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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.
Equine monoclonal antibodies recognize common epitopes on variants of equine infectious anaemia virus.
Immunology    December 1, 1990   Volume 71, Issue 4 592-594 
Perryman LE, O'Rourke KI, Mason PH, McGuire TC.Equine-murine xenohybridoma cells were produced using SP2/0 murine myeloma cells and splenic lymph node cells obtained from horses infected with 10(6) TCID50 of single cloned variants of equine infectious anaemia virus (EIAV). The xenohybridomas secreted equine IgG monoclonal antibodies reactive with EIAV in enzyme immunoassays employing purified virus. Seven antibodies were studied in detail. They bound to viral glycoproteins (gp90 or gp45) in radioimmunoprecipitation assays, and reacted with homologous EIAV as well as five other cloned variants of EIAV. When evaluated against a single cloned...
The open reading frame ORF S3 of equine infectious anemia virus is expressed during the viral life cycle.
Journal of virology    December 1, 1990   Volume 64, Issue 12 6319-6324 doi: 10.1128/JVI.64.12.6319-6324.1990
Saman E, Breugelmans K, Heyndrickx L, Merregaert J.The genome of equine infectious anemia virus (EIAV) contains several small open reading frames (ORFs), the importance of which in the development of the virus is not clear. We investigated the possibility that the largest of these ORFs (ORF S3) is expressed during the course of the viral infection. The ORF S3 information was expressed in Escherichia coli, and the antigen was used to raise monospecific antiserum. A 20-kDa protein expressed in cells producing EIAV was identified as the gene product of ORF S3. Furthermore, sera from EIAV-infected animals specifically recognized this protein, indi...
Isolations of African horse sickness virus from vector insects made during the 1988 epizootic in Spain.
Epidemiology and infection    October 1, 1990   Volume 105, Issue 2 447-454 doi: 10.1017/s0950268800048020
Mellor PS, Boned J, Hamblin C, Graham S.This paper describes the first isolations of African horse sickness virus (AHSV) from insects in Spain. Seven isolations of AHSV serotype 4 were made; four from Culicoides imicola a known vector of the virus elsewhere, two from mixed pools of Culicoides species not including C. imicola and one from blood engorged mosquitoes. Three further isolations of AHSV serotype 4 were also made from horses kept adjacent to the insect collecting sites. This work presents the first definitive identification of the vectors of AHSV in Spain during the 1987, 88 and 89 epizootics. Suggestions are also made conc...
Herpetic keratitis in a horse.
Equine veterinary journal. Supplement    September 1, 1990   Issue 10 15-17 doi: 10.1111/j.2042-3306.1990.tb04703.x
Miller TR, Gaskin JM, Whitley RD, Wittcoff ML.No abstract available
Aujeszky’s disease in a horse.
Zentralblatt fur Veterinarmedizin. Reihe B. Journal of veterinary medicine. Series B    September 1, 1990   Volume 37, Issue 7 532-538 doi: 10.1111/j.1439-0450.1990.tb01092.x
van den Ingh TS, Binkhorst GJ, Kimman TG, Vreeswijk J, Pol JM, van Oirschot JT.A horse with neurological signs and severe meningoencephalitis caused by Aujeszky's disease is described. The diagnosis was established by immunohistochemistry, DNA-in situ hybridization and serological tests. Aujeszky's disease virus antigen and Aujeszky's disease viral DNA were detected in neurons of the cerebrum. In the serum of the horse antibodies against Aujeszky's disease virus were detected in a virus neutralization test, in a blocking ELISA which specifically detects antibodies against the glycoprotein I (Ig) of the virus, in an indirect double sandwich ELISA and with colloidal gold i...
An indirect sandwich ELISA utilising F(ab’)2 fragments for the detection of African horsesickness virus.
Journal of virological methods    September 1, 1990   Volume 29, Issue 3 279-289 doi: 10.1016/0166-0934(90)90055-k
du Plessis DH, van Wyngaardt W, Bremer CW.African horsesickness virus (AHSV), an important disease of equines is caused by an orbivirus. Because of the need to contain the spread of the disease, it is often essential to make a rapid diagnosis. For this purpose, an ELISA capable of detecting viral antigen in animal tissue and in cell culture fluid was developed. Immobilised F(ab')2 fragments prepared by digestion of AHSV-specific IgG with pepsin were used to trap virus from tissue homogenates or cell culture supernatant. After addition of intact IgG as detecting antibody, Staphylococcus aureus protein A labelled with horseradish peroxi...
