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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.
Electron microscopy of equine respiratory viruses in organ cultures of equine fetal respiratory tract epithelium.
American journal of veterinary research    October 1, 1984   Volume 45, Issue 10 1953-1960 
O'Niell FD, Issel CJ, Henk WG.Organ cultures of equine fetal tracheal and nasal turbinate epithelium were inoculated with equine influenza virus-A1 (EIV-A1), equine herpesvirus-1 (EHV-1), or equine rhinovirus-1 (ERV-1). Infected organ cultures were processed for scanning and transmission electron microscopy at various intervals and were compared with noninfected controls. Organ cultures inoculated with ERV-1 appeared normal with the exception of rare island-like lesions in infected nasal turbinate. Virus particles were not seen in thin sections of organ cultures infected with ERV-1. The EHV-1 caused extensive loss of the e...
Pathogenicity of equine herpesvirus 1 subtype 2 for foals and adult pony mares.
Veterinary microbiology    October 1, 1984   Volume 9, Issue 6 533-542 doi: 10.1016/0378-1135(84)90015-4
Coignoul FL, Bertram TA, Cheville NF.Three pony mares and 4 pony foals were inoculated with a subtype 2 strain of equine herpesvirus 1. Foals had periods of fever 12 h and 2.5 days after inoculation and leukopenia, involving both neutrophils and lymphocytes, followed by leukocytosis. Mares had transient fever and leukopenia 24 hours after inoculation that were less severe than in foals. An increase in circulating virus-neutralizing antibody was seen in 2 of 3 inoculated mares, but not in foals. Attempts to isolate virus from blood were unsuccessful. These studies show that equine herpesvirus 1 subtype 2 is a mild pathogen for pon...
Experimental infection of horses and ponies by oral and intranasal routes with New York State reovirus type 3 and German reovirus types 1 and 3 equine isolates.
Zentralblatt fur Veterinarmedizin. Reihe B. Journal of veterinary medicine. Series B    October 1, 1984   Volume 31, Issue 9 707-717 doi: 10.1111/j.1439-0450.1984.tb01354.x
Conner M, Gillespie J, Schiff E, Holmes D, Frey M, Quick S.No abstract available
Antibodies to Berne virus in horses and other animals.
Veterinary microbiology    October 1, 1984   Volume 9, Issue 6 523-531 doi: 10.1016/0378-1135(84)90014-2
Weiss M, Steck F, Kaderli R, Horzinek MC.After inoculation into 2 foals, Berne virus induced neutralizing antibody, but did not cause clinical symptoms. In a horizontal study of seropositive mares and their offspring, a decline of maternal antibodies and a sudden synchronous seroconversion in all foals were observed, again without clinical symptoms. The virus is widespread in the Swiss horse population and has been so during the last decade; rises in antibody titers were noted in 9% of paired sera sampled at random. Positive reactions were also obtained in serum neutralization tests and ELISA using small numbers of horse sera from Ge...
Growth kinetics of equine respiratory tract viruses in cell and organ cultures.
American journal of veterinary research    October 1, 1984   Volume 45, Issue 10 1961-1966 
O'Niell FD, Issel CJ.Growth kinetics of equine influenza virus-A1, equine herpesvirus-1, and equine rhinovirus-1 were determined in susceptible cell monolayers and in organ cultures of equine fetal tracheal and nasal turbinate epithelium. Equine influenza virus-A1 was replicated in cell and organ cultures and was released more readily and for longer periods from nasal turbinate epithelium than from tracheal epithelium. Equine herpesvirus-1 was also replicated in cell and organ cultures. During the first 24 hours after inoculation, equine herpesvirus-1 was released more readily from tracheal epithelium than from na...
Immunologic relationships between equine herpesvirus type 1 (equine abortion virus) and type 4 (equine rhinopneumonitis virus).
American journal of veterinary research    October 1, 1984   Volume 45, Issue 10 1947-1952 
Fitzpatrick DR, Studdert MJ.The specificity of selected immune responses to equine herpesvirus type 1 (EHV-1) and type 4 (EHV-4) was examined in 3 colostrum-deprived specific-pathogen-free foals. Single foals were vaccinated with inactivated EHV-1, inactivated EHV-4, or control cell lysate plus adjuvant followed by successive intranasal challenge exposures with EHV-1 and EHV-4 or with EHV-4 and EHV-1. Vaccination with inactivated virus preparations elicited cellular immune responses and antibody which were augmented by subsequent challenge exposures. Cellular immune responses, as measured by in vitro lymphocyte blastogen...
