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Topic:Virus

The study of viral infections that affect equine species assesses the relationship between viruses and horses. Infections can lead to a range of clinical symptoms and may impact the health and performance of horses. Common equine viruses include Equine Influenza Virus, Equine Herpesvirus, and West Nile Virus, among others. Understanding the mechanisms of viral transmission, pathogenesis, and host immune responses is essential for developing effective prevention and treatment strategies. This page compiles peer-reviewed research studies and scholarly articles that explore the epidemiology, molecular biology, and clinical management of viral infections in horses.
[New species of the Acholeplasmataceae and Mycoplasmataceae families in horses]. Kirchhoff H.No abstract available
Histologic, immunofluorescent, and electron microscopic studies of equine dermis cells infected with an equine adenovirus.
American journal of veterinary research    March 1, 1974   Volume 35, Issue 3 431-436 
Ardans AA, Pritchett RF, Zee YC.No abstract available
[Experimental infection of the equine nasal mucosa with rhinopneumonitis virus (Herpesvirus equi 1)].
Berliner und Munchener tierarztliche Wochenschrift    February 15, 1974   Volume 87, Issue 4 61-66 
Teufel P, Grund S, Zeller R.No abstract available
Prevalence of antibodies to herpesvirus types 1 and 2, arteritis and infectious anemia viral antigens in equine serum.
American journal of veterinary research    February 1, 1974   Volume 35, Issue 2 181-185 
McGuire TC, Crawford TB, Henson JB.No abstract available
Equine infectious anemia. Henson JB, McGuire TC.No abstract available
Influenza infection in horse stocks caused by equine A-1 and Hong Kong subtype in Hungary.
Acta veterinaria Academiae Scientiarum Hungaricae    January 1, 1974   Volume 24, Issue 4 457-461 
Romváry J, Tanyi J, Máthé Z, Farkas E.No abstract available
Respiratory viral infections among thoroughbred horses in training during 1972.
Equine veterinary journal    January 1, 1974   Volume 6, Issue 1 19-24 doi: 10.1111/j.2042-3306.1974.tb03922.x
Powell DG, Burrows R, Goodridge D.No abstract available
Florida’s program against E.I.A. Campbell CL.No abstract available
Equine infectious anemia.
Modern veterinary practice    January 1, 1974   Volume 55, Issue 1 59 
No abstract available
History and geographic distribution of Venezuelan equine encephalitis.
Bulletin of the Pan American Health Organization    January 1, 1974   Volume 8, Issue 2 100-110 
Lord RD.No abstract available
Titration of precipitating antibody in equine infectious anemia.
National Institute of Animal Health quarterly    January 1, 1974   Volume 14, Issue 1 1-8 
Nakajima H, Fukunaga Y, Ushimi C.No abstract available
[Mutability of viruses of the equine encephalitis group under the influence of alkylating compounds. 2. Genetic characteristics of mutants of eastern and Venezuelan equine encephalitis viruses produced by formaldehyde and by N-nitroso-methyl-urea].
Revue roumaine de virologie    January 1, 1974   Volume 25, Issue 3 259-263 
Solianik RG, Fedorov IuV.No abstract available
Propagation of equine infectious anemia virus in horse kidney cell cultures.
National Institute of Animal Health quarterly    January 1, 1974   Volume 14, Issue 4 155-162 
Kono Y, Yoshino T.No abstract available
Equine herpesvirus 1: biological and biophysical comparison of two viruses from different clinical entities.
Intervirology    January 1, 1974   Volume 4, Issue 3 189-198 doi: 10.1159/000149857
Borgen HC, Ludwig H.No abstract available
Comparative aspects of equine herpesviruses.
The Cornell veterinarian    January 1, 1974   Volume 64, Issue 1 94-122 
Studdert MJ.No abstract available
Equine epizootic caused by influenza virus type A2/England 42/72.
Revue roumaine de virologie    January 1, 1974   Volume 25, Issue 3 207-210 
Bronitki A, Sărăţeanu D, Surdan C, Popescu A.No abstract available
Venezuelan equine encephalitis.
Advances in veterinary science and comparative medicine    January 1, 1974   Volume 18 79-116 
Johnson KM, Martin DH.No abstract available
Characterization of an equine adenovirus.