Comparative evaluation of the agar gel immunodiffusion test and two commercial ELISA kits for the serodiagnosis of equine infectious anemia.
Zentralblatt fur Veterinarmedizin. Reihe B. Journal of veterinary medicine. Series B    August 1, 1990   Volume 37, Issue 6 448-458 doi: 10.1111/j.1439-0450.1990.tb01082.x
Bürki F, Rossmanith E.Selected sets of serum samples of horses were tested blindly in a comparative investigation for antibodies against Equine Infectious Anemia (EIA) virus. Three commercial kits were used, a well-established agar-gel immuno-diffusion kit which our laboratory has been using routinely for 14 years on one hand, a competitive ELISA kit (CELISA) and a non-competitive ELISA kit on the other hand. The American EIA Reference Laboratory in Ames cotested 56 serum samples with the same 3 products, with highest-level correlation, thereby ascertaining full dependability of our own results. Five EIA experts su...
Cloning and characterization of cDNAs encoding equine infectious anemia virus tat and putative Rev proteins.
Journal of virology    August 1, 1990   Volume 64, Issue 8 3716-3725 doi: 10.1128/JVI.64.8.3716-3725.1990
Stephens RM, Derse D, Rice NR.We isolated and characterized six cDNA clones from an equine infectious anemia virus-infected cell line that displays a Rev-defective phenotype. With the exception of one splice site in one of the clones, all six cDNAs exhibited the same splicing pattern and consisted of four exons. Exon 1 contained the 5' end of the genome; exon 2 contained the tat gene from mid-genome; exon 3 consisted of a small section of env, near the 5' end of the env gene; and exon 4 contained the putative rev open reading frame from the 3' end of the genome. The structures of the cDNAs predict a bicistronic message in ...
African horse sickness: a continuing menace.
Journal of the American Veterinary Medical Association    June 15, 1990   Volume 196, Issue 12 2019-2021 
Brown CC, Dardiri AH.No abstract available
Rapid diagnosis of equine influenza.
The Veterinary record    June 2, 1990   Volume 126, Issue 22 550-551 
Anestad G, Maagaard O.During an epizootic of equine influenza in Norway caused by influenza A/equine (H3N8) virus the efficacy of rapid virus diagnosis by the indirect immunofluorescence technique was evaluated. The antiserum used in the test was a polyclonal influenza A virus antiserum with reactivity directed mainly against the common nucleoprotein and matrix protein. This antiserum possessed sufficient reactivity for the detection of virus-infected exfoliated nasopharyngeal cells. Nasopharyngeal smear samples from 92 horses were examined and a positive diagnosis was obtained for 57 (62 per cent). Paired serum sa...
Equine herpesvirus type 1: detection of viral DNA sequences in aborted fetuses with the polymerase chain reaction.
Veterinary microbiology    May 1, 1990   Volume 22, Issue 4 373-381 doi: 10.1016/0378-1135(90)90024-p
Ballagi-Pordány A, Klingeborn B, Flensburg J, Belák S.Primers and probes were selected from the gene encoding glycoprotein 13 (gp 13) of equine herpesvirus 1 (EHV-1). The polymerase chain reaction (PCR) was run on infected and noninfected cultured cells and on 63 specimens from 29 aborted equine fetuses. The results were evaluated by electrophoresis and dot-blot hybridization using an oligonucleotide probe labeled with biotin. In the infected samples electrophoresis showed a PCR product of about 280 base pairs. The dot-blot hybridization confirmed that this product contained EHV-1 DNA sequences. PCR took 4 h and hybridization another 14 h; the re...
Transcript analysis of the equine herpesvirus 1 glycoprotein B gene homologue and its expression by a recombinant vaccinia virus.
The Journal of general virology    May 1, 1990   Volume 71 ( Pt 5) 1119-1129 doi: 10.1099/0022-1317-71-5-1119
Bell CW, Boyle DB, Whalley JM.Transcript mapping of the equine herpesvirus 1 (EHV-1) glycoprotein B (gB) gene homologue by Northern blot, S1 nuclease and primer extension analyses indicated that two overlapping transcripts of 3.4 and 4.6 kb originated from the same strand and were transcribed from left to right between coordinates 0.40 and 0.43 of the EHV-1 genome. The 3.4 kb transcript encoded EHV-1 gB and the 5' RNA terminus was located approximately 30 bases downstream from a probable TATA element. The coding region of the gB gene homologue was reconstructed from two subclones using oligonucleotide mutagenesis and inser...
