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Structural proteins of equine infectious anemia virus and their antigenic activity.

Abstract: Using purified equine infectious anemia (EIA) virus labeled with 3H-glucosamine or 14C-protein hydrolysate, structural proteins were analyzed by sodium dodecyl sulfate-polyacrylamide gel electrophoresis. As a result, 2 glycoproteins and 10 proteins with molecular weights (mol wt) ranging from 12,000 to 115,000 daltons were demonstrated. Of 12 structural proteins, 3 proteins, namely a glycoprotein with mol wt of 76,000 (gp76) and 2 proteins with mol wt of 25,000 (p25) and 12,000 (p12), respectively, had distinct antigenic activity from one another in immunodiffusion. Development of antibodies against gp76 and p25 was compared in infected horses. The antibody to gp76 appeared earlier and stronger than to p25 in horses infected with the homologous virus strain. The fraction with glycoproteins was found to have hemagglutinating activity which was inhibited by the serum sample from horses infected with equine infectious anemia virus.
Publication Date: 1984-01-01 PubMed ID: 6322625
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  • Comparative Study
  • Journal Article

Summary

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The research article discusses the analysis of structural proteins of the Equine Infectious Anemia (EIA) virus using labeled compounds, in relation to their antigenic activity and the development of antibodies in infected horses.

Protein Analysis and Antigenic activity

The researchers used purified equine infectious anemia virus labeled with compounds like 3H-glucosamine or 14C-protein hydrolysate for their experiments. They were looking specifically at structural proteins, which are the building blocks of the virus. These proteins were analyzed through sodium dodecyl sulfate-polyacrylamide gel electrophoresis, a common laboratory technique to separate proteins based on their molecular weight.

  • Through this procedure, they found two types of glycoproteins and ten other proteins. Glycoproteins are proteins that have carbohydrates attached to them. These proteins had molecular weights ranging from 12,000 to 115,000 daltons. Dalton is a unit of measurement for atomic mass.
  • Among the 12 structural proteins, three had distinct antigenic activity from the others in immunodiffusion, a process used to detect and study immune responses. These three proteins were a glycoprotein with a molecular weight of 76,000 (gp76) and two proteins with molecular weights of 25,000 (p25) and 12,000 (p12).

Antibody Development

The development of antibodies, which are proteins produced by the immune system to fight against foreign substances like viruses, was compared in infected horses. According to the study:

  • The antibodies against the glycoprotein gp76 appeared earlier and stronger in horses infected with the homologous virus strain than those to the p25 protein.
  • It was also found that the fraction containing the glycoproteins had hemagglutinating activity. Hemagglutination is a process by which red blood cells clump together. This activity was inhibited by the serum sample from horses infected with equine infectious anemia virus, indicating a possible defense mechanism.

All in all, the research provides important insight into the structural proteins of the EIA virus and their role in immune response in horses. This could potentially help in the development of more effective treatments or vaccines against the disease.

Cite This Article

APA
Nishimura M, Nakajima H. (1984). Structural proteins of equine infectious anemia virus and their antigenic activity. Am J Vet Res, 45(1), 5-10.

Publication

ISSN: 0002-9645
NlmUniqueID: 0375011
Country: United States
Language: English
Volume: 45
Issue: 1
Pages: 5-10

Researcher Affiliations

Nishimura, M
    Nakajima, H

      MeSH Terms

      • Animals
      • Antibodies, Viral / analysis
      • Antigens, Viral / immunology
      • Centrifugation, Density Gradient
      • Electrophoresis, Polyacrylamide Gel
      • Equine Infectious Anemia / immunology
      • Glycoproteins / immunology
      • Horses
      • Immunodiffusion / veterinary
      • Infectious Anemia Virus, Equine / analysis
      • Infectious Anemia Virus, Equine / immunology
      • Molecular Weight
      • Sodium Dodecyl Sulfate
      • Viral Proteins / immunology

      Citations

      This article has been cited 3 times.
      1. Zheng YH, Sentsui H, Nakaya T, Kono Y, Ikuta K. In vivo dynamics of equine infectious anemia viruses emerging during febrile episodes: insertions/duplications at the principal neutralizing domain.. J Virol 1997 Jul;71(7):5031-9.
      2. Sellon DC. Equine infectious anemia.. Vet Clin North Am Equine Pract 1993 Aug;9(2):321-36.
        doi: 10.1016/s0749-0739(17)30399-1pubmed: 8395326google scholar: lookup
      3. 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