American journal of veterinary research    December 1, 1973   Volume 34, Issue 12 1587-1590 
England JJ, McChesney AE, Chow TL.No abstract available
Virus-like particles in an equine sarcoid cell line.
American journal of veterinary research    December 1, 1973   Volume 34, Issue 12 1601-1603 
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...
Equine abortion (herpes) virus: properties of the hemagglutinin in virus suspensions.
Virology    November 1, 1973   Volume 56, Issue 1 164-171 doi: 10.1016/0042-6822(73)90295-x
Klingeborn B, Dinter Z.No abstract available
[Study of some biological properties of influenza virus strains of poultry and horses isolated in the USSR].
Voprosy virusologii    November 1, 1973   Volume 18, Issue 6 705-709 
Osidze NG, Tkachenko AV, Bogautdinov ZF, Siurin VN.No abstract available
Immune response of equine fetus to coliphage T2.
American journal of veterinary research    October 1, 1973   Volume 34, Issue 10 1363-1364 
Martin BR, Larson KA.No abstract available
The characterisation of an equine adenovirus.
Australian veterinary journal    October 1, 1973   Volume 49, Issue 10 456-459 doi: 10.1111/j.1751-0813.1973.tb09291.x
Wilks CR, Studdert MJ.No abstract available
Equine herpesviruses: antigenic relationships and deoxyribonucleic acid densities.
Infection and immunity    October 1, 1973   Volume 8, Issue 4 621-627 doi: 10.1128/iai.8.4.621-627.1973
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 ...
Equine abortion (herpes) virus: evaluation of markers in a field vaccination trial.
Applied microbiology    October 1, 1973   Volume 26, Issue 4 566-569 doi: 10.1128/am.26.4.566-569.1973
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...
Possible evidence for interference with Venezuelan equine encephalitis virus vaccination of equines by pre-existing antibody to Eastern or Western Equine encephalitis virus, or both.
Applied microbiology    October 1, 1973   Volume 26, Issue 4 485-488 doi: 10.1128/am.26.4.485-488.1973
Calisher CH, Sasso DR, Sather GE.During 1971, an epizootic of Venezuelan equine encephalitis (VEE) reached the United States. Laboratory tests were performed on a large number of sick, healthy, unvaccinated, and vaccinated horses. Neutralization (N) tests in cell cultures revealed that 153 of 193 (79.3%) equines outside the state of Texas and 175 of 204 (85.8%) within Texas (82.6% overall) had detectable N antibody to VEE virus a week or more after vaccination. Twenty-six of 40 (65%) non-Texas equines and 18 of 29 (62%) Texas equines which had no detectable antibody against VEE virus a week or more after vaccination had N ant...
Quantitation of immunoglobulin-bearing lymphocytes and lymphocyte response to mitogens in horses persistently infected by equine infectious anemia virus.
Infection and immunity    October 1, 1973   Volume 8, Issue 4 679-682 doi: 10.1128/iai.8.4.679-682.1973
Banks KL, Henson JB.A defect in lymphocyte function could be responsible for persistent infection by the equine infectious anemia virus. The number of lymphocytes bearing surface immunoglobulin, as detected by immunofluorescence, and lymphocyte response to mitogens were the same in uninfected and equine infectious anemia-infected animals. A defect in T or B lymphocyte numbers or ability to respond to stimuli was not detected in this chronic virus disease.
Wildlife as sentinels for Venezuelan equine encephalomyelitis.
Journal of the American Veterinary Medical Association    September 15, 1973   Volume 163, Issue 6 657-661 
Bigler WJ, McLean RG.No abstract available
Preparation of equine infectious anemia antigens for diagnosis.
Japanese journal of microbiology    September 1, 1973   Volume 17, Issue 5 393-399 doi: 10.1111/j.1348-0421.1973.tb00790.x
Ueda S, Samejima T, Kuroda S, Nakamura J.No abstract available
Experimental infection of horses with enzootic and epizootic strains of Venezuelan equine encephalomyelitis virus.
The Journal of infectious diseases    September 1, 1973   Volume 128, Issue 3 271-282 doi: 10.1093/infdis/128.3.271
Walton TE, Alvarez O, Buckwalter RM, Johnson KM.No abstract available