Haematological measurements as an aid to early diagnosis and prognosis of respiratory viral infections in thoroughbred horses.
The Veterinary record    April 14, 1990   Volume 126, Issue 15 359-363 
Mason DK, Watkins KL, McNie JT, Luk CM.In late November 1988 large numbers of thoroughbred horses in training in Hong Kong developed a transient pyrexia with, in some cases, the clinical signs of viral respiratory disease. Serial blood samples for haematological examination were taken from 10 of the horses which were stabled in six different blocks. They had developed a high temperature within three days of each other and subsequently seroconverted to equine herpes virus 1 (EHV1). The absolute monocyte count was more than 0.5 x 10(9)/litre in all 10 within the first five days, and nine of them had a high neutrophil/lymphocyte ratio...
General health care and miscellaneous conditions of the racehorse.
The Veterinary clinics of North America. Equine practice    April 1, 1990   Volume 6, Issue 1 223-237 doi: 10.1016/s0749-0739(17)30564-3
McClure JM.This article provides an overview of general health care management procedures commonly dealt with by racetrack practitioners. Although some of the conditions discussed are similar to those observed in a non-racetrack practice, the manner in which they are approached usually varies because of the unique circumstances encountered in the racetrack setting.
[Concomitant activity of 2 bunyaviruses in horses in Argentina].
Revista Argentina de microbiologia    April 1, 1990   Volume 22, Issue 2 98-101 
Cámara A, Contigiani MS, Medeot SI.A serologic survey of horses for Kairi (KRI) and Cache Valley (CV), two related Bunyaviruses, was conducted simultaneously in Cordoba and Santa Fe provinces, Argentina, during late 1983 and 1984. The prevalence of neutralizing antibodies only for KRI was 13.3% and only for CV was 40.0%; but if the total positive sera for KRI and CV were taken into account, the prevalence reached 48.3 and 75.0%, respectively. The prevalence for CV was higher than for KRI in Cordoba (p less than 0.01), but both were similar in Santa Fe province. The demonstration of seroconversion in horses of the two zones for ...
Genetic drift of equine 2 influenza A virus (H3N8), 1963-1988: analysis by oligonucleotide mapping.
Veterinary microbiology    April 1, 1990   Volume 22, Issue 2-3 225-236 doi: 10.1016/0378-1135(90)90109-9
Berg M, Desselberger U, Abusugra IA, Klingeborn B, Linné T.Comparative analysis by RNA oligonucleotide fingerprints of total genomic RNA as well as the individual RNA segments of equine 2 influenza A virus strains from 1963, 1968, 1979, 1984, 1987 and 1988 revealed genetic diversity. Strains from the epizootic outbreak during 1978-1979 showed minor differences among their genomes. The Swedish isolates from 1979 up to 1988 showed increasing genomic heterogeneity indicating genetic drift.
Trajectory analysis of winds and vesicular stomatitis in North America, 1982-5.
Epidemiology and infection    April 1, 1990   Volume 104, Issue 2 313-328 doi: 10.1017/s0950268800059495
Sellers RF, Maarouf AR.Outbreaks of vesicular stomatitis, serotype New Jersey, during epidemics in the United States and northern Mexico, 1982-5, were examined by backward trajectories of winds to investigate spread and possible sources. The outbreaks selected for analysis did not involve introduction of disease by infected animals. The findings indicate that wind could have been responsible for carrying infection from northern Mexico to Arizona and New Mexico and thence to Colorado and Utah and on to Wyoming, Idaho and Montana. The results of these analyses are consistent with the findings from T1 RNAse fingerprint...
Pattern of transcription of the genome of equine infectious anemia virus.
Journal of virology    April 1, 1990   Volume 64, Issue 4 1839-1843 doi: 10.1128/JVI.64.4.1839-1843.1990
Noiman S, Yaniv A, Sherman L, Tronick SR, Gazit A.The pattern of expression of the equine infectious anemia virus (EIAV) genome in a persistently infected canine cell line was determined. Five EIAV-specific transcripts (8.2, 5.0, 4.0, 2, and 1.8 kilobases [kb]) were detected by using subgenomic restriction enzyme fragments of EIAV DNA and EIAV-specific oligonucleotides as probes. The 8.2-kb mRNA could be shown to represent viral genomic RNA, whereas the smaller transcripts were generated by splicing events. Evidence was obtained that indicated that each subgenomic RNA species shared a common 5'-splice donor. The 5.0-kb mRNA was found to be ex...
