Skip to main content
Journal of Virology logoLink to Journal of Virology
. 1976 Sep;19(3):1073–1079. doi: 10.1128/jvi.19.3.1073-1079.1976

Equine infectious anemia virus: evidence favoring classification as a retravirus.

H P Charman, S Bladen, R V Gilden, L Coggins
PMCID: PMC354947  PMID: 61283

Abstract

Equine infectious anemia virus (EIAV) has a density of 1.154 g/cm3 in sucrose a high-molecular-weight RNA similar in size to Rauscher murine leukemia virus, and an internal virion reverse transcriptase that utilizes the synthetic RNA template poly(rA) but not the synthetic DNA template poly(dA), both with (dT)12 as primer. Although capable of utilizing manganese at low concentrations (approximately 0.1 mM), EIAV reverse transcriptase showed highest activity in the presence of 9 mM magnesium. The major protein of EIAV has a slightly lower molecular weight than the comparable protein of type C viruses and co-electrophoresed with 125I-labeled p25 of Mason-Pfizer monkey virus. A reference horse serum with antibodies to the major EIAV protein reacted only with EIAV and not with other type C or non-type C retraviruses. Reciprocally, a broadly reactive serum to type C virus p30s and specific sera to a variety of non-type C retraviruses did not react with EIAV. We recommend the inclusion of EIAV in the family Retraviridae.

