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Infection and immunity1979; 23(2); 472-478; doi: 10.1128/iai.23.2.472-478.1979

Specificity of response to viral proteins in horses infected with equine infectious anemia virus.

Abstract: Three structural proteins of equine infectious anemia virus were purified, labeled with 125I, and utilized in radioimmunoassays with horse sera and antisera to heterologous retroviruses. Whereas radioimmunoassay titers for the major protein, p25, were 500- to 1,000-fold higher than titers in immunodiffusion, for clinical purposes these two procedures were equivalent. Antibodies to two low-molecular-weight proteins, p12 and p10, were also found in infected horses, but with a lower frequency and lower titers. As a rule, only sera positive for p25 also contained antibody to p12 and p10. Antisera to the major structural protein of other retroviruses did not precipitate equine infectious anemia virus p25. These sera include antibody to mammalian type C viruses, bovine leukemia virus, visna virus, mouse mammary tumor virus, squirrel monkey retrovirus, and Mason-Pfizer monkey virus.
Publication Date: 1979-02-01 PubMed ID: 217831PubMed Central: PMC414189DOI: 10.1128/iai.23.2.472-478.1979Google Scholar: Lookup
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  • Journal Article
  • Research Support
  • U.S. Gov't
  • P.H.S.

Summary

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The given research focuses on exploring the effects of equine infectious anemia virus on horses. The study sheds light on the immune response of infected horses towards three structural proteins of the virus, with further comparison and assessment of diagnostic procedures.

Investigation with Viral Proteins

  • The researchers began by purifying three structural proteins of the equine infectious anemia virus. These proteins were then labeled with 125I, a radioactive isotope of iodine, to be used in further experimentation.
  • These labelled proteins were used in radioimmunoassays along with horse sera (the liquid part of blood after clotting) and antisera to heterologous retroviruses (antibodies formed against other types of retroviruses). This process ensured efficient detection and measurement of antibodies produced by the horses in response to the equine infectious anemia virus.

Results and Analysis

  • The researchers found that radioimmunoassay titers (the highest dilution of serum that still reacts to the virus) for the major viral protein, p25, were 500- to 1,000-fold higher than titers detected in immunodiffusion, a technique used to observe the reaction between an antigen (i.e., the virus) and its specific antibody.
  • However, despite this difference in magnitude, the research claims both procedures to be equivalent for clinical purposes. The likely interpretation here is that although radioimmunoassay appears more sensitive in detecting antibodies, both methods are equally useful in a clinical scenario for diagnosing equine infectious anemia virus.
  • The study also detected antibodies to two other low-molecular-weight proteins, p12 and p10, in infected horses. These antibodies were found with lower frequency and lower titers compared to the p25 protein.
  • A notable observation was that, typically, only the sera positive for p25 also contained antibodies for p12 and p10, suggesting an order or dependency in the horse’s immune response to these viral proteins.

Comparative Assessment

  • In the course of this study, the researchers observed that antisera, formed against the primary structural protein of other retroviruses, did not precipitate (bind to and precipitate out from the solution) equine infectious anemia virus p25.
  • This included antibodies to various viruses like mammalian type C viruses, bovine leukemia virus, visna virus, mouse mammary tumor virus, squirrel monkey retrovirus, and Mason-Pfizer monkey virus. This finding implies specificity in the immune response to the equine infectious anemia virus, underscoring the unique nature of its proteins, especially p25.

Cite This Article

APA
Charman H, Long C, Coggins L. (1979). Specificity of response to viral proteins in horses infected with equine infectious anemia virus. Infect Immun, 23(2), 472-478. https://doi.org/10.1128/iai.23.2.472-478.1979

Publication

ISSN: 0019-9567
NlmUniqueID: 0246127
Country: United States
Language: English
Volume: 23
Issue: 2
Pages: 472-478

Researcher Affiliations

Charman, H
    Long, C
      Coggins, L

        MeSH Terms

        • Animals
        • Antibodies, Viral / analysis
        • Equine Infectious Anemia / immunology
        • Horses
        • Immunodiffusion
        • Infectious Anemia Virus, Equine / immunology
        • Radioimmunoassay
        • Retroviridae / immunology
        • Viral Proteins / immunology

