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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.
Serological and virological investigations of an equid herpesvirus 1 (EHV-1) abortion storm on a stud farm in 1985.
Journal of reproduction and fertility. Supplement    January 1, 1987   Volume 35 509-518 
Mumford JA, Rossdale PD, Jessett DM, Gann SJ, Ousey J, Cook RF.An extensive outbreak of EHV-1 abortions occurred on a stud farm in England in 1985. Of the 67 pregnant mares present on the stud farm, 31 were challenged with EHV-1, resulting in the loss of 22 fetuses or foals. Laboratory investigations revealed that the spread of the virus closely followed movement of apparently healthy mares (during the incubation period of the infection). During the outbreak mares were challenged 1-4 months before the expected foaling date. There was no relationship between the gestational age at the time of challenge and the subsequent outcome of infection in terms of ab...
Molecular pathogenesis of equine coital exanthema (ECE): temperature sensitivity (TS) and restriction endonuclease (RE) fragment profiles of several field isolates.
Archives of virology    January 1, 1987   Volume 92, Issue 3-4 293-299 doi: 10.1007/BF01317485
Bouchey D, Evermann J, Jacob RJ.Examination of six field isolates of equine herpesvirus 3, the causative agent of equine coital exanthema, indicates that all were temperature sensitive (ts) at the body temperature, 39 degrees C, of their host (Equine asinus and callabus) when grown in cell culture. The isolates were characterized by fingerprint analysis with the restriction endonucleases XbaI, EcoRI, BamHI and Hind III to establish possible epidemiologic relatedness. Three of the six isolates may be considered related. Variation in the mobility of the BamHI-A and Hind III-K fragments indicates that a small plaque isolate may...
Epidemiology of equine herpesvirus 2 (equine cytomegalovirus).
Journal of clinical microbiology    January 1, 1987   Volume 25, Issue 1 13-16 doi: 10.1128/jcm.25.1.13-16.1987
Browning GF, Studdert MJ.The epidemiology of equine herpesvirus 2 was examined by using restriction endonuclease DNA fingerprints to distinguish viruses isolated from two groups of horses. The first group consisted of three yearlings isolated from other horses but in contact with each other for 418 days, whereas the second comprised seven mares and their foals, which were sampled at monthly intervals from parturition until the foals were about 180 days old. There was a complex pattern of transmission, with 15 different viruses isolated from both groups. Four distinguishable viruses were isolated from the three yearlin...
Phagocytosis of horse erythrocytes treated with equine infectious anemia virus by cultivated horse leukocytes.
Archives of virology    January 1, 1987   Volume 95, Issue 1-2 67-77 doi: 10.1007/BF01311335
Sentsui H, Kono Y.Horse erythrocytes treated with equine infectious anemia virus hemagglutinin were phagocytized by cultivated horse leukocytes (mainly macrophage-like cells and partly polymorphonuclear cells) after incubation with fresh horse serum but not with inactivated horse serum. The phagocytosis began as soon as the erythrocytes were added to the leukocyte cultures, and the majority of the reaction proceeded within 30 minutes. Addition of antiserum showed a slightly suppressing but no enhancing effect on the phagocytosis. Phagocytosis seemed to be caused by the recognition of the third complement compon...
Arbovirus isolations from mosquitoes collected during and after the 1982-1983 epizootic of western equine encephalitis in Argentina.
The American journal of tropical medicine and hygiene    January 1, 1987   Volume 36, Issue 1 107-113 doi: 10.4269/ajtmh.1987.36.107
Mitchell CJ, Monath TP, Sabattini MS, Daffner JF, Cropp CB, Calisher CH, Darsie RF, Jakob WL.Mosquitoes were collected in Santa Fe and Rio Negro provinces, Argentina, in 1982-1983 during a western equine encephalitis (WEE) epizootic. Totals of 153,084 mosquitoes from Santa Fe Province and 484 from Rio Negro Province were tested for virus in 2,351 pools. Seventeen virus strains were isolated, all from Santa Fe collections, as follows: 4 WEE, 6 Venezuelan equine encephalitis, 1 St. Louis encephalitis, 2 Antequera, 1 Maguari, 1 Melao, 1 new vesiculovirus (Calchaqui), and 1 Gamboa. The WEE virus isolates were from Aedes albifasciatus, Anopheles albitarsis, Mansonia species, and Psorophora...
