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AIDS research and human retroviruses1993; 9(1); 7-11; doi: 10.1089/aid.1993.9.7

High prevalence of serum antibodies to equine infectious anemia virus reverse transcriptase.

Abstract: The immunogenicity of the equine infectious anemia virus (EIAV) reverse transcriptase (RT) was examined by immunoblot assay with recombinant EIAV RT. All of the 19 sera from EIAV-infected horses tested contained antibodies that recognized EIAV RT and directly inhibited the polymerase activity of the enzyme. An examination of sera obtained sequentially from two experimentally infected animals revealed that anti-RT antibodies arise early in infection and increase in level. The appearance of the antibodies correlated with progression toward the asymptomatic period of infection.
Publication Date: 1993-01-01 PubMed ID: 7678974DOI: 10.1089/aid.1993.9.7Google Scholar: Lookup
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  • Journal Article
  • Research Support
  • Non-U.S. Gov't
  • Research Support
  • U.S. Gov't
  • P.H.S.

Summary

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The research examined the significance of equine infectious anemia virus (EIAV) enzyme in horse serum, finding that horses infected with EIAV consistently produced antibodies capable of targeting and inhibiting the enzyme activity. Increase in these antibodies over time was found to be associated with the progression towards asymptomatic periods of the infection.

Overview of the Research

  • The research focused on understanding the immunogenicity – the ability to induce an immune response – of the reverse transcriptase (RT) enzyme of the equine infectious anemia virus (EIAV), a disease that affects horses.
  • The researchers examined the horse serum using an immunoblot assay, a method used to detect specific proteins in a sample, with the use of a genetically recreated (recombinant) EIAV RT.
  • Serum samples from nineteen horses with EIAV were tested.

Main Findings

  • The research found that all the tested samples from the EIAV-infected horses contained antibodies that could identify the EIAV RT.
  • More importantly, these antibodies were found to inhibit the polymerase activity of the RT enzyme. Polymerase activity refers to the process of creating new DNA or RNA molecules, which is crucial for the virus to replicate within the host.
  • The researchers also observed the production of antibodies over time in two experimentally infected horses.
  • It was found that the anti-RT antibodies arose early in the infection and their levels increased over time.

Significance of the Findings

  • The rise in antibody levels was found to correlate with a progression towards asymptomatic periods of the infection, suggesting a potential role of these antibodies in suppressing the disease symptoms.
  • This indicates that the equine immune system recognizes the virus’s RT enzyme as a threat and produces antibodies to shut down its function, thus limiting the spread and impact of the virus.
  • The understanding of the immune response to EIAV can potentially pave the way for novel therapeutics and vaccine strategies against EIAV, improving the health and longevity of horses.

Cite This Article

APA
DeVico AL, Issel CJ, Le Grice SF, Payne SL, Montelaro RC, Sarngadharan MG. (1993). High prevalence of serum antibodies to equine infectious anemia virus reverse transcriptase. AIDS Res Hum Retroviruses, 9(1), 7-11. https://doi.org/10.1089/aid.1993.9.7

Publication

ISSN: 0889-2229
NlmUniqueID: 8709376
Country: United States
Language: English
Volume: 9
Issue: 1
Pages: 7-11

Researcher Affiliations

DeVico, A L
  • Department of Cell Biology, Advanced BioScience Laboratories, Kensington, MD 20895.
Issel, C J
    Le Grice, S F
      Payne, S L
        Montelaro, R C
          Sarngadharan, M G

            MeSH Terms

            • Animals
            • Antibodies, Viral / blood
            • Cross Reactions
            • Equine Infectious Anemia / immunology
            • Horses
            • Immunoblotting
            • Infectious Anemia Virus, Equine / enzymology
            • Infectious Anemia Virus, Equine / immunology
            • RNA-Directed DNA Polymerase / immunology
            • Recombinant Proteins / immunology

            Grant Funding

            • AI-31147 / NIAID NIH HHS
            • N01-CP-73723 / NCI NIH HHS
            • N01-CP-74101 / NCI NIH HHS

            Citations

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