        References

        This article includes 30 references
        1. GREENWOOD FC, HUNTER WM, GLOVER JS. THE PREPARATION OF I-131-LABELLED HUMAN GROWTH HORMONE OF HIGH SPECIFIC RADIOACTIVITY.. Biochem J 1963 Oct;89(1):114-23.
          pubmed: 14097352doi: 10.1042/bj0890114google scholar: lookup
        2. Parker J, Pollard JW, Friesen JD, Stanners CP. Stuttering: high-level mistranslation in animal and bacterial cells.. Proc Natl Acad Sci U S A 1978 Mar;75(3):1091-5.
          pubmed: 349556doi: 10.1073/pnas.75.3.1091google scholar: lookup
        3. Charman HP, Bladen S, Gilden RV, Coggins L. Equine infectious anemia virus: evidence favoring classification as a retravirus.. J Virol 1976 Sep;19(3):1073-9.
          pubmed: 61283doi: 10.1128/JVI.19.3.1073-1079.1976google scholar: lookup
        4. O'Farrell PZ, Goodman HM, O'Farrell PH. High resolution two-dimensional electrophoresis of basic as well as acidic proteins.. Cell 1977 Dec;12(4):1133-41.
          pubmed: 23215doi: 10.1016/0092-8674(77)90176-3google scholar: lookup
        5. Hunter E, Bhown AS, Bennett JC. Amino-terminal amino acid sequence of the major structural polypeptides of avian retroviruses: sequence homology between reticuloendotheliosis virus p30 and p30s of mammalian retroviruses.. Proc Natl Acad Sci U S A 1978 Jun;75(6):2708-12.
          pubmed: 208072doi: 10.1073/pnas.75.6.2708google scholar: lookup
        6. Rice NR, Simek S, Ryder OA, Coggins L. Detection of proviral DNA in horse cells infected with equine infectious anemia virus.. J Virol 1978 Jun;26(3):577-83.
          pubmed: 209211doi: 10.1128/JVI.26.3.577-583.1978google scholar: lookup
        7. Long CW, Berzinski TR, Gilden RV. Immunologic studies of the low molecular weight DNA binding protein of murine oncornaviruses.. Int J Cancer 1977 Jun 15;19(6):843-50.
          pubmed: 194848doi: 10.1002/ijc.2910190616google scholar: lookup
        8. Cheevers WP, Archer BG, Crawford TB. Characterization of RNA from equine infectious anemia virus.. J Virol 1977 Nov;24(2):489-97.
          pubmed: 199735doi: 10.1128/JVI.24.2.489-497.1977google scholar: lookup
        9. Narayan O, Griffin DE, Chase J. Antigenic shift of visna virus in persistently infected sheep.. Science 1977 Jul 22;197(4301):376-8.
          pubmed: 195339doi: 10.1126/science.195339google scholar: lookup
        10. O'Farrell PZ, Goodman HM. Resolution of simian virus 40 proteins in whole cell extracts by two-dimensional electrophoresis: heterogeneity of the major capsid protein.. Cell 1976 Oct;9(2):289-98.
          pubmed: 184964doi: 10.1016/0092-8674(76)90119-7google scholar: lookup
        11. Huebner RJ, Gilden RV, Lane WT, Toni R, Trimmer RW, Hill PR. Suppression of murine type-C RNA virogenes by type-specific oncornavirus vaccines: prospects for prevention of cancer.. Proc Natl Acad Sci U S A 1976 Feb;73(2):620-4.
          pubmed: 174116doi: 10.1073/pnas.73.2.620google scholar: lookup
        12. Miller JM, Van der Maaten MJ. A complement-fixation test for the bovine leukemia (C-type) virus.. J Natl Cancer Inst 1974 Dec;53(6):1699-702.
          pubmed: 4373577
        13. Miller JM, Olson C. Precipitating antibody to an internal antigen of the C-type virus associated with bovine lymphosarcoma.. J Natl Cancer Inst 1972 Nov;49(5):1459-62.
          pubmed: 4346540
        14. Kono Y, Kobayashi K, Fukunaga Y. Antigenic drift of equine infectious anemia virus in chronically infected horses.. Arch Gesamte Virusforsch 1973;41(1):1-10.
          pubmed: 4123810doi: 10.1007/BF01249923google scholar: lookup
        15. Oroszlan S, Summers MR, Foreman C, Gilden RV. Murine type-C virus group-specific antigens: interstrain immunochemical, biophysical, and amino acid sequence differences.. J Virol 1974 Dec;14(6):1559-74.
        16. Malmquist WA, Barnett D, Becvar CS. Production of equine infectious anemia antigen in a persistently infected cell line.. Arch Gesamte Virusforsch 1973;42(4):361-70.
