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. 1989 Nov;63(11):4932–4937. doi: 10.1128/jvi.63.11.4932-4937.1989

Characterization of a simian hepatitis A virus (HAV): antigenic and genetic comparison with human HAV.

E A Brown 1, R W Jansen 1, S M Lemon 1
PMCID: PMC251140  PMID: 2552172

Abstract

PA21, a strain of hepatitis A virus (HAV) recovered from a naturally infected captive owl monkey, is indistinguishable from human HAV in polyclonal radioimmunoassays and cross-neutralization studies. However, cDNA-RNA hybridization has suggested a significant difference at the genomic level between PA21 and a reference human virus, HM175. Further characterization of this unique HAV was undertaken in an effort to determine the extent of genetic divergence from human HAV and its relation to the conserved antigenic structure of the virus. The close similarity between PA21 and HM175 antigens was confirmed with an extended panel of 18 neutralizing murine monoclonal antibodies: a reproducible difference in binding to the two viruses was detected with only one antibody (B5-B3). The nucleotide sequence of the P1 region of the PA21 genome had only 83.2% identity with HM175 virus, a difference approximately twice as great as that found between any two human strains. Most nucleotide changes were in third base positions, and the amino acid sequences of the capsid proteins were largely conserved. Amino acid replacements were clustered in the carboxy terminus of VP1 and the amino-terminal regions of VP2 and VP1. These data indicate that PA21 virus represents a unique genotype of HAV and suggest the existence of an ecologically isolated niche for HAV among feral owl monkeys.

