    288 1-287 and 289-8376
    289 1-288 and 290-8376
    290 1-289 and 291-8376
    291 1-290 and 292-8376
    292 1-291 and 293-8376
    293 1-292 and 294-8376
    294 1-293 and 295-8376
    295 1-294 and 296-8376
    296 1-295 and 297-8376
    297 1-296 and 298-8376
    298 1-297 and 299-8376
    299 1-298 and 300-8376
    300 1-299 and 301-8376
    301 1-300 and 302-8376
    302 1-301 and 303-8376
    303 1-302 and 304-8376
    304 1-303 and 305-8376
    305 1-304 and 306-8376
    306 1-305 and 307-8376
    307 1-306 and 308-8376
    308 1-307 and 309-8376
    309 1-308 and 310-8376
    310 1-309 and 311-8376
    311 1-310 and 312-8376
    312 1-311 and 313-8376
    313 1-312 and 314-8376
    314 1-313 and 315-8376
    315 1-314 and 316-8376
    316 1-315 and 317-8376
    317 1-316 and 318-8376
    318 1-317 and 319-8376
    319 1-318 and 320-8376
    320 1-319 and 321-8376
    321 1-320 and 322-8376
    322 1-321 and 323-8376
    323 1-322 and 324-8376
    324 1-323 and 325-8376
    325 1-324 and 326-8376
    326 1-325 and 327-8376
    327 1-326 and 328-8376
    328 1-327 and 329-8376
    329 1-328 and 330-8376
    330 1-329 and 331-8376
    331 1-330 and 332-8376
    332 1-331 and 333-8376
    333 1-332 and 334-8376
    334 1-333 and 335-8376
    335 1-334 and 336-8376
    336 1-335 and 337-8376
    337 1-336 and 338-8376
    338 1-337 and 339-8376
    339 1-338 and 340-8376
    340 1-339 and 341-8376
    341 1-340 and 342-8376
    342 1-341 and 343-8376
    343 1-342 and 344-8376
    344 1-343 and 345-8376
    345 1-344 and 346-8376
    346 1-345 and 347-8376
    347 1-346 and 348-8376
    348 1-347 and 349-8376
    349 1-348 and 350-8376
    350 1-349 and 351-8376
    351 1-350 and 352-8376
    352 1-351 and 353-8376
    353 1-352 and 354-8376
    354 1-353 and 355-8376
    355 1-354 and 356-8376
    356 1-355 and 357-8376
    357 1-356 and 358-8376
    358 1-357 and 359-8376
    359 1-358 and 360-8376
    360 1-359 and 361-8376
    361 1-360 and 362-8376
    362 1-361 and 363-8376
    363 1-362 and 364-8376
    364 1-363 and 365-8376
    365 1-364 and 366-8376
    366 1-365 and 367-8376
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    999 1-998 and 1000-8376
    1000 1-999 and 1001-8376
    1001 1-1000 and 1002-8376
    1002 1-1001 and 1003-8376
    1003 1-1002 and 1004-8376
    1004 1-1003 and 1005-8376
    1005 1-1004 and 1006-8376
    1006 1-1005 and 1007-8376
    1007 1-1006 and 1008-8376
    1008 1-1007 and 1009-8376
    1009 1-1008 and 1010-8376
    1010 1-1009 and 1011-8376
    1011 1-1010 and 1012-8376
    1012 1-1011 and 1013-8376
    1013 1-1012 and 1014-8376
    1014 1-1013 and 1015-8376
    1015 1-1014 and 1016-8376
    1016 1-1015 and 1017-8376
    1017 1-1016 and 1018-8376
    1018 1-1017 and 1019-8376
    1019 1-1018 and 1020-8376
    1020 1-1019 and 1021-8376
    1021 1-1020 and 1022-8376
    1022 1-1021 and 1023-8376
    1023 1-1022 and 1024-8376
    1024 1-1023 and 1025-8376
    1025 1-1024 and 1026-8376
    1026 1-1025 and 1027-8376
    1027 1-1026 and 1028-8376
    1028 1-1027 and 1029-8376
    1029 1-1028 and 1030-8376
    1030 1-1029 and 1031-8376
    1031 1-1030 and 1032-8376
    1032 1-1031 and 1033-8376
    1033 1-1032 and 1034-8376
    1034 1-1033 and 1035-8376
    1035 1-1034 and 1036-8376
    1036 1-1035 and 1037-8376
    1037 1-1036 and 1038-8376
    1038 1-1037 and 1039-8376
    1039 1-1038 and 1040-8376
    1040 1-1039 and 1041-8376
    1041 1-1040 and 1042-8376
    1042 1-1041 and 1043-8376
    1043 1-1042 and 1044-8376
    1044 1-1043 and 1045-8376
    1045 1-1044 and 1046-8376
    1046 1-1045 and 1047-8376
    1047 1-1046 and 1048-8376
    1048 1-1047 and 1049-8376
    1049 1-1048 and 1050-8376
    1050 1-1049 and 1051-8376
    1051 1-1050 and 1052-8376
    1052 1-1051 and 1053-8376
    1053 1-1052 and 1054-8376
    1054 1-1053 and 1055-8376
    1055 1-1054 and 1056-8376
    1056 1-1055 and 1057-8376
    1057 1-1056 and 1058-8376
    1058 1-1057 and 1059-8376
    1059 1-1058 and 1060-8376
    1060 1-1059 and 1061-8376
    1061 1-1060 and 1062-8376
    1062 1-1061 and 1063-8376
    1063 1-1062 and 1064-8376
    1064 1-1063 and 1065-8376
    1065 1-1064 and 1066-8376
    1066 1-1065 and 1067-8376
    1067 1-1066 and 1068-8376
    1068 1-1067 and 1069-8376
    1069 1-1068 and 1070-8376
    1070 1-1069 and 1071-8376
    1071 1-1070 and 1072-8376
    1072 1-1071 and 1073-8376
    1073 1-1072 and 1074-8376
    1074 1-1073 and 1075-8376
    1075 1-1074 and 1076-8376
    1076 1-1075 and 1077-8376
    1077 1-1076 and 1078-8376
    1078 1-1077 and 1079-8376
    1079 1-1078 and 1080-8376
    1080 1-1079 and 1081-8376
    1081 1-1080 and 1082-8376
    1082 1-1081 and 1083-8376
    1083 1-1082 and 1084-8376
    1084 1-1083 and 1085-8376
    1085 1-1084 and 1086-8376
    1086 1-1085 and 1087-8376
    1087 1-1086 and 1088-8376
    1088 1-1087 and 1089-8376
    1089 1-1088 and 1090-8376
    1090 1-1089 and 1091-8376
    1091 1-1090 and 1092-8376
    1092 1-1091 and 1093-8376
    1093 1-1092 and 1094-8376
    1094 1-1093 and 1095-8376
    1095 1-1094 and 1096-8376
    1096 1-1095 and 1097-8376
    1097 1-1096 and 1098-8376
    1098 1-1097 and 1099-8376
    1099 1-1098 and 1100-8376
    1100 1-1099 and 1101-8376
    1101 1-1100 and 1102-8376
    1102 1-1101 and 1103-8376
    1103 1-1102 and 1104-8376
    1104 1-1103 and 1105-8376
    1105 1-1104 and 1106-8376
    1106 1-1105 and 1107-8376
    1107 1-1106 and 1108-8376
    1108 1-1107 and 1109-8376
    1109 1-1108 and 1110-8376
    1110 1-1109 and 1111-8376
    1111 1-1110 and 1112-8376
    1112 1-1111 and 1113-8376
    1113 1-1112 and 1114-8376
    1114 1-1113 and 1115-8376
    1115 1-1114 and 1116-8376
    1116 1-1115 and 1117-8376
    1117 1-1116 and 1118-8376
    1118 1-1117 and 1119-8376
    1119 1-1118 and 1120-8376
    1120 1-1119 and 1121-8376
    1121 1-1120 and 1122-8376
    1122 1-1121 and 1123-8376
    1123 1-1122 and 1124-8376
    1124 1-1123 and 1125-8376
    1125 1-1124 and 1126-8376
    1126 1-1125 and 1127-8376
    1127 1-1126 and 1128-8376
    1128 1-1127 and 1129-8376
    1129 1-1128 and 1130-8376
    1130 1-1129 and 1131-8376
    1131 1-1130 and 1132-8376
    1132 1-1131 and 1133-8376
    1133 1-1132 and 1134-8376
    1134 1-1133 and 1135-8376
    1135 1-1134 and 1136-8376
    1136 1-1135 and 1137-8376
    1137 1-1136 and 1138-8376
    1138 1-1137 and 1139-8376
    1139 1-1138 and 1140-8376
    1140 1-1139 and 1141-8376
    1141 1-1140 and 1142-8376
    1142 1-1141 and 1143-8376
    1143 1-1142 and 1144-8376
    1144 1-1143 and 1145-8376
    1145 1-1144 and 1146-8376
    1146 1-1145 and 1147-8376
    1147 1-1146 and 1148-8376
    1148 1-1147 and 1149-8376
    1149 1-1148 and 1150-8376
    1150 1-1149 and 1151-8376
    1151 1-1150 and 1152-8376
    1152 1-1151 and 1153-8376
    1153 1-1152 and 1154-8376
    1154 1-1153 and 1155-8376
    1155 1-1154 and 1156-8376
    1156 1-1155 and 1157-8376
    1157 1-1156 and 1158-8376
    1158 1-1157 and 1159-8376
    1159 1-1158 and 1160-8376
    1160 1-1159 and 1161-8376
    1161 1-1160 and 1162-8376
    1162 1-1161 and 1163-8376
    1163 1-1162 and 1164-8376
    1164 1-1163 and 1165-8376
    1165 1-1164 and 1166-8376
    1166 1-1165 and 1167-8376
    1167 1-1166 and 1168-8376
    1168 1-1167 and 1169-8376
    1169 1-1168 and 1170-8376
    1170 1-1169 and 1171-8376
    1171 1-1170 and 1172-8376
    1172 1-1171 and 1173-8376
    1173 1-1172 and 1174-8376
    1174 1-1173 and 1175-8376
    1175 1-1174 and 1176-8376
    1176 1-1175 and 1177-8376
    1177 1-1176 and 1178-8376
    1178 1-1177 and 1179-8376
    1179 1-1178 and 1180-8376
    1180 1-1179 and 1181-8376
    1181 1-1180 and 1182-8376
    1182 1-1181 and 1183-8376
    1183 1-1182 and 1184-8376
    1184 1-1183 and 1185-8376
    1185 1-1184 and 1186-8376
    1186 1-1185 and 1187-8376
    1187 1-1186 and 1188-8376
    1188 1-1187 and 1189-8376
    1189 1-1188 and 1190-8376
    1190 1-1189 and 1191-8376
    1191 1-1190 and 1192-8376
    1192 1-1191 and 1193-8376
    1193 1-1192 and 1194-8376
    1194 1-1193 and 1195-8376
    1195 1-1194 and 1196-8376
    1196 1-1195 and 1197-8376
    1197 1-1196 and 1198-8376
    1198 1-1197 and 1199-8376
    1199 1-1198 and 1200-8376
    1200 1-1199 and 1201-8376
    1201 1-1200 and 1202-8376
    1202 1-1201 and 1203-8376
    1203 1-1202 and 1204-8376
    1204 1-1203 and 1205-8376
    1205 1-1204 and 1206-8376
    1206 1-1205 and 1207-8376
    1207 1-1206 and 1208-8376
    1208 1-1207 and 1209-8376
    1209 1-1208 and 1210-8376
    1210 1-1209 and 1211-8376
    1211 1-1210 and 1212-8376
    1212 1-1211 and 1213-8376
    1213 1-1212 and 1214-8376
    1214 1-1213 and 1215-8376
    1215 1-1214 and 1216-8376
    1216 1-1215 and 1217-8376
    1217 1-1216 and 1218-8376
    1218 1-1217 and 1219-8376
    1219 1-1218 and 1220-8376
    1220 1-1219 and 1221-8376
    1221 1-1220 and 1222-8376
    1222 1-1221 and 1223-8376
    1223 1-1222 and 1224-8376
    1224 1-1223 and 1225-8376
    1225 1-1224 and 1226-8376
    1226 1-1225 and 1227-8376
    1227 1-1226 and 1228-8376
    1228 1-1227 and 1229-8376
    1229 1-1228 and 1230-8376
    1230 1-1229 and 1231-8376
    1231 1-1230 and 1232-8376
    1232 1-1231 and 1233-8376
    1233 1-1232 and 1234-8376
    1234 1-1233 and 1235-8376
    1235 1-1234 and 1236-8376
    1236 1-1235 and 1237-8376
    1237 1-1236 and 1238-8376
    1238 1-1237 and 1239-8376
    1239 1-1238 and 1240-8376
    1240 1-1239 and 1241-8376
    1241 1-1240 and 1242-8376
    1242 1-1241 and 1243-8376
    1243 1-1242 and 1244-8376
    1244 1-1243 and 1245-8376
    1245 1-1244 and 1246-8376
    1246 1-1245 and 1247-8376
    1247 1-1246 and 1248-8376
    1248 1-1247 and 1249-8376
    1249 1-1248 and 1250-8376
    1250 1-1249 and 1251-8376
    1251 1-1250 and 1252-8376
    1252 1-1251 and 1253-8376
    1253 1-1252 and 1254-8376
    1254 1-1253 and 1255-8376
    1255 1-1254 and 1256-8376
    1256 1-1255 and 1257-8376
    1257 1-1256 and 1258-8376
    1258 1-1257 and 1259-8376
    1259 1-1258 and 1260-8376
    1260 1-1259 and 1261-8376
    1261 1-1260 and 1262-8376
    1262 1-1261 and 1263-8376
    1263 1-1262 and 1264-8376
    1264 1-1263 and 1265-8376
    1265 1-1264 and 1266-8376
    1266 1-1265 and 1267-8376
    1267 1-1266 and 1268-8376
    1268 1-1267 and 1269-8376
    1269 1-1268 and 1270-8376
    1270 1-1269 and 1271-8376
    1271 1-1270 and 1272-8376
    1272 1-1271 and 1273-8376
    1273 1-1272 and 1274-8376
    1274 1-1273 and 1275-8376
    1275 1-1274 and 1276-8376
    1276 1-1275 and 1277-8376
    1277 1-1276 and 1278-8376
    1278 1-1277 and 1279-8376
    1279 1-1278 and 1280-8376
    1280 1-1279 and 1281-8376
    1281 1-1280 and 1282-8376
    1282 1-1281 and 1283-8376
    1283 1-1282 and 1284-8376
    1284 1-1283 and 1285-8376
    1285 1-1284 and 1286-8376
    1286 1-1285 and 1287-8376
    1287 1-1286 and 1288-8376
    1288 1-1287 and 1289-8376
    1289 1-1288 and 1290-8376
    1290 1-1289 and 1291-8376
    1291 1-1290 and 1292-8376
    1292 1-1291 and 1293-8376
    1293 1-1292 and 1294-8376
    1294 1-1293 and 1295-8376
    1295 1-1294 and 1296-8376
    1296 1-1295 and 1297-8376
    1297 1-1296 and 1298-8376
    1298 1-1297 and 1299-8376
    1299 1-1298 and 1300-8376
    1300 1-1299 and 1301-8376
    1301 1-1300 and 1302-8376
    1302 1-1301 and 1303-8376
    1303 1-1302 and 1304-8376
    1304 1-1303 and 1305-8376
    1305 1-1304 and 1306-8376
    1306 1-1305 and 1307-8376
    1307 1-1306 and 1308-8376
    1308 1-1307 and 1309-8376
    1309 1-1308 and 1310-8376
    1310 1-1309 and 1311-8376
    1311 1-1310 and 1312-8376
    1312 1-1311 and 1313-8376
    1313 1-1312 and 1314-8376
    1314 1-1313 and 1315-8376
    1315 1-1314 and 1316-8376
    1316 1-1315 and 1317-8376
    1317 1-1316 and 1318-8376
    1318 1-1317 and 1319-8376
    1319 1-1318 and 1320-8376
    1320 1-1319 and 1321-8376
    1321 1-1320 and 1322-8376
    1322 1-1321 and 1323-8376
    1323 1-1322 and 1324-8376
    1324 1-1323 and 1325-8376
    1325 1-1324 and 1326-8376
    1326 1-1325 and 1327-8376
    1327 1-1326 and 1328-8376
    1328 1-1327 and 1329-8376
    1329 1-1328 and 1330-8376
    1330 1-1329 and 1331-8376
    1331 1-1330 and 1332-8376
    1332 1-1331 and 1333-8376
    1333 1-1332 and 1334-8376
    1334 1-1333 and 1335-8376
    1335 1-1334 and 1336-8376
    1336 1-1335 and 1337-8376
    1337 1-1336 and 1338-8376
    1338 1-1337 and 1339-8376
    1339 1-1338 and 1340-8376
    1340 1-1339 and 1341-8376
    1341 1-1340 and 1342-8376
    1342 1-1341 and 1343-8376
    1343 1-1342 and 1344-8376
    1344 1-1343 and 1345-8376
    1345 1-1344 and 1346-8376
    1346 1-1345 and 1347-8376
    1347 1-1346 and 1348-8376
    1348 1-1347 and 1349-8376
    1349 1-1348 and 1350-8376
    1350 1-1349 and 1351-8376
    1351 1-1350 and 1352-8376
    1352 1-1351 and 1353-8376
    1353 1-1352 and 1354-8376
    1354 1-1353 and 1355-8376
    1355 1-1354 and 1356-8376
    1356 1-1355 and 1357-8376
    1357 1-1356 and 1358-8376
    1358 1-1357 and 1359-8376
    1359 1-1358 and 1360-8376
    1360 1-1359 and 1361-8376
    1361 1-1360 and 1362-8376
    1362 1-1361 and 1363-8376
    1363 1-1362 and 1364-8376
    1364 1-1363 and 1365-8376
    1365 1-1364 and 1366-8376
    1366 1-1365 and 1367-8376
    1367 1-1366 and 1368-8376
    1368 1-1367 and 1369-8376
    1369 1-1368 and 1370-8376
    1370 1-1369 and 1371-8376
    1371 1-1370 and 1372-8376
    1372 1-1371 and 1373-8376
    1373 1-1372 and 1374-8376
    1374 1-1373 and 1375-8376
    1375 1-1374 and 1376-8376
    1376 1-1375 and 1377-8376
    1377 1-1376 and 1378-8376
    1378 1-1377 and 1379-8376
    1379 1-1378 and 1380-8376
    1380 1-1379 and 1381-8376
    1381 1-1380 and 1382-8376
    1382 1-1381 and 1383-8376
    1383 1-1382 and 1384-8376
    1384 1-1383 and 1385-8376
    1385 1-1384 and 1386-8376
    1386 1-1385 and 1387-8376
    1387 1-1386 and 1388-8376
    1388 1-1387 and 1389-8376
    1389 1-1388 and 1390-8376
    1390 1-1389 and 1391-8376
    1391 1-1390 and 1392-8376
    1392 1-1391 and 1393-8376
    1393 1-1392 and 1394-8376
    1394 1-1393 and 1395-8376
    1395 1-1394 and 1396-8376
    1396 1-1395 and 1397-8376
    1397 1-1396 and 1398-8376
    1398 1-1397 and 1399-8376
    1399 1-1398 and 1400-8376
    1400 1-1399 and 1401-8376
    1401 1-1400 and 1402-8376
    1402 1-1401 and 1403-8376
    1403 1-1402 and 1404-8376
    1404 1-1403 and 1405-8376
    1405 1-1404 and 1406-8376
    1406 1-1405 and 1407-8376
    1407 1-1406 and 1408-8376
    1408 1-1407 and 1409-8376
    1409 1-1408 and 1410-8376
    1410 1-1409 and 1411-8376
    1411 1-1410 and 1412-8376
    1412 1-1411 and 1413-8376
    1413 1-1412 and 1414-8376
    1414 1-1413 and 1415-8376
    1415 1-1414 and 1416-8376
    1416 1-1415 and 1417-8376
    1417 1-1416 and 1418-8376
    1418 1-1417 and 1419-8376
    1419 1-1418 and 1420-8376
    1420 1-1419 and 1421-8376
    1421 1-1420 and 1422-8376
    1422 1-1421 and 1423-8376
    1423 1-1422 and 1424-8376
    1424 1-1423 and 1425-8376
    1425 1-1424 and 1426-8376
    1426 1-1425 and 1427-8376
    1427 1-1426 and 1428-8376
    1428 1-1427 and 1429-8376
    1429 1-1428 and 1430-8376
    1430 1-1429 and 1431-8376
    1431 1-1430 and 1432-8376
    1432 1-1431 and 1433-8376
    1433 1-1432 and 1434-8376
    1434 1-1433 and 1435-8376
    1435 1-1434 and 1436-8376
    1436 1-1435 and 1437-8376
    1437 1-1436 and 1438-8376
    1438 1-1437 and 1439-8376
    1439 1-1438 and 1440-8376
    1440 1-1439 and 1441-8376
    1441 1-1440 and 1442-8376
    1442 1-1441 and 1443-8376
    1443 1-1442 and 1444-8376
    1444 1-1443 and 1445-8376
    1445 1-1444 and 1446-8376
    1446 1-1445 and 1447-8376
    1447 1-1446 and 1448-8376
    1448 1-1447 and 1449-8376
    1449 1-1448 and 1450-8376
    1450 1-1449 and 1451-8376
    1451 1-1450 and 1452-8376
    1452 1-1451 and 1453-8376
    1453 1-1452 and 1454-8376
    1454 1-1453 and 1455-8376
    1455 1-1454 and 1456-8376
    1456 1-1455 and 1457-8376
    1457 1-1456 and 1458-8376
    1458 1-1457 and 1459-8376
    1459 1-1458 and 1460-8376
    1460 1-1459 and 1461-8376
    1461 1-1460 and 1462-8376
    1462 1-1461 and 1463-8376
    1463 1-1462 and 1464-8376
    1464 1-1463 and 1465-8376
    1465 1-1464 and 1466-8376
    1466 1-1465 and 1467-8376
    1467 1-1466 and 1468-8376
    1468 1-1467 and 1469-8376
    1469 1-1468 and 1470-8376
    1470 1-1469 and 1471-8376
    1471 1-1470 and 1472-8376
    1472 1-1471 and 1473-8376
    1473 1-1472 and 1474-8376
    1474 1-1473 and 1475-8376
    1475 1-1474 and 1476-8376
    1476 1-1475 and 1477-8376
    1477 1-1476 and 1478-8376
    1478 1-1477 and 1479-8376
    1479 1-1478 and 1480-8376
    1480 1-1479 and 1481-8376
    1481 1-1480 and 1482-8376
    1482 1-1481 and 1483-8376
    1483 1-1482 and 1484-8376
    1484 1-1483 and 1485-8376
    1485 1-1484 and 1486-8376
    1486 1-1485 and 1487-8376
    1487 1-1486 and 1488-8376
    1488 1-1487 and 1489-8376
    1489 1-1488 and 1490-8376
    1490 1-1489 and 1491-8376
    1491 1-1490 and 1492-8376
    1492 1-1491 and 1493-8376
    1493 1-1492 and 1494-8376
    1494 1-1493 and 1495-8376
    1495 1-1494 and 1496-8376
    1496 1-1495 and 1497-8376
    1497 1-1496 and 1498-8376
    1498 1-1497 and 1499-8376
    1499 1-1498 and 1500-8376
    1500 1-1499 and 1501-8376
    1501 1-1500 and 1502-8376
    1502 1-1501 and 1503-8376
    1503 1-1502 and 1504-8376
    1504 1-1503 and 1505-8376
    1505 1-1504 and 1506-8376
    1506 1-1505 and 1507-8376
    1507 1-1506 and 1508-8376
    1508 1-1507 and 1509-8376
    1509 1-1508 and 1510-8376
    1510 1-1509 and 1511-8376
    1511 1-1510 and 1512-8376
    1512 1-1511 and 1513-8376