Biotin-labeled antigen sandwich enzyme-linked immunosorbent assay (BLA-S-ELISA) for the detection of Japanese encephalitis antibody in human and a variety of animal sera.
Journal of immunological methods    September 4, 1984   Volume 72, Issue 2 401-409 doi: 10.1016/0022-1759(84)90008-5
Chang HC, Takashima I, Arikawa J, Hashimoto N.A biotin-labeled antigen (BLA) was adapted to a sandwich enzyme-linked immunosorbent assay (S-ELISA) for detection of Japanese encephalitis (JE) antibody in a variety of animal sera. JE antigen was fixed on the wells of a microplate and became bound to the specific antibody which could react with a peroxidase-labeled avidin conjugate and azino-di-(3-ethylbenzthiazolin sulfonic acid) (ABTS) as a substrate. The BLA-S-ELISA could simultaneously detect JE antibody in all hemagglutination inhibition (HI) positive sera from man, swine, monkey, horse, cattle, rabbit, rat, mouse and pigeon by using th...
Equine adenovirus 1 isolated from cauda equina neuritis.
Research in veterinary science    September 1, 1984   Volume 37, Issue 2 252-254 
Edington N, Wright JA, Patel JR, Edwards GB, Griffiths L.Equine adenovirus 1 was recovered after four to six passages from two out of three cases of cauda equina neuritis (CEN) using kidney monolayers. Similar treatment of lumbo-sacral spinal cord from six normal horses did not yield adenovirus. All three cases of CEN had antibodies to the neuritogenic myelin protein P2 while immunofluorescence demonstrated that autologous IgG bound to the myelin of affected nerves. Adenovirus was not detected in neural tissue by immunofluorescence.
Detection of eastern equine encephalomyelitis virus and Highlands J virus antigens within mosquito pools by enzyme immunoassay (EIA). II. Retrospective field test of the EIA.
The American journal of tropical medicine and hygiene    September 1, 1984   Volume 33, Issue 5 973-980 doi: 10.4269/ajtmh.1984.33.973
Hildreth SW, Beaty BJ, Maxfield HK, Gilfillan RF, Rosenau BJ.Enzyme immunoassays (EIAs) for eastern equine encephalomyelitis (EEE) and Highlands J (HJ) virus antigens were compared in a retrospective study with standard virus isolation procedures (VIP) for detection of alpha virus-infected mosquito pools. The original VIP was a plaque assay in chick embryo cell culture, and was performed in the years from 1979 to 1981. Using the original VIP as the reference standard, the sensitivity rate of the EIA was 0.7674 and the false negative rate was 0.2326. However, when the storage age and the initial virus titer of the sample were considered, the sensitivity ...
Antigenic variation during persistent infection by equine infectious anemia virus, a retrovirus.
The Journal of biological chemistry    August 25, 1984   Volume 259, Issue 16 10539-10544 
Montelaro RC, Parekh B, Orrego A, Issel CJ.The recurrent nature of equine infectious anemia has been attributed to relatively rapid antigenic variations in equine infectious anemia virus (EIAV) during persistent infection under selective immune pressures. This model was tested by serological and biochemical analysis of virus isolates recovered from separate febrile episodes in two experimentally infected ponies. Neutralization assays employing immune sera from the experimentally infected ponies demonstrated that distinct antigenic strains of virus predominate during sequential febrile episodes in a single pony. Analysis of the test str...
Enzyme-linked immunosorbent assay for detection of equine infectious anemia antibody to purified P26 viral protein.
American journal of veterinary research    August 1, 1984   Volume 45, Issue 8 1542-1543 
Shen DT, Gorham JR, McGuire TC.An indirect enzyme-linked immunosorbent assay (ELISA) was developed for the detection of equine infectious anemia (EIA) antibody in horse sera. Purified P26 viral protein was the antigen; alkaline phosphatase linked to rabbit anti-horse immunoglobulin G was the conjugate. The ELISA detected EIA antibodies in horse sera as early as 11 to 14 days after experimental inoculations. There was full agreement between the results of ELISA and the agar-gel immunodiffusion tests on EIA proficiency test sera. The ELISA readily detected EIA antibody in horse sera that had weak positive reactions on agar-ge...