[Influenza or equine herpes virus (EHV)?].
Tijdschrift voor diergeneeskunde    March 15, 1990   Volume 115, Issue 6 272 
van Maanen C, Binkhorst GJ.No abstract available
Distribution of neutralizing antibodies to California and Bunyamwera serogroup viruses in horses and rodents in California.
The American journal of tropical medicine and hygiene    March 1, 1990   Volume 42, Issue 3 282-290 doi: 10.4269/ajtmh.1990.42.282
Campbell GL, Reeves WC, Hardy JL, Eldridge BF.Neutralization tests were done on sera from 141 horses from high elevation regions of California. Antibody prevalences to Jamestown Canyon, snowshoe hare, and California encephalitis viruses in the California serogroup and Northway virus in the Bunyamwera serogroup were 55%, 43%, 18%, and 46%, respectively. In 51 horses from rural low elevation regions, seroprevalences were 31%, 35%, 35%, and 37%, respectively. Twenty-four horses from a suburban lowland area were seronegative, except for a single horse with a low titer to snowshoe hare virus. Seroprevalence to Jamestown Canyon and snowshoe har...
One way protection between equid herpesvirus 1 and 4 in vivo.
Research in veterinary science    March 1, 1990   Volume 48, Issue 2 235-239 
Edington N, Bridges CG.Two groups each of six sibling ponies were exposed to sequential infections with equid herpesvirus 1 or 4 (EHV-1 or EHV-4) at four or five month intervals. Two exposures to EHV-4 did not significantly reduce virus shedding or pyrexia when the ponies were subsequently exposed to EHV-1. However, two sequential infections with EHV-1 completely protected against challenge with EHV-4. Virus neutralising antibody in each group did not increase until 21 days after primary exposure and was subtype specific. However, complement fixing antibody rose within seven days after inoculation with EHV-1, and 14...
Intracellular proteins of feline immunodeficiency virus and their antigenic relationship with equine infectious anaemia virus proteins.
The Journal of general virology    March 1, 1990   Volume 71 ( Pt 3) 739-743 doi: 10.1099/0022-1317-71-3-739
Egberink HF, Ederveen J, Montelaro RC, Pedersen NC, Horzinek MC, Koolen MJ.Feline immunodeficiency virus (FIV) grown in cat lymphocyte and thymocyte cultures was labelled with L-[35S]methionine or [3H]glucosamine and virus-coded proteins were identified using immunoprecipitation. Polypeptides with apparent Mr values of 15K, 24K, 43K, 50K, 120K and 160K were detected. An additional polypeptide of 10K was detected by Western blot analysis. The two highest Mr species sometimes appeared as one band, of which only the 120K polypeptide was glycosylated. In the presence of tunicamycin gp120 was no longer detectable and a non-glycosylated precursor of 75K was found instead. ...
Induction of immune response and protection from equine viral arteritis (EVA) by formalin inactivated-virus vaccine for EVA in horses.
Zentralblatt fur Veterinarmedizin. Reihe B. Journal of veterinary medicine. Series B    March 1, 1990   Volume 37, Issue 2 135-141 doi: 10.1111/j.1439-0450.1990.tb01036.x
Fukunaga Y, Wada R, Matsumura T, Sugiura T, Imagawa H.Thirty-nine horses included 3 pregnant mares were examined by inoculating with formalin inactivated-virus vaccine for EVA. Antibody response of horses after one dose vaccination was somewhat poor and 50% effective inoculum dose of the vaccine should be included 10(8.4) pfu of virus before inactivation. After 2 doses given at an interval of 4 weeks, the horses developed such high titer of SN antibody as up to 1:5,120. The SN titer declined rather rapidly, but supplemental administration of the vaccine at an interval of more than 2 months elicited a prompt antibody response and SN titers persist...
Experimental infection of ponies with equine influenza (H3N8) viruses by intranasal inoculation or exposure to aerosols.