    1513 1-1512 and 1514-8376
    1514 1-1513 and 1515-8376
    1515 1-1514 and 1516-8376
    1516 1-1515 and 1517-8376
    1517 1-1516 and 1518-8376
    1518 1-1517 and 1519-8376
    1519 1-1518 and 1520-8376
    1520 1-1519 and 1521-8376
    1521 1-1520 and 1522-8376
    1522 1-1521 and 1523-8376
    1523 1-1522 and 1524-8376
    1524 1-1523 and 1525-8376
    1525 1-1524 and 1526-8376
    1526 1-1525 and 1527-8376
    1527 1-1526 and 1528-8376
    1528 1-1527 and 1529-8376
    1529 1-1528 and 1530-8376
    1530 1-1529 and 1531-8376
    1531 1-1530 and 1532-8376
    1532 1-1531 and 1533-8376
    1533 1-1532 and 1534-8376
    1534 1-1533 and 1535-8376
    1535 1-1534 and 1536-8376
    1536 1-1535 and 1537-8376
    1537 1-1536 and 1538-8376
    1538 1-1537 and 1539-8376
    1539 1-1538 and 1540-8376
    1540 1-1539 and 1541-8376
    1541 1-1540 and 1542-8376
    1542 1-1541 and 1543-8376
    1543 1-1542 and 1544-8376
    1544 1-1543 and 1545-8376
    1545 1-1544 and 1546-8376
    1546 1-1545 and 1547-8376
    1547 1-1546 and 1548-8376
    1548 1-1547 and 1549-8376
    1549 1-1548 and 1550-8376
    1550 1-1549 and 1551-8376
    1551 1-1550 and 1552-8376
    1552 1-1551 and 1553-8376
    1553 1-1552 and 1554-8376
    1554 1-1553 and 1555-8376
    1555 1-1554 and 1556-8376
    1556 1-1555 and 1557-8376
    1557 1-1556 and 1558-8376
    1558 1-1557 and 1559-8376
    1559 1-1558 and 1560-8376
    1560 1-1559 and 1561-8376
    1561 1-1560 and 1562-8376
    1562 1-1561 and 1563-8376
    1563 1-1562 and 1564-8376
    1564 1-1563 and 1565-8376
    1565 1-1564 and 1566-8376
    1566 1-1565 and 1567-8376
    1567 1-1566 and 1568-8376
    1568 1-1567 and 1569-8376
    1569 1-1568 and 1570-8376
    1570 1-1569 and 1571-8376
    1571 1-1570 and 1572-8376
    1572 1-1571 and 1573-8376
    1573 1-1572 and 1574-8376
    1574 1-1573 and 1575-8376
    1575 1-1574 and 1576-8376
    1576 1-1575 and 1577-8376
    1577 1-1576 and 1578-8376
    1578 1-1577 and 1579-8376
    1579 1-1578 and 1580-8376
    1580 1-1579 and 1581-8376
    1581 1-1580 and 1582-8376
    1582 1-1581 and 1583-8376
    1583 1-1582 and 1584-8376
    1584 1-1583 and 1585-8376
    1585 1-1584 and 1586-8376
    1586 1-1585 and 1587-8376
    1587 1-1586 and 1588-8376
    1588 1-1587 and 1589-8376
    1589 1-1588 and 1590-8376
    1590 1-1589 and 1591-8376
    1591 1-1590 and 1592-8376
    1592 1-1591 and 1593-8376
    1593 1-1592 and 1594-8376
    1594 1-1593 and 1595-8376
    1595 1-1594 and 1596-8376
    1596 1-1595 and 1597-8376
    1597 1-1596 and 1598-8376
    1598 1-1597 and 1599-8376
    1599 1-1598 and 1600-8376
    1600 1-1599 and 1601-8376
    1601 1-1600 and 1602-8376
    1602 1-1601 and 1603-8376
    1603 1-1602 and 1604-8376
    1604 1-1603 and 1605-8376
    1605 1-1604 and 1606-8376
    1606 1-1605 and 1607-8376
    1607 1-1606 and 1608-8376
    1608 1-1607 and 1609-8376
    1609 1-1608 and 1610-8376
    1610 1-1609 and 1611-8376
    1611 1-1610 and 1612-8376
    1612 1-1611 and 1613-8376
    1613 1-1612 and 1614-8376
    1614 1-1613 and 1615-8376
    1615 1-1614 and 1616-8376
    1616 1-1615 and 1617-8376
    1617 1-1616 and 1618-8376
    1618 1-1617 and 1619-8376
    1619 1-1618 and 1620-8376
    1620 1-1619 and 1621-8376
    1621 1-1620 and 1622-8376
    1622 1-1621 and 1623-8376
    1623 1-1622 and 1624-8376
    1624 1-1623 and 1625-8376
    1625 1-1624 and 1626-8376
    1626 1-1625 and 1627-8376
    1627 1-1626 and 1628-8376
    1628 1-1627 and 1629-8376
    1629 1-1628 and 1630-8376
    1630 1-1629 and 1631-8376
    1631 1-1630 and 1632-8376
    1632 1-1631 and 1633-8376
    1633 1-1632 and 1634-8376
    1634 1-1633 and 1635-8376
    1635 1-1634 and 1636-8376
    1636 1-1635 and 1637-8376
    1637 1-1636 and 1638-8376
    1638 1-1637 and 1639-8376
    1639 1-1638 and 1640-8376
    1640 1-1639 and 1641-8376
    1641 1-1640 and 1642-8376
    1642 1-1641 and 1643-8376
    1643 1-1642 and 1644-8376
    1644 1-1643 and 1645-8376
    1645 1-1644 and 1646-8376
    1646 1-1645 and 1647-8376
    1647 1-1646 and 1648-8376
    1648 1-1647 and 1649-8376
    1649 1-1648 and 1650-8376
    1650 1-1649 and 1651-8376
    1651 1-1650 and 1652-8376
    1652 1-1651 and 1653-8376
    1653 1-1652 and 1654-8376
    1654 1-1653 and 1655-8376
    1655 1-1654 and 1656-8376
    1656 1-1655 and 1657-8376
    1657 1-1656 and 1658-8376
    1658 1-1657 and 1659-8376
    1659 1-1658 and 1660-8376
    1660 1-1659 and 1661-8376
    1661 1-1660 and 1662-8376
    1662 1-1661 and 1663-8376
    1663 1-1662 and 1664-8376
    1664 1-1663 and 1665-8376
    1665 1-1664 and 1666-8376
    1666 1-1665 and 1667-8376
    1667 1-1666 and 1668-8376
    1668 1-1667 and 1669-8376
    1669 1-1668 and 1670-8376
    1670 1-1669 and 1671-8376
    1671 1-1670 and 1672-8376
    1672 1-1671 and 1673-8376
    1673 1-1672 and 1674-8376
    1674 1-1673 and 1675-8376
    1675 1-1674 and 1676-8376
    1676 1-1675 and 1677-8376
    1677 1-1676 and 1678-8376
    1678 1-1677 and 1679-8376
    1679 1-1678 and 1680-8376
    1680 1-1679 and 1681-8376
    1681 1-1680 and 1682-8376
    1682 1-1681 and 1683-8376
    1683 1-1682 and 1684-8376
    1684 1-1683 and 1685-8376
    1685 1-1684 and 1686-8376
    1686 1-1685 and 1687-8376
    1687 1-1686 and 1688-8376
    1688 1-1687 and 1689-8376
    1689 1-1688 and 1690-8376
    1690 1-1689 and 1691-8376
    1691 1-1690 and 1692-8376
    1692 1-1691 and 1693-8376
    1693 1-1692 and 1694-8376
    1694 1-1693 and 1695-8376
    1695 1-1694 and 1696-8376
    1696 1-1695 and 1697-8376
    1697 1-1696 and 1698-8376
    1698 1-1697 and 1699-8376
    1699 1-1698 and 1700-8376
    1700 1-1699 and 1701-8376
    1701 1-1700 and 1702-8376
    1702 1-1701 and 1703-8376
    1703 1-1702 and 1704-8376
    1704 1-1703 and 1705-8376
    1705 1-1704 and 1706-8376
    1706 1-1705 and 1707-8376
    1707 1-1706 and 1708-8376
    1708 1-1707 and 1709-8376
    1709 1-1708 and 1710-8376
    1710 1-1709 and 1711-8376
    1711 1-1710 and 1712-8376
    1712 1-1711 and 1713-8376
    1713 1-1712 and 1714-8376
    1714 1-1713 and 1715-8376
    1715 1-1714 and 1716-8376
    1716 1-1715 and 1717-8376
    1717 1-1716 and 1718-8376
    1718 1-1717 and 1719-8376
    1719 1-1718 and 1720-8376
    1720 1-1719 and 1721-8376
    1721 1-1720 and 1722-8376
    1722 1-1721 and 1723-8376
    1723 1-1722 and 1724-8376
    1724 1-1723 and 1725-8376
    1725 1-1724 and 1726-8376
    1726 1-1725 and 1727-8376
    1727 1-1726 and 1728-8376
    1728 1-1727 and 1729-8376
    1729 1-1728 and 1730-8376
    1730 1-1729 and 1731-8376
    1731 1-1730 and 1732-8376
    1732 1-1731 and 1733-8376
    1733 1-1732 and 1734-8376
    1734 1-1733 and 1735-8376
    1735 1-1734 and 1736-8376
    1736 1-1735 and 1737-8376
    1737 1-1736 and 1738-8376
    1738 1-1737 and 1739-8376
    1739 1-1738 and 1740-8376
    1740 1-1739 and 1741-8376
    1741 1-1740 and 1742-8376
    1742 1-1741 and 1743-8376
    1743 1-1742 and 1744-8376
    1744 1-1743 and 1745-8376
    1745 1-1744 and 1746-8376
    1746 1-1745 and 1747-8376
    1747 1-1746 and 1748-8376
    1748 1-1747 and 1749-8376
    1749 1-1748 and 1750-8376
    1750 1-1749 and 1751-8376
    1751 1-1750 and 1752-8376
    1752 1-1751 and 1753-8376
    1753 1-1752 and 1754-8376
    1754 1-1753 and 1755-8376
    1755 1-1754 and 1756-8376
    1756 1-1755 and 1757-8376
    1757 1-1756 and 1758-8376
    1758 1-1757 and 1759-8376
    1759 1-1758 and 1760-8376
    1760 1-1759 and 1761-8376
    1761 1-1760 and 1762-8376
    1762 1-1761 and 1763-8376
    1763 1-1762 and 1764-8376
    1764 1-1763 and 1765-8376
    1765 1-1764 and 1766-8376
    1766 1-1765 and 1767-8376
    1767 1-1766 and 1768-8376
    1768 1-1767 and 1769-8376
    1769 1-1768 and 1770-8376
    1770 1-1769 and 1771-8376
    1771 1-1770 and 1772-8376
    1772 1-1771 and 1773-8376
    1773 1-1772 and 1774-8376
    1774 1-1773 and 1775-8376
    1775 1-1774 and 1776-8376
    1776 1-1775 and 1777-8376
    1777 1-1776 and 1778-8376
    1778 1-1777 and 1779-8376
    1779 1-1778 and 1780-8376
    1780 1-1779 and 1781-8376
    1781 1-1780 and 1782-8376
    1782 1-1781 and 1783-8376
    1783 1-1782 and 1784-8376
    1784 1-1783 and 1785-8376
    1785 1-1784 and 1786-8376
    1786 1-1785 and 1787-8376
    1787 1-1786 and 1788-8376
    1788 1-1787 and 1789-8376
    1789 1-1788 and 1790-8376
    1790 1-1789 and 1791-8376
    1791 1-1790 and 1792-8376
    1792 1-1791 and 1793-8376
    1793 1-1792 and 1794-8376
    1794 1-1793 and 1795-8376
    1795 1-1794 and 1796-8376
    1796 1-1795 and 1797-8376
    1797 1-1796 and 1798-8376
    1798 1-1797 and 1799-8376
    1799 1-1798 and 1800-8376
    1800 1-1799 and 1801-8376
    1801 1-1800 and 1802-8376
    1802 1-1801 and 1803-8376
    1803 1-1802 and 1804-8376
    1804 1-1803 and 1805-8376
    1805 1-1804 and 1806-8376
    1806 1-1805 and 1807-8376
    1807 1-1806 and 1808-8376
    1808 1-1807 and 1809-8376
    1809 1-1808 and 1810-8376
    1810 1-1809 and 1811-8376
    1811 1-1810 and 1812-8376
    1812 1-1811 and 1813-8376
    1813 1-1812 and 1814-8376
    1814 1-1813 and 1815-8376
    1815 1-1814 and 1816-8376
    1816 1-1815 and 1817-8376
    1817 1-1816 and 1818-8376
    1818 1-1817 and 1819-8376
    1819 1-1818 and 1820-8376
    1820 1-1819 and 1821-8376
    1821 1-1820 and 1822-8376
    1822 1-1821 and 1823-8376
    1823 1-1822 and 1824-8376
    1824 1-1823 and 1825-8376
    1825 1-1824 and 1826-8376
    1826 1-1825 and 1827-8376
    1827 1-1826 and 1828-8376
    1828 1-1827 and 1829-8376
    1829 1-1828 and 1830-8376
    1830 1-1829 and 1831-8376
    1831 1-1830 and 1832-8376
    1832 1-1831 and 1833-8376
    1833 1-1832 and 1834-8376
    1834 1-1833 and 1835-8376
    1835 1-1834 and 1836-8376
    1836 1-1835 and 1837-8376
    1837 1-1836 and 1838-8376
    1838 1-1837 and 1839-8376
    1839 1-1838 and 1840-8376
    1840 1-1839 and 1841-8376
    1841 1-1840 and 1842-8376
    1842 1-1841 and 1843-8376
    1843 1-1842 and 1844-8376
    1844 1-1843 and 1845-8376
    1845 1-1844 and 1846-8376
    1846 1-1845 and 1847-8376
    1847 1-1846 and 1848-8376
    1848 1-1847 and 1849-8376
    1849 1-1848 and 1850-8376
    1850 1-1849 and 1851-8376
    1851 1-1850 and 1852-8376
    1852 1-1851 and 1853-8376
    1853 1-1852 and 1854-8376
    1854 1-1853 and 1855-8376
    1855 1-1854 and 1856-8376
    1856 1-1855 and 1857-8376
    1857 1-1856 and 1858-8376
    1858 1-1857 and 1859-8376
    1859 1-1858 and 1860-8376
    1860 1-1859 and 1861-8376
    1861 1-1860 and 1862-8376
    1862 1-1861 and 1863-8376
    1863 1-1862 and 1864-8376
    1864 1-1863 and 1865-8376
    1865 1-1864 and 1866-8376
    1866 1-1865 and 1867-8376
    1867 1-1866 and 1868-8376
    1868 1-1867 and 1869-8376
    1869 1-1868 and 1870-8376
    1870 1-1869 and 1871-8376
    1871 1-1870 and 1872-8376
    1872 1-1871 and 1873-8376
    1873 1-1872 and 1874-8376
    1874 1-1873 and 1875-8376
    1875 1-1874 and 1876-8376
    1876 1-1875 and 1877-8376
    1877 1-1876 and 1878-8376
    1878 1-1877 and 1879-8376
    1879 1-1878 and 1880-8376
    1880 1-1879 and 1881-8376
    1881 1-1880 and 1882-8376
    1882 1-1881 and 1883-8376
    1883 1-1882 and 1884-8376
    1884 1-1883 and 1885-8376
    1885 1-1884 and 1886-8376
    1886 1-1885 and 1887-8376
    1887 1-1886 and 1888-8376
    1888 1-1887 and 1889-8376
    1889 1-1888 and 1890-8376
    1890 1-1889 and 1891-8376
    1891 1-1890 and 1892-8376
    1892 1-1891 and 1893-8376
    1893 1-1892 and 1894-8376
    1894 1-1893 and 1895-8376
    1895 1-1894 and 1896-8376
    1896 1-1895 and 1897-8376
    1897 1-1896 and 1898-8376
    1898 1-1897 and 1899-8376
    1899 1-1898 and 1900-8376
    1900 1-1899 and 1901-8376
    1901 1-1900 and 1902-8376
    1902 1-1901 and 1903-8376
    1903 1-1902 and 1904-8376
    1904 1-1903 and 1905-8376
    1905 1-1904 and 1906-8376
    1906 1-1905 and 1907-8376
    1907 1-1906 and 1908-8376
    1908 1-1907 and 1909-8376
    1909 1-1908 and 1910-8376
    1910 1-1909 and 1911-8376
    1911 1-1910 and 1912-8376
    1912 1-1911 and 1913-8376
    1913 1-1912 and 1914-8376
    1914 1-1913 and 1915-8376
    1915 1-1914 and 1916-8376
    1916 1-1915 and 1917-8376
    1917 1-1916 and 1918-8376
    1918 1-1917 and 1919-8376
    1919 1-1918 and 1920-8376
    1920 1-1919 and 1921-8376
    1921 1-1920 and 1922-8376
    1922 1-1921 and 1923-8376
    1923 1-1922 and 1924-8376
    1924 1-1923 and 1925-8376
    1925 1-1924 and 1926-8376
    1926 1-1925 and 1927-8376
    1927 1-1926 and 1928-8376
    1928 1-1927 and 1929-8376
    1929 1-1928 and 1930-8376
    1930 1-1929 and 1931-8376
    1931 1-1930 and 1932-8376
    1932 1-1931 and 1933-8376
    1933 1-1932 and 1934-8376
    1934 1-1933 and 1935-8376
    1935 1-1934 and 1936-8376
    1936 1-1935 and 1937-8376
    1937 1-1936 and 1938-8376
    1938 1-1937 and 1939-8376
    1939 1-1938 and 1940-8376
    1940 1-1939 and 1941-8376
    1941 1-1940 and 1942-8376
    1942 1-1941 and 1943-8376
    1943 1-1942 and 1944-8376
    1944 1-1943 and 1945-8376
    1945 1-1944 and 1946-8376
    1946 1-1945 and 1947-8376
    1947 1-1946 and 1948-8376
    1948 1-1947 and 1949-8376
    1949 1-1948 and 1950-8376
    1950 1-1949 and 1951-8376
    1951 1-1950 and 1952-8376
    1952 1-1951 and 1953-8376
    1953 1-1952 and 1954-8376
    1954 1-1953 and 1955-8376
    1955 1-1954 and 1956-8376
    1956 1-1955 and 1957-8376
    1957 1-1956 and 1958-8376
    1958 1-1957 and 1959-8376
    1959 1-1958 and 1960-8376
    1960 1-1959 and 1961-8376
    1961 1-1960 and 1962-8376
    1962 1-1961 and 1963-8376
    1963 1-1962 and 1964-8376
    1964 1-1963 and 1965-8376
    1965 1-1964 and 1966-8376
    1966 1-1965 and 1967-8376
    1967 1-1966 and 1968-8376
    1968 1-1967 and 1969-8376
    1969 1-1968 and 1970-8376
    1970 1-1969 and 1971-8376
    1971 1-1970 and 1972-8376
    1972 1-1971 and 1973-8376
    1973 1-1972 and 1974-8376
    1974 1-1973 and 1975-8376
    1975 1-1974 and 1976-8376
    1976 1-1975 and 1977-8376
    1977 1-1976 and 1978-8376
    1978 1-1977 and 1979-8376
    1979 1-1978 and 1980-8376
    1980 1-1979 and 1981-8376
    1981 1-1980 and 1982-8376
    1982 1-1981 and 1983-8376
    1983 1-1982 and 1984-8376
    1984 1-1983 and 1985-8376
    1985 1-1984 and 1986-8376
    1986 1-1985 and 1987-8376
    1987 1-1986 and 1988-8376
    1988 1-1987 and 1989-8376
    1989 1-1988 and 1990-8376
    1990 1-1989 and 1991-8376
    1991 1-1990 and 1992-8376
    1992 1-1991 and 1993-8376
    1993 1-1992 and 1994-8376
    1994 1-1993 and 1995-8376
    1995 1-1994 and 1996-8376
    1996 1-1995 and 1997-8376
    1997 1-1996 and 1998-8376
    1998 1-1997 and 1999-8376
    1999 1-1998 and 2000-8376
    2000 1-1999 and 2001-8376
    2001 1-2000 and 2002-8376
    2002 1-2001 and 2003-8376
    2003 1-2002 and 2004-8376
    2004 1-2003 and 2005-8376
    2005 1-2004 and 2006-8376
    2006 1-2005 and 2007-8376
    2007 1-2006 and 2008-8376
    2008 1-2007 and 2009-8376
    2009 1-2008 and 2010-8376
    2010 1-2009 and 2011-8376
    2011 1-2010 and 2012-8376
    2012 1-2011 and 2013-8376
    2013 1-2012 and 2014-8376
    2014 1-2013 and 2015-8376
    2015 1-2014 and 2016-8376
    2016 1-2015 and 2017-8376
    2017 1-2016 and 2018-8376
    2018 1-2017 and 2019-8376
    2019 1-2018 and 2020-8376
    2020 1-2019 and 2021-8376
    2021 1-2020 and 2022-8376
    2022 1-2021 and 2023-8376
    2023 1-2022 and 2024-8376
    2024 1-2023 and 2025-8376
    2025 1-2024 and 2026-8376
    2026 1-2025 and 2027-8376
    2027 1-2026 and 2028-8376
    2028 1-2027 and 2029-8376
    2029 1-2028 and 2030-8376
    2030 1-2029 and 2031-8376
    2031 1-2030 and 2032-8376
    2032 1-2031 and 2033-8376
    2033 1-2032 and 2034-8376
    2034 1-2033 and 2035-8376
    2035 1-2034 and 2036-8376
    2036 1-2035 and 2037-8376
    2037 1-2036 and 2038-8376
    2038 1-2037 and 2039-8376
    2039 1-2038 and 2040-8376
    2040 1-2039 and 2041-8376
    2041 1-2040 and 2042-8376
    2042 1-2041 and 2043-8376
    2043 1-2042 and 2044-8376
    2044 1-2043 and 2045-8376
    2045 1-2044 and 2046-8376
    2046 1-2045 and 2047-8376
    2047 1-2046 and 2048-8376
    2048 1-2047 and 2049-8376
    2049 1-2048 and 2050-8376
    2050 1-2049 and 2051-8376
    2051 1-2050 and 2052-8376
    2052 1-2051 and 2053-8376
    2053 1-2052 and 2054-8376
    2054 1-2053 and 2055-8376
    2055 1-2054 and 2056-8376
    2056 1-2055 and 2057-8376
    2057 1-2056 and 2058-8376
    2058 1-2057 and 2059-8376
    2059 1-2058 and 2060-8376
    2060 1-2059 and 2061-8376
    2061 1-2060 and 2062-8376
    2062 1-2061 and 2063-8376
    2063 1-2062 and 2064-8376
    2064 1-2063 and 2065-8376
    2065 1-2064 and 2066-8376
    2066 1-2065 and 2067-8376
    2067 1-2066 and 2068-8376
    2068 1-2067 and 2069-8376
    2069 1-2068 and 2070-8376
    2070 1-2069 and 2071-8376
    2071 1-2070 and 2072-8376
    2072 1-2071 and 2073-8376
    2073 1-2072 and 2074-8376
    2074 1-2073 and 2075-8376
    2075 1-2074 and 2076-8376
    2076 1-2075 and 2077-8376
    2077 1-2076 and 2078-8376
    2078 1-2077 and 2079-8376
    2079 1-2078 and 2080-8376
    2080 1-2079 and 2081-8376
    2081 1-2080 and 2082-8376
    2082 1-2081 and 2083-8376
    2083 1-2082 and 2084-8376
    2084 1-2083 and 2085-8376
    2085 1-2084 and 2086-8376
    2086 1-2085 and 2087-8376
    2087 1-2086 and 2088-8376
    2088 1-2087 and 2089-8376
    2089 1-2088 and 2090-8376
    2090 1-2089 and 2091-8376
    2091 1-2090 and 2092-8376
    2092 1-2091 and 2093-8376
    2093 1-2092 and 2094-8376
    2094 1-2093 and 2095-8376
    2095 1-2094 and 2096-8376
    2096 1-2095 and 2097-8376
    2097 1-2096 and 2098-8376
    2098 1-2097 and 2099-8376
    2099 1-2098 and 2100-8376