Full text

PDF
1073

Images in this article

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Charman H. P., Gardner M. B., McAllister R. M., Kim N., Gilden R. V. Humoral immune responses of cats to mammalian type-C virus p30s. Int J Cancer. 1976 Jan 15;17(1):98–108. doi: 10.1002/ijc.2910170114. [DOI] [PubMed] [Google Scholar]
  2. Charman H. P., Kim N., Gilden R. V., Hardy W. D., Jr, Essex M. Humoral immune responses of cats to feline leukemia virus: comparison of responses to the major structural protein p30 and to a virus-specific cell membrane antigen (FOCMA). J Natl Cancer Inst. 1976 Apr;56(4):859–861. doi: 10.1093/jnci/56.4.859. [DOI] [PubMed] [Google Scholar]
  3. Charman H. P., Kim N., White M., Marquardt H., Gilden R. V., Kawakami T. Natural and experimentally induced antibodies to defined mammalian type-C virus proteins in primates. J Natl Cancer Inst. 1975 Dec;55(6):1419–1424. doi: 10.1093/jnci/55.6.1419. [DOI] [PubMed] [Google Scholar]
  4. Coggins L., Norcross N. L., Nusbaum S. R. Diagnosis of equine infectious anemia by immunodiffusion test. Am J Vet Res. 1972 Jan;33(1):11–18. [PubMed] [Google Scholar]
  5. Dailey M. O., Hunter R. L. The role of lipid in the induction of hapten-specific delayed hypersensitivity and contact sensitivity. J Immunol. 1974 Apr;112(4):1526–1534. [PubMed] [Google Scholar]
  6. Dalton A. J., Heine U. I., Melnick J. L. Symposium: characterization of oncornaviruses and related viruses--a report. J Natl Cancer Inst. 1975 Oct;55(4):941–943. doi: 10.1093/jnci/55.4.941. [DOI] [PubMed] [Google Scholar]
  7. Diglio C. A., Ferrer J. F. Induction of syncytia by the bovine C-type leukemia virus. Cancer Res. 1976 Mar;36(3):1056–1067. [PubMed] [Google Scholar]
  8. Fine D. L., Landon J. C., Pienta R. J., Kubicek M. T., Valerio M. G., Loeb W. F., Chopra H. C. Responses of infant rhesus monkeys to inoculation with Mason-Pfizer monkey virus materials. J Natl Cancer Inst. 1975 Mar;54(3):651–658. [PubMed] [Google Scholar]
  9. Fuccillo D. A., Kurent J. E., Sever J. L. Slow virus diseases. Annu Rev Microbiol. 1974;28(0):231–234. doi: 10.1146/annurev.mi.28.100174.001311. [DOI] [PubMed] [Google Scholar]
  10. GREENWOOD F. C., HUNTER W. M., GLOVER J. S. THE PREPARATION OF I-131-LABELLED HUMAN GROWTH HORMONE OF HIGH SPECIFIC RADIOACTIVITY. Biochem J. 1963 Oct;89:114–123. doi: 10.1042/bj0890114. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Gardner M. B., Henderson B. E., Officer J. E., Rongey R. W., Parker J. C., Oliver C., Estes J. D., Huebner R. J. A spontaneous lower motor neuron disease apparently caused by indigenous type-C RNA virus in wild mice. J Natl Cancer Inst. 1973 Oct;51(4):1243–1254. doi: 10.1093/jnci/51.4.1243. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Gilden R. V., Long C. W., Hanson M., Toni R., Charman H. P., Oroszlan S., Miller J. M., Van der Maaten M. J. Characteristics of the major internal protein and RNA-dependent DNA polymerase of bovine leukaemia virus. J Gen Virol. 1975 Dec;29(3):305–314. doi: 10.1099/0022-1317-29-3-305. [DOI] [PubMed] [Google Scholar]
  13. Haase A. T., Baringer J. R. The structural polypeptides of RNA slow viruses. Virology. 1974 Jan;57(1):238–250. doi: 10.1016/0042-6822(74)90124-x. [DOI] [PubMed] [Google Scholar]
  14. Hardy W. D., Jr, Hess P. W., MacEwen E. G., McClelland A. J., Zuckerman E. E., Essex M., Cotter S. M., Jarrett O. Biology of feline leukemia virus in the natural environment. Cancer Res. 1976 Feb;36(2 Pt 2):582–588. [PubMed] [Google Scholar]
  15. Howk R. S., Rye L. A., Killeen L. A., Scolnick E. M., Parks W. P. Characterization and separation of viral DNA polymerase in mouse milk. Proc Natl Acad Sci U S A. 1973 Jul;70(7):2117–2121. doi: 10.1073/pnas.70.7.2117. [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. Hruska J. F., Takemoto K. K. Biochemical properties of a hamster syncytium-forming ("foamy") virus. J Natl Cancer Inst. 1975 Mar;54(3):601–605. [PubMed] [Google Scholar]
  17. Hunter R. L., Strickland F. Immunization with a lipid-conjugated membrane antigen to suppress growth of a fibrosarcoma induced by simian virus 40. J Natl Cancer Inst. 1975 May;54(5):1157–1163. doi: 10.1093/jnci/54.5.1157. [DOI] [PubMed] [Google Scholar]
