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[Use of the immunoenzyme test ELISA-NS3 to distinguish horses infected by African horsesickness virus from vaccinated horses].

Abstract: A vaccination protocol involving three horses, with five repeated injections of inactivated serotype 4 African horse sickness virus, was undertaken to determine a possible threshold for the appearance of antibodies against the non-structural protein NS3. Using an indirect enzyme-linked immunosorbent assay, with the recombinant NS3 protein as an antigen, the authors detected a response to NS3 as of the second injection for the first horse and after four injections for the second horse. No response to NS3 was detected for the third horse. The results show that the inactivated vaccine is insufficiently purified to eliminate the non-structural protein NS3. Therefore using the NS3 protein as a marker did not enable differentiation between vaccinated and infected horses.
Publication Date: 1999-12-10 PubMed ID: 10588005
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  • English Abstract
  • Journal Article

Summary

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The research aimed to develop a test that could tell the difference between horses that were vaccinated against the African Horsesickness Virus (AHS) and those that are infected with it. Using the protein NS3 as a marker did not work as hoped because the vaccine used did not entirely eliminate this protein.

Background

  • African Horsesickness Virus (AHS) is a deadly virus that affects horses, and there is an inactivated vaccine available for it.
  • Vaccines are usually designed to simulate an infection, so the immune system generates antibodies that can fight off the actual virus.
  • It can be challenging to distinguish between animals that have been vaccinated and those that have been naturally infected because both groups will have antibodies against the virus.
  • Scientists were trying to use a protein called NS3, found in the AHS virus, as a marker to tell the difference between vaccinated and infected horses.

Methodology

  • The researchers undertook a protocol involving three horses and five repeated injections of inactivated serotype 4 AHS virus.
  • They aimed to determine the threshold for the onset of antibodies against NS3.
  • An indirect enzyme-linked immunosorbent assay (ELISA), which is a test used to detect and measure antibodies in the blood, was used.
  • The recombinant NS3 protein served as an antigen in this test, which is a substance that triggers the immune system to produce antibodies.

Findings

  • After multiple injections, horses one and two generated a response to NS3, detected using the ELISA. The third horse did not produce a reaction to NS3.
  • These results show that horses receiving the inactivated vaccine can still produce antibodies against NS3, implying the vaccine did not wholly remove this protein.

Implications

  • Using NS3 as a marker was thus unhelpful in distinguishing between horses that have been vaccinated and those infected with the virus.
  • This study suggests that the vaccine needs to be further purified or refined to entirely eliminate NS3, which could help in the differentiation between vaccinated and infected horses in the future.

Cite This Article

APA
Idrissi Bougrine S, Fassi Fihri O, el Harrak M, Fassi Fehri MM. (1999). [Use of the immunoenzyme test ELISA-NS3 to distinguish horses infected by African horsesickness virus from vaccinated horses]. Rev Sci Tech, 18(3), 618-626.

Publication

ISSN: 0253-1933
NlmUniqueID: 8712301
Country: France
Language: fre
Volume: 18
Issue: 3
Pages: 618-626

Researcher Affiliations

Idrissi Bougrine, S
  • Institut agronomique et vétérinaire Hassan II, Département de microbiologie, immunologie et maladies contagieuses, Rabat-Instituts, Maroc.
Fassi Fihri, O
    el Harrak, M
      Fassi Fehri, M M

        MeSH Terms

        • African Horse Sickness / diagnosis
        • African Horse Sickness / immunology
        • African Horse Sickness / prevention & control
        • African Horse Sickness Virus / immunology
        • Animals
        • Antibodies, Viral / blood
        • Antigens, Viral / immunology
        • Enzyme-Linked Immunosorbent Assay / veterinary
        • Horses
        • Neutralization Tests / veterinary
        • Recombinant Proteins / immunology
        • Vaccination / veterinary
        • Vaccines, Inactivated / immunology
        • Viral Nonstructural Proteins / immunology
        • Viral Vaccines / immunology

        Citations

        This article has been cited 2 times.
        1. Wen Y, Cheng A, Wang M, Ge H, Shen C, Liu S, Xiang J, Jia R, Zhu D, Chen X, Lian B, Chang H, Zhou Y. A Thymidine Kinase recombinant protein-based ELISA for detecting antibodies to Duck Plague Virus. Virol J 2010 Apr 23;7:77.
          doi: 10.1186/1743-422X-7-77pubmed: 20416075google scholar: lookup
        2. Mohd Jaafar F, Attoui H, Gallian P, Biagini P, Cantaloube JF, de Micco P, de Lamballerie X. Recombinant VP7-based enzyme-linked immunosorbent assay for detection of immunoglobulin G antibodies to Colorado tick fever virus. J Clin Microbiol 2003 May;41(5):2102-5.