    2100 1-2099 and 2101-8376
    2101 1-2100 and 2102-8376
    2102 1-2101 and 2103-8376
    2103 1-2102 and 2104-8376
    2104 1-2103 and 2105-8376
    2105 1-2104 and 2106-8376
    2106 1-2105 and 2107-8376
    2107 1-2106 and 2108-8376
    2108 1-2107 and 2109-8376
    2109 1-2108 and 2110-8376
    2110 1-2109 and 2111-8376
    2111 1-2110 and 2112-8376
    2112 1-2111 and 2113-8376
    2113 1-2112 and 2114-8376
    2114 1-2113 and 2115-8376
    2115 1-2114 and 2116-8376
    2116 1-2115 and 2117-8376
    2117 1-2116 and 2118-8376
    2118 1-2117 and 2119-8376
    2119 1-2118 and 2120-8376
    2120 1-2119 and 2121-8376
    2121 1-2120 and 2122-8376
    2122 1-2121 and 2123-8376
    2123 1-2122 and 2124-8376
    2124 1-2123 and 2125-8376
    2125 1-2124 and 2126-8376
    2126 1-2125 and 2127-8376
    2127 1-2126 and 2128-8376
    2128 1-2127 and 2129-8376
    2129 1-2128 and 2130-8376
    2130 1-2129 and 2131-8376
    2131 1-2130 and 2132-8376
    2132 1-2131 and 2133-8376
    2133 1-2132 and 2134-8376
    2134 1-2133 and 2135-8376
    2135 1-2134 and 2136-8376
    2136 1-2135 and 2137-8376
    2137 1-2136 and 2138-8376
    2138 1-2137 and 2139-8376
    2139 1-2138 and 2140-8376
    2140 1-2139 and 2141-8376
    2141 1-2140 and 2142-8376
    2142 1-2141 and 2143-8376
    2143 1-2142 and 2144-8376
    2144 1-2143 and 2145-8376
    2145 1-2144 and 2146-8376
    2146 1-2145 and 2147-8376
    2147 1-2146 and 2148-8376
    2148 1-2147 and 2149-8376
    2149 1-2148 and 2150-8376
    2150 1-2149 and 2151-8376
    2151 1-2150 and 2152-8376
    2152 1-2151 and 2153-8376
    2153 1-2152 and 2154-8376
    2154 1-2153 and 2155-8376
    2155 1-2154 and 2156-8376
    2156 1-2155 and 2157-8376
    2157 1-2156 and 2158-8376
    2158 1-2157 and 2159-8376
    2159 1-2158 and 2160-8376
    2160 1-2159 and 2161-8376
    2161 1-2160 and 2162-8376
    2162 1-2161 and 2163-8376
    2163 1-2162 and 2164-8376
    2164 1-2163 and 2165-8376
    2165 1-2164 and 2166-8376
    2166 1-2165 and 2167-8376
    2167 1-2166 and 2168-8376
    2168 1-2167 and 2169-8376
    2169 1-2168 and 2170-8376
    2170 1-2169 and 2171-8376
    2171 1-2170 and 2172-8376
    2172 1-2171 and 2173-8376
    2173 1-2172 and 2174-8376
    2174 1-2173 and 2175-8376
    2175 1-2174 and 2176-8376
    2176 1-2175 and 2177-8376
    2177 1-2176 and 2178-8376
    2178 1-2177 and 2179-8376
    2179 1-2178 and 2180-8376
    2180 1-2179 and 2181-8376
    2181 1-2180 and 2182-8376
    2182 1-2181 and 2183-8376
    2183 1-2182 and 2184-8376
    2184 1-2183 and 2185-8376
    2185 1-2184 and 2186-8376
    2186 1-2185 and 2187-8376
    2187 1-2186 and 2188-8376
    2188 1-2187 and 2189-8376
    2189 1-2188 and 2190-8376
    2190 1-2189 and 2191-8376
    2191 1-2190 and 2192-8376
    2192 1-2191 and 2193-8376
    2193 1-2192 and 2194-8376
    2194 1-2193 and 2195-8376
    2195 1-2194 and 2196-8376
    2196 1-2195 and 2197-8376
    2197 1-2196 and 2198-8376
    2198 1-2197 and 2199-8376
    2199 1-2198 and 2200-8376
    2200 1-2199 and 2201-8376
    2201 1-2200 and 2202-8376
    2202 1-2201 and 2203-8376
    2203 1-2202 and 2204-8376
    2204 1-2203 and 2205-8376
    2205 1-2204 and 2206-8376
    2206 1-2205 and 2207-8376
    2207 1-2206 and 2208-8376
    2208 1-2207 and 2209-8376
    2209 1-2208 and 2210-8376
    2210 1-2209 and 2211-8376
    2211 1-2210 and 2212-8376
    2212 1-2211 and 2213-8376
    2213 1-2212 and 2214-8376
    2214 1-2213 and 2215-8376
    2215 1-2214 and 2216-8376
    2216 1-2215 and 2217-8376
    2217 1-2216 and 2218-8376
    2218 1-2217 and 2219-8376
    2219 1-2218 and 2220-8376
    2220 1-2219 and 2221-8376
    2221 1-2220 and 2222-8376
    2222 1-2221 and 2223-8376
    2223 1-2222 and 2224-8376
    2224 1-2223 and 2225-8376
    2225 1-2224 and 2226-8376
    2226 1-2225 and 2227-8376
    2227 1-2226 and 2228-8376
    2228 1-2227 and 2229-8376
    2229 1-2228 and 2230-8376
    2230 1-2229 and 2231-8376
    2231 1-2230 and 2232-8376
    2232 1-2231 and 2233-8376
    2233 1-2232 and 2234-8376
    2234 1-2233 and 2235-8376
    2235 1-2234 and 2236-8376
    2236 1-2235 and 2237-8376
    2237 1-2236 and 2238-8376
    2238 1-2237 and 2239-8376
    2239 1-2238 and 2240-8376
    2240 1-2239 and 2241-8376
    2241 1-2240 and 2242-8376
    2242 1-2241 and 2243-8376
    2243 1-2242 and 2244-8376
    2244 1-2243 and 2245-8376
    2245 1-2244 and 2246-8376
    2246 1-2245 and 2247-8376
    2247 1-2246 and 2248-8376
    2248 1-2247 and 2249-8376
    2249 1-2248 and 2250-8376
    2250 1-2249 and 2251-8376
    2251 1-2250 and 2252-8376
    2252 1-2251 and 2253-8376
    2253 1-2252 and 2254-8376
    2254 1-2253 and 2255-8376
    2255 1-2254 and 2256-8376
    2256 1-2255 and 2257-8376
    2257 1-2256 and 2258-8376
    2258 1-2257 and 2259-8376
    2259 1-2258 and 2260-8376
    2260 1-2259 and 2261-8376
    2261 1-2260 and 2262-8376
    2262 1-2261 and 2263-8376
    2263 1-2262 and 2264-8376
    2264 1-2263 and 2265-8376
    2265 1-2264 and 2266-8376
    2266 1-2265 and 2267-8376
    2267 1-2266 and 2268-8376
    2268 1-2267 and 2269-8376
    2269 1-2268 and 2270-8376
    2270 1-2269 and 2271-8376
    2271 1-2270 and 2272-8376
    2272 1-2271 and 2273-8376
    2273 1-2272 and 2274-8376
    2274 1-2273 and 2275-8376
    2275 1-2274 and 2276-8376
    2276 1-2275 and 2277-8376
    2277 1-2276 and 2278-8376
    2278 1-2277 and 2279-8376
    2279 1-2278 and 2280-8376
    2280 1-2279 and 2281-8376
    2281 1-2280 and 2282-8376
    2282 1-2281 and 2283-8376
    2283 1-2282 and 2284-8376
    2284 1-2283 and 2285-8376
    2285 1-2284 and 2286-8376
    2286 1-2285 and 2287-8376
    2287 1-2286 and 2288-8376
    2288 1-2287 and 2289-8376
    2289 1-2288 and 2290-8376
    2290 1-2289 and 2291-8376
    2291 1-2290 and 2292-8376
    2292 1-2291 and 2293-8376
    2293 1-2292 and 2294-8376
    2294 1-2293 and 2295-8376
    2295 1-2294 and 2296-8376
    2296 1-2295 and 2297-8376
    2297 1-2296 and 2298-8376
    2298 1-2297 and 2299-8376
    2299 1-2298 and 2300-8376
    2300 1-2299 and 2301-8376
    2301 1-2300 and 2302-8376
    2302 1-2301 and 2303-8376
    2303 1-2302 and 2304-8376
    2304 1-2303 and 2305-8376
    2305 1-2304 and 2306-8376
    2306 1-2305 and 2307-8376
    2307 1-2306 and 2308-8376
    2308 1-2307 and 2309-8376
    2309 1-2308 and 2310-8376
    2310 1-2309 and 2311-8376
    2311 1-2310 and 2312-8376
    2312 1-2311 and 2313-8376
    2313 1-2312 and 2314-8376
    2314 1-2313 and 2315-8376
    2315 1-2314 and 2316-8376
    2316 1-2315 and 2317-8376
    2317 1-2316 and 2318-8376
    2318 1-2317 and 2319-8376
    2319 1-2318 and 2320-8376
    2320 1-2319 and 2321-8376
    2321 1-2320 and 2322-8376
    2322 1-2321 and 2323-8376
    2323 1-2322 and 2324-8376
    2324 1-2323 and 2325-8376
    2325 1-2324 and 2326-8376
    2326 1-2325 and 2327-8376
    2327 1-2326 and 2328-8376
    2328 1-2327 and 2329-8376
    2329 1-2328 and 2330-8376
    2330 1-2329 and 2331-8376
    2331 1-2330 and 2332-8376
    2332 1-2331 and 2333-8376
    2333 1-2332 and 2334-8376
    2334 1-2333 and 2335-8376
    2335 1-2334 and 2336-8376
    2336 1-2335 and 2337-8376
    2337 1-2336 and 2338-8376
    2338 1-2337 and 2339-8376
    2339 1-2338 and 2340-8376
    2340 1-2339 and 2341-8376
    2341 1-2340 and 2342-8376
    2342 1-2341 and 2343-8376
    2343 1-2342 and 2344-8376
    2344 1-2343 and 2345-8376
    2345 1-2344 and 2346-8376
    2346 1-2345 and 2347-8376
    2347 1-2346 and 2348-8376
    2348 1-2347 and 2349-8376
    2349 1-2348 and 2350-8376
    2350 1-2349 and 2351-8376
    2351 1-2350 and 2352-8376
    2352 1-2351 and 2353-8376
    2353 1-2352 and 2354-8376
    2354 1-2353 and 2355-8376
    2355 1-2354 and 2356-8376
    2356 1-2355 and 2357-8376
    2357 1-2356 and 2358-8376
    2358 1-2357 and 2359-8376
    2359 1-2358 and 2360-8376
    2360 1-2359 and 2361-8376
    2361 1-2360 and 2362-8376
    2362 1-2361 and 2363-8376
    2363 1-2362 and 2364-8376
    2364 1-2363 and 2365-8376
    2365 1-2364 and 2366-8376
    2366 1-2365 and 2367-8376
    2367 1-2366 and 2368-8376
    2368 1-2367 and 2369-8376
    2369 1-2368 and 2370-8376
    2370 1-2369 and 2371-8376
    2371 1-2370 and 2372-8376
    2372 1-2371 and 2373-8376
    2373 1-2372 and 2374-8376
    2374 1-2373 and 2375-8376
    2375 1-2374 and 2376-8376
    2376 1-2375 and 2377-8376
    2377 1-2376 and 2378-8376
    2378 1-2377 and 2379-8376
    2379 1-2378 and 2380-8376
    2380 1-2379 and 2381-8376
    2381 1-2380 and 2382-8376
    2382 1-2381 and 2383-8376
    2383 1-2382 and 2384-8376
    2384 1-2383 and 2385-8376
    2385 1-2384 and 2386-8376
    2386 1-2385 and 2387-8376
    2387 1-2386 and 2388-8376
    2388 1-2387 and 2389-8376
    2389 1-2388 and 2390-8376
    2390 1-2389 and 2391-8376
    2391 1-2390 and 2392-8376
    2392 1-2391 and 2393-8376
    2393 1-2392 and 2394-8376
    2394 1-2393 and 2395-8376
    2395 1-2394 and 2396-8376
    2396 1-2395 and 2397-8376
    2397 1-2396 and 2398-8376
    2398 1-2397 and 2399-8376
    2399 1-2398 and 2400-8376
    2400 1-2399 and 2401-8376
    2401 1-2400 and 2402-8376
    2402 1-2401 and 2403-8376
    2403 1-2402 and 2404-8376
    2404 1-2403 and 2405-8376
    2405 1-2404 and 2406-8376
    2406 1-2405 and 2407-8376
    2407 1-2406 and 2408-8376
    2408 1-2407 and 2409-8376
    2409 1-2408 and 2410-8376
    2410 1-2409 and 2411-8376
    2411 1-2410 and 2412-8376
    2412 1-2411 and 2413-8376
    2413 1-2412 and 2414-8376
    2414 1-2413 and 2415-8376
    2415 1-2414 and 2416-8376
    2416 1-2415 and 2417-8376
    2417 1-2416 and 2418-8376
    2418 1-2417 and 2419-8376
    2419 1-2418 and 2420-8376
    2420 1-2419 and 2421-8376
    2421 1-2420 and 2422-8376
    2422 1-2421 and 2423-8376
    2423 1-2422 and 2424-8376
    2424 1-2423 and 2425-8376
    2425 1-2424 and 2426-8376
    2426 1-2425 and 2427-8376
    2427 1-2426 and 2428-8376
    2428 1-2427 and 2429-8376
    2429 1-2428 and 2430-8376
    2430 1-2429 and 2431-8376
    2431 1-2430 and 2432-8376
    2432 1-2431 and 2433-8376
    2433 1-2432 and 2434-8376
    2434 1-2433 and 2435-8376
    2435 1-2434 and 2436-8376
    2436 1-2435 and 2437-8376
    2437 1-2436 and 2438-8376
    2438 1-2437 and 2439-8376
    2439 1-2438 and 2440-8376
    2440 1-2439 and 2441-8376
    2441 1-2440 and 2442-8376
    2442 1-2441 and 2443-8376
    2443 1-2442 and 2444-8376
    2444 1-2443 and 2445-8376
    2445 1-2444 and 2446-8376
    2446 1-2445 and 2447-8376
    2447 1-2446 and 2448-8376
    2448 1-2447 and 2449-8376
    2449 1-2448 and 2450-8376
    2450 1-2449 and 2451-8376
    2451 1-2450 and 2452-8376
    2452 1-2451 and 2453-8376
    2453 1-2452 and 2454-8376
    2454 1-2453 and 2455-8376
    2455 1-2454 and 2456-8376
    2456 1-2455 and 2457-8376
    2457 1-2456 and 2458-8376
    2458 1-2457 and 2459-8376
    2459 1-2458 and 2460-8376
    2460 1-2459 and 2461-8376
    2461 1-2460 and 2462-8376
    2462 1-2461 and 2463-8376
    2463 1-2462 and 2464-8376
    2464 1-2463 and 2465-8376
    2465 1-2464 and 2466-8376
    2466 1-2465 and 2467-8376
    2467 1-2466 and 2468-8376
    2468 1-2467 and 2469-8376
    2469 1-2468 and 2470-8376
    2470 1-2469 and 2471-8376
    2471 1-2470 and 2472-8376
    2472 1-2471 and 2473-8376
    2473 1-2472 and 2474-8376
    2474 1-2473 and 2475-8376
    2475 1-2474 and 2476-8376
    2476 1-2475 and 2477-8376
    2477 1-2476 and 2478-8376
    2478 1-2477 and 2479-8376
    2479 1-2478 and 2480-8376
    2480 1-2479 and 2481-8376
    2481 1-2480 and 2482-8376
    2482 1-2481 and 2483-8376
    2483 1-2482 and 2484-8376
    2484 1-2483 and 2485-8376
    2485 1-2484 and 2486-8376
    2486 1-2485 and 2487-8376
    2487 1-2486 and 2488-8376
    2488 1-2487 and 2489-8376
    2489 1-2488 and 2490-8376
    2490 1-2489 and 2491-8376
    2491 1-2490 and 2492-8376
    2492 1-2491 and 2493-8376
    2493 1-2492 and 2494-8376
    2494 1-2493 and 2495-8376
    2495 1-2494 and 2496-8376
    2496 1-2495 and 2497-8376
    2497 1-2496 and 2498-8376
    2498 1-2497 and 2499-8376
    2499 1-2498 and 2500-8376
    2500 1-2499 and 2501-8376
    2501 1-2500 and 2502-8376
    2502 1-2501 and 2503-8376
    2503 1-2502 and 2504-8376
    2504 1-2503 and 2505-8376
    2505 1-2504 and 2506-8376
    2506 1-2505 and 2507-8376
    2507 1-2506 and 2508-8376
    2508 1-2507 and 2509-8376
    2509 1-2508 and 2510-8376
    2510 1-2509 and 2511-8376
    2511 1-2510 and 2512-8376
    2512 1-2511 and 2513-8376
    2513 1-2512 and 2514-8376
    2514 1-2513 and 2515-8376
    2515 1-2514 and 2516-8376
    2516 1-2515 and 2517-8376
    2517 1-2516 and 2518-8376
    2518 1-2517 and 2519-8376
    2519 1-2518 and 2520-8376
    2520 1-2519 and 2521-8376
    2521 1-2520 and 2522-8376
    2522 1-2521 and 2523-8376
    2523 1-2522 and 2524-8376
    2524 1-2523 and 2525-8376
    2525 1-2524 and 2526-8376
    2526 1-2525 and 2527-8376
    2527 1-2526 and 2528-8376
    2528 1-2527 and 2529-8376
    2529 1-2528 and 2530-8376
    2530 1-2529 and 2531-8376
    2531 1-2530 and 2532-8376
    2532 1-2531 and 2533-8376
    2533 1-2532 and 2534-8376
    2534 1-2533 and 2535-8376
    2535 1-2534 and 2536-8376
    2536 1-2535 and 2537-8376
    2537 1-2536 and 2538-8376
    2538 1-2537 and 2539-8376
    2539 1-2538 and 2540-8376
    2540 1-2539 and 2541-8376
    2541 1-2540 and 2542-8376
    2542 1-2541 and 2543-8376
    2543 1-2542 and 2544-8376
    2544 1-2543 and 2545-8376
    2545 1-2544 and 2546-8376
    2546 1-2545 and 2547-8376
    2547 1-2546 and 2548-8376
    2548 1-2547 and 2549-8376
    2549 1-2548 and 2550-8376
    2550 1-2549 and 2551-8376
    2551 1-2550 and 2552-8376
    2552 1-2551 and 2553-8376
    2553 1-2552 and 2554-8376
    2554 1-2553 and 2555-8376
    2555 1-2554 and 2556-8376
    2556 1-2555 and 2557-8376
    2557 1-2556 and 2558-8376
    2558 1-2557 and 2559-8376
    2559 1-2558 and 2560-8376
    2560 1-2559 and 2561-8376
    2561 1-2560 and 2562-8376
    2562 1-2561 and 2563-8376
    2563 1-2562 and 2564-8376
    2564 1-2563 and 2565-8376
    2565 1-2564 and 2566-8376
    2566 1-2565 and 2567-8376
    2567 1-2566 and 2568-8376
    2568 1-2567 and 2569-8376
    2569 1-2568 and 2570-8376
    2570 1-2569 and 2571-8376
    2571 1-2570 and 2572-8376
    2572 1-2571 and 2573-8376
    2573 1-2572 and 2574-8376
    2574 1-2573 and 2575-8376
    2575 1-2574 and 2576-8376
    2576 1-2575 and 2577-8376
    2577 1-2576 and 2578-8376
    2578 1-2577 and 2579-8376
    2579 1-2578 and 2580-8376
    2580 1-2579 and 2581-8376
    2581 1-2580 and 2582-8376
    2582 1-2581 and 2583-8376
    2583 1-2582 and 2584-8376
    2584 1-2583 and 2585-8376
    2585 1-2584 and 2586-8376
    2586 1-2585 and 2587-8376
    2587 1-2586 and 2588-8376
    2588 1-2587 and 2589-8376
    2589 1-2588 and 2590-8376
    2590 1-2589 and 2591-8376
    2591 1-2590 and 2592-8376
    2592 1-2591 and 2593-8376
    2593 1-2592 and 2594-8376
    2594 1-2593 and 2595-8376
    2595 1-2594 and 2596-8376
    2596 1-2595 and 2597-8376
    2597 1-2596 and 2598-8376
    2598 1-2597 and 2599-8376
    2599 1-2598 and 2600-8376
    2600 1-2599 and 2601-8376
    2601 1-2600 and 2602-8376
    2602 1-2601 and 2603-8376
    2603 1-2602 and 2604-8376
    2604 1-2603 and 2605-8376
    2605 1-2604 and 2606-8376
    2606 1-2605 and 2607-8376
    2607 1-2606 and 2608-8376
    2608 1-2607 and 2609-8376
    2609 1-2608 and 2610-8376
    2610 1-2609 and 2611-8376
    2611 1-2610 and 2612-8376
    2612 1-2611 and 2613-8376
    2613 1-2612 and 2614-8376
    2614 1-2613 and 2615-8376
    2615 1-2614 and 2616-8376
    2616 1-2615 and 2617-8376
    2617 1-2616 and 2618-8376
    2618 1-2617 and 2619-8376
    2619 1-2618 and 2620-8376
    2620 1-2619 and 2621-8376
    2621 1-2620 and 2622-8376
    2622 1-2621 and 2623-8376
    2623 1-2622 and 2624-8376
    2624 1-2623 and 2625-8376
    2625 1-2624 and 2626-8376
    2626 1-2625 and 2627-8376
    2627 1-2626 and 2628-8376
    2628 1-2627 and 2629-8376
    2629 1-2628 and 2630-8376
    2630 1-2629 and 2631-8376
    2631 1-2630 and 2632-8376
    2632 1-2631 and 2633-8376
    2633 1-2632 and 2634-8376
    2634 1-2633 and 2635-8376
    2635 1-2634 and 2636-8376
    2636 1-2635 and 2637-8376
    2637 1-2636 and 2638-8376
    2638 1-2637 and 2639-8376
    2639 1-2638 and 2640-8376
    2640 1-2639 and 2641-8376
    2641 1-2640 and 2642-8376
    2642 1-2641 and 2643-8376
    2643 1-2642 and 2644-8376
    2644 1-2643 and 2645-8376
    2645 1-2644 and 2646-8376
    2646 1-2645 and 2647-8376
    2647 1-2646 and 2648-8376
    2648 1-2647 and 2649-8376
    2649 1-2648 and 2650-8376
    2650 1-2649 and 2651-8376
    2651 1-2650 and 2652-8376
    2652 1-2651 and 2653-8376
    2653 1-2652 and 2654-8376
    2654 1-2653 and 2655-8376
    2655 1-2654 and 2656-8376
    2656 1-2655 and 2657-8376
    2657 1-2656 and 2658-8376
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    2911 1-2910 and 2912-8376
    2912 1-2911 and 2913-8376
    2913 1-2912 and 2914-8376
    2914 1-2913 and 2915-8376
    2915 1-2914 and 2916-8376
    2916 1-2915 and 2917-8376
    2917 1-2916 and 2918-8376
    2918 1-2917 and 2919-8376
    2919 1-2918 and 2920-8376
    2920 1-2919 and 2921-8376
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    2922 1-2921 and 2923-8376
    2923 1-2922 and 2924-8376
    2924 1-2923 and 2925-8376
    2925 1-2924 and 2926-8376
    2926 1-2925 and 2927-8376
    2927 1-2926 and 2928-8376
    2928 1-2927 and 2929-8376
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    2932 1-2931 and 2933-8376
    2933 1-2932 and 2934-8376
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    2935 1-2934 and 2936-8376
    2936 1-2935 and 2937-8376
    2937 1-2936 and 2938-8376