[Differentiation of equine influenza viruses subtype 2 with monoclonal antibodies].
Tierarztliche Praxis. Supplement    January 1, 1987   Volume 2 41-46 
Eichhorn W.Infections and clinical diseases caused by equine 2 influenza A viruses are observed worldwide. The frequency of these outbreaks supports the hypothesis that antigenic variation of the surface proteins may play an important role. For the demonstration of these variations, monoclonal antibodies (Mabs) were prepared. They are directed against the hemagglutinin or the neuraminidase of the prototype strain a/eq/Miami/1/63. In hemagglutination-inhibition assays with Mabs two reaction patterns were observed: four Mabs inhibited 14 out of 17 strains tested. Another Mab recognized the hemagglutinin of...
Epizootic vesicular stomatitis in Colorado, 1982: infection in occupational risk groups.
The American journal of tropical medicine and hygiene    January 1, 1987   Volume 36, Issue 1 177-182 doi: 10.4269/ajtmh.1987.36.177
Reif JS, Webb PA, Monath TP, Emerson JK, Poland JD, Kemp GE, Cholas G.In 1982-1983, an epizootic of vesicular stomatitis occurred in the western United States. Veterinarians, research workers, and regulatory personnel who were exposed to vesicular stomatitis virus were examined for patterns of human infection and prevalence of vesicular stomatitis New Jersey serotype neutralizing antibody. Insight into the mechanism of transmission was sought by comparing activities of antibody-positive and antibody-negative persons. A statistically significant risk factor was a history of infected animals sneezing in the face of serosurvey participants. Elevated odds ratios wer...
Getah virus isolations from mosquitoes collected at two horse habitations in the western areas of Japan.
Nihon juigaku zasshi. The Japanese journal of veterinary science    December 1, 1986   Volume 48, Issue 6 1191-1197 doi: 10.1292/jvms1939.48.1191
Kumanomido T, Fukunaga Y, Kamada M, Imagawa H, Ando Y, Wada R, Nitta M, Akiyama Y.No abstract available
Equine viral rhinopneumonitis.
Revue scientifique et technique (International Office of Epizootics)    December 1, 1986   Volume 5, Issue 4 837-867 doi: 10.20506/rst.5.4.273
Bryans JT, Allen GP.No abstract available
Identification of Aedes campestris from New Mexico: with notes on the isolation of western equine encephalitis and other arboviruses.
Journal of the American Mosquito Control Association    December 1, 1986   Volume 2, Issue 4 529-534 
Clark GG, Crabbs CL, Bailey CL, Calisher CH, Craig GB.An arbovirus survey was conducted during August 1985 at White Sands Missile Range in southcentral New Mexico following a suspected arboviral disease epizootic among feral horses. A total of 20,566 mosquitoes (18,505 females and 2,061 males) and 8,900 biting gnats were collected and assayed for virus. Female mosquitoes were principally Aedes campestris (54.8%), Aedes dorsalis (30.4%) and Culex tarsalis (13.2%). Arboviruses were not isolated from biting gnats, but mosquitoes yielded a total of 37 viral isolates, including western equine encephalitis (WEE) (18), California serogroup (15), Cache V...
Nucleotide and deduced amino acid sequence of the influenza neuraminidase genes of two equine serotypes.
Virology    December 1, 1986   Volume 155, Issue 2 460-468 doi: 10.1016/0042-6822(86)90207-2
Dale B, Brown R, Miller J, White RT, Air GM, Cordell B.Equine influenza is caused by two serotypes of type A influenza virus, EIV-A1 and EIV-A2. The complete nucleotide sequence of the neuraminidase (NA) genes of both the A1 (N7 subtype) and A2 (N8 subtype) serotype has been determined following cloning of full-length viral NA cDNAs into pBR322. Analysis of the deduced amino acid sequences reveals that the N7 and N8 genes share expected extensive homologies with the previously sequenced N1, N2, and N9 NA subtypes. These homologies include conservation of basic NA gene and protein structure, cysteine residues, potential glycosylation sites, and res...
Lentivirus genomic organization: the complete nucleotide sequence of the env gene region of equine infectious anemia virus.
