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Archives of virology1999; 144(4); 817-827; doi: 10.1007/s007050050547

Phylogenetic characterization of a highly attenuated strain of equine arteritis virus from the semen of a persistently infected standardbred stallion.

Abstract: An avirulent, novel variant of equine arteritis virus (EAV; CA95G) was isolated from the semen of a persistently infected Standardbred stallion. The CA95G virus caused subclinical infection and seroconversion in susceptible horses, and virus was isolated only once from blood and nasal secretions collected from 6 experimentally infected horses. Sequence analysis of genes encoding the known EAV structural proteins shows that this highly attenuated strain of EAV is genetically similar to virulent field strains of EAV and, in particular, to a strain of EAV that was isolated during an outbreak of equine viral arteritis in western Canada in 1986. Not only is the carrier stallion the critical natural reservoir of EAV, but genetic diversity of the virus is generated in the course of persistent infection of carrier stallions. The subtle genetic changes that facilitate and maintain persistent EAV infection of the stallion's reproductive tract likely influence phenotypic properties of the virus such as virulence.
Publication Date: 1999-06-12 PubMed ID: 10365172DOI: 10.1007/s007050050547Google Scholar: Lookup
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  • Journal Article
  • Research Support
  • Non-U.S. Gov't
  • Research Support
  • U.S. Gov't
  • Non-P.H.S.

Summary

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This research article delves into the genetic analysis and characterization of a weakened or ‘attenuated’ strain of the equine arteritis virus (EAV) named CA95G. It was found in the semen of a Standardbred stallion that was persistently infected with the virus. Despite its weakened form, this strain was capable of causing a non-symptomatic infection and an immune response in susceptible horses.

Analysis of the CA95G Strain

  • The researchers isolated the novel CA95G strain of EAV from the semen of a persistently infected Standardbred stallion.
  • This strain was found to cause subclinical infection, meaning the horses showed no apparent symptoms, however, the immune response was evident as seroconversion took place. Seroconversion is the process of developing detectable antibodies in the blood that are specifically directed towards an invading pathogen.
  • Interestingly, the CA95G virus was only isolated once from the blood and nasal secretions of 6 horses that were deliberately infected as part of the study.

Comparative Genetic Analysis

  • The researchers conducted a sequence analysis of the genes that code for known EAV structural proteins. This was done to compare the genetic material of the CA95G strain with that of virulent field strains of EAV.
  • They discovered that the highly attenuated CA95G strain was genetically similar to virulent strains of EAV, particularly one strain that was isolated during an outbreak of equine viral arteritis in western Canada in 1986.

Persistent Infection and Virus Diversity

  • The study also underlined that carrier stallions act as natural reservoirs for EAV. This means that the horses can harbor the virus for an extended period, helping in its spread.
  • Moreover, genetic diversity of the virus is generated during the course of persistent infection in carrier stallions. In other words, as the virus remains in the stallion’s system for longer, its genetic makeup undergoes changes.
  • These subtle genetic changes that maintain the persistent EAV infection in the stallion’s reproductive tract are likely to influence the behavior of the virus, for instance, its virulence or severity.

Cite This Article

APA
Patton JF, Balasuriya UB, Hedges JF, Schweidler TM, Hullinger PJ, MacLachlan NJ. (1999). Phylogenetic characterization of a highly attenuated strain of equine arteritis virus from the semen of a persistently infected standardbred stallion. Arch Virol, 144(4), 817-827. https://doi.org/10.1007/s007050050547

Publication

ISSN: 0304-8608
NlmUniqueID: 7506870
Country: Austria
Language: English
Volume: 144
Issue: 4
Pages: 817-827

Researcher Affiliations

Patton, J F
  • Department of Pathology, Microbiology and Immunology, School of Veterinary Medicine, University of California, Davis, USA.
Balasuriya, U B
    Hedges, J F
      Schweidler, T M
        Hullinger, P J
          MacLachlan, N J

            MeSH Terms

            • Animals
            • Arterivirus Infections / physiopathology
            • Arterivirus Infections / veterinary
            • Arterivirus Infections / virology
            • Equartevirus / classification
            • Equartevirus / genetics
            • Equartevirus / isolation & purification
            • Horse Diseases / blood
            • Horse Diseases / physiopathology
            • Horse Diseases / virology
            • Horses / virology
            • Male
            • Molecular Sequence Data
            • Nasal Mucosa / virology
            • Open Reading Frames
            • Phylogeny
            • Semen / virology

            Citations

            This article has been cited 9 times.
            1. Balasuriya UB, Zhang J, Go YY, MacLachlan NJ. Experiences with infectious cDNA clones of equine arteritis virus: lessons learned and insights gained. Virology 2014 Aug;462-463:388-403.
              doi: 10.1016/j.virol.2014.04.029pubmed: 24913633google scholar: lookup
            2. 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
            3. 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
            4. 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
            5. 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
            6. Echeverría MG, Díaz S, Metz GE, Serena MS, Panei CJ, Nosetto E. Genetic typing of equine arteritis virus isolates from Argentina. Virus Genes 2007 Oct;35(2):313-20.
              doi: 10.1007/s11262-007-0081-4pubmed: 17294142google scholar: lookup
            7. MacLachlan NJ, Balasuriya UB. Equine viral arteritis. Adv Exp Med Biol 2006;581:429-33.
              doi: 10.1007/978-0-387-33012-9_77pubmed: 17037573google scholar: lookup
            8. Tobiasch E, Kehm R, Bahr U, Tidona CA, Jakob NJ, Handermann M, Darai G, Giese M. Large envelope glycoprotein and nucleocapsid protein of equine arteritis virus (EAV) induce an immune response in Balb/c mice by DNA vaccination; strategy for developing a DNA-vaccine against EAV-infection. Virus Genes 2001 Mar;22(2):187-99.
              doi: 10.1023/a:1008175525254pubmed: 11324756google scholar: lookup
            9. Hedges JF, Balasuriya UB, Timoney PJ, McCollum WH, MacLachlan NJ. Genetic divergence with emergence of novel phenotypic variants of equine arteritis virus during persistent infection of stallions. J Virol 1999 May;73(5):3672-81.