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Selected References

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  1. Binn L. N., Lemon S. M., Marchwicki R. H., Redfield R. R., Gates N. L., Bancroft W. H. Primary isolation and serial passage of hepatitis A virus strains in primate cell cultures. J Clin Microbiol. 1984 Jul;20(1):28–33. doi: 10.1128/jcm.20.1.28-33.1984. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Burke D. S., Heisey G. B. Wild Malaysian cynomolgus monkeys are exposed to hepatitis A virus. Am J Trop Med Hyg. 1984 Sep;33(5):940–944. doi: 10.4269/ajtmh.1984.33.940. [DOI] [PubMed] [Google Scholar]
  3. Cohen J. I., Rosenblum B., Ticehurst J. R., Daemer R. J., Feinstone S. M., Purcell R. H. Complete nucleotide sequence of an attenuated hepatitis A virus: comparison with wild-type virus. Proc Natl Acad Sci U S A. 1987 Apr;84(8):2497–2501. doi: 10.1073/pnas.84.8.2497. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Cohen J. I., Ticehurst J. R., Purcell R. H., Buckler-White A., Baroudy B. M. Complete nucleotide sequence of wild-type hepatitis A virus: comparison with different strains of hepatitis A virus and other picornaviruses. J Virol. 1987 Jan;61(1):50–59. doi: 10.1128/jvi.61.1.50-59.1987. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. De Chastonay J., Siegl G. Replicative events in hepatitis A virus-infected MRC-5 cells. Virology. 1987 Apr;157(2):268–275. doi: 10.1016/0042-6822(87)90269-8. [DOI] [PubMed] [Google Scholar]
  6. Deinhardt F. Hepatitis in primates. Adv Virus Res. 1976;20:113–157. doi: 10.1016/s0065-3527(08)60503-5. [DOI] [PubMed] [Google Scholar]
  7. Deinhardt F., Peterson D., Cross G., Wolfe L., Holmes A. W. Hepatitis in marmosets. Am J Med Sci. 1975 Jul-Aug;270(1):73–80. doi: 10.1097/00000441-197507000-00011. [DOI] [PubMed] [Google Scholar]
  8. Devereux J., Haeberli P., Smithies O. A comprehensive set of sequence analysis programs for the VAX. Nucleic Acids Res. 1984 Jan 11;12(1 Pt 1):387–395. doi: 10.1093/nar/12.1part1.387. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Diamond D. C., Wimmer E., von der Helm K., Deinhardt F. The genomic map of hepatitis A virus: an alternate analysis. Microb Pathog. 1986 Apr;1(2):217–219. doi: 10.1016/0882-4010(86)90023-9. [DOI] [PubMed] [Google Scholar]
  10. Dienstag J. L., Davenport F. M., McCollum R. W., Hennessy A. V., Klatskin G., Purcell R. H. Nonhuman primate-associated viral hepatitis type A. Serologic evidence of hepatitis A virus infection. JAMA. 1976 Aug 2;236(5):462–464. [PubMed] [Google Scholar]
  11. Dienstag J. L., Feinstone S. M., Purcell R. H., Hoofnagle J. H., Barker L. F., London W. T., Popper H., Peterson J. M., Kapikian A. Z. Experimental infection of chimpanzees with hepatitis A virus. J Infect Dis. 1975 Nov;132(5):532–545. doi: 10.1093/infdis/132.5.532. [DOI] [PubMed] [Google Scholar]
  12. Gubler U., Hoffman B. J. A simple and very efficient method for generating cDNA libraries. Gene. 1983 Nov;25(2-3):263–269. doi: 10.1016/0378-1119(83)90230-5. [DOI] [PubMed] [Google Scholar]
  13. Jansen R. W., Newbold J. E., Lemon S. M. Complete nucleotide sequence of a cell culture-adapted variant of hepatitis A virus: comparison with wild-type virus with restricted capacity for in vitro replication. Virology. 1988 Apr;163(2):299–307. doi: 10.1016/0042-6822(88)90270-x. [DOI] [PubMed] [Google Scholar]
  14. LeDuc J. W., Lemon S. M., Keenan C. M., Graham R. R., Marchwicki R. H., Binn L. N. Experimental infection of the New World owl monkey (Aotus trivirgatus) with hepatitis A virus. Infect Immun. 1983 May;40(2):766–772. doi: 10.1128/iai.40.2.766-772.1983. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. Lemon S. M., Binn L. N. Antigenic relatedness of two strains of hepatitis A virus determined by cross-neutralization. Infect Immun. 1983 Oct;42(1):418–420. doi: 10.1128/iai.42.1.418-420.1983. [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. Lemon S. M., Binn L. N. Serum neutralizing antibody response to hepatitis A virus. J Infect Dis. 1983 Dec;148(6):1033–1039. doi: 10.1093/infdis/148.6.1033. [DOI] [PubMed] [Google Scholar]
  17. Lemon S. M., Chao S. F., Jansen R. W., Binn L. N., LeDuc J. W. Genomic heterogeneity among human and nonhuman strains of hepatitis A virus. J Virol. 1987 Mar;61(3):735–742. doi: 10.1128/jvi.61.3.735-742.1987. [DOI] [PMC free article] [PubMed] [Google Scholar]