Virology    December 1, 1986   Volume 155, Issue 2 309-321 doi: 10.1016/0042-6822(86)90195-9
Rushlow K, Olsen K, Stiegler G, Payne SL, Montelaro RC, Issel CJ.The nucleotide sequence of the envelope (env) gene region of equine infectious anemia virus (EIAV), a member of the lentivirus subfamily of retroviruses, has been determined from a clone of integrated proviral DNA for which the gag and pol sequences have been reported previously. The env gene is 859 codons in length and the sequence reported here is consistent with the published biochemical properties of EIAV glycoproteins. The env gene region of EIAV shares considerable structural similarities but negligible sequence homologies with the env genes of other members of the lentivirus subfamily, ...
Abortion and perinatal foal mortality associated with equine herpesvirus type 1 in a herd of Grevy’s zebra.
Journal of the American Veterinary Medical Association    November 1, 1986   Volume 189, Issue 9 1185-1186 
Wolff PL, Meehan TP, Basgall EJ, Allen GP, Sundberg JP.No abstract available
Shedding and interspecies type sero-reactivity of the envelope glycopolypeptide gp120 of the human immunodeficiency virus.
The Journal of general virology    November 1, 1986   Volume 67 ( Pt 11) 2533-2538 doi: 10.1099/0022-1317-67-11-2533
Schneider J, Kaaden O, Copeland TD, Oroszlan S, Hunsmann G.Two glycopolypeptides with molecular weights 160,000 and 120,000 (gp120) are regularly recognized by human immunodeficiency virus (HIV)-specific antisera in lysates of cells persistently infected with HIV. In the present study, gp120 was characterized as the major envelope glycopolypeptide of HIV. Gp120 was identified as the external viral glycoprotein by radiosequencing and by its presence in purified virus. However gp120 was predominantly shed as a soluble protein into the culture fluid. Furthermore gp120 was precipitated by sera from horses infected with equine infectious anaemia virus (EIA...
Use of indirect and competitive ELISAs to compare isolates of equine influenza A virus.
Journal of virological methods    November 1, 1986   Volume 14, Issue 3-4 253-265 doi: 10.1016/0166-0934(86)90027-3
Denyer MS, Crowther JR.Antigenic differences within equine-1 and equine-2 isolates of influenza were studied by haemagglutination inhibition tests, indirect ELISA and competition ELISA, using the same antisera. Better differentiation was obtained with the competition ELISA than with the other two tests. All three methods produced similar relationships within the equine-1 isolates but differed in their ability to differentiate the equine-2 isolates where the competition ELISA was superior and produced epidemiologically sensible results. In all three tests, post-infection ferret and horse sera were more useful in disc...
Mortality of captive whooping cranes caused by eastern equine encephalitis virus.
Journal of the American Veterinary Medical Association    November 1, 1986   Volume 189, Issue 9 1006-1010 
Dein FJ, Carpenter JW, Clark GG, Montali RJ, Crabbs CL, Tsai TF, Docherty DE.Of 39 captive whooping cranes (Grus americana), 7 died during a 7-week period (Sept 17 through Nov 4, 1984) at the Patuxent Wildlife Research Center, Laurel, Md. Before their deaths, 4 cranes did not develop clinical signs, whereas the other 3 cranes were lethargic and ataxic, with high aspartate transaminase, gamma-glutamyl transferase, and lactic acid dehydrogenase activities, and high uric acid concentrations. Necropsies indicated that the birds had ascites, intestinal mucosal discoloration, fat depletion, hepatomegaly, splenomegaly, and visceral gout. Microscopically, extensive necrosis an...
Molecular cloning and physical characterization of integrated equine infectious anemia virus: molecular and immunologic evidence of its close relationship to ovine and caprine lentiviruses.
Virology    October 15, 1986   Volume 154, Issue 1 1-8 doi: 10.1016/0042-6822(86)90424-1
Yaniv A, Dahlberg J, Gazit A, Sherman L, Chiu IM, Tronick SR, Aaronson SA.Molecular clones of the integrated form of the genome of equine infectious anemia virus (EIAV), the etiologic agent of a naturally occurring, worldwide disease of horses, were obtained. The restriction map of a full-length genome was determined. Additional evidence for the close evolutionary relationship between EIAV and a prototype lentivirus (caprine arthritis encephalitis virus) was acquired by Southern blotting and immunological analyses. An interspecies radioimmunoassay was developed in which EIAV and ovine and caprine lentiviruses could be detected equally well. These studies make availa...
Enzyme-linked immunosorbent assay for the detection of antibodies to equid herpesvirus type 1 (EHV-1).
