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Journal of comparative pathology1998; 117(3); 201-208; doi: 10.1016/s0021-9975(97)80015-1

Venereal infection of mares by equine arteritis virus and use of killed vaccine against the infection.

Abstract: Venereal infection with equine arteritis virus (EAV) was established in each of seven mares by inoculation via the cervix with 20 ml of viral suspension (> or = 8 x 10(6) plaque-forming units; PFU), following treatment with prostaglandin and oestradiol. A dose of < or = 8 x 10(5) PFU produced infection in only five of eight mares. Serum neutralizing antibody developed in mares manifesting clinical signs of equine viral arteritis (EVA), and a weak antibody was detectable in one apparently healthy mare inoculated with 8 x 10(5) PFU. Virus isolation was demonstrated not only in the buffy coat but also in nasal swabs of infected mares. EAV was isolated frequently from the body tissues of the mares (killed 10 to 34 days post-inoculation) up to day 12, but rarely from the reproductive tissues later than day 12. The virus persisted longest in the splenic and deep inguinal lymph nodes, followed by the spleen and internal iliac lymph nodes. Four mares immunized with a killed vaccine for EVA showed no clinical disease after venereal challenge with EAV; the virus was recovered from the buffy coat of three mares and from the nasal swab of one of them, but not from the remaining animal.
Publication Date: 1998-02-03 PubMed ID: 9447481DOI: 10.1016/s0021-9975(97)80015-1Google Scholar: Lookup
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  • Journal Article

Summary

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The researchers studied the venereal infection of horses by the Equine Arteritis Virus (EAV), and the impact of a killed vaccine designed to combat this infection and observed its clinical implications among the infected mares.

Introduction and Methodology

  • The study focused on understanding the venereal infection caused by Equine Arteritis Virus (EAV) amongst mares. Seven mares were artificially infected with EAV by inoculating them with greater than 8 million plaque-forming units (PFU) of viral suspension through their cervix after treatment with prostaglandin and oestradiol.
  • The researchers used a lesser dose of less or equal to 800,000 PFU (Plaque Forming Units) to infect another group of eight mares as a control.
  • As a part of a vaccination test, four mares were immunized with a killed vaccine for Equine Viral Arteritis (EVA)

Observations and Findings

  • Infection was confirmed in all seven mares with higher dose inoculation, whereas only five out of eight mares were found infected when given the lesser dose.
  • All the mares showing clinical signs developed Serum neutralizing antibodies, which are immune system proteins that neutralize the pathogen’s effect. There was indication of weak antibody detection in one seemingly healthy mare that was inoculated with 800,000 PFU.
  • The presence of EAV was evident not only in the buffy coat (layer of white blood cells and platelets) but also within the nasal swabs of the infected mares.
  • The isolation of the virus was frequently discovered in the body tissues of the mares up until day 12 post-inoculation, but rarely after day 12 within reproductive tissues.
  • The virus was detected for the longest duration in the splenic and deep inguinal lymph nodes, followed by the spleen and internal iliac lymph nodes.

Impact of the Killed Vaccine

  • The four mares that were immunized with the killed EVA vaccine showed no clinical signs of disease after being later infected with EAV.
  • Virus presence was observed from the buffy coats of three of these vaccinated mares and within the nasal swab of one of them, but the virus was not found in the rest.

This study indicates that venereal infection with EAV in mares can be effectively prevented using the killed EVA vaccine, while further suggesting that the virus mainly persists in the splenic and lymph node regions until 12 days post-inoculation.

Cite This Article

APA
Fukunaga Y, Wada R, Imagawa H, Kanemaru T. (1998). Venereal infection of mares by equine arteritis virus and use of killed vaccine against the infection. J Comp Pathol, 117(3), 201-208. https://doi.org/10.1016/s0021-9975(97)80015-1

Publication

ISSN: 0021-9975
NlmUniqueID: 0102444
Country: England
Language: English
Volume: 117
Issue: 3
Pages: 201-208

Researcher Affiliations

Fukunaga, Y
  • Epizootic Research Station, Japan Racing Association, Tochigi.
Wada, R
    Imagawa, H
      Kanemaru, T

        MeSH Terms

        • Animals
        • Arterivirus Infections / immunology
        • Arterivirus Infections / transmission
        • Arterivirus Infections / veterinary
        • Equartevirus / immunology
        • Equartevirus / isolation & purification
        • Female
        • Horse Diseases / immunology
        • Horse Diseases / transmission
        • Horse Diseases / virology
        • Horses
        • Sexually Transmitted Diseases, Viral / immunology
        • Sexually Transmitted Diseases, Viral / veterinary
        • Uterine Cervical Diseases / immunology
        • Uterine Cervical Diseases / veterinary
        • Vaccination / veterinary
        • Vaccines, Inactivated / immunology