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    2939 1-2938 and 2940-8376
    2940 1-2939 and 2941-8376
    2941 1-2940 and 2942-8376
    2942 1-2941 and 2943-8376
    2943 1-2942 and 2944-8376
    2944 1-2943 and 2945-8376
    2945 1-2944 and 2946-8376
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    2949 1-2948 and 2950-8376
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    2952 1-2951 and 2953-8376
    2953 1-2952 and 2954-8376
    2954 1-2953 and 2955-8376
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    2956 1-2955 and 2957-8376
    2957 1-2956 and 2958-8376
    2958 1-2957 and 2959-8376
    2959 1-2958 and 2960-8376
    2960 1-2959 and 2961-8376
    2961 1-2960 and 2962-8376
    2962 1-2961 and 2963-8376
    2963 1-2962 and 2964-8376
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    2965 1-2964 and 2966-8376
    2966 1-2965 and 2967-8376
    2967 1-2966 and 2968-8376
    2968 1-2967 and 2969-8376
    2969 1-2968 and 2970-8376
    2970 1-2969 and 2971-8376
    2971 1-2970 and 2972-8376
    2972 1-2971 and 2973-8376
    2973 1-2972 and 2974-8376
    2974 1-2973 and 2975-8376
    2975 1-2974 and 2976-8376
    2976 1-2975 and 2977-8376
    2977 1-2976 and 2978-8376
    2978 1-2977 and 2979-8376
    2979 1-2978 and 2980-8376
    2980 1-2979 and 2981-8376
    2981 1-2980 and 2982-8376
    2982 1-2981 and 2983-8376
    2983 1-2982 and 2984-8376
    2984 1-2983 and 2985-8376
    2985 1-2984 and 2986-8376
    2986 1-2985 and 2987-8376
    2987 1-2986 and 2988-8376
    2988 1-2987 and 2989-8376
    2989 1-2988 and 2990-8376
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    2992 1-2991 and 2993-8376
    2993 1-2992 and 2994-8376
    2994 1-2993 and 2995-8376
    2995 1-2994 and 2996-8376
    2996 1-2995 and 2997-8376
    2997 1-2996 and 2998-8376
    2998 1-2997 and 2999-8376
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    3003 1-3002 and 3004-8376
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    3008 1-3007 and 3009-8376
    3009 1-3008 and 3010-8376
    3010 1-3009 and 3011-8376
    3011 1-3010 and 3012-8376
    3012 1-3011 and 3013-8376
    3013 1-3012 and 3014-8376
    3014 1-3013 and 3015-8376
    3015 1-3014 and 3016-8376
    3016 1-3015 and 3017-8376
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    3018 1-3017 and 3019-8376
    3019 1-3018 and 3020-8376
    3020 1-3019 and 3021-8376
    3021 1-3020 and 3022-8376
    3022 1-3021 and 3023-8376
    3023 1-3022 and 3024-8376
    3024 1-3023 and 3025-8376
    3025 1-3024 and 3026-8376
    3026 1-3025 and 3027-8376
    3027 1-3026 and 3028-8376
    3028 1-3027 and 3029-8376
    3029 1-3028 and 3030-8376
    3030 1-3029 and 3031-8376
    3031 1-3030 and 3032-8376
    3032 1-3031 and 3033-8376
    3033 1-3032 and 3034-8376
    3034 1-3033 and 3035-8376
    3035 1-3034 and 3036-8376
    3036 1-3035 and 3037-8376
    3037 1-3036 and 3038-8376
    3038 1-3037 and 3039-8376
    3039 1-3038 and 3040-8376
    3040 1-3039 and 3041-8376
    3041 1-3040 and 3042-8376
    3042 1-3041 and 3043-8376
    3043 1-3042 and 3044-8376
    3044 1-3043 and 3045-8376
    3045 1-3044 and 3046-8376
    3046 1-3045 and 3047-8376
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    3057 1-3056 and 3058-8376
    3058 1-3057 and 3059-8376
    3059 1-3058 and 3060-8376
    3060 1-3059 and 3061-8376
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    3062 1-3061 and 3063-8376
    3063 1-3062 and 3064-8376
    3064 1-3063 and 3065-8376
    3065 1-3064 and 3066-8376
    3066 1-3065 and 3067-8376
    3067 1-3066 and 3068-8376
    3068 1-3067 and 3069-8376
    3069 1-3068 and 3070-8376
    3070 1-3069 and 3071-8376
    3071 1-3070 and 3072-8376
    3072 1-3071 and 3073-8376
    3073 1-3072 and 3074-8376
    3074 1-3073 and 3075-8376
    3075 1-3074 and 3076-8376
    3076 1-3075 and 3077-8376
    3077 1-3076 and 3078-8376
    3078 1-3077 and 3079-8376
    3079 1-3078 and 3080-8376
    3080 1-3079 and 3081-8376
    3081 1-3080 and 3082-8376
    3082 1-3081 and 3083-8376
    3083 1-3082 and 3084-8376
    3084 1-3083 and 3085-8376
    3085 1-3084 and 3086-8376
    3086 1-3085 and 3087-8376
    3087 1-3086 and 3088-8376
    3088 1-3087 and 3089-8376
    3089 1-3088 and 3090-8376
    3090 1-3089 and 3091-8376
    3091 1-3090 and 3092-8376
    3092 1-3091 and 3093-8376
    3093 1-3092 and 3094-8376
    3094 1-3093 and 3095-8376
    3095 1-3094 and 3096-8376
    3096 1-3095 and 3097-8376
    3097 1-3096 and 3098-8376
    3098 1-3097 and 3099-8376
    3099 1-3098 and 3100-8376
    3100 1-3099 and 3101-8376
    3101 1-3100 and 3102-8376
    3102 1-3101 and 3103-8376
    3103 1-3102 and 3104-8376
    3104 1-3103 and 3105-8376
    3105 1-3104 and 3106-8376
    3106 1-3105 and 3107-8376
    3107 1-3106 and 3108-8376
    3108 1-3107 and 3109-8376
    3109 1-3108 and 3110-8376
    3110 1-3109 and 3111-8376
    3111 1-3110 and 3112-8376
    3112 1-3111 and 3113-8376
    3113 1-3112 and 3114-8376
    3114 1-3113 and 3115-8376
    3115 1-3114 and 3116-8376
    3116 1-3115 and 3117-8376
    3117 1-3116 and 3118-8376
    3118 1-3117 and 3119-8376
    3119 1-3118 and 3120-8376
    3120 1-3119 and 3121-8376
    3121 1-3120 and 3122-8376
    3122 1-3121 and 3123-8376
    3123 1-3122 and 3124-8376
    3124 1-3123 and 3125-8376
    3125 1-3124 and 3126-8376
    3126 1-3125 and 3127-8376
    3127 1-3126 and 3128-8376
    3128 1-3127 and 3129-8376
    3129 1-3128 and 3130-8376
    3130 1-3129 and 3131-8376
    3131 1-3130 and 3132-8376
    3132 1-3131 and 3133-8376
    3133 1-3132 and 3134-8376
    3134 1-3133 and 3135-8376
    3135 1-3134 and 3136-8376
    3136 1-3135 and 3137-8376
    3137 1-3136 and 3138-8376
    3138 1-3137 and 3139-8376
    3139 1-3138 and 3140-8376
    3140 1-3139 and 3141-8376
    3141 1-3140 and 3142-8376
    3142 1-3141 and 3143-8376
    3143 1-3142 and 3144-8376
    3144 1-3143 and 3145-8376
    3145 1-3144 and 3146-8376
    3146 1-3145 and 3147-8376
    3147 1-3146 and 3148-8376
    3148 1-3147 and 3149-8376
    3149 1-3148 and 3150-8376
    3150 1-3149 and 3151-8376
    3151 1-3150 and 3152-8376
    3152 1-3151 and 3153-8376
    3153 1-3152 and 3154-8376
    3154 1-3153 and 3155-8376
    3155 1-3154 and 3156-8376
    3156 1-3155 and 3157-8376
    3157 1-3156 and 3158-8376
    3158 1-3157 and 3159-8376
    3159 1-3158 and 3160-8376
    3160 1-3159 and 3161-8376
    3161 1-3160 and 3162-8376
    3162 1-3161 and 3163-8376
    3163 1-3162 and 3164-8376
    3164 1-3163 and 3165-8376
    3165 1-3164 and 3166-8376
    3166 1-3165 and 3167-8376
    3167 1-3166 and 3168-8376
    3168 1-3167 and 3169-8376
    3169 1-3168 and 3170-8376
    3170 1-3169 and 3171-8376
    3171 1-3170 and 3172-8376
    3172 1-3171 and 3173-8376
    3173 1-3172 and 3174-8376
    3174 1-3173 and 3175-8376
    3175 1-3174 and 3176-8376
    3176 1-3175 and 3177-8376
    3177 1-3176 and 3178-8376
    3178 1-3177 and 3179-8376
    3179 1-3178 and 3180-8376
    3180 1-3179 and 3181-8376
    3181 1-3180 and 3182-8376
    3182 1-3181 and 3183-8376
    3183 1-3182 and 3184-8376
    3184 1-3183 and 3185-8376
    3185 1-3184 and 3186-8376
    3186 1-3185 and 3187-8376
    3187 1-3186 and 3188-8376
    3188 1-3187 and 3189-8376
    3189 1-3188 and 3190-8376
    3190 1-3189 and 3191-8376
    3191 1-3190 and 3192-8376
    3192 1-3191 and 3193-8376
    3193 1-3192 and 3194-8376
    3194 1-3193 and 3195-8376
    3195 1-3194 and 3196-8376
    3196 1-3195 and 3197-8376
    3197 1-3196 and 3198-8376
    3198 1-3197 and 3199-8376
    3199 1-3198 and 3200-8376
    3200 1-3199 and 3201-8376
    3201 1-3200 and 3202-8376
    3202 1-3201 and 3203-8376
    3203 1-3202 and 3204-8376
    3204 1-3203 and 3205-8376
    3205 1-3204 and 3206-8376
    3206 1-3205 and 3207-8376
    3207 1-3206 and 3208-8376
    3208 1-3207 and 3209-8376
    3209 1-3208 and 3210-8376
    3210 1-3209 and 3211-8376
    3211 1-3210 and 3212-8376
    3212 1-3211 and 3213-8376
    3213 1-3212 and 3214-8376
    3214 1-3213 and 3215-8376
    3215 1-3214 and 3216-8376
    3216 1-3215 and 3217-8376
    3217 1-3216 and 3218-8376
    3218 1-3217 and 3219-8376
    3219 1-3218 and 3220-8376
    3220 1-3219 and 3221-8376
    3221 1-3220 and 3222-8376
    3222 1-3221 and 3223-8376
    3223 1-3222 and 3224-8376
    3224 1-3223 and 3225-8376
    3225 1-3224 and 3226-8376
    3226 1-3225 and 3227-8376
    3227 1-3226 and 3228-8376
    3228 1-3227 and 3229-8376
    3229 1-3228 and 3230-8376
    3230 1-3229 and 3231-8376
    3231 1-3230 and 3232-8376
    3232 1-3231 and 3233-8376
    3233 1-3232 and 3234-8376
    3234 1-3233 and 3235-8376
    3235 1-3234 and 3236-8376
    3236 1-3235 and 3237-8376
    3237 1-3236 and 3238-8376
    3238 1-3237 and 3239-8376
    3239 1-3238 and 3240-8376
    3240 1-3239 and 3241-8376
    3241 1-3240 and 3242-8376
    3242 1-3241 and 3243-8376
    3243 1-3242 and 3244-8376
    3244 1-3243 and 3245-8376
    3245 1-3244 and 3246-8376
    3246 1-3245 and 3247-8376
    3247 1-3246 and 3248-8376
    3248 1-3247 and 3249-8376
    3249 1-3248 and 3250-8376
    3250 1-3249 and 3251-8376
    3251 1-3250 and 3252-8376
    3252 1-3251 and 3253-8376
    3253 1-3252 and 3254-8376
    3254 1-3253 and 3255-8376
    3255 1-3254 and 3256-8376
    3256 1-3255 and 3257-8376
    3257 1-3256 and 3258-8376
    3258 1-3257 and 3259-8376
    3259 1-3258 and 3260-8376
    3260 1-3259 and 3261-8376
    3261 1-3260 and 3262-8376
    3262 1-3261 and 3263-8376
    3263 1-3262 and 3264-8376
    3264 1-3263 and 3265-8376
    3265 1-3264 and 3266-8376
    3266 1-3265 and 3267-8376
    3267 1-3266 and 3268-8376
    3268 1-3267 and 3269-8376
    3269 1-3268 and 3270-8376
    3270 1-3269 and 3271-8376
    3271 1-3270 and 3272-8376
    3272 1-3271 and 3273-8376
    3273 1-3272 and 3274-8376
    3274 1-3273 and 3275-8376
    3275 1-3274 and 3276-8376
    3276 1-3275 and 3277-8376
    3277 1-3276 and 3278-8376
    3278 1-3277 and 3279-8376
    3279 1-3278 and 3280-8376
    3280 1-3279 and 3281-8376
    3281 1-3280 and 3282-8376
    3282 1-3281 and 3283-8376
    3283 1-3282 and 3284-8376
    3284 1-3283 and 3285-8376
    3285 1-3284 and 3286-8376
    3286 1-3285 and 3287-8376
    3287 1-3286 and 3288-8376
    3288 1-3287 and 3289-8376
    3289 1-3288 and 3290-8376
    3290 1-3289 and 3291-8376
    3291 1-3290 and 3292-8376
    3292 1-3291 and 3293-8376
    3293 1-3292 and 3294-8376
    3294 1-3293 and 3295-8376
    3295 1-3294 and 3296-8376
    3296 1-3295 and 3297-8376
    3297 1-3296 and 3298-8376
    3298 1-3297 and 3299-8376
    3299 1-3298 and 3300-8376
    3300 1-3299 and 3301-8376
    3301 1-3300 and 3302-8376
    3302 1-3301 and 3303-8376
    3303 1-3302 and 3304-8376
    3304 1-3303 and 3305-8376
    3305 1-3304 and 3306-8376
    3306 1-3305 and 3307-8376
    3307 1-3306 and 3308-8376
    3308 1-3307 and 3309-8376
    3309 1-3308 and 3310-8376
    3310 1-3309 and 3311-8376
    3311 1-3310 and 3312-8376
    3312 1-3311 and 3313-8376
    3313 1-3312 and 3314-8376
    3314 1-3313 and 3315-8376
    3315 1-3314 and 3316-8376
    3316 1-3315 and 3317-8376
    3317 1-3316 and 3318-8376
    3318 1-3317 and 3319-8376
    3319 1-3318 and 3320-8376
    3320 1-3319 and 3321-8376
    3321 1-3320 and 3322-8376
    3322 1-3321 and 3323-8376
    3323 1-3322 and 3324-8376
    3324 1-3323 and 3325-8376
    3325 1-3324 and 3326-8376
    3326 1-3325 and 3327-8376
    3327 1-3326 and 3328-8376
    3328 1-3327 and 3329-8376
    3329 1-3328 and 3330-8376
    3330 1-3329 and 3331-8376
    3331 1-3330 and 3332-8376
    3332 1-3331 and 3333-8376
    3333 1-3332 and 3334-8376
    3334 1-3333 and 3335-8376
    3335 1-3334 and 3336-8376
    3336 1-3335 and 3337-8376
    3337 1-3336 and 3338-8376
    3338 1-3337 and 3339-8376
    3339 1-3338 and 3340-8376
    3340 1-3339 and 3341-8376
    3341 1-3340 and 3342-8376
    3342 1-3341 and 3343-8376
    3343 1-3342 and 3344-8376
    3344 1-3343 and 3345-8376
    3345 1-3344 and 3346-8376
    3346 1-3345 and 3347-8376
    3347 1-3346 and 3348-8376
    3348 1-3347 and 3349-8376
    3349 1-3348 and 3350-8376
    3350 1-3349 and 3351-8376
    3351 1-3350 and 3352-8376
    3352 1-3351 and 3353-8376
    3353 1-3352 and 3354-8376
    3354 1-3353 and 3355-8376
    3355 1-3354 and 3356-8376
    3356 1-3355 and 3357-8376
    3357 1-3356 and 3358-8376
    3358 1-3357 and 3359-8376
    3359 1-3358 and 3360-8376
    3360 1-3359 and 3361-8376
    3361 1-3360 and 3362-8376
    3362 1-3361 and 3363-8376
    3363 1-3362 and 3364-8376
    3364 1-3363 and 3365-8376
    3365 1-3364 and 3366-8376
    3366 1-3365 and 3367-8376
    3367 1-3366 and 3368-8376
    3368 1-3367 and 3369-8376
    3369 1-3368 and 3370-8376
    3370 1-3369 and 3371-8376
    3371 1-3370 and 3372-8376
    3372 1-3371 and 3373-8376
    3373 1-3372 and 3374-8376
    3374 1-3373 and 3375-8376
    3375 1-3374 and 3376-8376
    3376 1-3375 and 3377-8376
    3377 1-3376 and 3378-8376
    3378 1-3377 and 3379-8376
    3379 1-3378 and 3380-8376
    3380 1-3379 and 3381-8376
    3381 1-3380 and 3382-8376
    3382 1-3381 and 3383-8376
    3383 1-3382 and 3384-8376
    3384 1-3383 and 3385-8376
    3385 1-3384 and 3386-8376
    3386 1-3385 and 3387-8376
    3387 1-3386 and 3388-8376
    3388 1-3387 and 3389-8376
    3389 1-3388 and 3390-8376
    3390 1-3389 and 3391-8376
    3391 1-3390 and 3392-8376
    3392 1-3391 and 3393-8376
    3393 1-3392 and 3394-8376
    3394 1-3393 and 3395-8376
    3395 1-3394 and 3396-8376
    3396 1-3395 and 3397-8376
    3397 1-3396 and 3398-8376
    3398 1-3397 and 3399-8376
    3399 1-3398 and 3400-8376
    3400 1-3399 and 3401-8376
    3401 1-3400 and 3402-8376
    3402 1-3401 and 3403-8376
    3403 1-3402 and 3404-8376
    3404 1-3403 and 3405-8376
    3405 1-3404 and 3406-8376
    3406 1-3405 and 3407-8376
    3407 1-3406 and 3408-8376
    3408 1-3407 and 3409-8376
    3409 1-3408 and 3410-8376
    3410 1-3409 and 3411-8376
    3411 1-3410 and 3412-8376
    3412 1-3411 and 3413-8376
    3413 1-3412 and 3414-8376
    3414 1-3413 and 3415-8376
    3415 1-3414 and 3416-8376
    3416 1-3415 and 3417-8376
    3417 1-3416 and 3418-8376
    3418 1-3417 and 3419-8376
    3419 1-3418 and 3420-8376
    3420 1-3419 and 3421-8376
    3421 1-3420 and 3422-8376
    3422 1-3421 and 3423-8376
    3423 1-3422 and 3424-8376
    3424 1-3423 and 3425-8376
    3425 1-3424 and 3426-8376
    3426 1-3425 and 3427-8376
    3427 1-3426 and 3428-8376
    3428 1-3427 and 3429-8376
    3429 1-3428 and 3430-8376
    3430 1-3429 and 3431-8376
    3431 1-3430 and 3432-8376
    3432 1-3431 and 3433-8376
    3433 1-3432 and 3434-8376
    3434 1-3433 and 3435-8376
    3435 1-3434 and 3436-8376
    3436 1-3435 and 3437-8376
    3437 1-3436 and 3438-8376
    3438 1-3437 and 3439-8376
    3439 1-3438 and 3440-8376
    3440 1-3439 and 3441-8376
    3441 1-3440 and 3442-8376
    3442 1-3441 and 3443-8376
    3443 1-3442 and 3444-8376
    3444 1-3443 and 3445-8376
    3445 1-3444 and 3446-8376
    3446 1-3445 and 3447-8376
    3447 1-3446 and 3448-8376
    3448 1-3447 and 3449-8376
    3449 1-3448 and 3450-8376
    3450 1-3449 and 3451-8376
    3451 1-3450 and 3452-8376
    3452 1-3451 and 3453-8376
    3453 1-3452 and 3454-8376
    3454 1-3453 and 3455-8376
    3455 1-3454 and 3456-8376
    3456 1-3455 and 3457-8376
    3457 1-3456 and 3458-8376
    3458 1-3457 and 3459-8376
    3459 1-3458 and 3460-8376
    3460 1-3459 and 3461-8376
    3461 1-3460 and 3462-8376
    3462 1-3461 and 3463-8376
    3463 1-3462 and 3464-8376
    3464 1-3463 and 3465-8376
    3465 1-3464 and 3466-8376
    3466 1-3465 and 3467-8376
    3467 1-3466 and 3468-8376
    3468 1-3467 and 3469-8376
    3469 1-3468 and 3470-8376
    3470 1-3469 and 3471-8376
    3471 1-3470 and 3472-8376
    3472 1-3471 and 3473-8376
    3473 1-3472 and 3474-8376
    3474 1-3473 and 3475-8376
    3475 1-3474 and 3476-8376
    3476 1-3475 and 3477-8376
    3477 1-3476 and 3478-8376
    3478 1-3477 and 3479-8376
    3479 1-3478 and 3480-8376
    3480 1-3479 and 3481-8376
    3481 1-3480 and 3482-8376
    3482 1-3481 and 3483-8376
    3483 1-3482 and 3484-8376
    3484 1-3483 and 3485-8376
    3485 1-3484 and 3486-8376
    3486 1-3485 and 3487-8376
    3487 1-3486 and 3488-8376
    3488 1-3487 and 3489-8376
    3489 1-3488 and 3490-8376
    3490 1-3489 and 3491-8376
    3491 1-3490 and 3492-8376
    3492 1-3491 and 3493-8376
    3493 1-3492 and 3494-8376
    3494 1-3493 and 3495-8376
    3495 1-3494 and 3496-8376
    3496 1-3495 and 3497-8376
    3497 1-3496 and 3498-8376
    3498 1-3497 and 3499-8376
    3499 1-3498 and 3500-8376
    3500 1-3499 and 3501-8376
    3501 1-3500 and 3502-8376
    3502 1-3501 and 3503-8376
    3503 1-3502 and 3504-8376
    3504 1-3503 and 3505-8376
    3505 1-3504 and 3506-8376
    3506 1-3505 and 3507-8376
    3507 1-3506 and 3508-8376
    3508 1-3507 and 3509-8376
    3509 1-3508 and 3510-8376
    3510 1-3509 and 3511-8376
    3511 1-3510 and 3512-8376
    3512 1-3511 and 3513-8376
    3513 1-3512 and 3514-8376
    3514 1-3513 and 3515-8376
    3515 1-3514 and 3516-8376
    3516 1-3515 and 3517-8376
    3517 1-3516 and 3518-8376
    3518 1-3517 and 3519-8376
    3519 1-3518 and 3520-8376
    3520 1-3519 and 3521-8376
    3521 1-3520 and 3522-8376
    3522 1-3521 and 3523-8376
    3523 1-3522 and 3524-8376
    3524 1-3523 and 3525-8376
    3525 1-3524 and 3526-8376
    3526 1-3525 and 3527-8376
    3527 1-3526 and 3528-8376
    3528 1-3527 and 3529-8376
    3529 1-3528 and 3530-8376
    3530 1-3529 and 3531-8376
    3531 1-3530 and 3532-8376
    3532 1-3531 and 3533-8376
    3533 1-3532 and 3534-8376
    3534 1-3533 and 3535-8376
    3535 1-3534 and 3536-8376
