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Topic:Virology

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.
Natural equine viral arteritis in foals.
Schweizer Archiv fur Tierheilkunde    October 1, 1981   Volume 123, Issue 10 523-533 
Golnik W, Michalska Z, Michalak T.No abstract available
Antigenic and structural conservation of herpesvirus DNA-binding proteins.
The Journal of general virology    October 1, 1981   Volume 56, Issue Pt 2 409-419 doi: 10.1099/0022-1317-56-2-409
Littler E, Yeo J, Killington RA, Purifoy DJ, Powell KL.Previously, we have shown a common antigen of several herpesviruses (pseudorabies virus, equine abortion virus and bovine mammillitis virus) to be antigenically related to the major DNA-binding proteins of herpes simplex virus types 1 and 2. In this study we have purified the cross-reacting polypeptide from cells infected with pseudorabies virus, equine abortion virus and bovine mammillitis virus and shown the cross-reacting protein to be a major DNA-binding protein for each virus. Tryptic peptide analysis of the cross-reacting DNA-binding proteins of all five viruses has shown structural simi...
Isolation and identification of African horsesickness virus from naturally infected dogs in Upper Egypt.
Canadian journal of comparative medicine : Revue canadienne de medecine comparee    October 1, 1981   Volume 45, Issue 4 392-396 
Salama SA, Dardiri AH, Awad FI, Soliman AM, Amin MM.African horsesickness virus was isolated from blood samples of street dogs in Aswan Province in Arab Republic of Egypt. Of six isolated "dog strain" African horsesickness viruses, three viruses designated D2, D6 and D10 have been identified as type 9 African horsesickness virus. Methods of isolation, tissue culture adaptation, serological indentification and typing are described. Horses experimentally infected with dog viruses showed febrile reaction and characteristic clinical and pathological signs of African horsesickness. Reisolation of African horsesickness virus type 9 was achieved from ...
Studies with equine infectious anemia virus: transmission attempts by mosquitoes and survival of virus on vector mouthparts and hypodermic needles, and in mosquito tissue culture.
American journal of veterinary research    September 1, 1981   Volume 42, Issue 9 1469-1473 
Williams DL, Issel CJ, Steelman CD, Adams WV, Benton CV.Biological and mechanical transmission trials with Psorophora columbiae (Dyar and Knab) and Aedes sollicitans (Walker) and ponies acutely infected with equine infectious anemia virus (EIAV) were negative. The EIAV antigen was detected by radioimmunoassay in Ae sollicitans immediately after the mosquitoes had fed on an acutely ill pony, but not 14 days after feeding. Psorophora columbiae mosquitoes had detectable EIAV antigen as determined by radioimmunoassay 24 hours after they fed on an acutely ill pony; this antigen was not detected again until 6 days after feeding and was still detected 14 ...
Stability of viability and immunizing potency of lyophilized, modified equine arteritis live-virus vaccine.
American journal of veterinary research    September 1, 1981   Volume 42, Issue 9 1501-1505 
Harry TO, McCollum WH.The Bucyrus strain of equine arteritis virus, previously modified to avirulence and vaccinal virus by 131 serial passages in primary cell cultures of horse kidney followed by 111 passages in primary cell cultures of rabbit kidney, was further passaged in cultures of the E. Derm (NBL-6) cell line, a continuous diploid cell line. Pools of the 16th and 25th passages of the virus in this last equine dermal cell line were lyophilized and stored in lots at 37 C, 23 to 28 C, 4C, and -20 C. The viability of the vaccinal virus deteriorated rapidly during storage at 37 C and at 23 to 28 C, but was relat...
Isolation of picornavirus from horses associated with Getah virus infection.
Nihon juigaku zasshi. The Japanese journal of veterinary science    August 1, 1981   Volume 43, Issue 4 569-572 doi: 10.1292/jvms1939.43.569
Fukunaga Y, Kumanomido T, Imagawa H, Ando Y, Kamada M, Wada R, Akiyama Y.No abstract available
Intestinal threshold of an enzootic strain of Venezuelan encephalitis virus in Culex (Melanoconion) taeniopus mosquitoes and its implications to vector competency and vertebrate amplifying hosts.