  18. Lemon S. M., Jansen R. W., Newbold J. E. Infectious hepatitis A virus particles produced in cell culture consist of three distinct types with different buoyant densities in CsCl. J Virol. 1985 Apr;54(1):78–85. doi: 10.1128/jvi.54.1.78-85.1985. [DOI] [PMC free article] [PubMed] [Google Scholar]
  19. Lemon S. M., LeDuc J. W., Binn L. N., Escajadillo A., Ishak K. G. Transmission of hepatitis A virus among recently captured Panamanian owl monkeys. J Med Virol. 1982;10(1):25–36. doi: 10.1002/jmv.1890100105. [DOI] [PubMed] [Google Scholar]
  20. Lemon S. M. Type A viral hepatitis. New developments in an old disease. N Engl J Med. 1985 Oct 24;313(17):1059–1067. doi: 10.1056/NEJM198510243131706. [DOI] [PubMed] [Google Scholar]
  21. Linemeyer D. L., Menke J. G., Martin-Gallardo A., Hughes J. V., Young A., Mitra S. W. Molecular cloning and partial sequencing of hepatitis A viral cDNA. J Virol. 1985 May;54(2):247–255. doi: 10.1128/jvi.54.2.247-255.1985. [DOI] [PMC free article] [PubMed] [Google Scholar]
  22. Minor P. D., Ferguson M., Evans D. M., Almond J. W., Icenogle J. P. Antigenic structure of polioviruses of serotypes 1, 2 and 3. J Gen Virol. 1986 Jul;67(Pt 7):1283–1291. doi: 10.1099/0022-1317-67-7-1283. [DOI] [PubMed] [Google Scholar]
  23. Najarian R., Caput D., Gee W., Potter S. J., Renard A., Merryweather J., Van Nest G., Dina D. Primary structure and gene organization of human hepatitis A virus. Proc Natl Acad Sci U S A. 1985 May;82(9):2627–2631. doi: 10.1073/pnas.82.9.2627. [DOI] [PMC free article] [PubMed] [Google Scholar]
  24. Nüesch J., Krech S., Siegl G. Detection and characterization of subgenomic RNAs in hepatitis A virus particles. Virology. 1988 Aug;165(2):419–427. doi: 10.1016/0042-6822(88)90585-5. [DOI] [PMC free article] [PubMed] [Google Scholar]
  25. Pattison C. P., Maynard J. E., Bryan J. S. Subhuman primate-associated hepatitis. J Infect Dis. 1975 Oct;132(4):478–478. doi: 10.1093/infdis/132.4.478. [DOI] [PubMed] [Google Scholar]
  26. Paul A. V., Tada H., von der Helm K., Wissel T., Kiehn R., Wimmer E., Deinhardt F. The entire nucleotide sequence of the genome of human hepatitis A virus (isolate MBB). Virus Res. 1987 Aug;8(2):153–171. doi: 10.1016/0168-1702(87)90026-8. [DOI] [PubMed] [Google Scholar]
  27. Ping L. H., Jansen R. W., Stapleton J. T., Cohen J. I., Lemon S. M. Identification of an immunodominant antigenic site involving the capsid protein VP3 of hepatitis A virus. Proc Natl Acad Sci U S A. 1988 Nov;85(21):8281–8285. doi: 10.1073/pnas.85.21.8281. [DOI] [PMC free article] [PubMed] [Google Scholar]
  28. Rico-Hesse R., Pallansch M. A., Nottay B. K., Kew O. M. Geographic distribution of wild poliovirus type 1 genotypes. Virology. 1987 Oct;160(2):311–322. doi: 10.1016/0042-6822(87)90001-8. [DOI] [PubMed] [Google Scholar]
  29. Robertson B. H., Brown V. K., Bradley D. W. Nucleic acid sequence of the VP1 region of attenuated MS-1 hepatitis A virus. Virus Res. 1987 Nov;8(4):309–316. doi: 10.1016/0168-1702(87)90003-7. [DOI] [PubMed] [Google Scholar]
  30. Sanger F., Nicklen S., Coulson A. R. DNA sequencing with chain-terminating inhibitors. Proc Natl Acad Sci U S A. 1977 Dec;74(12):5463–5467. doi: 10.1073/pnas.74.12.5463. [DOI] [PMC free article] [PubMed] [Google Scholar]
  31. Siegl G., Frösner G. G. Characterization and classification of virus particles associated with hepatitis A. I. Size, density, and sedimentation. J Virol. 1978 Apr;26(1):40–47. doi: 10.1128/jvi.26.1.40-47.1978. [DOI] [PMC free article] [PubMed] [Google Scholar]
  32. Smith M. S., Swanepoel P. J., Bootsma M. Hepatitis A in non-human primates in nature. Lancet. 1980 Dec 6;2(8206):1241–1242. doi: 10.1016/s0140-6736(80)92495-2. [DOI] [PubMed] [Google Scholar]
  33. Ticehurst J. R., Racaniello V. R., Baroudy B. M., Baltimore D., Purcell R. H., Feinstone S. M. Molecular cloning and characterization of hepatitis A virus cDNA. Proc Natl Acad Sci U S A. 1983 Oct;80(19):5885–5889. doi: 10.1073/pnas.80.19.5885. [DOI] [PMC free article] [PubMed] [Google Scholar]
  34. Weitz M., Siegl G. Variation among hepatitis A virus strains. I. Genomic variation detected by T1 oligonucleotide mapping. Virus Res. 1985 Dec;4(1):53–67. doi: 10.1016/0168-1702(85)90020-6. [DOI] [PubMed] [Google Scholar]

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