    3536 1-3535 and 3537-8376
    3537 1-3536 and 3538-8376
    3538 1-3537 and 3539-8376
    3539 1-3538 and 3540-8376
    3540 1-3539 and 3541-8376
    3541 1-3540 and 3542-8376
    3542 1-3541 and 3543-8376
    3543 1-3542 and 3544-8376
    3544 1-3543 and 3545-8376
    3545 1-3544 and 3546-8376
    3546 1-3545 and 3547-8376
    3547 1-3546 and 3548-8376
    3548 1-3547 and 3549-8376
    3549 1-3548 and 3550-8376
    3550 1-3549 and 3551-8376
    3551 1-3550 and 3552-8376
    3552 1-3551 and 3553-8376
    3553 1-3552 and 3554-8376
    3554 1-3553 and 3555-8376
    3555 1-3554 and 3556-8376
    3556 1-3555 and 3557-8376
    3557 1-3556 and 3558-8376
    3558 1-3557 and 3559-8376
    3559 1-3558 and 3560-8376
    3560 1-3559 and 3561-8376
    3561 1-3560 and 3562-8376
    3562 1-3561 and 3563-8376
    3563 1-3562 and 3564-8376
    3564 1-3563 and 3565-8376
    3565 1-3564 and 3566-8376
    3566 1-3565 and 3567-8376
    3567 1-3566 and 3568-8376
    3568 1-3567 and 3569-8376
    3569 1-3568 and 3570-8376
    3570 1-3569 and 3571-8376
    3571 1-3570 and 3572-8376
    3572 1-3571 and 3573-8376
    3573 1-3572 and 3574-8376
    3574 1-3573 and 3575-8376
    3575 1-3574 and 3576-8376
    3576 1-3575 and 3577-8376
    3577 1-3576 and 3578-8376
    3578 1-3577 and 3579-8376
    3579 1-3578 and 3580-8376
    3580 1-3579 and 3581-8376
    3581 1-3580 and 3582-8376
    3582 1-3581 and 3583-8376
    3583 1-3582 and 3584-8376
    3584 1-3583 and 3585-8376
    3585 1-3584 and 3586-8376
    3586 1-3585 and 3587-8376
    3587 1-3586 and 3588-8376
    3588 1-3587 and 3589-8376
    3589 1-3588 and 3590-8376
    3590 1-3589 and 3591-8376
    3591 1-3590 and 3592-8376
    3592 1-3591 and 3593-8376
    3593 1-3592 and 3594-8376
    3594 1-3593 and 3595-8376
    3595 1-3594 and 3596-8376
    3596 1-3595 and 3597-8376
    3597 1-3596 and 3598-8376
    3598 1-3597 and 3599-8376
    3599 1-3598 and 3600-8376
    3600 1-3599 and 3601-8376
    3601 1-3600 and 3602-8376
    3602 1-3601 and 3603-8376
    3603 1-3602 and 3604-8376
    3604 1-3603 and 3605-8376
    3605 1-3604 and 3606-8376
    3606 1-3605 and 3607-8376
    3607 1-3606 and 3608-8376
    3608 1-3607 and 3609-8376
    3609 1-3608 and 3610-8376
    3610 1-3609 and 3611-8376
    3611 1-3610 and 3612-8376
    3612 1-3611 and 3613-8376
    3613 1-3612 and 3614-8376
    3614 1-3613 and 3615-8376
    3615 1-3614 and 3616-8376
    3616 1-3615 and 3617-8376
    3617 1-3616 and 3618-8376
    3618 1-3617 and 3619-8376
    3619 1-3618 and 3620-8376
    3620 1-3619 and 3621-8376
    3621 1-3620 and 3622-8376
    3622 1-3621 and 3623-8376
    3623 1-3622 and 3624-8376
    3624 1-3623 and 3625-8376
    3625 1-3624 and 3626-8376
    3626 1-3625 and 3627-8376
    3627 1-3626 and 3628-8376
    3628 1-3627 and 3629-8376
    3629 1-3628 and 3630-8376
    3630 1-3629 and 3631-8376
    3631 1-3630 and 3632-8376
    3632 1-3631 and 3633-8376
    3633 1-3632 and 3634-8376
    3634 1-3633 and 3635-8376
    3635 1-3634 and 3636-8376
    3636 1-3635 and 3637-8376
    3637 1-3636 and 3638-8376
    3638 1-3637 and 3639-8376
    3639 1-3638 and 3640-8376
    3640 1-3639 and 3641-8376
    3641 1-3640 and 3642-8376
    3642 1-3641 and 3643-8376
    3643 1-3642 and 3644-8376
    3644 1-3643 and 3645-8376
    3645 1-3644 and 3646-8376
    3646 1-3645 and 3647-8376
    3647 1-3646 and 3648-8376
    3648 1-3647 and 3649-8376
    3649 1-3648 and 3650-8376
    3650 1-3649 and 3651-8376
    3651 1-3650 and 3652-8376
    3652 1-3651 and 3653-8376
    3653 1-3652 and 3654-8376
    3654 1-3653 and 3655-8376
    3655 1-3654 and 3656-8376
    3656 1-3655 and 3657-8376
    3657 1-3656 and 3658-8376
    3658 1-3657 and 3659-8376
    3659 1-3658 and 3660-8376
    3660 1-3659 and 3661-8376
    3661 1-3660 and 3662-8376
    3662 1-3661 and 3663-8376
    3663 1-3662 and 3664-8376
    3664 1-3663 and 3665-8376
    3665 1-3664 and 3666-8376
    3666 1-3665 and 3667-8376
    3667 1-3666 and 3668-8376
    3668 1-3667 and 3669-8376
    3669 1-3668 and 3670-8376
    3670 1-3669 and 3671-8376
    3671 1-3670 and 3672-8376
    3672 1-3671 and 3673-8376
    3673 1-3672 and 3674-8376
    3674 1-3673 and 3675-8376
    3675 1-3674 and 3676-8376
    3676 1-3675 and 3677-8376
    3677 1-3676 and 3678-8376
    3678 1-3677 and 3679-8376
    3679 1-3678 and 3680-8376
    3680 1-3679 and 3681-8376
    3681 1-3680 and 3682-8376
    3682 1-3681 and 3683-8376
    3683 1-3682 and 3684-8376
    3684 1-3683 and 3685-8376
    3685 1-3684 and 3686-8376
    3686 1-3685 and 3687-8376
    3687 1-3686 and 3688-8376
    3688 1-3687 and 3689-8376
    3689 1-3688 and 3690-8376
    3690 1-3689 and 3691-8376
    3691 1-3690 and 3692-8376
    3692 1-3691 and 3693-8376
    3693 1-3692 and 3694-8376
    3694 1-3693 and 3695-8376
    3695 1-3694 and 3696-8376
    3696 1-3695 and 3697-8376
    3697 1-3696 and 3698-8376
    3698 1-3697 and 3699-8376
    3699 1-3698 and 3700-8376
    3700 1-3699 and 3701-8376
    3701 1-3700 and 3702-8376
    3702 1-3701 and 3703-8376
    3703 1-3702 and 3704-8376
    3704 1-3703 and 3705-8376
    3705 1-3704 and 3706-8376
    3706 1-3705 and 3707-8376
    3707 1-3706 and 3708-8376
    3708 1-3707 and 3709-8376
    3709 1-3708 and 3710-8376
    3710 1-3709 and 3711-8376
    3711 1-3710 and 3712-8376
    3712 1-3711 and 3713-8376
    3713 1-3712 and 3714-8376
    3714 1-3713 and 3715-8376
    3715 1-3714 and 3716-8376
    3716 1-3715 and 3717-8376
    3717 1-3716 and 3718-8376
    3718 1-3717 and 3719-8376
    3719 1-3718 and 3720-8376
    3720 1-3719 and 3721-8376
    3721 1-3720 and 3722-8376
    3722 1-3721 and 3723-8376
    3723 1-3722 and 3724-8376
    3724 1-3723 and 3725-8376
    3725 1-3724 and 3726-8376
    3726 1-3725 and 3727-8376
    3727 1-3726 and 3728-8376
    3728 1-3727 and 3729-8376
    3729 1-3728 and 3730-8376
    3730 1-3729 and 3731-8376
    3731 1-3730 and 3732-8376
    3732 1-3731 and 3733-8376
    3733 1-3732 and 3734-8376
    3734 1-3733 and 3735-8376
    3735 1-3734 and 3736-8376
    3736 1-3735 and 3737-8376
    3737 1-3736 and 3738-8376
    3738 1-3737 and 3739-8376
    3739 1-3738 and 3740-8376
    3740 1-3739 and 3741-8376
    3741 1-3740 and 3742-8376
    3742 1-3741 and 3743-8376
    3743 1-3742 and 3744-8376
    3744 1-3743 and 3745-8376
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    3954 1-3953 and 3955-8376
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    3965 1-3964 and 3966-8376
    3966 1-3965 and 3967-8376
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    3968 1-3967 and 3969-8376
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    3970 1-3969 and 3971-8376
    3971 1-3970 and 3972-8376
    3972 1-3971 and 3973-8376
    3973 1-3972 and 3974-8376
    3974 1-3973 and 3975-8376
    3975 1-3974 and 3976-8376
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    3989 1-3988 and 3990-8376
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    3993 1-3992 and 3994-8376
    3994 1-3993 and 3995-8376
    3995 1-3994 and 3996-8376
    3996 1-3995 and 3997-8376
    3997 1-3996 and 3998-8376
    3998 1-3997 and 3999-8376
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    4003 1-4002 and 4004-8376
    4004 1-4003 and 4005-8376
    4005 1-4004 and 4006-8376
    4006 1-4005 and 4007-8376
    4007 1-4006 and 4008-8376
    4008 1-4007 and 4009-8376
    4009 1-4008 and 4010-8376
    4010 1-4009 and 4011-8376
    4011 1-4010 and 4012-8376
    4012 1-4011 and 4013-8376
    4013 1-4012 and 4014-8376
    4014 1-4013 and 4015-8376
    4015 1-4014 and 4016-8376
    4016 1-4015 and 4017-8376
    4017 1-4016 and 4018-8376
    4018 1-4017 and 4019-8376
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    4020 1-4019 and 4021-8376
    4021 1-4020 and 4022-8376
    4022 1-4021 and 4023-8376
    4023 1-4022 and 4024-8376
    4024 1-4023 and 4025-8376
    4025 1-4024 and 4026-8376
    4026 1-4025 and 4027-8376
    4027 1-4026 and 4028-8376
    4028 1-4027 and 4029-8376
    4029 1-4028 and 4030-8376
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    4031 1-4030 and 4032-8376
    4032 1-4031 and 4033-8376
    4033 1-4032 and 4034-8376
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    4039 1-4038 and 4040-8376
    4040 1-4039 and 4041-8376
    4041 1-4040 and 4042-8376
    4042 1-4041 and 4043-8376
    4043 1-4042 and 4044-8376
    4044 1-4043 and 4045-8376
    4045 1-4044 and 4046-8376
    4046 1-4045 and 4047-8376
    4047 1-4046 and 4048-8376
    4048 1-4047 and 4049-8376
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    4053 1-4052 and 4054-8376
    4054 1-4053 and 4055-8376
    4055 1-4054 and 4056-8376
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    4064 1-4063 and 4065-8376
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    4066 1-4065 and 4067-8376
    4067 1-4066 and 4068-8376
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    4070 1-4069 and 4071-8376
    4071 1-4070 and 4072-8376
    4072 1-4071 and 4073-8376
    4073 1-4072 and 4074-8376
    4074 1-4073 and 4075-8376
    4075 1-4074 and 4076-8376
    4076 1-4075 and 4077-8376
    4077 1-4076 and 4078-8376
    4078 1-4077 and 4079-8376
    4079 1-4078 and 4080-8376
    4080 1-4079 and 4081-8376
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    4083 1-4082 and 4084-8376
    4084 1-4083 and 4085-8376
    4085 1-4084 and 4086-8376
    4086 1-4085 and 4087-8376
    4087 1-4086 and 4088-8376
    4088 1-4087 and 4089-8376
    4089 1-4088 and 4090-8376
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    4091 1-4090 and 4092-8376
    4092 1-4091 and 4093-8376
    4093 1-4092 and 4094-8376
    4094 1-4093 and 4095-8376
    4095 1-4094 and 4096-8376
    4096 1-4095 and 4097-8376
    4097 1-4096 and 4098-8376
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    4100 1-4099 and 4101-8376
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    4102 1-4101 and 4103-8376
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    4106 1-4105 and 4107-8376
    4107 1-4106 and 4108-8376
    4108 1-4107 and 4109-8376
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    4110 1-4109 and 4111-8376
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    4112 1-4111 and 4113-8376
    4113 1-4112 and 4114-8376
    4114 1-4113 and 4115-8376
    4115 1-4114 and 4116-8376
    4116 1-4115 and 4117-8376
    4117 1-4116 and 4118-8376
    4118 1-4117 and 4119-8376
    4119 1-4118 and 4120-8376
    4120 1-4119 and 4121-8376
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    4122 1-4121 and 4123-8376
    4123 1-4122 and 4124-8376
    4124 1-4123 and 4125-8376
    4125 1-4124 and 4126-8376
    4126 1-4125 and 4127-8376
    4127 1-4126 and 4128-8376
    4128 1-4127 and 4129-8376
    4129 1-4128 and 4130-8376
    4130 1-4129 and 4131-8376
    4131 1-4130 and 4132-8376
    4132 1-4131 and 4133-8376
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    4134 1-4133 and 4135-8376
    4135 1-4134 and 4136-8376
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    4137 1-4136 and 4138-8376
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    4140 1-4139 and 4141-8376
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    4142 1-4141 and 4143-8376
    4143 1-4142 and 4144-8376
    4144 1-4143 and 4145-8376
    4145 1-4144 and 4146-8376
    4146 1-4145 and 4147-8376
    4147 1-4146 and 4148-8376
    4148 1-4147 and 4149-8376
    4149 1-4148 and 4150-8376
    4150 1-4149 and 4151-8376
    4151 1-4150 and 4152-8376
    4152 1-4151 and 4153-8376
    4153 1-4152 and 4154-8376
    4154 1-4153 and 4155-8376
    4155 1-4154 and 4156-8376
    4156 1-4155 and 4157-8376
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    4158 1-4157 and 4159-8376
    4159 1-4158 and 4160-8376
    4160 1-4159 and 4161-8376
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    4162 1-4161 and 4163-8376
    4163 1-4162 and 4164-8376
    4164 1-4163 and 4165-8376
    4165 1-4164 and 4166-8376
    4166 1-4165 and 4167-8376
    4167 1-4166 and 4168-8376
    4168 1-4167 and 4169-8376
    4169 1-4168 and 4170-8376
    4170 1-4169 and 4171-8376
    4171 1-4170 and 4172-8376
    4172 1-4171 and 4173-8376
    4173 1-4172 and 4174-8376
    4174 1-4173 and 4175-8376
    4175 1-4174 and 4176-8376
    4176 1-4175 and 4177-8376
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    4178 1-4177 and 4179-8376
    4179 1-4178 and 4180-8376
    4180 1-4179 and 4181-8376
    4181 1-4180 and 4182-8376
    4182 1-4181 and 4183-8376
    4183 1-4182 and 4184-8376
    4184 1-4183 and 4185-8376
    4185 1-4184 and 4186-8376
    4186 1-4185 and 4187-8376
    4187 1-4186 and 4188-8376
    4188 1-4187 and 4189-8376
    4189 1-4188 and 4190-8376
    4190 1-4189 and 4191-8376
    4191 1-4190 and 4192-8376
    4192 1-4191 and 4193-8376
    4193 1-4192 and 4194-8376
    4194 1-4193 and 4195-8376
    4195 1-4194 and 4196-8376
    4196 1-4195 and 4197-8376
    4197 1-4196 and 4198-8376
    4198 1-4197 and 4199-8376
    4199 1-4198 and 4200-8376
    4200 1-4199 and 4201-8376
    4201 1-4200 and 4202-8376
    4202 1-4201 and 4203-8376
    4203 1-4202 and 4204-8376
    4204 1-4203 and 4205-8376
    4205 1-4204 and 4206-8376
    4206 1-4205 and 4207-8376
    4207 1-4206 and 4208-8376
    4208 1-4207 and 4209-8376
    4209 1-4208 and 4210-8376
    4210 1-4209 and 4211-8376
    4211 1-4210 and 4212-8376
    4212 1-4211 and 4213-8376
    4213 1-4212 and 4214-8376
    4214 1-4213 and 4215-8376
    4215 1-4214 and 4216-8376
    4216 1-4215 and 4217-8376
    4217 1-4216 and 4218-8376
    4218 1-4217 and 4219-8376
    4219 1-4218 and 4220-8376
    4220 1-4219 and 4221-8376
    4221 1-4220 and 4222-8376
    4222 1-4221 and 4223-8376
    4223 1-4222 and 4224-8376
    4224 1-4223 and 4225-8376
    4225 1-4224 and 4226-8376
    4226 1-4225 and 4227-8376
    4227 1-4226 and 4228-8376
    4228 1-4227 and 4229-8376
    4229 1-4228 and 4230-8376
    4230 1-4229 and 4231-8376
    4231 1-4230 and 4232-8376
    4232 1-4231 and 4233-8376
    4233 1-4232 and 4234-8376
    4234 1-4233 and 4235-8376
    4235 1-4234 and 4236-8376
    4236 1-4235 and 4237-8376
    4237 1-4236 and 4238-8376
    4238 1-4237 and 4239-8376
    4239 1-4238 and 4240-8376
    4240 1-4239 and 4241-8376
    4241 1-4240 and 4242-8376
    4242 1-4241 and 4243-8376
    4243 1-4242 and 4244-8376
    4244 1-4243 and 4245-8376
    4245 1-4244 and 4246-8376
    4246 1-4245 and 4247-8376
    4247 1-4246 and 4248-8376
    4248 1-4247 and 4249-8376
    4249 1-4248 and 4250-8376
    4250 1-4249 and 4251-8376
    4251 1-4250 and 4252-8376
    4252 1-4251 and 4253-8376
    4253 1-4252 and 4254-8376
    4254 1-4253 and 4255-8376
    4255 1-4254 and 4256-8376
    4256 1-4255 and 4257-8376
    4257 1-4256 and 4258-8376
    4258 1-4257 and 4259-8376
    4259 1-4258 and 4260-8376
    4260 1-4259 and 4261-8376
    4261 1-4260 and 4262-8376
    4262 1-4261 and 4263-8376
    4263 1-4262 and 4264-8376
    4264 1-4263 and 4265-8376
    4265 1-4264 and 4266-8376
    4266 1-4265 and 4267-8376
    4267 1-4266 and 4268-8376
    4268 1-4267 and 4269-8376
    4269 1-4268 and 4270-8376
    4270 1-4269 and 4271-8376
    4271 1-4270 and 4272-8376
    4272 1-4271 and 4273-8376
    4273 1-4272 and 4274-8376
    4274 1-4273 and 4275-8376
    4275 1-4274 and 4276-8376
    4276 1-4275 and 4277-8376
    4277 1-4276 and 4278-8376
    4278 1-4277 and 4279-8376
    4279 1-4278 and 4280-8376
    4280 1-4279 and 4281-8376
    4281 1-4280 and 4282-8376
    4282 1-4281 and 4283-8376
    4283 1-4282 and 4284-8376
    4284 1-4283 and 4285-8376
    4285 1-4284 and 4286-8376
    4286 1-4285 and 4287-8376
    4287 1-4286 and 4288-8376
    4288 1-4287 and 4289-8376
    4289 1-4288 and 4290-8376
    4290 1-4289 and 4291-8376
    4291 1-4290 and 4292-8376
    4292 1-4291 and 4293-8376
    4293 1-4292 and 4294-8376
    4294 1-4293 and 4295-8376
    4295 1-4294 and 4296-8376
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    4316 1-4315 and 4317-8376
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    4405 1-4404 and 4406-8376
    4406 1-4405 and 4407-8376
    4407 1-4406 and 4408-8376
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    4416 1-4415 and 4417-8376
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    4418 1-4417 and 4419-8376
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    4431 1-4430 and 4432-8376
    4432 1-4431 and 4433-8376
    4433 1-4432 and 4434-8376
    4434 1-4433 and 4435-8376
    4435 1-4434 and 4436-8376
    4436 1-4435 and 4437-8376
    4437 1-4436 and 4438-8376
    4438 1-4437 and 4439-8376
    4439 1-4438 and 4440-8376
    4440 1-4439 and 4441-8376
    4441 1-4440 and 4442-8376
    4442 1-4441 and 4443-8376
    4443 1-4442 and 4444-8376
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    4445 1-4444 and 4446-8376
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    4447 1-4446 and 4448-8376
    4448 1-4447 and 4449-8376
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    4454 1-4453 and 4455-8376
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    4457 1-4456 and 4458-8376
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    4473 1-4472 and 4474-8376
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    4475 1-4474 and 4476-8376
    4476 1-4475 and 4477-8376
    4477 1-4476 and 4478-8376
    4478 1-4477 and 4479-8376
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    4480 1-4479 and 4481-8376
    4481 1-4480 and 4482-8376
    4482 1-4481 and 4483-8376
    4483 1-4482 and 4484-8376
    4484 1-4483 and 4485-8376
    4485 1-4484 and 4486-8376
    4486 1-4485 and 4487-8376
    4487 1-4486 and 4488-8376
    4488 1-4487 and 4489-8376