Nihon juigaku zasshi. The Japanese journal of veterinary science    October 1, 1986   Volume 48, Issue 5 1045-1048 doi: 10.1292/jvms1939.48.1045
Hohdatsu T, Eiki T, Ide S, Yamagishi H.No abstract available
Transmissibility and abortogenic effect of equine viral arteritis in mares.
Journal of the American Veterinary Medical Association    October 1, 1986   Volume 189, Issue 7 769-771 
Cole JR, Hall RF, Gosser HS, Hendricks JB, Pursell AR, Senne DA, Pearson JE, Gipson CA.A group of 14 pregnant mares was exposed via contact to 4 mares bred to stallions infected with equine viral arteritis virus. There was a demonstrable febrile response in each donor mare and in 12 of the pregnant mares. All 18 mares became seropositive after exposure. Equine viral arteritis virus was isolated from the nasopharynx of 5 pregnant mares, but not from the donor mares. Ten of the pregnant mares aborted, and virus was isolated from fetal specimens or placenta of 8.
Hemagglutination-inhibiting antibodies to equine influenza viruses in Japanese horses and antigenic variation of the viruses.
The Kitasato archives of experimental medicine    September 1, 1986   Volume 59, Issue 3 49-55 
Kudo H, Ohde H, Yamanaka T, Ohtsuka Y, Matumoto M.No abstract available
Respiratory disease in foals and the epizootiology of equine herpesvirus type 2 infection.
New Zealand veterinary journal    September 1, 1986   Volume 34, Issue 9 152-155 doi: 10.1080/00480169.1986.35331
Fu ZF, Robinson AJ, Horner GW, Dickinson LG, Grimmett JB, Marshall RB.The epizootiology of equine herpesvirus type 2 (EHV-2) infection was investigated in Thoroughbred foals on a stud farm which in previous years had suffered economic loss due to respiratory disease. Sixteen pairs of foals and their dams were selected for this study and all of the foals became infected with EHV-2 by two to four months of age. These animals responded serologically to the virus infection as detected by an enzyme-linked immunosorbent assay (ELISA). EHV-2 infection persisted in these foals for two to six months with constant or intermittent virus recovery. This persistent infection ...
Preliminary characterisation of torovirus-like particles of humans: comparison with Berne virus of horses and Breda virus of calves.
Journal of medical virology    September 1, 1986   Volume 20, Issue 1 67-78 doi: 10.1002/jmv.1890200109
Beards GM, Brown DW, Green J, Flewett TH.Pleomorphic virus-like particles have been observed by electron microscopy in the faeces of children and adults with diarrhoea. Some of these particles were approximately 100 nm in diameter and had a "fringe" of closely applied peplomers approximately 10 nm long; they closely resembled Berne virus of horses and Breda virus of calves, the two representatives of a newly proposed family called the Toroviridae. In one sample a toroidal nucleoprotein-like structure was observed within the particles. For two samples a buoyant density of 1.14 g/ml was determined by centrifugation through a sucrose de...
Cloning and fine mapping the DNA of equine herpesvirus type one defective interfering particles.
Virology    September 1, 1986   Volume 153, Issue 2 188-200 doi: 10.1016/0042-6822(86)90022-x
Baumann RP, Staczek J, O'Callaghan DJ.Equine herpesvirus type one (EHV-1) defective interfering (DI) particle DNA fragments were inserted into the XbaI site of the plasmid vector pACYC184. Five DI XbaI fragments, which ranged in molecular weight from 4.5 to 6.7 MDa, were selected for detailed analysis. Each DI DNA clone was labeled with 32P-deoxynucleotides by nick translation and hybridized to genomic digests of EHV-1 standard (STD) DNA bound to nitrocellulose. All five clones were shown to hybridize to DNA sequences derived from the left terminus (0.0-0.04 map units) of the long (L) region and from the short (S) region inverted ...
Responses of horses vaccinated with avirulent modified-live equine arteritis virus propagated in the E. Derm (NBL-6) cell line to nasal inoculation with virulent virus.
American journal of veterinary research    September 1, 1986   Volume 47, Issue 9 1931-1934 
McCollum WH.Nineteen horses with no prior experience with equine arteritis virus (EAV) were inoculated IM with an avirulent live-virus vaccine against equine viral arteritis; the vaccinal virus had been passaged serially 131 times in primary cell cultures of equine kidney, 111 times in primary cell cultures of rabbit kidney, and 16 times in an equine dermis cell line (EAV HK-131/RK-111/ED-16). Three or 4 of the vaccinated horses each, along with appropriate nonvaccinated controls, were inoculated nasally with virulent EAV at each of months 3, 6, 9, 12, 18, and 24 after they were vaccinated. The following ...