Genomic alterations associated with persistent infections by equine infectious anaemia virus, a retrovirus.
The Journal of general virology    August 1, 1984   Volume 65 ( Pt 8) 1395-1399 doi: 10.1099/0022-1317-65-8-1395
Payne S, Parekh B, Montelaro RC, Issel CJ.The unique periodic nature of equine infectious anaemia (EIA) is believed to result from the ability of the infecting virus. EIAV, to undergo relatively rapid antigenic variations which circumvent host immune responses resulting in distinct virus populations in sequential clinical episodes in the persistently infected horse. This model was examined by oligonucleotide mapping comparisons of the RNA genomes of selected isolates of EIAV. Variations in oligonucleotide maps could be reproducibly demonstrated (i) after adaptation of the laboratory strain of EIAV to replication in a pony, (ii) after ...
Antigenic reactivity of the major glycoprotein of equine infectious anemia virus, a retrovirus.
Virology    July 30, 1984   Volume 136, Issue 2 368-374 doi: 10.1016/0042-6822(84)90173-9
Montelaro RC, West M, Issel CJ.The immunogenic contributions of the carbohydrate and peptide portions of the major envelope glycoprotein of equine infections anemia virus, EIAV gp90, were analyzed by measuring the effects of specific glycosidase and protease digestions on the reactivity of the glycoprotein with immune sera from infected horses. The results of both direct and competitive radioimmunoassay demonstrated that immune sera contained antibodies reactive with both the carbohydrate and protein moieties of EIAV gp90, with the predominant reactivity apparently against the gp90 peptide epitopes. These results contrast w...
Microneutralization test in PK(15) cells for assay of antibodies to louping ill virus.
Journal of clinical microbiology    July 1, 1984   Volume 20, Issue 1 128-130 doi: 10.1128/jcm.20.1.128-130.1984
Timoney PJ, Geraghty VP, Harrington AM, Dillon PB.A microneutralization test in PK(15) cells was developed to measure the neutralizing antibody response of a group of ponies experimentally challenged with louping ill virus. Viral cytopathic effect was maximal after 6 days of incubation, at which point titration endpoints were clear-cut and readily determinable. The assay compared favorably with the mouse neutralization test for accuracy and ease of performance.
Pathology of maternal genital tract, placenta, and fetus in equine viral arteritis.
Veterinary pathology    May 1, 1984   Volume 21, Issue 3 333-340 doi: 10.1177/030098588402100311
Coignoul FL, Cheville NF.Six pregnant mares were given equine viral arteritis virus intravenously. Tissues from genital tracts, placentae, and fetuses were examined by light and electron microscopy to study the mechanism of abortion. Four mares which died with acute disease had diffuse vacuolation of endometrial epithelium and systemic necrotizing vasculitis. Two of these mares had dead fetuses and two had live fetuses; virus was isolated from tissues of one live fetus. Placentae of mares dying from acute disease did not have lesions attributable to infection; virus was isolated from two of these placentae. One of the...
Ultrastructural comparison of Oncovirinae (type C), Spumavirinae, and Lentivirinae: three subfamilies of Retroviridae found in farm animals.
Journal of the National Cancer Institute    May 1, 1984   Volume 72, Issue 5 1075-1084 
Bouillant AM, Becker SA.The successive steps of maturation of seven retroviruses from five species of farm animals and one retrovirus from a mouse were compared in cell cultures. The viruses included three type C oncoviruses, one spumavirus, and three lentiviruses. Although members of the 3 subfamilies shared some gross morphologic features such as budding on plasma membranes, core, and surface projections, differences were noted in the ultrastructural detail of these features. Type C oncoviruses did not show any structural differentiation in identifiable form in the cytoplasm as opposed to characteristic features ob...
Equine cytomegalovirus: structural proteins of virions and nucleocapsids.
