Analyze Diet
Comparative immunology, microbiology and infectious diseases2003; 26(4); 251-260; doi: 10.1016/S0147-9571(02)00054-1

The serologic response of horses to equine arteritis virus as determined by competitive enzyme-linked immunosorbent assays (c-ELISAs) to structural and non-structural viral proteins.

Abstract: In an effort to further characterize the humoral immune response of horses to equine arteritis virus (EAV), direct and competitive enzyme-linked immunosorbent assays (c-ELISAs) were developed using monoclonal and polyclonal anti-sera to structural (G(L), N and M) and non-structural (nsp1) viral proteins. A nsp1-specific monoclonal antibody was produced to facilitate development of a c-ELISA to this protein. Data obtained using the various c-ELISAs confirm that the M protein is a major target of the antibody response of horses to EAV. However, none of the c-ELISAs that were developed were as sensitive in detecting EAV-specific antibodies in horse sera as the existing serum neutralization test.
Publication Date: 2003-04-05 PubMed ID: 12676125DOI: 10.1016/S0147-9571(02)00054-1Google Scholar: Lookup
The Equine Research Bank provides access to a large database of publicly available scientific literature. Inclusion in the Research Bank does not imply endorsement of study methods or findings by Mad Barn.
  • Journal Article
  • Research Support
  • Non-U.S. Gov't

Summary

This research summary has been generated with artificial intelligence and may contain errors and omissions. Refer to the original study to confirm details provided. Submit correction.

This study sought to further investigate the immune response of horses to equine arteritis virus (EAV) by developing direct and competitive enzyme-linked immunosorbent assays to identify structural and non-structural viral proteins. Though they were not as sensitive as existing methods, these new processes confirmed that the M protein is a major target of the horse’s immune response to EAV.

Development of New Assays

  • The research focused on improving the understanding of the horse’s immune system’s response to the equine arteritis virus (EAV).
  • An effort was made to develop direct and competitive enzyme-linked immunosorbent assays (c-ELISAs), which are laboratory tests widely used to detect and measure specific proteins or antibodies.
  • Both monoclonal and polyclonal antisera were used in these tests to pinpoint structural (G(L), N, and M) and non-structural (nsp1) viral proteins.
  • A unique monoclonal antibody targeting the non-structural protein nsp1 was also produced to facilitate the construction of a c-ELISA for this protein.

Findings and Conclusions

  • The data obtained using the different c-ELISAs showed that the M protein is a primary target of the horse’s antibody response to EAV.
  • This reaffirms the importance of the M protein within the virus and could be significant for furthering our understanding of the horse’s immune response mechanism to EAV.
  • However, despite these new developments, none of the newly designed c-ELISAs were as sensitive in detecting EAV-specific antibodies in horse serum as the pre-existing serum neutralization test.
  • This suggests that while the new c-ELISAs contribute to our understanding of the horse’s immune response to EAV, the development of even more sensitive tests in the future might still be necessary.

Cite This Article

APA
Wagner HM, Balasuriya UB, James MacLachlan N. (2003). The serologic response of horses to equine arteritis virus as determined by competitive enzyme-linked immunosorbent assays (c-ELISAs) to structural and non-structural viral proteins. Comp Immunol Microbiol Infect Dis, 26(4), 251-260. https://doi.org/10.1016/S0147-9571(02)00054-1

Publication

ISSN: 0147-9571
NlmUniqueID: 7808924
Country: England
Language: English
Volume: 26
Issue: 4
Pages: 251-260

Researcher Affiliations

Wagner, H M
  • Bernard and Gloria Salick Equine Viral Disease Laboratory, Department of Pathology, Microbiology, and Immunology, School of Veterinary Medicine, University of California at Davis, One Shields Avenue, 95616, Davis, CA, USA
Balasuriya, U B R
    James MacLachlan, N

      MeSH Terms

      • Animals
      • Antibodies, Monoclonal / immunology
      • Antibodies, Viral / immunology
      • Arterivirus Infections / immunology
      • Arterivirus Infections / veterinary
      • Cell Line
      • Cricetinae
      • Enzyme-Linked Immunosorbent Assay
      • Equartevirus / immunology
      • Horse Diseases / immunology
      • Horses / immunology
      • Viral Nonstructural Proteins / immunology
      • Viral Structural Proteins / immunology