The American journal of tropical medicine and hygiene    July 1, 1981   Volume 30, Issue 4 862-869 doi: 10.4269/ajtmh.1981.30.862
Scherer WF, Cupp EW, Lok JB, Brenner RJ, Ordonez JV.The minimal intestinal dose of an enzootic strain of Venezuelan encephalitis (VE) virus for Culex (Melanoconion) taeniopus mosquitoes caught at a marsh habitat of VE virus in Guatemala was less than five plaque forming units (pfu) of virus. Ingestion of this dose of virus in blood of viremic hamsters resulted in transmission of virus to other hamsters. This low intestinal threshold of an enzootic strain of VE virus indicates that the natural Guatemalan population of Cu. (Mel.) taeniopus can acquire VE virus from vertebrates that have viremia levels as low as 1,000-5,000 pfu/ml of blood, provid...
Equine influenza in the Netherlands during the winter of 1978-1979; antigenic drift of the A-equi 2 virus.
The veterinary quarterly    April 15, 1981   Volume 3, Issue 2 80-84 doi: 10.1080/01652176.1981.9693801
van Oirschot JT, Masurel N, Huffels AD, Anker WJ.Influenza virus A-equi 2(Heq2Neq2) caused an epizootic in the Netherlands in the winter of 1978-1979. Horses vaccinated with A/Equi/Praha/56 (HEq1Neq1) and A/Equi/Miami/63 (Heq2Neq2) were also infected and showed clinical signs. The virus involved showed a marked antigenic drift from the prototype and vaccine strain A/Equi/Miami/63 (Heq2Neq2). Infection of ferrets with the Dutch/79 isolates gave rise to high haemagglutination-inhibition antibody titres to a number of A-Equi 2-1963, 1968 and 1979 viruses. The incorporation of this virus into future influenza vaccines should be considered.
The diagnosis of viral disease in equine practice.
The Veterinary record    March 21, 1981   Volume 108, Issue 12 249-251 doi: 10.1136/vr.108.12.249
No abstract available
Differentiation of sub-types of equine herpesvirus I by restriction endonuclease analysis.
Australian veterinary journal    March 1, 1981   Volume 57, Issue 3 148-149 doi: 10.1111/j.1751-0813.1981.tb00495.x
Sabine M, Robertson GR, Whalley JM.No abstract available
Venezuelan equine encephalitis virus: horse virulence of P-676 and MF-8 small and minute plaques.
The American journal of tropical medicine and hygiene    March 1, 1981   Volume 30, Issue 2 444-448 doi: 10.4269/ajtmh.1981.30.444
Justines G, Oro G, Alvarez O.The P-676 and MF-8 epizootic strains of Venezuelan equine encephalitis (VEE) virus were found to contain a minute plaque (MP), different from the predominant small plaque (SP) present in these virus strains. The MP and SP were stable after passages in Vero cells, mice, or horses. Equines were inoculated with the SP or MP of the P-676 and MF-8 strains. Inoculation of either P-676 SP or MP into horses induced high fever and viremia but no signs of encephalitis or death. Four horses infected with MF-8 SP became very ill, with high fever and viremia; three of the inoculated animals died. Four hors...
Central nervous system demyelination in Venezuelan equine encephalomyelitis infection.
Journal of the neurological sciences    March 1, 1981   Volume 49, Issue 3 397-418 doi: 10.1016/0022-510x(81)90030-7
Dal Canto MC, Rabinowitz SG.Arboviruses are important pathogens for both animals and humans. Venezuelan equine encephalomyelitis virus (VEEV) is an arbovirus whose pathogenicity for grey matter structures has been previously studied. To our knowledge, the present study is the first to describe extensive inflammation and demyelination in spinal cord white matter of mice infected with VEEV. To probe a possible immunepathogenesis of white matter alterations in this infection, nude mice and heterozygous controls were similarly infected. Whereas controls still showed inflammatory demyelination, nude mice showed no white matte...
Equine cytomegalovirus: cultural characteristics and properties of viral DNA.
Virology    February 1, 1981   Volume 109, Issue 1 106-119 doi: 10.1016/0042-6822(81)90475-x
Wharton JH, Henry BE, O'Callaghan DJ.No abstract available
Surveillance for immunity against equine influenza virus infections.
Comparative immunology, microbiology and infectious diseases    January 1, 1981   Volume 4, Issue 3-4 267-278 doi: 10.1016/0147-9571(81)90012-6
Bürki F, Lamatsch O.No abstract available
Propagation of equine infectious anemia virus in horse cell cultures.
Virologie    January 1, 1981   Volume 32, Issue 1 23-27 
Grădinaru DA, Stirbu C, Păltineanu D, Mironescu D, Manolescu N.The Wyoming strain of equine infectious anemia virus was adapted to cell cultures by 7 passages in horse leukocytes and 14 passages in fetal equine dermal and kidney cells. The virus was made evident by electron microscopy and immunodiffusion tests with antigens prepared from culture fluids.