          pubmed: 4358259doi: 10.1007/BF01250717google scholar: lookup
        17. Umphenour NW, Kemen MJ, Coggins L. Equine infectious anemia: a retrospective study of an epizootic.. J Am Vet Med Assoc 1974 Jan 1;164(1):66-9.
          pubmed: 4358831
        18. Coggins L, Norcross NL, Nusbaum SR. Diagnosis of equine infectious anemia by immunodiffusion test.. Am J Vet Res 1972 Jan;33(1):11-8.
          pubmed: 4333633
        19. Gilden RV. Interrelationships among RNA tumor viruses and host cells.. Adv Cancer Res 1975;22:157-202.
          pubmed: 56125doi: 10.1016/s0065-230x(08)60177-3google scholar: lookup
        20. Barbacid M, Stephenson JR, Aaronson SA. gag Gene of mammalian type-C RNA tumour viruses.. Nature 1976 Aug 12;262(5569):554-9.
          pubmed: 60707doi: 10.1038/262554a0google scholar: lookup
        21. Chapman HP, White MH, Rahman R, Gilden RV. Species and interspecies radioimmunoassays for rat type C virus p30: interviral comparisons and assay of human tumor extracts.. J Virol 1975 Jan;17(1):51-9.
          pubmed: 54444doi: 10.1128/JVI.17.1.51-59.1976google scholar: lookup
        22. Gilden RV, Long CW, Hanson M, Toni R, Charman HP, Oroszlan S, Miller JM, Van der Maaten MJ. Characteristics of the major internal protein and RNA-dependent DNA polymerase of bovine leukaemia virus.. J Gen Virol 1975 Dec;29(3):305-14.
          pubmed: 54405doi: 10.1099/0022-1317-29-3-305google scholar: lookup
        23. O'Farrell PH. High resolution two-dimensional electrophoresis of proteins.. J Biol Chem 1975 May 25;250(10):4007-21.
          pubmed: 236308
        24. Charman HP, Kim N, White M, Marquardt H, Gilden RV, Kawakami T. Natural and experimentally induced antibodies to defined mammalian type-C virus proteins in primates.. J Natl Cancer Inst 1975 Dec;55(6):1419-24.
          pubmed: 173868doi: 10.1093/jnci/55.6.1419google scholar: lookup
        25. Toma B, Laude H, Goret P. [Purification and study of equine infectious anemia virus antigens, produced in vivo or in cultured cells].. C R Acad Hebd Seances Acad Sci D 1975 Sep 1;281(9):591-4.
          pubmed: 174831
        26. Charman HP, Kim N, Gilden RV, Hardy WD 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):859-61.
          pubmed: 176414doi: 10.1093/jnci/56.4.859google scholar: lookup
        27. Charman HP, Gardner MB, McAllister RM, Kim N, Gilden RV. Humoral immune responses of cats to mammalian type-C virus p30s.. Int J Cancer 1976 Jan 15;17(1):98-108.
          pubmed: 175024doi: 10.1002/ijc.2910170114google scholar: lookup
        28. Gruber J. Purification, concentration, and inactivation of Venezuelan equine encephalitis virus.. Appl Microbiol 1970 Sep;20(3):427-32.
          pubmed: 4922154doi: 10.1128/am.20.3.427-432.1970google scholar: lookup
        29. Strand M, August JT. Structural proteins of ribonucleic acid tumor viruses. Purification of envelope, core, and internal components.. J Biol Chem 1976 Jan 25;251(2):559-64.
          pubmed: 942719
        30. Laemmli UK. Cleavage of structural proteins during the assembly of the head of bacteriophage T4.. Nature 1970 Aug 15;227(5259):680-5.
          pubmed: 5432063doi: 10.1038/227680a0google scholar: lookup

        Citations

        This article has been cited 3 times.
        1. Sellon DC, Fuller FJ, McGuire TC. The immunopathogenesis of equine infectious anemia virus. Virus Res 1994 May;32(2):111-38.
          doi: 10.1016/0168-1702(94)90038-8pubmed: 8067050google scholar: lookup
        2. Montelaro RC, Lohrey N, Parekh B, Blakeney EW, Issel CJ. Isolation and comparative biochemical properties of the major internal polypeptides of equine infectious anemia virus. J Virol 1982 Jun;42(3):1029-38.
        3. Zhu JC, Cook JH, Dahmani M, Riley SP. The host calcium system contributes to intracellular Rickettsia pathogenesis. Infect Immun 2025 Oct 14;93(10):e0036325.
          doi: 10.1128/iai.00363-25pubmed: 40838898google scholar: lookup