Virology    April 15, 1984   Volume 134, Issue 1 184-195 doi: 10.1016/0042-6822(84)90284-8
Caughman GB, Staczek J, O'Callaghan DJ.Enveloped virions and nucleocapsids of equine cytomegalovirus (ECMV; equine herpesvirus type 2) have been purified from the supernatants and the nuclear extracts of infected rabbit kidney (RK) cells, respectively, and their structural protein compositions have been analyzed. Sodium dodecyl sulfate-polyacrylamide gel electrophoresis analysis revealed that ECMV nucleocapsids were composed of nine proteins (average molecular weights = 148K, 52K, 49.5K, 46K, 43.5K, 38.5K, 27K, 20K, and 18K), which together constituted 89% of the total nucleocapsid protein on the basis of incorporated 3H-labeled am...
Trials of an inactivated equid herpesvirus 1 vaccine: challenge with a subtype 1 virus.
The Veterinary record    April 14, 1984   Volume 114, Issue 15 369-374 doi: 10.1136/vr.114.15.369
Burrows R, Goodridge D, Denyer MS.Vaccinated yearlings , two-year-old and in-foal pony mares with appropriate controls were exposed to aerosols of a subtype 1 virus one to two months after two or three vaccinations; all became infected. No obvious differences in the febrile responses, clinical signs and subsequent abortions were found between vaccinated and control mares. All vaccinated yearlings and two-year-old ponies developed a febrile respiratory disease but this was less severe than that suffered by the controls and the amounts and duration of virus shedding were reduced.
Trials of an inactivated equid herpesvirus 1 vaccine: challenge with a subtype 2 virus.
The Veterinary record    April 14, 1984   Volume 114, Issue 15 375-381 doi: 10.1136/vr.114.15.375
Mumford JA, Bates J.Serological responses following two and three doses of an inactivated equid herpesvirus 1 ( EHV -1) vaccine containing a subtype 1 strain were examined in yearling ponies. Complement fixing antibody responses were significantly higher against the subtype 1 vaccine strain than against a subtype 2 virus. Complement fixing antibody responses declined rapidly after the second dose of vaccine and had returned to almost pre-vaccination levels eight weeks after the second dose of vaccine. Complement fixing antibody titres to the heterologous subtype 2 strain increased after each successive dose of va...
Plaque assay of equine influenza virus.
Veterinary microbiology    April 1, 1984   Volume 9, Issue 2 187-192 doi: 10.1016/0378-1135(84)90034-8
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.
Herpesvirus diseases of veterinary importance.
Clinics in dermatology    April 1, 1984   Volume 2, Issue 2 147-151 doi: 10.1016/0738-081x(84)90073-7
Chang TW.No abstract available
Correlation of influenza A virus nucleoprotein genes with host species.
Virology    March 1, 1984   Volume 133, Issue 2 438-442 doi: 10.1016/0042-6822(84)90410-0
Bean WJ.The RNAs coding for the nucleoproteins of a panel of influenza isolates from human and nonhuman hosts were compared by RNA-RNA hybridization to determine the extent of genetic diversity of this protein and to determine if related nucleoproteins (NP) are consistently found in viruses from certain hosts. Five nucleoprotein groups were defined. Group 1 contains nearly all of the avian influenza viruses, group 2 includes only certain viruses isolated from gulls, group 3 includes all recent equine influenza strains, group 4 contains only equine/Prague/1/56, and group 5 contains all human and swine ...
[The neurological form of EVH1 in horses].
Tijdschrift voor diergeneeskunde    February 1, 1984   Volume 109, Issue 3 94 
van Oirschot JT, Binkhorst JT, Breukink HJ.No abstract available
Carriers of equine infectious anemia virus.
Journal of the American Veterinary Medical Association    February 1, 1984   Volume 184, Issue 3 279-281 
Coggins L.Presently available data continue to support the idea that once a horse is infected with equine infectious anemia virus it remains infected indefinitely. Infection may not always be demonstrated by inoculation of plasma, serum, or whole blood transfusions into susceptible recipients, but transfusions of fresh whole blood will be infective in at least 95% of the horses testing positive in the agar gel immunodiffusion test. For detection of infectivity in a small percentage of inapparent carriers, it appears necessary to inoculate washed leukocytes collected over a period of time.
Studies on equine infectious anemia virus transmission by insects.