Demonstration of the carrier state in naturally acquired equine arteritis virus infection in the stallion.
Research in veterinary science    September 1, 1986   Volume 41, Issue 2 279-280 
Timoney PJ, McCollum WH, Roberts AW, Murphy TW.The chronic carrier state was virologically confirmed in 15 thoroughbred stallions naturally infected with equine arteritis virus based on the results of test matings and, or, isolations of the virus from semen. Carrier stallions were shown to shed equine arteritis virus in the semen for at least one to two years. Existence of a short-term or convalescent carrier state was also demonstrated in five additional stallions. The frequency of the long-term carrier state in stallions naturally infected with equine arteritis virus was 35 per cent; it varied considerably between groups of stallions on ...
[Concentration of the Venezuelan equine encephalomyelitis virus in a 2-phase system of water-soluble polymers].
Voprosy virusologii    September 1, 1986   Volume 31, Issue 5 584-587 
Pomelova VG, Gaĭdamovich SIa, Demenev VA, Kadoshnikov IuP.A three-step concentration of Venezuelan equine encephalomyelitis (VEE) virus from tissue culture fluid was carried out in a two-phase system of polyethyleneglycol (PEG)--sodium dextran sulphate (SDS). The concentration method was based on the dependence of virus distribution coefficient upon NaCl content in the system which allowed alternating transfer of the virus from one phase of the system into the other. The infectious activity of the virus increased approximately 100-fold after the first step, 190-fold after the second, and 300-fold after the third step. The process of concentration was...
Identification and antigenic comparison of equine arteritis virus isolated from an outbreak of epidemic abortion of mares.
Zentralblatt fur Veterinarmedizin. Reihe B. Journal of veterinary medicine. Series B    August 1, 1986   Volume 33, Issue 6 413-417 doi: 10.1111/j.1439-0450.1986.tb00051.x
Golnik W, Moraillon A, Golnik J.No abstract available
Equine herpesvirus type 1 infection–a reply.
New Zealand veterinary journal    August 1, 1986   Volume 34, Issue 8 136 doi: 10.1080/00480169.1986.35324
Fu ZF, Robinson AJ.No abstract available
Equine arteritis virus-induced polypeptide synthesis.
The Journal of general virology    August 1, 1986   Volume 67 ( Pt 8) 1543-1549 doi: 10.1099/0022-1317-67-8-1543
van Berlo MF, Rottier PJ, Spaan WJ, Horzinek MC.Intracellular virus-specific proteins induced by equine arteritis virus (EAV) have been compared with in vitro translation products of virion and intracellular EAV RNAs. In infected BHK-21 cells, the two major virion proteins (C and E1) and polypeptides with mol. wt. of 60,000 (p60), 42,000 (p42) and 30,000 (p30) were found. There were no indications that the viral proteins were processed from a larger precursor as shown by pulse-chase, amino acid analogue and protease inhibitor experiments. The six polyadenylated RNAs that occur in EAV-infected cells were isolated and translated in an mRNA-de...
Intracellular equine arteritis virus (EAV)-specific RNAs contain common sequences.
Virology    July 30, 1986   Volume 152, Issue 2 492-496 doi: 10.1016/0042-6822(86)90154-6
van Berlo MF, Rottier PJ, Horzinek MC, van der Zeijst BA.Equine arteritis virus (EAV) is a nonarthropod-borne togavirus. Six virus-specific RNA species have been found in EAV-infected cells having the following molecular weights: 4.3 X 10(6) (RNA1), 1.3 X 10(6) (RNA2), 0.9 X 10(6) (RNA3), 0.7 X 10(6) (RNA4), 0.3 X 10(6) (RNA5), and 0.2 X 10(6) (RNA6). RNA1 comigrates with the viral genome (M. F. Van Berlo, M. C. Horzinek, and B. A. M. Van der Zeijst, 1982, Virology 118, 345-352). All RNAs hybridized with a radio-labeled cDNA probe representing RNA6, indicating that they contain common sequences. To study this homology in more detail, RNase T1 oligon...