Virology in horses encompasses the study of viruses that affect equine species, including their biology, transmission, and impact on horse health. This field investigates viral pathogens that can lead to a range of diseases, from respiratory infections to neurological disorders. Common viruses affecting horses include equine influenza virus, equine herpesvirus, and West Nile virus. Understanding these viruses involves examining their genetic makeup, modes of transmission, and interactions with the equine immune system. This page compiles peer-reviewed research studies and scholarly articles that explore the epidemiology, pathogenesis, and control measures of viral infections in horses.
Gorelkin L, Jahrling PB.Pancreatic tissue from hamsters inoculated with a virulent strain of Venezuelan equine encephalomyelitis virus (VEE) was studied sequentially with fluorescent antibody, light and electron microscopic technics. Progressive viral growth and cellular necrosis in the pancreas were demonstrated. Pancreatic infection resulted from both viremia and direct extension from the spleen across contaminated serosal planes. Mature viruses traversed the endothelium within endothelial vesicles and were associated with acinar as well as islet cells.
Joncas JH, Gilker JC, Chagnon A.The relative value of heterophil agglutinins (HA) and of specific EBV antibodies in the diagnosis of infectious mononucleosis (IM) was assessed in 108 cases of the disease and in 280 controls. Among the 108 cases 93 were HA-positive by sheep cells in at least one of their sera, while 15 were HA-negative by the same test. Among the 280 controls false-positive HA tests were not encountered except in eight cases with the horse cell microtitre tests. With one of the two slide tests at least two false-positive tests and 12 false-negative tests were also found but these sera had low titres in microt...
England JJ, Watson RE, Larson KA.On electron microscopic examination of a cell line derived from an equine sarcoid, intracytoplasmic oncornavirus-like particles were seen. Cells treated with idoxuridine-dimethyl sulfoxide (idu-dmso) had a two- to four-fold increase in the number of particles as compared with nontreated cells or cells treated with dmso alone. The intracytoplasmic virus-like particles were double membrane structures measuring 80 to 100 nm. in diameter. Particles were seen extracelluarly or budding from the cell membrane into the extracellular space. These extracellular particles were 100 nm. in diameter and con...
Plummer G, Goodheart CR, Studdert MJ.Equine herpesviruses with a deoxyribonucleic acid density of 1.716 to 1.717 g/cm(3) were compared with one another by the plaque-reduction test and by the rate of development of cytopathic effect as indicated by plaque size in rabbit kidney cultures. Of the 19 isolates studied, the 9 which had already been tentatively labeled equine abortion viruses were serologically similar to one another; each of them grew more quickly than did any of the other 10 isolates although the mean plaque sizes formed a series of gradations with no clear hiatus which would permit the unequivocal delineation of the ...
Klingeborn B.Twelve mares were vaccinated with attenuated equine abortion virus (EAV) strain RAC-H. Two nonvaccinated mares served as controls. In at least three mares the vaccination appeared to coincide with a natural infection. This was indicated by characterization of the EAV isolated from nasal secretions of six vaccinated mares, a nonvaccinated control, and also from the lung, spleen, and liver of a fetus aborted by a vaccinated mare. The relative sensitivity of the isolated EAV to dithiothreitol was used to distinguish the RAC-H strain and wild-type virus. Of the 10 EAV isolates, four were recognize...
Sinclair R, Binns MM, Chirnside ED, Mumford JA.The N-terminal fragment comprising residues +1 to +50 (gB1-50) of equine herpesvirus type 1 (EHV-1) glycoprotein B was expressed as a glutathione S-transferase fusion protein in Escherichia coli. Recombinant gB1-50 (rgB1-50) was recognized in immunoblots by sera from rabbits immunized with EHV-1 and by convalescent-phase sera from horses with natural EHV-1 infections. An enzyme-linked immunosorbent assay (ELISA) for monitoring antibody levels against EHV-1 was developed by using rgB1-50, and its specificity was assessed with a panel of reference antisera against other equine viruses. A specifi...
Uppal PK, Yadav MP, Singh BK, Prasad S.A progenital disease encountered at one equine stud farm at Bangalore in Southern India during 1987 was investigated and confirmed as equine coital exanthema on the basis of characteristic lesions and clinical symptoms, isolation of equine herpes virus-3 (EHV-3) from the scabs collected from animals having active lesions and demonstration of neutralizing antibodies in the sera of recovered mares and stallion. This is the first authenticated report of the occurrence of equine coital exanthema in India due to EHV-3.
Thompson DB, Spradborw PB, Studdert M.Some details of the clinical and postmortem findings of an Arab foal that died as a consequence of adenoviral pneumonia superimposed on a combined immunodeficiency disease are provided. The foal was the 17th in a series of similar deaths that occurred on a farm since 1959. An adenovirus, which by haemagglutination inhibition and serum neutralisation tests was antigenically similar to 2 other equine adenoviruses isolated in Australia, was isolated from a nasal swab taken from the foal when it was 23 days of age.
Weremowicz S, Parzych R, Malicki K.Summary
The outbreak of equine influenza in Poland in 1980 was caused by an equine influenza virus antigenically related to the strain A/equine/Miami/63/Heq2, Neq2. This was confirmed by isolation of six strains of influenza virus from horses suffering from the acute form of the disease. About 45 % and 69 % of positive results were obtained in the HI test performed with sera taken from convalescent and affected animals, respectively. A relatively high level of antibodies against newly isolated equine influenza virus strains was found in 50 % of serum samples taken from the grooms. A relativ...
Yamagishi H, Ide S, Eiki T, Eiguchi Y, Nagamine T, Igarashi Y, Yoshioka I, Matumoto M.ESK cells, a stable cell line derived from a swine embryo kidney, were found to be a good medium for plaque formation of the Prague and Miami strains of equine influenza virus. Factors influencing the plaque formation were investigated and a plaque assay for these viruses was worked out. The method is not only simple enough for routine use, but also is as sensitive as the egg inoculation method. The method was readily adapted for a neutralization test.