Distribution of ribonucleic acid coliphages in animals.
Applied and environmental microbiology    January 1, 1981   Volume 41, Issue 1 164-168 doi: 10.1128/aem.41.1.164-168.1981
Osawa S, Furuse K, Watanabe I.To determine the distribution pattern of ribonucleic acid (RNA) coliphages (classified by serological groups I through IV) in animal sources, we isolated RNA phages from (i) feces samples from domestic animals (cows, pigs, horses, and fowls), some other animals in a zoological garden, and humans, (ii) the gastrointestinal contents of cows and pigs, and (iii) sewage samples from treatment plants in slaughter houses. These samples were then analyzed serologically. The concentration of RNA phages in the first and second kinds of material was fairly low (10 to 10(3) plaque-forming units per origin...
In vitro host range of equine infectious anemia virus.
Intervirology    January 1, 1981   Volume 16, Issue 4 225-232 doi: 10.1159/000149271
Benton CV, Brown BL, Harshman JS, Gilden RV.Equine infectious anemia virus (EIAV) was successfully inoculated onto cell cultures of canine and feline origin, resulting in chronic infections in these cultures. Infection of equine cell cultures, which were the previous sole in vitro source demonstrated for virus production, was also performed for comparative purposes. Determination of the nature of the virus produced in the heterologous as well as the equine cells was accomplished in several ways. SDS-PAGE of purified virus from the different cell lines indicated very similar protein composition. Immunological identity was observed in gel...
Equine infectious anemia virus, a putative lentivirus, contains polypeptides analogous to prototype-C oncornaviruses.
Virology    December 1, 1980   Volume 107, Issue 2 520-525 doi: 10.1016/0042-6822(80)90319-0
Parekh B, Issel CJ, Montelaro RC.No abstract available
Response of pregnant mares to equine herpesvirus 1 (EHV1).
The Cornell veterinarian    October 1, 1980   Volume 70, Issue 4 391-400 
Gleeson LJ, Coggins L.Twenty-one pregnant mares were inoculated with EHV1. Nineteen became infected as evidenced by clinical signs and/or viremia but only one mare aborted a virus-infected fetus. The viremias were leukocyte-associated and appeared to be non-productive, latent infections of these cells. Infectivity, detectable by cocultivation, persisted in the circulating leukocytes for as long as 9 days without resulting in abortion. The data suggest that it is extremely difficult to evaluate the efficacy of vaccines in preventing EHV1 (Rhinopneumonitis) abortion due to the paucity of non-exposed mares, lack of te...
An epidemic of Getah virus infection among racehorses: properties of the virus.
Research in veterinary science    September 1, 1980   Volume 29, Issue 2 162-167 
Kono Y, Sentsui H, Ito Y.A virus (Sakai) which had been recovered from an outbreak of disease in horses was found to be a small spherical enveloped RNA virus with a diameter of approximately 70 nm and a buoyant density of 1.22 g per ml. It grew well and produced a cytopathic effect in a variety of cell cultures; it was sensitive to organic solvents, heat and low pH. It agglutinated goose erythrocytes in a 0.35 M sodium chloride solution at an optimum pH of 6.2 and was antigenically identical or closely related to Getah virus, a member of the alphavirus subgroup of the Togaviridae.
An epidemic of Getah virus infection among racehorses: isolation of the virus.
Research in veterinary science    September 1, 1980   Volume 29, Issue 2 157-161 
Sentsui H, Kono Y.During the autumn of 1978 a disease characterised by fever and occasionally by exanthema and/or oedema of the limbs was seen in approximately 13 per cent of horses in a training stable in the Kanto district of Japan. A virus was isolated by the intracerebral inoculation of one-day-old mice from blood and nasal swabs taken from naturally and experimentally infected horses. The virus was subsequently passaged in two monkey kidney cell lines in which it produced complete cytopathic changes. Infected horses developed neutralising, complement fixing and haemagglutinin inhibiting antibodies to the v...
Fifty years of equine venereology.
Equine veterinary journal    July 1, 1980   Volume 12, Issue 3 99-100 doi: 10.1111/j.2042-3306.1980.tb03392.x
No abstract available
Enzyme-linked immunosorbent assay, using staphylococcal protein A for detecting virus antibodies.