      Citations

      This article has been cited 17 times.
      1. Thieulent CJ, Sarkar S, Carossino M, Bhowmik M, Zhu H, Balasuriya UBR. Cell Surface Vimentin Is an Attachment Factor That Facilitates Equine Arteritis Virus Infection In Vitro. Viruses 2026 Jan 15;18(1).
        doi: 10.3390/v18010113pubmed: 41600875google scholar: lookup
      2. Bhat S, Karunakaran S, Frossard JP, Choudhury B, Steinbach F. Genetic characterization of equine arteritis virus associated with outbreaks in the UK, 2019. J Gen Virol 2025 Dec;106(12).
        doi: 10.1099/jgv.0.002181pubmed: 41334982google scholar: lookup
      3. Thieulent CJ, Carossino M, Balasuriya UBR, Graves K, Bailey E, Eberth J, Canisso IF, Andrews FM, Keowen ML, Go YY. Development of a TaqMan(®) Allelic Discrimination qPCR Assay for Rapid Detection of Equine CXCL16 Allelic Variants Associated With the Establishment of Long-Term Equine Arteritis Virus Carrier State in Stallions. Front Genet 2022;13:871875.
        doi: 10.3389/fgene.2022.871875pubmed: 35495124google scholar: lookup
      4. Li Y, Firth AE, Brierley I, Cai Y, Napthine S, Wang T, Yan X, Kuhn JH, Fang Y. Programmed -2/-1 Ribosomal Frameshifting in Simarteriviruses: an Evolutionarily Conserved Mechanism. J Virol 2019 Aug 15;93(16).
        doi: 10.1128/JVI.00370-19pubmed: 31167906google scholar: lookup
      5. Bannai H, Nemoto M, Tsujimura K, Yamanaka T, Kokado H, Kondo T. Evaluation of two enzyme-linked immunosorbent assays for the detection of antibodies against equine arteritis virus. J Equine Sci 2018 Dec;29(4):111-115.
        doi: 10.1294/jes.29.111pubmed: 30607135google scholar: lookup
      6. Sarkar S, Bailey E, Go YY, Cook RF, Kalbfleisch T, Eberth J, Chelvarajan RL, Shuck KM, Artiushin S, Timoney PJ, Balasuriya UB. Allelic Variation in CXCL16 Determines CD3+ T Lymphocyte Susceptibility to Equine Arteritis Virus Infection and Establishment of Long-Term Carrier State in the Stallion. PLoS Genet 2016 Dec;12(12):e1006467.
        doi: 10.1371/journal.pgen.1006467pubmed: 27930647google scholar: lookup
      7. Sarkar S, Chelvarajan L, Go YY, Cook F, Artiushin S, Mondal S, Anderson K, Eberth J, Timoney PJ, Kalbfleisch TS, Bailey E, Balasuriya UB. Equine Arteritis Virus Uses Equine CXCL16 as an Entry Receptor. J Virol 2016 Jan 13;90(7):3366-84.
        doi: 10.1128/JVI.02455-15pubmed: 26764004google scholar: lookup
      8. Go YY, Li Y, Chen Z, Han M, Yoo D, Fang Y, Balasuriya UB. Equine arteritis virus does not induce interferon production in equine endothelial cells: identification of nonstructural protein 1 as a main interferon antagonist. Biomed Res Int 2014;2014:420658.
        doi: 10.1155/2014/420658pubmed: 24967365google scholar: lookup
      9. Balasuriya UB, Go YY, MacLachlan NJ. Equine arteritis virus. Vet Microbiol 2013 Nov 29;167(1-2):93-122.
        doi: 10.1016/j.vetmic.2013.06.015pubmed: 23891306google scholar: lookup
      10. Zhang J, Go YY, Huang CM, Meade BJ, Lu Z, Snijder EJ, Timoney PJ, Balasuriya UB. Development and characterization of an infectious cDNA clone of the modified live virus vaccine strain of equine arteritis virus. Clin Vaccine Immunol 2012 Aug;19(8):1312-21.
        doi: 10.1128/CVI.00302-12pubmed: 22739697google scholar: lookup
      11. Go YY, Bailey E, Cook DG, Coleman SJ, Macleod JN, Chen KC, Timoney PJ, Balasuriya UB. Genome-wide association study among four horse breeds identifies a common haplotype associated with in vitro CD3+ T cell susceptibility/resistance to equine arteritis virus infection. J Virol 2011 Dec;85(24):13174-84.
        doi: 10.1128/JVI.06068-11pubmed: 21994447google scholar: lookup
      12. Go YY, Snijder EJ, Timoney PJ, Balasuriya UB. Characterization of equine humoral antibody response to the nonstructural proteins of equine arteritis virus. Clin Vaccine Immunol 2011 Feb;18(2):268-79.
        doi: 10.1128/CVI.00444-10pubmed: 21147938google scholar: lookup
      13. Go YY, Zhang J, Timoney PJ, Cook RF, Horohov DW, Balasuriya UB. Complex interactions between the major and minor envelope proteins of equine arteritis virus determine its tropism for equine CD3+ T lymphocytes and CD14+ monocytes. J Virol 2010 May;84(10):4898-911.
        doi: 10.1128/JVI.02743-09pubmed: 20219931google scholar: lookup
      14. Zhang J, Stein DA, Timoney PJ, Balasuriya UB. Curing of HeLa cells persistently infected with equine arteritis virus by a peptide-conjugated morpholino oligomer. Virus Res 2010 Jun;150(1-2):138-42.
      15. Zhang J, Timoney PJ, MacLachlan NJ, McCollum WH, Balasuriya UB. Persistent equine arteritis virus infection in HeLa cells. J Virol 2008 Sep;82(17):8456-64.
        doi: 10.1128/JVI.01249-08pubmed: 18579588google scholar: lookup
      16. Go YY, Wong SJ, Branscum AJ, Demarest VL, Shuck KM, Vickers ML, Zhang J, McCollum WH, Timoney PJ, Balasuriya UB. Development of a fluorescent-microsphere immunoassay for detection of antibodies specific to equine arteritis virus and comparison with the virus neutralization test. Clin Vaccine Immunol 2008 Jan;15(1):76-87.
        doi: 10.1128/CVI.00388-07pubmed: 18032597google scholar: lookup
      17. van den Born E, Posthuma CC, Gultyaev AP, Snijder EJ. Discontinuous subgenomic RNA synthesis in arteriviruses is guided by an RNA hairpin structure located in the genomic leader region. J Virol 2005 May;79(10):6312-24.