    4489 1-4488 and 4490-8376
    4490 1-4489 and 4491-8376
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    4492 1-4491 and 4493-8376
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    4504 1-4503 and 4505-8376
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    4506 1-4505 and 4507-8376
    4507 1-4506 and 4508-8376
    4508 1-4507 and 4509-8376
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    4510 1-4509 and 4511-8376
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    4514 1-4513 and 4515-8376
    4515 1-4514 and 4516-8376
    4516 1-4515 and 4517-8376
    4517 1-4516 and 4518-8376
    4518 1-4517 and 4519-8376
    4519 1-4518 and 4520-8376
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    4521 1-4520 and 4522-8376
    4522 1-4521 and 4523-8376
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    4524 1-4523 and 4525-8376
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    4526 1-4525 and 4527-8376
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    4528 1-4527 and 4529-8376
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    4532 1-4531 and 4533-8376
    4533 1-4532 and 4534-8376
    4534 1-4533 and 4535-8376
    4535 1-4534 and 4536-8376
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    4537 1-4536 and 4538-8376
    4538 1-4537 and 4539-8376
    4539 1-4538 and 4540-8376
    4540 1-4539 and 4541-8376
    4541 1-4540 and 4542-8376
    4542 1-4541 and 4543-8376
    4543 1-4542 and 4544-8376
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    4552 1-4551 and 4553-8376
    4553 1-4552 and 4554-8376
    4554 1-4553 and 4555-8376
    4555 1-4554 and 4556-8376
    4556 1-4555 and 4557-8376
    4557 1-4556 and 4558-8376
    4558 1-4557 and 4559-8376
    4559 1-4558 and 4560-8376
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    4575 1-4574 and 4576-8376
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    4593 1-4592 and 4594-8376
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    4595 1-4594 and 4596-8376
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    4616 1-4615 and 4617-8376
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    4702 1-4701 and 4703-8376
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    4705 1-4704 and 4706-8376
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    4710 1-4709 and 4711-8376
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    4715 1-4714 and 4716-8376
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    4718 1-4717 and 4719-8376
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    4773 1-4772 and 4774-8376
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    4803 1-4802 and 4804-8376
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    4816 1-4815 and 4817-8376
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    4820 1-4819 and 4821-8376
    4821 1-4820 and 4822-8376
    4822 1-4821 and 4823-8376
    4823 1-4822 and 4824-8376
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    4826 1-4825 and 4827-8376
    4827 1-4826 and 4828-8376
    4828 1-4827 and 4829-8376
    4829 1-4828 and 4830-8376
    4830 1-4829 and 4831-8376
    4831 1-4830 and 4832-8376
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    5576 1-5575 and 5577-8376
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    8096 1-8095 and 8097-8376
    8097 1-8096 and 8098-8376
    8098 1-8097 and 8099-8376
    8099 1-8098 and 8100-8376
    8100 1-8099 and 8101-8376
    8101 1-8100 and 8102-8376
    8102 1-8101 and 8103-8376
    8103 1-8102 and 8104-8376
    8104 1-8103 and 8105-8376
    8105 1-8104 and 8106-8376
    8106 1-8105 and 8107-8376
    8107 1-8106 and 8108-8376
    8108 1-8107 and 8109-8376
    8109 1-8108 and 8110-8376
    8110 1-8109 and 8111-8376
    8111 1-8110 and 8112-8376
    8112 1-8111 and 8113-8376
    8113 1-8112 and 8114-8376
    8114 1-8113 and 8115-8376
    8115 1-8114 and 8116-8376
    8116 1-8115 and 8117-8376
    8117 1-8116 and 8118-8376
    8118 1-8117 and 8119-8376
    8119 1-8118 and 8120-8376
    8120 1-8119 and 8121-8376
    8121 1-8120 and 8122-8376
    8122 1-8121 and 8123-8376
    8123 1-8122 and 8124-8376
    8124 1-8123 and 8125-8376
    8125 1-8124 and 8126-8376
    8126 1-8125 and 8127-8376
    8127 1-8126 and 8128-8376
    8128 1-8127 and 8129-8376
    8129 1-8128 and 8130-8376
    8130 1-8129 and 8131-8376
    8131 1-8130 and 8132-8376
    8132 1-8131 and 8133-8376
    8133 1-8132 and 8134-8376
    8134 1-8133 and 8135-8376
    8135 1-8134 and 8136-8376
    8136 1-8135 and 8137-8376
    8137 1-8136 and 8138-8376
    8138 1-8137 and 8139-8376
    8139 1-8138 and 8140-8376
    8140 1-8139 and 8141-8376
    8141 1-8140 and 8142-8376
    8142 1-8141 and 8143-8376
    8143 1-8142 and 8144-8376
    8144 1-8143 and 8145-8376
    8145 1-8144 and 8146-8376
    8146 1-8145 and 8147-8376
    8147 1-8146 and 8148-8376
    8148 1-8147 and 8149-8376
    8149 1-8148 and 8150-8376
    8150 1-8149 and 8151-8376
    8151 1-8150 and 8152-8376
    8152 1-8151 and 8153-8376
    8153 1-8152 and 8154-8376
    8154 1-8153 and 8155-8376
    8155 1-8154 and 8156-8376
    8156 1-8155 and 8157-8376
    8157 1-8156 and 8158-8376
    8158 1-8157 and 8159-8376
    8159 1-8158 and 8160-8376
    8160 1-8159 and 8161-8376
    8161 1-8160 and 8162-8376
    8162 1-8161 and 8163-8376
    8163 1-8162 and 8164-8376
    8164 1-8163 and 8165-8376
    8165 1-8164 and 8166-8376
    8166 1-8165 and 8167-8376
    8167 1-8166 and 8168-8376
    8168 1-8167 and 8169-8376
    8169 1-8168 and 8170-8376
    8170 1-8169 and 8171-8376
    8171 1-8170 and 8172-8376
    8172 1-8171 and 8173-8376
    8173 1-8172 and 8174-8376
    8174 1-8173 and 8175-8376
    8175 1-8174 and 8176-8376
    8176 1-8175 and 8177-8376
    8177 1-8176 and 8178-8376
    8178 1-8177 and 8179-8376
    8179 1-8178 and 8180-8376
    8180 1-8179 and 8181-8376
    8181 1-8180 and 8182-8376
    8182 1-8181 and 8183-8376
    8183 1-8182 and 8184-8376
    8184 1-8183 and 8185-8376
    8185 1-8184 and 8186-8376
    8186 1-8185 and 8187-8376
    8187 1-8186 and 8188-8376
    8188 1-8187 and 8189-8376
    8189 1-8188 and 8190-8376
    8190 1-8189 and 8191-8376
    8191 1-8190 and 8192-8376
    8192 1-8191 and 8193-8376
    8193 1-8192 and 8194-8376
    8194 1-8193 and 8195-8376
    8195 1-8194 and 8196-8376
    8196 1-8195 and 8197-8376
    8197 1-8196 and 8198-8376
    8198 1-8197 and 8199-8376
    8199 1-8198 and 8200-8376
    8200 1-8199 and 8201-8376
    8201 1-8200 and 8202-8376
    8202 1-8201 and 8203-8376
    8203 1-8202 and 8204-8376
    8204 1-8203 and 8205-8376
    8205 1-8204 and 8206-8376
    8206 1-8205 and 8207-8376
    8207 1-8206 and 8208-8376
    8208 1-8207 and 8209-8376
    8209 1-8208 and 8210-8376
    8210 1-8209 and 8211-8376
    8211 1-8210 and 8212-8376
    8212 1-8211 and 8213-8376
    8213 1-8212 and 8214-8376
    8214 1-8213 and 8215-8376
    8215 1-8214 and 8216-8376
    8216 1-8215 and 8217-8376
    8217 1-8216 and 8218-8376
    8218 1-8217 and 8219-8376
    8219 1-8218 and 8220-8376
    8220 1-8219 and 8221-8376
    8221 1-8220 and 8222-8376
    8222 1-8221 and 8223-8376
    8223 1-8222 and 8224-8376
    8224 1-8223 and 8225-8376
    8225 1-8224 and 8226-8376
    8226 1-8225 and 8227-8376
    8227 1-8226 and 8228-8376
    8228 1-8227 and 8229-8376
    8229 1-8228 and 8230-8376
    8230 1-8229 and 8231-8376
    8231 1-8230 and 8232-8376
    8232 1-8231 and 8233-8376
    8233 1-8232 and 8234-8376
    8234 1-8233 and 8235-8376
    8235 1-8234 and 8236-8376
    8236 1-8235 and 8237-8376
    8237 1-8236 and 8238-8376
    8238 1-8237 and 8239-8376
    8239 1-8238 and 8240-8376
    8240 1-8239 and 8241-8376
    8241 1-8240 and 8242-8376
    8242 1-8241 and 8243-8376
    8243 1-8242 and 8244-8376
    8244 1-8243 and 8245-8376
    8245 1-8244 and 8246-8376
    8246 1-8245 and 8247-8376
    8247 1-8246 and 8248-8376
    8248 1-8247 and 8249-8376
    8249 1-8248 and 8250-8376
    8250 1-8249 and 8251-8376
    8251 1-8250 and 8252-8376
    8252 1-8251 and 8253-8376
    8253 1-8252 and 8254-8376
    8254 1-8253 and 8255-8376
    8255 1-8254 and 8256-8376
    8256 1-8255 and 8257-8376
    8257 1-8256 and 8258-8376
    8258 1-8257 and 8259-8376
    8259 1-8258 and 8260-8376
    8260 1-8259 and 8261-8376
    8261 1-8260 and 8262-8376
    8262 1-8261 and 8263-8376
    8263 1-8262 and 8264-8376
    8264 1-8263 and 8265-8376
    8265 1-8264 and 8266-8376
    8266 1-8265 and 8267-8376
    8267 1-8266 and 8268-8376
    8268 1-8267 and 8269-8376
    8269 1-8268 and 8270-8376
    8270 1-8269 and 8271-8376
    8271 1-8270 and 8272-8376
    8272 1-8271 and 8273-8376
    8273 1-8272 and 8274-8376
    8274 1-8273 and 8275-8376
    8275 1-8274 and 8276-8376
    8276 1-8275 and 8277-8376
    8277 1-8276 and 8278-8376
    8278 1-8277 and 8279-8376
    8279 1-8278 and 8280-8376
    8280 1-8279 and 8281-8376
    8281 1-8280 and 8282-8376
    8282 1-8281 and 8283-8376
    8283 1-8282 and 8284-8376
    8284 1-8283 and 8285-8376
    8285 1-8284 and 8286-8376
    8286 1-8285 and 8287-8376
    8287 1-8286 and 8288-8376
    8288 1-8287 and 8289-8376
    8289 1-8288 and 8290-8376
    8290 1-8289 and 8291-8376
    8291 1-8290 and 8292-8376
    8292 1-8291 and 8293-8376
    8293 1-8292 and 8294-8376
    8294 1-8293 and 8295-8376
    8295 1-8294 and 8296-8376
    8296 1-8295 and 8297-8376
    8297 1-8296 and 8298-8376
    8298 1-8297 and 8299-8376
    8299 1-8298 and 8300-8376
    8300 1-8299 and 8301-8376
    8301 1-8300 and 8302-8376
    8302 1-8301 and 8303-8376
    8303 1-8302 and 8304-8376
    8304 1-8303 and 8305-8376
    8305 1-8304 and 8306-8376
    8306 1-8305 and 8307-8376
    8307 1-8306 and 8308-8376
    8308 1-8307 and 8309-8376
    8309 1-8308 and 8310-8376
    8310 1-8309 and 8311-8376
    8311 1-8310 and 8312-8376
    8312 1-8311 and 8313-8376
    8313 1-8312 and 8314-8376
    8314 1-8313 and 8315-8376
    8315 1-8314 and 8316-8376
    8316 1-8315 and 8317-8376
    8317 1-8316 and 8318-8376
    8318 1-8317 and 8319-8376
    8319 1-8318 and 8320-8376
    8320 1-8319 and 8321-8376
    8321 1-8320 and 8322-8376
    8322 1-8321 and 8323-8376
    8323 1-8322 and 8324-8376
    8324 1-8323 and 8325-8376
    8325 1-8324 and 8326-8376
    8326 1-8325 and 8327-8376
    8327 1-8326 and 8328-8376
    8328 1-8327 and 8329-8376
    8329 1-8328 and 8330-8376
    8330 1-8329 and 8331-8376
    8331 1-8330 and 8332-8376
    8332 1-8331 and 8333-8376
    8333 1-8332 and 8334-8376
    8334 1-8333 and 8335-8376
    8335 1-8334 and 8336-8376
    8336 1-8335 and 8337-8376
    8337 1-8336 and 8338-8376
    8338 1-8337 and 8339-8376
    8339 1-8338 and 8340-8376
    8340 1-8339 and 8341-8376
    8341 1-8340 and 8342-8376
    8342 1-8341 and 8343-8376
    8343 1-8342 and 8344-8376
    8344 1-8343 and 8345-8376
    8345 1-8344 and 8346-8376
    8346 1-8345 and 8347-8376
    8347 1-8346 and 8348-8376
    8348 1-8347 and 8349-8376
    8349 1-8348 and 8350-8376
    8350 1-8349 and 8351-8376
    8351 1-8350 and 8352-8376
    8352 1-8351 and 8353-8376
    8353 1-8352 and 8354-8376
    8354 1-8353 and 8355-8376
    8355 1-8354 and 8356-8376
    8356 1-8355 and 8357-8376
    8357 1-8356 and 8358-8376
    8358 1-8357 and 8359-8376
    8359 1-8358 and 8360-8376
    8360 1-8359 and 8361-8376
    8361 1-8360 and 8362-8376
    8362 1-8361 and 8363-8376
    8363 1-8362 and 8364-8376
    8364 1-8363 and 8365-8376
    8365 1-8364 and 8366-8376
    8366 1-8365 and 8367-8376
    8367 1-8366 and 8368-8376
    8368 1-8367 and 8369-8376
    8369 1-8368 and 8370-8376
    8370 1-8369 and 8371-8376
    8371 1-8370 and 8372-8376
    8372 1-8371 and 8373-8376
    8373 1-8372 and 8374-8376
    8374 1-8373 and 8375-8376
    8375 1-8374 and 8376
    8376 1-8375
  • Thus the invention includes each of the 35074500 possible pairs of SEQ IDs 1-8376 (1&2, 1&3, 1&4, 1&5 . . . 1&8375, 1&8376, 2&3, 2&4, 2&5 . . . 2&8375, 2&8376, 3&4 . . . 1000&1001, 1000&1002 . . . 1000&8376 . . . 8374&8375, 8374&8376, 8373&8376) although, for reasons of space, these are not listed in full here.
  • Details as to how the molecules which make up the SEQ IDs 1-4056 can be produced and used can be found from the relevant international applications and these details need not be repeated here. Similar principles apply to SEQ IDs 4057-8376.
  • SEQ IDs 1-8376 in the compositions of the invention may he supplemented or substituted with molecules comprising sequences homologous (ie. having sequence identity) to SEQ IDs 1-8376. Depending on the particular sequence, the degree of identity is preferably greater than 50% (eg. 65%, 80%, 90%, or more), and include mutants and allelic variants. Sequence identity between the proteins is preferably determined by the Smith-Waterman homology search algorithm as implemented in the MPSRCH program (Oxford Molecular), using an affine gap search with parameters gap open penalty=2 and gap extension penalty=1.
  • SEQ IDs 1-8376 in the compositions of the invention may be supplemented or substituted with molecules comprising fragments of SEQ IDs 1-8376. Such fragments should comprise at least n consecutive monomers from the molecules and, depending on the particular sequence, n is either (i) 7 or more for protein molecules (eg. 8, 10, 12, 14, 16, 18, 20 or more), preferably such that the fragment comprises an epitope from the sequence, or (ii) 10 or more for nucleic acid molecules ( eg 12, 14, 15, 18, 20, 25. 30, 35, 40 or more).
  • Where the composition includes a protein that exists in different nascent and mature forms, the mature form of the protein is preferably used. For example, the mature form of the NspA protein (SEQ IDs 4008-4033: WO096/29412: FIG. 29) lacking the signal peptide may be used.
  • In the case of protein molecules. SEQ IDs 1-8376 in the compositions of the invention may be supplemented or substituted with an antibody that binds to the protein. This antibody may be monoclonal or polyclonal.
  • In the case of nucleic acid molecules. SEQ IDs 1-8376 in the compositions of the invention may be supplemented or substituted with nucleic acid which can hybridise to the Neisserial nucleic acid, preferably under “high stringency” conditions (eg. 65° C. in a 0.1×SSC. 0.5% SDS solution).
  • It will be appreciated that any nucleic acid in the compositions can take various forms (eg. single stranded, double stranded, vectors, probes etc.). In addition, the term “nucleic acid” includes DNA and RNA, and also their analogues, such as those containing modified backbones, and also peptide nucleic acids (PNA) etc.
  • In certain embodiments, the composition comprises molecules from different Neisseria species, such as one or more N. meningitidis molecule and one or more N. gonorrhoeae molecule. In some embodiments, the composition may comprise molecules from different serogroups and/or strains of the same species, such as strains A and B of N. meningitidis. Further embodiments comprise mixtures of one or more N. meningitidis molecules from different strains and also one or more N. gonorrhoeae molecules.
  • Many proteins are relatively conserved between different species, serogroups and strains of N. meningitidis and N. gonorrhoeae (eg. SEQ IDs 52, 54, 58). PCT/IB00/00642 includes a more detailed experimental analysis of conserved regions in these proteins. To ensure maximum cross-strain recognition and reactivity, regions of proteins that are conserved between different Neisserial species, serogroups and strains can he used in the compositions of the present invention. The invention therefore provides proteins which comprise stretches of amino acid sequence that are shared across the majority of Neisseria. particularly N. meningitidis and N. gonorrhoeae. Preferably, therefore, the composition comprises a protein comprising a fragment of a Neisserial protein (preferably a protein from SEQ IDs 1-8376, or more preferably SEQ IDs 1-4002), wherein said fragment consists of n consecutive conserved amino acids. Depending on the particular protein, u is 7 or more (eg. 8, 10, 12, 14, 16, 18, 20 or more). The fragment preferably comprises an antigenic or immunogenic region of the Neisserial protein. A “conserved” amino acid is one that is present in a particular Neisserial protein in at least x% of Neisseria (or, preferably, in at least of combined N. meningitidis and N. gonorrhoeae strains). The value of x may be 50% or more eg. 66%, 75%, 80%, 90%, 95% or even 100% (ie. the amino acid is found in the protein in question in all Neisseria). In order to determine whether an amino acid is “conserved” in a particular Neisserial protein, it is necessary to compare that amino acid residue in the sequences of the protein in question from a plurality of different Neisseria (a “reference population”). Suitable definitions of “reference populations” can be found in PCT/IB00/00642. Amino acid sequences of different Neissieriae can easily be compared using computers. This will typically involve the alignment of a number of sequences using an algorithm such as CLUSTAL [Thompson el al. (1994) Nucleic Acids Res 22:4673-4680: Trends Biochem Sci (1998) 23:403-405] or, preferably. PILEUP [part of the GCG Wisconsin package, preferably version 9.0]. Conserved amino acids are readily apparent in a multiple sequence alignment—at the amino acid position in question a majority of the aligned sequences will contain a particular amino acid. Conserved amino acids can he made more visually apparent by using a program such as BOXSHADE [available, for instance, at the NIH on-line], PRETTYBOX [GCG Wisconsin, version 10] or JALVIEW [available on-line at EBI].