American journal of veterinary research    June 1, 1980   Volume 41, Issue 6 978-980 
Potgieter LN, Rouse BT, Webb-Martin TA.A modification of the indirect enzyme-linked immunosorbent assay (ELISA) was developed which used staphylococcal protein A linked to horseradish peroxidase. Virus antibodies in equine, bovine, porcine, feline, canine, lagomorphic (rabbit), and human sera were detected, using the indirect ELISA in which the antiglobulin enzyme conjugate was replaced by protein A linked to horseradish peroxidase. Results of the ELISA were compared with the results of the serum-virus neutralization test. The application of the test in laboratories performing serologic assays with sera from diverse animal species ...
Biochemical characterization of equine herpesvirus type 3-induced deoxythymidine kinase purified from lytically infected horse embryo dermal fibroblasts.
Journal of virology    May 1, 1980   Volume 34, Issue 2 474-483 doi: 10.1128/JVI.34.2.474-483.1980
McGowan JJ, Allen GP, Barnett JM, Gentry GA.Infection of horse KyED cells with equine herpesvirus type 3 (EHV-3) resulted in a sevenfold increase in cytosol deoxythymidine kinase (dTK) activity. The EHV-3 dTK was purified from KyED cytosol dTK by affinity chromatography on deoxythymidine-Sepharose and characterized with respect to its electrophoretic mobility, molecular weight, substrate specificity, phosphate donor specificity, and immunological specificity. The purified EHV-3 dTK migrated in polyacrylamide gels with an Rf of 0.30 and sedimented in glycerol gradients with an S value of 5.13, corresponding to a molecular weight of 83,00...
Significant antigenic drift within the influenza equi 2 subtype in Sweden.
The Veterinary record    April 19, 1980   Volume 106, Issue 16 363-364 doi: 10.1136/vr.106.16.363
Klingeborn B, Rockborn G, Dinter Z.No abstract available
Negative contrast electron microscopic techniques for diagnosis of viruses of veterinary importance.
The Cornell veterinarian    April 1, 1980   Volume 70, Issue 2 125-135 
England JJ, Reed DE.Negative contrast electron microscopy (NCEM) was utilized as a routine tool in the diagnosis of viral infections of domestic and wild animals. Viruses identified by this technique were observed in infected culture systems or clinical specimens from several species including horses, cattle, sheep, dogs, cats, pigs, deer, Rocky Mountain bighorn sheep, antelope, and several avian species. Viruses were identified by NCEM based on their size, morphology, and symmetry and consisted of adenoviruses, herpesviruses, paramyxoviruses, myxoviruses, picornaviruses, parvoviruses, coronaviruses, reoviruses, ...
[European Pharmacopoeia and the test of equine influenza vaccines (author’s transl)].
Comparative immunology, microbiology and infectious diseases    January 1, 1980   Volume 3, Issue 1-2 101-104 doi: 10.1016/0147-9571(80)90044-2
Pilet C, Poirier J.No abstract available
Equine influenza–a segment in influenza virus ecology.
Comparative immunology, microbiology and infectious diseases    January 1, 1980   Volume 3, Issue 1-2 45-59 doi: 10.1016/0147-9571(80)90038-7
Tůmová B.No abstract available
Virus and its relationship to the “poor performance” syndrome.
Equine veterinary journal    January 1, 1980   Volume 12, Issue 1 3-9 doi: 10.1111/j.2042-3306.1980.tb02285.x
Mumford JA, Rossdale PD.Racehorses perform badly for many different reasons. Trainers often expect clinicians to determine the cause in individual cases and, more especially, where most of the immates of the stable are apparently affected by loss of form. Clinical examinations may reveal signs including fever, serous nasal discharge and the occasional cough. Haematology and blood biochemistry are commonly used aids to diagnosis in the field and may be helpful, but there is a need for facilities for virological investigations to be made readily available for use by clinicans as an adjunct to more commonplace laborator...
Persistence in nature of influenza virus A/eq/Praha/56 (Heq1Neq1).
Acta virologica    January 1, 1980   Volume 24, Issue 1 63-67 
Tåmová B, Stumpa A, Zakopal J, Vĕzníková D, Mensík J.Equine influenza occurred in Czechoslovakia 14 years after the last epizootic in horses that had returned from abroad. Six strains A (Heq1Neq1) antigenically related to, but not identical with, strain A/eq/Praha/56 were isolated from 10 washings. Seroconversion was demonstrated with paired sera, but the antibody increase was more marked against the newly isolated strain.
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