  18. Ihle J. N., Hanna M. G., Jr, Roberson L. E., Kenney F. T. Autogenous immunity to endogenous RNA tumor virus. Identification of antibody reactivity to select viral antigens. J Exp Med. 1974 Jun 1;139(6):1568–1581. doi: 10.1084/jem.139.6.1568. [DOI] [PMC free article] [PubMed] [Google Scholar]
  19. Kemen M. J., Jr, Coggins L. Equine infectious anemia: transmission from infected mares to foals. J Am Vet Med Assoc. 1972 Sep 1;161(5):496–499. [PubMed] [Google Scholar]
  20. Malmquist W. A., Barnett D., Becvar C. S. Production of equine infectious anemia antigen in a persistently infected cell line. Arch Gesamte Virusforsch. 1973;42(4):361–370. doi: 10.1007/BF01250717. [DOI] [PubMed] [Google Scholar]
  21. Michalides R., Schlom J., Dahlberg J., Perk K. Biochemical properties of the bromodeoxyuridine-induced guinea pig virus. J Virol. 1975 Oct;16(4):1039–1050. doi: 10.1128/jvi.16.4.1039-1050.1975. [DOI] [PMC free article] [PubMed] [Google Scholar]
  22. Nakajima H., Tanaka S., Ushimi C. Physicochemical studies of equine infectious anemia virus. IV. Determination of the nucleic acid type in the virus. Arch Gesamte Virusforsch. 1970;31(3):273–280. doi: 10.1007/BF01253762. [DOI] [PubMed] [Google Scholar]
  23. Nakajima H., Yoshino T., Ushimi C. Equine infectious anemia virus from infected horse serum. Infect Immun. 1974 Sep;10(3):667–668. doi: 10.1128/iai.10.3.667-668.1974. [DOI] [PMC free article] [PubMed] [Google Scholar]
  24. Norcross N. L., Coggins L. Characterization of an equine infectious anemia antigen extracted from infected horse spleen tissue. Infect Immun. 1971 Nov;4(5):528–531. doi: 10.1128/iai.4.5.528-531.1971. [DOI] [PMC free article] [PubMed] [Google Scholar]
  25. Okabe H., Gilden R. V., Hatanaka M. RD 114 virus-specific sequences in feline cellular RNA: detection and characterization. J Virol. 1973 Nov;12(5):984–994. doi: 10.1128/jvi.12.5.984-994.1973. [DOI] [PMC free article] [PubMed] [Google Scholar]
  26. Okabe H., Gilden R. V., Hatanaka M. Specificity of the DNA product of RNA-dependent DNA polymerase in type C viruses: 3. Analysis of viruses derived from Syrian hamsters. Proc Natl Acad Sci U S A. 1974 Aug;71(8):3278–3282. doi: 10.1073/pnas.71.8.3278. [DOI] [PMC free article] [PubMed] [Google Scholar]
  27. Oroszlan S., Summers M. R., Foreman C., Gilden R. V. Murine type-C virus group-specific antigens: interstrain immunochemical, biophysical, and amino acid sequence differences. J Virol. 1974 Dec;14(6):1559–1574. doi: 10.1128/jvi.14.6.1559-1574.1974. [DOI] [PMC free article] [PubMed] [Google Scholar]
  28. Scolnick E., Rands E., Aaronson S. A., Todaro G. J. RNA-dependent DNA polymerase activity in five RNA viruses: divalent cation requirements. Proc Natl Acad Sci U S A. 1970 Dec;67(4):1789–1796. doi: 10.1073/pnas.67.4.1789. [DOI] [PMC free article] [PubMed] [Google Scholar]
  29. Tajima M., Nakajima H., Ito Y. Electron microscopy of equine infectious anemia virus. J Virol. 1969 Oct;4(4):521–527. doi: 10.1128/jvi.4.4.521-527.1969. [DOI] [PMC free article] [PubMed] [Google Scholar]
  30. Tronick S. R., Stephenson J. R., Aaronson S. A. Immunological properties of two polypeptides of Mason-Pfizer monkey virus. J Virol. 1974 Jul;14(1):125–132. doi: 10.1128/jvi.14.1.125-132.1974. [DOI] [PMC free article] [PubMed] [Google Scholar]
  31. Umphenour N. W., Kemen M. J., Coggins L. Equine infectious anemia: a retrospective study of an epizootic. J Am Vet Med Assoc. 1974 Jan 1;164(1):66–69. [PubMed] [Google Scholar]
  32. Verma I. M., Meuth N. L., Fan H., Baltimore D. Hamster leukemia virus: lack of endogenous DNA synthesis and unique structure of its DNA polymerase. J Virol. 1974 May;13(5):1075–1082. doi: 10.1128/jvi.13.5.1075-1082.1974. [DOI] [PMC free article] [PubMed] [Google Scholar]
  33. Weber K., Osborn M. The reliability of molecular weight determinations by dodecyl sulfate-polyacrylamide gel electrophoresis. J Biol Chem. 1969 Aug 25;244(16):4406–4412. [PubMed] [Google Scholar]
  34. Yen J., Ahmed M., Lyles J., Larson D., Mayyasi S. A. Competition radioimmunoassay for mason-pfizer monkey virus: comparison with recent isolates. Int J Cancer. 1975 Apr 15;15(4):632–639. doi: 10.1002/ijc.2910150412. [DOI] [PubMed] [Google Scholar]

Articles from Journal of Virology are provided here courtesy of American Society for Microbiology (ASM)

RESOURCES