  • Specific compositions according to the invention therefore include those comprising:
      • two or more biological molecules selected from SEQ IDs 1-4002:
      • one or more biological molecules selected from SEQ IDs 1-4002 combined with one or more biological molecules selected from SEQ IDs 4003-8376:
      • one or more biological molecules selected from SEQ IDs 1-4002 combined with the NspA protein as disclosed in WO96/29412: see also FIG. 29 herein), preferably in mature form:
      • one or more biological molecules selected from SEQ IDs 1-8376 (preferably SEQ IDs 1-4002) combined with transferring binding protein A (TbpA) and/or B (TbpB), such as the TbpA and TbpB disclosed in WO00/25811 (or immunogenic fragments thereof).
      • one or more fragments of proteins selected from SEQ IDs 1-4002, with the fragment preferably comprising a stretch of conserved amino acids;
      • a combination of different proteins, wherein the combination as a whole includes one or more proteins that is recognised by each strain in a reference population, although each individual protein in the combination may not itself be recognised by each strain in the reference population ie. each member of a reference population recognises at least one protein in the combination.
  • The invention also provides the compositions of the invention for use as medicaments (eg. as immunogenic compositions or vaccines) or as diagnostic reagents. It also provides the use of the compositions in the manufacture of: (i) a medicament for treating or preventing infection due to Neisserial bacteria: (ii) a diagnostic reagent for detecting the presence of Neisserial bacteria or of antibodies raised against Neisserial bacteria; and/or (iii) a reagent which can raise antibodies against Neisserial bacteria.
  • The invention also provides a method of treating a patient, comprising administering to the patient a therapeutically effective amount of a composition according to the invention.
  • The invention further provides a process for producing a composition according to the invention, comprising the step of bringing one or more of SEQ IDs 1-8376 into combination with one or more other of SEQ IDs 1-8376.
    • BRIEF DESCRIPTION OF THE DRAWINGS
  • FIGS. 1A-1B shows SDS-PAGE results for the expression of ORFs 6, 7, 13, 65-1, 72, 73-1, 105-1, 137-1, 143-1 and 147-1. The left-hand lanes show molecular weight markers (set M1).
  • FIGS. 2A-2C shows (FIG. 2A) SDS-PAGE results for ORF9 (FIG. 2B) the positions of the N. meningitidis immunoreactive band in a Western blot against a N. meningitidis outer membrane vesicle preparation (FIG. 2C) FACS analysis.
  • FIG. 3 shows SDS-PAGE results for the expression of ORFs 2-1, 5-1, 22-1, 132-1 and 4. The left-hand lanes show molecular weight markers (set M1).
  • FIGS. 4 to 28 show a hydrophilicity plot (upper), antigenic index (middle), and AMPHI regions (lower) for ORFs 2, 5, 6, 7, 9, 13a, 15, 22, 23, 27, 28, 32, 65, 72, 73, 76, 79, 89, 105, 106-1, 132, 137, 138, 143 and 147.
  • FIGS. 29A-29C shows sequence variability of NspA from various strains of meningococeus B. These sequences may he used as alternatives to the NspA of WO 96/29412 (SEQ IDs 4008-4033).
  • FIGS. 30A-30B shows the binding of polyclonal anti-rNspA by indirect fluorescence flow cytometry to encapsulated and non-encapsulated menB strains. FIGS. 31A-31E shows similar data for encapsulated strains 8047. CU385 & M986 (FIGS. 31A-31B) and non-encapsulated strains BZ232. MC58, NG3/88 & NGB 165 (FIGS. 31C-E).
  • FIG. 32 shows a model of NspA secondary structure.
  • FIGS. 33A-33I shows FACS analysis of non-encapsulated strain M7 (FIG. 33A) ethanol-treated (to disrupt the capsule) strains 2996, N44776, MC58, 1000, BZ232, BZ133, NG6/88, BZ198, NG3/88, 297-0, BZ147 and BZ169 (FIGS. 33B-33I).
  • FIGS. 34A-34C shows FACS analysis of M7 strain using a pentavalent mixture at 1:400 (FIG. 34A), 1:200 (FIG. 34B), & 1:100 (FIG. 34C) dilutions.
  • FIGS. 35A-35B show FACS for the individual antigens 287, 919, and 953 and combinations thereof.
    •  EXAMPLES Example 1 Expressing and Purification Experiments
  • ORFs 6, 7, 13, 65-1, 72, 73-1, 105-1, 137-1, 143-1 and 147-1 disclosed in WO99/24578 were expressed in E. coli and purified, as set out in the following table:
  • ORF His-fusion GST-fusion Purification MW (kDa)
     6 + GST-fusion 23
     7 + + GST-fusion 28
     13 + GST-fusion 10
     65-1 + UST-fusion 32
     72 + His-fusion 13.5
     73-1 + GST-fusion 13
    105-1 + + His-fusion 32
    137-1 + GST-fusion 31
    143-1 + + His-fusion 23.5
    147-1 − + His-fusion 32
    NOTE:
    ORF73-1 was expressed as a fragment (amino acids 41-161)
  • The protocols used to express these ten ORFs were essentially the same as those described in WO99/24578, using pGEX and pET vectors. Examples of the PCR primers used to amplify the ORFs are in the following table:
  • Restriction
    ORF Primer Sequence sites
    ORF65-1 Forward CGCGGATCCCATATG- BamHI-NdeI
    TTTATGAACAAATTTT
    CC
    Reverse CCCGCTCGAG-TTTGC XhoI
    TTTCGATAGAACGG
    ORF73-1 Forward CGCGGATCCCATATG- BamHI-NdeI
    GCCGGCGTGCTGATG
    Reverse CCCGCTCGAG-TTCAT XhoI
    CTTTTTCATGTTCG
    ORF105-1 Forward CGCGGATCCCATATG- BamHI-NdeI
    CCGACCGTCCGTT
    Reverse CCCGCTCGAG-TAAAC XhoI
    GAATGCCGTCCAG
    ORF143-1 Forward CGCGGATCCCATATG- BamHI-NdeI
    GAATCAACACTTTCAC
    Reverse CCCGCTCGAG-CACGC XhoI
    GGTTGCTGTAAC
    ORF147-1 Forward CCGGAATTCTACATAT EcoRI-NdeI
    G-TTTCAGAAACATTT
    GCAG
    Reverse CCCGCTCGAG-TTTGT XhoI
    TTTTCCAAGACAGAG
  • SDS-PAGE results :he ten expressed ORFs are shown in FIG. 1.
  • The ORF7-His fusion was used to immunise mice. The sera were used in an ELLSA assay, essentially as described in WO99 24578, and gave possitive results.
  • The following proteins were also expressed and purified results not shown:
  • Expressed Fragment
    His-fusion GST-fusion as a amino acid
    ORF expression expression fragment positions
    orf1 (s) - - -   43-1087
    orf1 (β) n.d. - - 1051-1457
    orf35-1 - - -
    orf41 n.d. n.d. -  25-619
    orf46 - - -  25-433
    orf61 n.d. n.d. -   1-575
    orf83-1 - - -  15-313
    orf100-1 n.d. - -  21-376
    orf114-1 n.d. - -    1-1423
    orf124-1 n.d. n.d. -
    orf131-1 n.d. - -  22-135
  • The following PCR primers were used to amplify these ORFs:
  • Restriction
    ORF Primer Sequence sites
    ORF1 (s) Forward CGCGGATCCGCTAGC- BamHI-NheI
    GGACACACTTATTTCG
    G
    Reverse CCCGCTCGAG-CAGCG XhoI
    CGTCAAGGCTT
    ORF1 (β) Forward CGCGGATCCGCTAGC- BamHI-NheI
    GAGTTCCGCCTGCATA
    A
    Reverse CCCGCTCGAG-CCAGC XhoI
    GGTAGCCTAATT
    ORF35-1 Forward CGCGGATCCGCTAGC- BamHI-NheI
    AGGGGCGACGACGTG
    Reverse CCCGCTCGAG-AAACA XhoI
    GCCATTTGAGCGA
    ORF41 Forward CGCGGATCCCATATG- BamHI-NdeI
    TATTTGAAACAGCTCC
    AAG
    Reverse CCCGCTCGAG-TTCTG XhoI
    GGTGAATGTTA
    ORF46 Forward CGCGGATCCCATATG- BamHI-NdeI
    TCAGATTTGGCAAACG
    ATC
    Reverse CCCGCTCGAG-CGTAT XhoI
    CATATTTCACGTGC
    ORF61 Forward CGCGGATCCGCTAGC- BamHI-NheI
    ACGGTTTTGAAGCTTT
    CGC
    Reverse CCCGCTCGAG-AATGA XhoI
    CGAGGTTGTCCG
    ORF83-1 Forward CGCGGATCCCATATG- BamHI-NdeI
    TGCGGCACACTGACCG
    Reverse CCCGCTCGAG-GCCGC XhoI
    CTTTGCGGC
    ORF100-1 Forward CGCGGATCCCATATG- BamHI-NdeI
    TCGGGCATTTACACCG
    G
    Reverse CCCGCTCGAG-TTCGT XhoI
    CGAAAACCTTTGC
    ORF114-1 Forward CGCGGATCCCATATG- BamHI-NdeI
    AATAAAGGTTTACATC
    GCAT
    Reverse CCCGCTCGAG-AATCG XhoI
    CTGCACCGGCT
    ORF124-1 Forward CGCGGATCCCATATG- BamHI-NdeI
    ACTGCCTTTTCGACA
    Reverse CCCGCTCGAG-GCGTG XhoI
    AAGCGTCAGGA
    ORF131-1 Forward CGCGGATCCCATATG- BamHI-NdeI
    TGCCGGCTGGCGGG
    Reverse CCCGCTCGAG-CCAGC XhoI
    GGACGCGTTC
  • Each of these ORFs can be combined with one or more of SEQ IDs 1-8376.
    • Example 2 ORF9 Expression and Purification
  • ORF9 disclosed in WO99/24578 was cloned in the pET vector and expressed in E. coli. The purified ORF-His fusion protein was analysed by SDS-PAGE, as shown in FIG. 2A. Mice were immunised with the purified ORF9-His and sera were used Western blot analysis (FIG. 2B). FACS analysis FIG. 2C), and ELISA assay. The protocols used were essentially the same as those set out in WO99/24578.
  • The results confirm that ORF9 is a surface-exposed protein, ORF9 is suitable for combining with one or more other of SEQ IDs 1-8376.
    • Example 3 Further Expression Experiments
  • Further expression and purification experiments were carried out in E. coli for ORFs 2-1, 5-1, 22-1 and 132-1 disclosed in WO99/74578, as set out in the following table:
  • His-fusion GST-fusion Expressed as a Fragment amino
    ORF expression expression fragment acid positions
    orf1 (s) — — —  43-1087
    orf1 (β) n.d. — — 1051-1457
    orf35-1 — — —
    orf41 n.d. n.d. —  25-619
    orf46 — — —  25-433
    orf61 n.d. n.d. —   1-575
  • The protocols used to express these four ORFs were essentially the same as those described in WO99/24578. using pGEX and pET vectors. Examples of the PCR primers used to amplify the ORFs are in the following table:
  • Restriction
    ORF Printer Sequence sites
    ORF5-1 Forward CGCGGATCCGCTAGC- BamHI-NheI
    GACGGCGCACAACCGA
    Reverse CCCGCTCGAG-TGTTT XhoI
    GGCGGATGGGG
    ORF22-1 Forward CGCGGATCCCATATG- BamHI-NdeI
    ATTAAAATCAAAAAAG
    GTC
    Reverse CCCGCTCGAG-GCCTT XhoI
    CCTTCTCAATGG
    ORF132-1 Forward CGCGGATCCCATATG- BamHI-NdeI
    AAAGAAGCGGGGTTTG
    AA
    Reverse CCCGCTCGAG-TCTCA XhoI
    AAGCTTCCAGCAG
  • SDS-PAGE results for the four expressed ORFs are shown in FIG. 3.
  • Each of these ORFs can be combined with one or more of SEQ IDs 1-8376.
    • Example 4 ORF4 Lipoprotein Expression and Purification
  • ORF-4 is disclosed in WO99/24578 as containing a lipopeptide signal sequence (LPSS). The full length ORF was amplified using the following PCR primers:
  • orf4-L for
    CGCGGATCCCATATGAAAACCTTCTTCAAAACC
    orf4-L rev
    CCCGCTCGAGTTATTTGGCTGCGCCTTC
  • The amplified DNA fragment was cloned into the vector pET21b+ for expression as a C-terminus His-tagged fusion. A log phase culture of E. coli containing pET21b+orf4-LPSS was induced with 1.0 mM IPTF for 3 h at 30° C. collected by centrifugation for 10 min at 8000 g, and resuspended in PBS. The suspension was sonicated on ice and Triton X-114 added to a final concentration of 0.6% (v/v). The material was incubated on ice for 20 minutes then warmed to 37° C. until phase separation occurred (indicated by a high degree of cloudiness). After centrifugation for 10 min at 10,000 g at 20° C. the upper aqueous phase was discarded, and the lower detergent phase collected without disrupting the bacterial pellet. To the detergent phase was added 13 volumes of 20 mM Histidine, 2 mM EDTA, 30 mM NaCl (pH 5.8). This was centrifuged for 10 min at 4° C. and the supernatant combined batchwise at 4° C. for 30 min. with Q Sepharose Fast Flow resin (Pharmacia). The mixture was centrifuged, the supernatant retained and the resin washed with 20 mM Histidine, 2mM EDTA, 30 mM NaCl (pH 5.8). Triton X-100 0.3% (v/v) and eluted with 1 M NaCl in the same buffer. The majority of Orf4 lipoprotein was found in the supernatant obtained after binding. Final purification was accomplished by chromatography on Hi-Trap™ O (Pharmacia). The binding-supernatant was adjusted to pH 7.0 by the addition of 0.1M HCl and applied to a Hi-Trap™ Q column equilibrated with 50 mM Tris-HCl (pH 7.0). 2 mM EDTA, 0.3% Triton X-100. 10 mM NaCl. The column was washed with 5.0 ml of the equilibration buffer and a NaCl gradient from 10 mM to 1M was applied. Two electrophoretically distinct forms of the protein eluted. One in the wash and the other in the NaCl gradient between 150 mM, and 300 mM NaCl. The protein obtained in the wash was used for immunization of mice. This form of the protein probably represents the fully processed, lipidated molecule.
  • The 31 kDa purified lipoprotein can be seen in FIG. 3, ORF4 is suitable for combining with one or more other of SEQ IDs 1-8376.
    • Example 5 Computer Prediction
  • Computer analysis of ORFs 2, 5, 6a, 7, 9, 13a, 15, 22, 23, 27, 28, 32, 65, 72, 73, 76, 79, 89, 105, 106-1, 132, 137, 138, 143 and 147 as disclosed in WO99/24578) was performed. FIGS. 4 to 28 show, for each of these ORFs, a hydrophilicity plot (upper), an antigenic index plot (middle), and an AMPHI analysis (lower). The AMPHI program has been used to predict T-cell epitopes [Gao et al. (1989) J. Immunol. 143:3007; Roberts et al. (1996) AIDS Res Hum Retrovir 12:593; Quakyi et al. (1992) Scand J Immunol suppl.11:9) and is available in the Protean package of DNASTAR. Inc. (1228 South Park Street. Madison, Wis. 53715 USA).
  • Each of these ORFs can be combined with one or more other of SEQ IDs 1-8376.
    • Example 6 Tetravalent Mixture
  • A mixture of proteins 919 (WO99/57280), 225 (WO99/57280), ORF4 (WO99/24578, example 26) and ORF40 (WO99/36544, example 1) was produced and assessed by ELISA and FACS. The ELISA titres against 13 test strains were as follows:
  •
    Strain M7 conF 2996 MC58 BZ133 BZ232 H44/76 1000
    Titre 38176 7892 17216 41488 17945 83990 6575
    Strain BZ198 NG6/88 BZ169 BZ147 NG3/88 297-0
    Titre 3329 59275 — — 12877 25640
  • The FACS results are shown in FIG. 33. It is evident that the tetravalent mixture gives excellent results, regardless of the particular menB strain used. In addition, antisera raised against the mixture in strain 2996 is bactericidal at up to 1:2048 dilution.
    • Example 7 Pentavalent Mixture
  • A mixture of proteins ORF4-L (the lipidated protein—see example 4 above). ORF37 (WO99/24578, example 1). ORF40 (WO99/36544, example 1), 502 (WO99/57280, pages 687-690) and 8 (WO99/57280, pages 165-167) was produced, The ELISA titres against 13 test strains were as follows:
  •
    Strain M7 conF 2996 MC58 BZ133 BZ232 H44/76 1000
    Titre — — 25428 — 58300 >109350 >109350
    Strain BZ198 NG6/88 BZ169 BZ147 NG3/88 297-0
    Titre 10999 109532 42888 28324 104212 33996
  • The FACS results are shown in FIG. 34. It is evident that the pentavalent mixture gives excellent results, regardless of the particular menB strain used. In addition, antisera raised against the mixture in strain 2996 is bacteriostatic.
    • Example 8 Trivalent Mixture
  • Proteins ORF1 (e.g. example 77 of WO99/24578: see also WO99/55873), ‘287’ (e.g. FIG. 21 of WO99/57280; also SEQ IDs 3103-3108 therein) and ‘919’ (e.g. WO99/57280 FIG. 23 and SEQ IDs 3069-3074 therein) were combined and adjuvanted with Al(OH)3. The proteins were from the 2996 strain of MenB.
  • This mixture was also combined with a MenC polysaccharide conjugate antigen [e.g. Costantino el al. (1992) Vaccine 10:691-698]. OMVs were used as controls.
  • The mixture was used in a bactericidal assay against the homologous strain and also heterologous MenB strains. Titres were as follows:
  • 2996 BZ133 BZ232 1000 MC58 NGH38
    Trivalent 2048 2048 4 <4 64 4
    +MenC 2048 >32000 4 128 1024 128
    Control 32765 4096 8192 16384 16384 8192
    • Example 9 Proteins 287, 919 and 953
  • Proteins 287, 919 and 953 are disclosed in WO99/57280. These proteins from N. meningitidis serogroup B strain 2996 were expressed and tested in a bactericidal assay against strain 2996, alone and in combinations. OMVs from 2996 were used as a positive control.
  • Antigen 287 919 953 Control
    Titre 8192 2048 128 65536
    Combination 287 + 919 287 + 953 919 + 953 287 + 919 + 953
    Titre 32000 8192 8192 8192
  • FIG. 35 shows FACS data for the individual antigens and for the four combinations.
  • It is evident that the antigen mixtures are more effective than the antigens in isolation on and, in particular, that combinations of 919+953 give surprisingly good results.
  • The individual antigens from 2996 and combinations were also tested against different serogroup A, B & C strains (i.e. heterologous challenge). Bactericidal titres were as follows:
  • Serogroup B (MenB) strains MenA MenC
    Antigen
    2996 BZ133 BZ232 MC58 NGH38 F6124 C11
    287 8192 >4096 256 1024 2048 1024 2048
    919 2048 — 1024 — — — —
    953 128 — — — — — —
    287 + 919 32000 >4096 512  512 1024 512 >2048
    287 + 953 8192 >4096 1024  512 2048 2048 >2048
    919 + 953 8192 — 8192 — — — —
    Trivalent 8192 >2048 256 — 1024 >2048 >2048
    Control 65536 — 8192 2048 — 2048 32768
  • It is apparent that the antigen mixtures are useful in conferring cross-strain activity.
  • In a second set of experiments, titres for the individual antigens were as follows:
  • Serogroup B (MenB) strains MenA MenC
    Antigen
    2996 BZ133 BZ232 MC58 NGH38 F6124 C11
    287 16000 2048 16 512 >2048 64 1024
    919 16000 — 2048 — — — —
    953 2048 — 16 — — — —
  • The three proteins used in this example were expressed and used in the following forms:
      • (1) Protein 287 was expressed in E. coli as a GST fusion:
      • (2) Protein 919 was expressed in E. coli without its leader peptide, without its mature N-terminal cysteine, and without any fusion partners (“919-untag”); and
      • (3) Protein 953 was expressed using a histidine tag.
  • Three immunisations were administered with Freund's adjuvants—the first included CFA, and the final two included WA.
    • Example 10 further Polyvalent Combinations
  • Further combinations of antigens were tested in CD1 mice:
  • Bactericidal
    Antigens * Adjuvant FACS ELISA acitivity
    919-his + Orf4-his + Freund +++ + 8192
    225-his + Orf40-his
    Orf-4-L + Orf37-GST + Freund +++ + Bacteriostatic
    Orf40-his + 502-his + 8-his
    919-untag + 791-his + Freund +++ + 4096
    792-his
    919-untag + 287-GST + Freund +++ + 8192
    953-his
    919-untag + 287-GST Freund +++ + 32000
    287-GST + 953-his Freund +++ + 8192
    919-untag + 953-his Freund +++ + 8192
    919-untag + Orf1-his + Al(OH)3 +++ + 2048
    287-GST
    919-untag + Orf1-his + 287- Al(OH)3 +++ + 2048
    GST + MenC glycoconj.
    Orf-46.1-his + 287-GST Al(OH)3 n.d. + 128
    * : “his” indicates expression and immunisation with a histidine-tagged protein;
    “ORF4-L” is the lipidated form of ORF4;
    “GST” indicates expression and immunisation with a GST fusion protein;
    “919-untag” is as defined in Example 9;
    “MenC glycoconj” is the MenC glycoconjugate described in Example 8.
  • Further combinations of antigens were tested in guinea pigs:
  • Bactericidal
    Antigens Adjuvant FACS ELISA activity
    919-his + 287-GST + 953- Freund + + 4096
    his + Orf46.1-his
    919-untage + 287-GST + 953-his Freund + + 4096
    287-GST + 953-his Al(OH)3 n.d. + 256
  • Evidently the combinations give excellent immunological results.
    • Example 11 NspA Combinations
  • NspA protein is disclosed in WO96/29412, and is represented herein as SEQ IDs 4008-4033. The academic literature disclosure of this protein [Martin et al. (1997) Exp. Med 185 1173-1183] reported the protein to be highly conserved between Neisseria strains (99% cross-reactivity of anti-NspA antibodies with 250 meningococcal A, B & C strains) and also efficient protection against deadly challenge with live bacteria. There have also been reports that NspA adsorbed on alum elicits serum meningococcal bactericidal antibody responses in rabbits and monkeys [Martin et al. (1998) Abstracts of 11th International pathogenic Neisseria conference, page 198]. On the basis of these data, rNspA (recombinant NspA) is being developed as a vaccine for the prevention of meningococcal disease caused by all serogroups.