Equine veterinary journal    March 1, 1990   Volume 22, Issue 2 93-98 doi: 10.1111/j.2042-3306.1990.tb04217.x
Mumford JA, Hannant D, Jessett DM.Infection of seronegative Welsh mountain ponies was established by intranasal instillation or exposure to nebulised aerosol of egg grown H3N8 viruses. Pyrexia and coughing were noted following intranasal instillation and high titres of virus were recovered from the nasopharynx. Exposure to aerosol resulted in more severe clinical signs characterised by high temperatures, dyspnoea, anorexia and coughing; lower levels of virus were recovered from the nasopharynx. The severity of clinical signs and the kinetics of virus shedding were dose-related with the minimal infectious dose being 10(2)EID50/...
Three-dimensional structures of maturable and abortive capsids of equine herpesvirus 1 from cryoelectron microscopy.
Journal of virology    February 1, 1990   Volume 64, Issue 2 563-573 doi: 10.1128/JVI.64.2.563-573.1990
Baker TS, Newcomb WW, Booy FP, Brown JC, Steven AC.Cryoelectron microscopy and three-dimensional computer reconstruction techniques have been used to compare the structures of two types of DNA-free capsids of equine herpesvirus 1 at a resolution of 4.5 nm. "Light" capsids are abortive, whereas "intermediate" capsids are related to maturable intracellular precursors. Their T = 16 icosahedral outer shells, approximately 125 nm in diameter, are indistinguishable and may be described in terms of three layers of density, totalling 15 nm in thickness. The outermost layer consists of protruding portions of both the hexon and the penton capsomers, ris...
Suppression of lymphocyte reactivity by culture supernatant from horse embryos and endometrium.
Biology of reproduction    February 1, 1990   Volume 42, Issue 2 294-300 doi: 10.1095/biolreprod42.2.294
Watson ED.The mechanisms that permit maternal tolerance of the conceptus allograft during early pregnancy in the mare have not been investigated. Embryos and endometria were collected from mares 14 days after ovulation and cultured for 20.5 h. The effect of addition of culture supernatant on incorporation of [3H]thymidine by equine peripheral blood lymphocytes was studied. Culture supernatant from endometrium of nonpregnant mares did not affect lymphocyte blastogenesis, but supernatant from both embryos and endometrium of pregnant mares reduced concanavalin A (Con A)- and phytohemagglutinin-induced blas...
[Current information on the subject of African horse sickness (AHS)].
Schweizer Archiv fur Tierheilkunde    January 1, 1990   Volume 132, Issue 4 205-210 
Kihm U, Ackermann M.The objective of the present review was to summarize current knowledge of African horse sickness (AHS), based on available literature (which is nonetheless relatively scant) and recent information obtained from the O.I.E. Brief description is made of the biology of AHS virus (an arbovirus, transmitted by Culicoides imicola), isolation of the agent, diagnosis by serotyping procedures, and preventive measures (such as protection of horses from insect infestation, or vaccination programs) which may be taken. The recent outbreaks in Spain, Portugal, and Morocco, have demonstrated that much more re...
[A rapid isolation of Venezuelan equine encephalomyelitis virus using the lanthanide immunofluorescence assay].
Voprosy virusologii    January 1, 1990   Volume 35, Issue 1 77-79 
Kharitonenkov IG, Gaĭdamovich SIa, Pomelova VG, Sokolova MV, Lavrova NA, Leonov SV, Zlobin VN.No abstract available
[New types of virus infections of domestic animals in the German Democratic Republic. 1. Serologic survey studies of the distribution of equine torovirus infections in the GDR].
Archiv fur experimentelle Veterinarmedizin    January 1, 1990   Volume 44, Issue 2 251-253 
Liebermann H.Sera collected from 124 horses were checked by means of the serum neutralisation test against equine Bern virus. Torovirusspecific antibodies were recordable from 35 percent of all horses tested. These results are likely to suggest that toroviruses are widespread in the GDR and occur not only in horses but in other domestic animals and in man, as well.
Temperature sensitivity of equine herpesvirus isolates: a brief review.
SAAS bulletin, biochemistry and biotechnology    January 1, 1990   Volume 3 124-128 
Jacob RJ, Price R, Bouchey D, Davis T, Borchelt J.This article reviews the findings on temperature sensitivity of equine herpesvirus isolates with an emphasis on equine herpesvirus 3, etiological agent of equine coital exanthema. The hypothesis is presented that the relative apathogenic nature of this herpesvirus may be an indirect result of its inability to synthesize and/or process glycoproteins needed by the virus to produce infectious virions at the normal body temperature of its natural host. It is suggested that equine herpesvirus 3 is the more evolved and naturally attenuated member of the equine herpesviruses.