Journal of the American Veterinary Medical Association    February 1, 1984   Volume 184, Issue 3 293-297 
Issel CJ, Foil LD.There are several factors involved in the mechanical transmission of equine infectious anemia (EIA) virus by insects. Large hematophagous insects, especially tabanids, which feed from extravascular sites (ie, pool feeding) appear to be the most efficient vectors. The biology of the host-seeking and blood-feeding behavior of the vectors are important variables that have been overlooked in the mechanical transmission of pathogens like EIA virus. The biology, population levels, and diversity of the vectors, in addition to the clinical status and proximity of EIA virus-infected horses maintained w...
Isolation and characteristics of an equine reovirus type 3 and an antibody prevalence survey to reoviruses in horses located in New York State.
Veterinary microbiology    February 1, 1984   Volume 9, Issue 1 15-25 doi: 10.1016/0378-1135(84)90075-0
Conner M, Kalica A, Kita J, Quick S, Schiff E, Joubert J, Gillespie J.Reoviruses have been isolated from a number of species including human, bovine, feline, canine and equine. In most species they seem to produce mild to inapparent disease. We have isolated a reovirus type 3 from a foal with diarrhea. The virus designated the Ralph strain has been propagated in both the MA-104 and A-72 cell lines. The strain produced cytoplasmic inclusion bodies in these cell cultures. Tissue-cultured virus fixed complement in the presence of reovirus antibodies, but failed to do so in the presence of rotavirus antiserum. By electron microscopy the viral particle measured +/- 6...
Coestablishment of persistent infection and oncogenic transformation of hamster embryo cells by equine cytomegalovirus.
Virology    January 30, 1984   Volume 132, Issue 2 339-351 doi: 10.1016/0042-6822(84)90040-0
Staczek J, Wharton JH, Dauenhauer SA, O'Callaghan DJ.Semipermissive, primary hamster embryo (HE) cells were morphologically transformed in vitro by infection with UV-irradiated equine cytomegalovirus (equine herpesvirus type 2; ECMV). Cell lines (designated EC-1-3) were established independently from foci and were shown to exhibit growth and biological properties typically associated with transformed cells: altered morphology, loss of contact inhibition, increased saturation density, decreased generation time, immortality in culture, normal growth in low concentrations of serum, colony formation in soft agar, and resistance to ECMV superinfectio...
[Current virus diseases in horses. Diseases in foals and respiratory tract infections].
Tierarztliche Praxis    January 1, 1984   Volume 12, Issue 4 481-488 
Mayr A, Thein P.At the moment, horse praxis is confronted by two disease complexes which are difficult to fight against as well in prophylaxis as in therapy, but which get an increasing importance. First they concern virus infections of the foals and second primary virus-caused respiratory diseases. Foals get infected during the embryonal/fetal development, in the perinatal or postnatal period. Normally the infection is caused by latent infected, clinical healthy mares, or in the postnatal period by ubiquitous, normally opportunistic socalled problem-viruses, i.e. equine herpes-viruses 1 and 2, rota-, corona-...
Borna disease of horses. An immunohistological and virological study of naturally infected animals.
Acta neuropathologica    January 1, 1984   Volume 64, Issue 3 213-221 doi: 10.1007/BF00688111
Gosztonyi G, Ludwig H.The brains of eight horses that had suffered from natural Borna disease were examined with virologic, immunohistological, and electron-microscopic methods. All brains harbored infectious virus as shown by inoculation of experimental animals. Regional assessment of the infectivity exhibited the highest titers in the hippocampus and piriform cortex and the lowest in the cerebellum. Conventional histology yielded pathologic alterations very similar to those of the classical description of the disease. Immunohistology demonstrated the highest amounts of Borna disease virus-specific antigen in the ...
Detection of equine infectious anemia virus in horse leukocyte cultures derived from horses in various stages of equine infectious anemia viral infection.
American journal of veterinary research    January 1, 1984   Volume 45, Issue 1 20-25 
Evans KS, Carpenter SL, Sevoian M.The enzyme-linked immunosorbent assay (ELISA) antigen-positive and agar-gel immunodiffusion test (AGID)-negative horses do not have infective equine infectious anemia (EIA) virus. The ELISA testing of horse leukocyte culture (HLC) supernatants did detect EIA virus in a HLC that was infected with the Wyoming strain of EIA virus and in HLC derived from horses in febrile, acute, or subacute stages of EIA infection. In supernatants of HLC derived from chronic and inapparent carrier horses, EIA virus was not detected with ELISA. Direct fluorescent antibody tests detected EIA virus in HLC infected w...