  • Despite sequence conservation, however, it has surprisingly been discovered that rNspA cell surface epitopes are detected on only 65% of the serogroup B strains tested below, and susceptibility to anti-NspA bactericidal activity is also less than that reported by Martin et al. These results contrast with Martin et al., and suggest that a rNspA-based meningococcal B vaccines will need to be supplemented with additional antigens in order to be effective.
  • The N. meningitidis strains tested in this example were isolated from patients residing in different countries over a period of more than 30 years (see table on page 72). These strains were selected to be representative of widely divergent ‘clonal’ groups, as defined by multilocus isoenzyme typing [Seiler et al. (1996) Mol. Microbiol. 19:841-856] and/or multilocus sequence typing [Maiden et al. (1998) PNAS USA 95:3140-45]. Strain M7, which is derived from strain NMB, contains a transposon insertion that blocks capsular polysaccharide biosynthesis [Stephens et al. (1991) Infect. Immun. 59:4097-4102], but all the other strains are encapsulated.
  • Based on the nucleotide sequence in Martin et al. (1997), PCR primers were designed and the NspA gene from strain 8047 was amplified. The sequence, including the promoter region, was cloned into pSK+ plasmid (rNspA). A plasmid pTrc.NspA.1 encoding a protein in which a portion of the signal sequence has been replaced with a poly-histidine tag was also used. Both plasmids were expressed in E. coli strain BL21(DE3) and the proteins were purified. In E. coli, rNspA is secreted, rather than being associated with the outer membrane. The protein was partially purified from the culture medium by precipitation with 55% w/v ammonium sulphate, and had an apparent MW of 18.6 kDa, confirmed by Western Blot.
  • The two forms of NspA (rNspA and denature His-tage NspA) were injected into 6-week old female CD-1 mice to raise antisera. The ability of these to bind to the surface of N. meningitidis strain B was determined using flow cytometric detection of indirect fluorescence assay [Granoff et at (1998) J. Immunol 160:5028-36]. The results for strains NMB and M7 (an acapsulated mutant of NMB) are shown in FIG. 30. As expected, anti-group B polysaccharide mAb SEAM-3 [Granoff et al] only binds to the encapsulated strain, whereas the positive anti-P1.2 (PorA) control mAb binds to both strains. The antisera raised against rNspA is able to bind both strains. Antisera against the His-tag NspA gave negative results, however. These antisera were also negative for strains 8047. CU385 and M986 (FIG. 31A), but by Western Blot these antisera gave positive results.
  • These data suggest that antibodies prepared using His-tag NspA recognise epitopes that are present in denatured NspA, but not native NspA as found on the cell-surface in vivo. In contrast, antibodies prepared against rNspA seem to recognise conformational NspA epitopes.
  • The flow cytometric assay was applied to the strains shown in the table on page 72. FIG. 31A shows that murine antibodies raised against rNspA bind to the surface of strain 8047 (the strain from which the nspA gene was cloned) and strain CU385, but not to M986, FIG. 31B shows similar negative results for strains BZ232, MC58, NG3/88 and N(31)165. In all of these negative cases, however, the anticapsular mAb control was positive.
  • The table on page 72 summarises the flow cytometry results. Although NspA is reported o be accessible at the surface of all intact N. meningitidis strains tested [Martin et al. (1997) J. Exp. Med 185 1173-1183: Plante et al. (1999) Infect. Immun. 67:2855-61], only 11 of the 17 test strains (65%) reacted with the anti-rNspA sera. There was no apparent relationship between cell-surface expression in a given strain and classification (by serotype, subtype, or electrophoretic type), or with year or country of isolation.
  • In an attempt to explain the differences in reactivity with the anti-rNspA sera, the nspA genes from five of the six negative strains (BX232, NG3/88, NGP165. M136 & M986) and from three of the positive strains (8047, CU385 & NG6/88) were sequenced. The sequence for the sixth negative strain (MC58) was already available from the complete genome sequence.
  • The nspA sequences for all ten strains were highly conserved, varying at most by 5 nucleotides from the prototype sequence of Martin et al. The most variant protein had only 3 amino acid differences (see FIG. 29). With one exception, all of the amino acid variants involved the same respective residues in discrete segments of the protein. These include the signal peptide, which is not present in the mature protein, and two short segments in the 50 C-terminal residues. These differences do not explain the antisera results, as there are examples of identical variant sequences in strains that were positive and those that were negative (compare M136 & 8047; NGI'165 & NG6/88; MC58 & CU385).
  • As neither lack of the gene nor polymorphism explained the antiserum results, the amount of NspA protein in the outer membranes of five strains (8047, CU385 & NG6/88—all positive for anti-rNspA; M986 & M136—both negative) were tested. Bacterial cell pellets were extracted with lauryl sarcosinate, and the insoluble outer membrane fractions were analysed. An 18.6 kDa band was seen for all five strains, and this was cross-reactive with anti-His-tag-NspA by Western Blot. Thus strain differences in nspA expression also failed to explain the results.
  • The ability of anti-rNspA to bind to the bacterial cell surface could be influenced by the amount of polysaccharide capsule present. The quantity of capsular polysaccharide produced by the 17 test strains was therefore assessed by inhibition ELISA.
  • Extracts of capsular polysaccharide were prepared based on a method described by Corn et al. [J. Infect. Dis. (1993) 167:356-64]. Individual bacterial clones were grown to an OD620 0.5-0.7 in 7 mL of Mueller-Hinton broth. Bacteria were collected by centrifugation at 5000 g for 15 min, washed in 0.6 mL of 10 mM Hepes, pH 8.0, and then resuspended in 0.6 mL of the same buffer containing 10 mM EDTA and incubated at 37° C. for 1 hr. The cells were pelleted at 10,000 g for 1 minute and the relative amount of meningococcal B polysaccharide antigen released into the supernatant was determined by an inhibition ELISA, performed as described by Azmi et al. [Infect. Immun. (1995) 63:1906-13]. The solid phase antigen in the ELISA was meningococcal B polysaccharide-ADH-biotin absorbed to avidin-coated microtiter plates [Granoff et al.]. The meningococcal B polysaccharide-reactive human paraprotein LIP [Azmi et al.] was used as the primary antibody (0.2 μg/ml). In the absence of inhibitor, this concentration of antibody was sufficient to given an OD of ˜0.7 to 1.0 after 30 minutes incubation with substrate [Azmi et al.] The titre of polysaccharide released into the supernatant was measured by determining the dilution of supernatant that resulted in 50% inhibition of antibody binding. Controls in this assay included an EDTA extract prepared from the strain M7, which does not produce any capsular polysaccharide, and purified meningococal B polysaccharide. To ensure that all of the capsular polysaccharide was released by the EDTA treatment, the same inhibition ELISA was performed using the cell pellet resuspended in the same buffer and volume as the capsule extract. The observable inhibitory activity from the cell pellet was between 0 and 10% of the activity observed in the capsule extracts with the latter, higher percentage coming from cell pellets of strains that produce the largest amounts of capsule.
  • The results for each strain are shown in the table on page 72. On average, the six negative anti-rNspA, strains produced three-fold more capsular polysaccharide than the eleven positive strains (respective reciprocal geometric mean dilutions of 676 vs 224, p<0.05). This may explain the results obtained with the antiserum—conceivably, the presence of larger amounts of capsule could interfere with the ability of the anti-rNspA antibody to bind to NspA epitopes which, in strains with lower amounts of capsule, are accessible.
  • The complement-dependent bactericidal activity of the anti-rNspA antisera were tested using an assay similar to that described by Mandrell et al. [J. Infect. Dis. (1995) 172:1279-89]. The complement source was human serum from a healthy adult with no detectable anti-capsular antibody to group B polysaccharide and no intrinsic bactericidal activity against the test strain. Serum bactericidal titres were defined as the serum dilution resulting in a 50% decrease in CFU/ml after 60 minutes incubation of bacteria in the reaction mixture, compared to the control CFU/ml at time zero.
  • Typically, bacteria incubated with a negative control antibody showed a 150-200% increase in CFU/ml during the 60 minutes of incubation. The positive control antibody [anti-capsular IgG2a mAb SEAM 12, Granoff et al.] showed complement-mediated bactericidal activity against all 17 strains. In contrast, the six strains that were negative for anti-rNspA antisera binding by flow assay were resistant, showing no bactericidal or bacteriostatic effects. Ten of the other eleven positive strains were either killed by complement and the antisera (SWZ107, J351, CU385, NG6/88, BZ198, H44/76, NMB & 8047) or were inhibited (H355 & S3446); strain 1000, however, was not affected.
  • The ability of the anti-rNspA antisera to confer passive protection against meningococcal B bacteremia was tested in infant rats using a method adapted from Saukkonen [J. Infect. Dis. (1988) 158:209-212]. Briefly, 6-7 day old rats were randomly distributed to nursing mothers. Groups of 5-6 animals were challenged IP with 100 μl of approximately 5000 CFU of N. meningitidis group B bacteria. One strain negative for NspA surface epitopes (M986) and one positive strain (8047) were tested, each of which having been passaged three times in infant rats. Immediately before administration, the bacterial suspension was mixed with different dilutions of test or control antibody (positive control: anticapsular mAb; negative control: anti-E. coli). 18 hours after challenge, blood specimens were obtained from the heart. Aliquots were plated onto chocolate agar, and CFU/ml was determined after overnight incubation at 37° C. in 5% CO2.
  • The protective activities of the various co-administered antibodies were as follows:
  • Dose per Blood culture
    rat CFU/ml CFU/ml
    Antibody or serum Positive/ (mean × (% of
    treatment dilution Strain total 10−3) control)
    Anticapsular mAb 2 μg M986 0/6 <1 <1
    Anti-rNspA 1:5 M986 6/6  44a 45
    Anti-rNspA 1:25 M986 6/6  93a 95
    Anti-E.coli 1:5 M986 6/6  98a —
    control
    Anticapsular mAb
    2 μg 8047 0/5 <1 <1
    Anti-rNspA 1:5 8047 1/6 0.2b 2
    Anti-rNspA 1:25 8047 1/5 0.4b 4
    Anti-E.coli 1:5 8047 6/6  10b —
    control
    ap > 0.5, compared to geometric mean CFU/ml of control rats
    bp < 0.001, compared to geometric mean CFU/ml of control rats
  • As can be seen, a dose of 2 μg per rat of the positive anticapsular control was protective against both strains. A 1:5 or 1:25 dilution of anti-rNspA antiserum protected against bacteremia caused by strain 8047. Neither dilution was effective in preventing M986 bacteremia, however.
  • Despite the positive conclusions of Martin et al., therefore, NspA does not seem to be effective in preventing meningococcal B infection. Approximately one third of strains have decreased cell-surface expression of NspA epitopes when grown in vitro, are resistant to anti-NspA induced complement-mediated bacteriolysis, and are resistant to passive antiserum immunisation. These strains produce large amounts of capsular polysaccharide, and would thus be expected to have the greatest virulence. The ability of a vaccine containing only NspA to confer broad protective immunity against meningococcal B thus has to be doubted.
  • Compositions comprising NspA [SEC) IDs 4008-4033; FIG. 29] therefore advantageously comprise further antigens. A preferred aspect of the invention is thus a combination of NspA protein with one or more further Neisserial antigens.
    • Example 12 NspA Fragments
  • A model of the secondary structure of NspA is shown in FIG. 32, containing eight transmembrane β-strands and 4 surface-exposed connecting loops. This fits the pattern of alternating hydrophobic and hydrophilic amino acids in NspA, which is characteristic of many β-barrel porins [Weiss et al. (1990) FEBS Letts 267:268-272]
  • The grey shaded areas in the model indicate segments that are >40% identical and >70% similar to encoded amino acid sequences of opacity proteins (Opa) from N. meningitidis, N. gonorrhoeae, N. flavius, N sicca. and H. Influenzae identified in a BLAST search of the non-redundant GenBank CDS. The alternating sequences are predicted amphiphilic β-strands; vertical segments correspond to transmembrane segments; the top of the figure corresponds to surface exposed segments, labelled as loops 1 to 4.
  • According to Martin et al., the only significant homology between the deduced amino acid sequence of NspA and those of other proteins are weak homologies with the Neisseria opacity protein (Opa) family in two small segments (˜20 amino acids) near the C-terminal end of the protein. However, separate comparisons of the N- and C-termini of NspA with GenBank reveals a high degree of homology (>40% identity and >70% similarity) between NspA and Opa proteins from N. meningitidis, N. gonorrhoeae, N. flavius, N. sicca, and H. influenzae. The Opa proteins are thought to he integral membrane proteins that have eight transmembrane segments and a β-barrel topology in the membrane similar to that of porin [Merker et al. (1997) Mol. Microbial. 23:281-293]. The presence of NspA in detergent-insoluble membrane preparations indicate that NspA is located in the outer membrane, which would be consistent with the Opa-like membrane topology shown in the model. In addition, the segments of NspA that are most homologous to those of the Opa proteins are the putative transmembrane segments indicated in the shaded areas of FIG. 32.
  • The opacity proteins of Neisseria can, under certain circumstances, elicit protective antibody. However, problems with limited antibody accessibility of the opacity proteins in encapsulated bacteria, variability of amino acid sequences in exposed loop segments, and phase variation of protein expression during clinical infection, have limited the ability of Opa to elicit protective antibody consistently [Maloniy et al, (1998) J. infect, Dis. 172:1279-89]. In contrast, there appears to be little or no sequence variation in the surface exposed loops of NspA in FIG. 32. However, it was recently reported that a panel of anti-N. meningitidis NspA monoclonal antibodies that reacted with all meningococcal strains tested reacted with only a limited number of N. gonorrhoeae strains, even though the respective amino acid sequences in the two species are 92% identical. When the respective NspA sequences of the meningococcal and gonococcal strains are compared (FIG. 29), all of the respective amino acid differences result in changes in hydrophobicity or charge, and are located in the putative surface exposed connecting loops (FIG. 32). This finding suggests that the connecting loops in NspA, which are highly conserved in N. meningitidis, may be important epitopes for antibodies that bind to native NspA. These segments of the molecule, therefore, would appear to be of greatest interest with respect to interacting with protective antibody. However, the putative surface loops of NspA are relatively small (10-14 amino acids) compared to, for example, the highly immunogenic external loops of PorA and ON (24 to 45 amino acids). The shorter length of the loops may limit the accessibility of NspA surface epitopes for binding interactions with serum antibody, especially in the presence of abundant capsular polysaccharide.
  • Accordingly, the invention provides the fragments of NspA that are exposed on the cell-surface in FIG. 32, namely SSSLGSAKG, NYKAPSTDFKLY, NRASVDLGGSDSFSQT and NYIGKVNTVKNVRSG, and also provides corresponding fragments from allelic variants of NspA. In addition, the invention provides sub-sequences of these fragments, comprising 7 or more contiguous amino acids from the fragments. The invention further provides proteins comprising these fragments. Nucleic acid encoding these fragments and proteins is also provided.
  • These NspA fragments, proteins comprising the fragments, and nucleic acid, may be used in the compositions of the invention, in particular as substitutes for full-length NspA. In a further aspect, these fragments, proteins and nucleic acids may be used as products in isolation, that is to say they need not exclusively be used in combination with other biological molecules.
  • It will be appreciated that the invention has been described by means of example only, and that modifications may be made whilst remaining within the spirit and scope of the invention.
  • Reactivity of anti-rNspA polyclonal antisera with native NspA exposed on the surface of live, encapsulated, Neisseria meningitidis B bacteria in relation to susceptibility to bacteriolvsis and cansular production.
  • Polysaccharide
    Meningococcal B Strains NspA Cell Anti-rNspA Capsule
    Serologic Surface Bactericidal Production
    Strain Country Year Classification ET Complex Reactivity c Activity d (l/titer) (l/titer ± SE)
    SWZ107 a Switzerland 1980 4: P1.2 104 Positive ≧64 28 ± 4
    NG6/88 a Norway 1988 NT: P1.1 173 Positive 4 115 ± 23
    CU385 b Cuba 1980 4: P1.15 5 Positive 4 116 ± 1 
    IH5341 Finland 1985 15: P1.7.16 ND Positive 16 176 ± 61
    BZ198 Netherlands 1986 NT: P- 154 Positive ≧64 362 ± 1 
    NMB US 1968 2b: P1.2, 5 ND Positive 16 244 ± 20
    8047 US 1978 2b: P1.2 ND Positive 16 1125 ± 50 
    H44/76 Norway 1976 15: P1.7, 16 5 Positive 24  99 ± 16
    1000 d USSR 1989 NT: P1.5 61 Positive <4 287 ± 12
    S3446 b US 1972 14: P1.23, 14 11 (A1 cluster) Positive <4 (static = 16)  585 ± 151
    H355 b Norway 1973 15: P1.15 11 cluster Positive <4 (static = 4)   656 ± 141
    BZ232 a Netherlands 1964 NT: P1.2 76 Negative <4 1493 ± 18 
    NG3/88 a Norway 1988 8: P1.1 A4 cluster Negative <4  498 ± 105
    MC58 UK 1985 15: P1.7, 16b 5 Negative <4  627 ± 121
    M136 b US 1968 11: P1.15 D1 cluster Negative <4 1056 ± 81 
    M986 b US 1963 2a: P1.5, 2 B2 cluster Negative <4 1442 ± 206
    NGP165 Norway 1974 NT: P1.2 37 Negative <4 138 ± 6 
    a Denotes strains that have been characterized further by multilocus sequence typing [Maiden, 1998].
    b Denotes strains obtained from the Frasch collection, US FDA. 8047 was obtained from W. Zollinger, Walter Reed Army Institute of Research, Washington, D.C. MC58 is the strain selected by TIGR for genomic sequencing. J351 was obtained from M. Sarvas, National Public Health Institute, Helsinki, Finland. The remaining strains are from the collection described by Seiler et al. [Seiler, 1996]. ET data are from Caugnant et al. [j. Infect. Dis. (1990) 162: 867-874], and Seiler et al.
    c By indirect fluorescence flow cytometry with anti-rNspA antisera.
    d Dilution of anti-rNspA antisera that when incubated for 60 min. with bacterial cells and 20% human complement yielded ≧50% decrease in CFU/ml, compared to that at time 0. “Static” refers to strains that were inhibited but not killed in the assay (≧50% but <100% survival at 60 mins).
    e Titre defined as dilution of capsule extract giving 50% inhibition of antibody binding to meningococcal B polysaccharide antigen in an ELISA.

Claims (31)

1. (canceled)
2. A method of inducing a bactericidal immune response in an animal, comprising administering to the animal a composition which comprises
(a) an immunologically effective amount of a protein lacking an N-terminal cysteine having at least 95% identity to the amino acid sequence of the mature form of SEQ ID NO: 3518; and
(b) an immunologically effective amount of an N. meningitidis protein comprising an amino acid sequence having at least 90% sequence identity to SEQ ID NO: 7645.
3. The method of claim 2, wherein the composition consists essentially of (a) and (b).
4. The method of claim 2, wherein the composition does not further comprise a protein having an amino acid sequence of at least 80% identity to SEQ ID NO: 3516.
5. The method according to claim 2, wherein the protein lacking an N-terminal cysteine is a recombinant protein.
6. The method according to claim 2, wherein the protein lacking an N-terminal cysteine is expressed as a fusion protein.
7. The method according to claim 2, wherein the protein lacking the N-terminal cysteine is fused to a GST protein or a HIS-tag.
8. The method according to claim 2, wherein the protein lacking an N-terminal cysteine and the N. meningitidis protein are from different strains of Neisseria meningitidis.
9. The method according to claim 2, wherein the composition additionally comprises an adjuvant or buffer suitable for a medicament.
10. The method according to claim 2, wherein the composition additionally comprises an adjuvant.
11. The method according to claim 2, wherein the composition further comprises aluminum hydroxide.
12. The method according to claim 2, wherein the composition further comprises a third Neisseria meningitidis biological molecule different than (a) and (b).
13. The method according to claim 2, wherein the composition is administered by injection.
14. The method according to claim 2, wherein the composition is a vaccine.
15. The method according to claim 2, wherein the animal is a human patient.
16. A method of eliciting bactericidal antibodies against N. meningitidis bacteria in an animal, comprising administering to the animal a composition which comprises
(a) an immunologically effective amount of a protein lacking an N-terminal cysteine having at least 95% identity to the amino acid sequence of the mature form of SEQ ID NO: 3518; and
(b) an immunologically effective amount of an N. meningitidis protein comprising an amino acid sequence having at least 90% sequence identity to SEQ ID NO: 7645.
17. The method according to claim 16, wherein the composition consists essentially of (a) and (b).
18. The method according to claim 16, wherein the composition does not comprise a protein having an amino acid sequence of at least 80% identity to SEQ ID NO: 3516 obtained from strain 2996.
19. The method according to claim 16, wherein the protein lacking an N-terminal cysteine is expressed as a fusion protein.
20. The method according to claim 16, wherein the protein lacking an N-terminal cysteine and the N. meningitidis protein are from different strains of Neisseria meningitidis.
21. The method according to claim 16, wherein the composition additionally comprises an adjuvant or buffer suitable for a medicament.
22. The method according to claim 16, wherein the composition further comprises aluminum hydroxide.
23. The method according to claim 16, wherein the composition further comprises a third Neisseria meningitidis biological molecule different than (a) and (b).
24. The method according to claim 16, wherein the composition is administered by injection.
25. The method according to claim 16, wherein the composition is a vaccine.
26. The method according to claim 16, wherein the animal is a human patient.
27. A method of eliciting bactericidal antibodies against N. meningitidis bacteria in an animal, comprising administering by injection to the animal a composition which comprises
(a) an immunologically effective amount of a protein lacking an N-terminal cysteine having at least 95% identity to the amino acid sequence of the mature form of SEQ ID NO: 3518; and
(b) an immunologically effective amount of an N. meningitidis protein comprising an amino acid sequence having at least 90% sequence identity to SEQ ID NO: 7645,
(c) a buffer suitable for a medicament, and
(d) aluminum hydroxide,
wherein the protein lacking an N-terminal cysteine and the N. meningitidis protein are from different strains of Neisseria meningitidis, thereby eliciting bactericidal antibodies against Neisseria meningitidis bacteria in the animal.
28. The method of claim 27, wherein the immune response induced by the protein lacking an N-terminal cysteine is bactericidal against at least three strains of Neisseria meningitidis in the animal, thereby eliciting bactericidal antibodies against at least three strains of Neisseria meningitidis in the animal.
29. The method according to claim 27, wherein the composition consists essentially of (a) and (b).
30. The method according to claim 27, wherein the composition does not further comprise a protein having an amino acid sequence of at least 80% identity to SEQ ID NO: 3516.
31. The method according to claim 27, wherein the composition does not comprise a protein having an amino acid sequence of at least 80% identity to SEQ ID NO: 3516 obtained from strain 2996.
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