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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.
[Study of precipitogens of equine infectious anemia virus]. Toma B, Goret P.No abstract available
[Microbiological studies on herpesvirus infections in the upper respiratory tract of the horse].
DTW. Deutsche tierarztliche Wochenschrift    February 1, 1973   Volume 80, Issue 3 49-52 
Floer W, Schmidt R, Petzoldt K.No abstract available
[Standardization of the hemagglutination-inhibition test for two equine influenza viruses]. Bürki F, Sibalin M.No abstract available
[Identification of the equine rhinopneumonitis virus isolated from aborted fetuses].
Veterinarno-meditsinski nauki    January 1, 1973   Volume 10, Issue 5 95-101 
Kharalambiev Kh, Ognianov D, Maklaklŭn P.No abstract available
Resistance of horses infected chronically with equine infectious anemia virus against reinfection.
National Institute of Animal Health quarterly    January 1, 1973   Volume 13, Issue 4 173-181 
Kono Y, Fukunaga Y, Kobayashi K.No abstract available
Antigenic drift of equine infectious anemia virus in chronically infected horses.
Archiv fur die gesamte Virusforschung    January 1, 1973   Volume 41, Issue 1 1-10 doi: 10.1007/BF01249923
Kono Y, Kobayashi K, Fukunaga Y.No abstract available
Structural proteins of equine arteritis virus.
Archiv fur die gesamte Virusforschung    January 1, 1973   Volume 40, Issue 3 177-188 doi: 10.1007/BF01242536
Hyllseth B.No abstract available
Physicochemical studies of equine infectious anemia virus. V. Effect of ultraviolet irradiation on virus infectivity.
Archiv fur die gesamte Virusforschung    January 1, 1973   Volume 41, Issue 1 135-137 doi: 10.1007/BF01249939
Nakajima H, Mizuno Y, Yasuda K, Ushimi C.No abstract available
Lyophilized combination pools of enterovirus equine antisera: preparation and test procedures for the identification of field strains of 42 enteroviruses.
Bulletin of the World Health Organization    January 1, 1973   Volume 48, Issue 3 263-268 
Melnick JL, Rennick V, Hampil B, Schmidt NJ, Ho HH.This paper describes the preparation of 8 dried pools (designated A to H) of sera. Each pool is composed of 10 or 11 of 42 individual enterovirus equine sera and contains 500 antibody units of each serum component per 0.1 ml. Procedures for using the antiserum pools are given, and guidance is provided for interpreting the results of serum neutralization tests in identifying field isolates.
Excretion of equine infectious anemia virus from horses infected with the virus.
National Institute of Animal Health quarterly    January 1, 1973   Volume 13, Issue 4 182-186 
Kono Y, Fukunaga Y, Kobayashi K.No abstract available
The complement-requiring neutralization of equine arteritis virus by late antisera.
Virology    January 1, 1973   Volume 51, Issue 1 71-77 doi: 10.1016/0042-6822(73)90366-8
Radwan AI, Burger D.No abstract available
Diagnosis of mixed infections with myxovirus influenzae A equi 2 and herpes virus equi 1 among Danish stud horses.
Acta veterinaria Scandinavica    January 1, 1973   Volume 14, Issue 2 205-218 doi: 10.1186/BF03547437
Jensen K.Examination of nasopharyngeal secretion and organ material from clinical cases of respiratory diseases in horses, using inoculation of embryonated hen eggs and rabbit and horse kidney cell cultures, resulted in the isolation of influenza virus and herpes virus. In 2 cases, both viruses were present in the same specimen. On the basis of the physio-chemical, cytological and serological criteria, the viruses were found to be identical with influenza virus type A equi 2 and herpes virus equi type 1. The methods for serological diagnosis and characterization of the influenza and herpes viruses are ...
WHO collaborative studies on enterovirus reference antisera; fourth report.
Bulletin of the World Health Organization    January 1, 1973   Volume 48, Issue 4 381-396 
Melnick JL, Hampil B.This paper summarizes the results of the fourth part of a comprehensive programme undertaken by the WHO International Reference Centre for Enteroviruses and other laboratories for the testing of enterovirus equine antisera prepared for long-term use as reference antisera. The studies were designed to appraise the specificity of the immune serum of horses inoculated with prototype enteroviruses (coxsackievirus types A2, 4, 8, 10, 11, 14-16, 18-21, and 24, and echoviruses E21, 27, 30, 31, and 33). Tests for neutralizing antibody were performed against the homologous viruses and against available...
[Demonstration of complement fixing antibodies in equine rhinovirus equine 1 infection].
Zentralblatt fur Veterinarmedizin. Reihe B. Journal of veterinary medicine. Series B    December 1, 1972   Volume 19, Issue 10 840-847 
Teufel P, Becker W.No abstract available
[Detection of the virus of equine rhinopneumonia by immunoluminescence].
Veterinariia    November 1, 1972   Volume 11 53-54 
Iurov KP, Kriukov NN.No abstract available
Development of an equine herpesvirus in two cell culture systems: light and electron microscopy.
Infection and immunity    November 1, 1972   Volume 6, Issue 5 865-876 doi: 10.1128/iai.6.5.865-876.1972
Fong CK, Hsiung GD.Development of equine herpesvirus strain 82A was studied in cells from primary horse kidney (HOK) cultures and an equine dermis (ED) cell strain. HOK and ED cells are equally susceptible to the 82A virus infection and yield about the same amount of infectious virus. Intranuclear inclusions were present in both cell systems, but a ring-shaped syncytial formation was observed only in infected ED cells. Ultrastructural studies revealed the presence of dense granules 30 nm in diameter and characteristic star-like clusters of granules in the infected HOK cells, but these granules were rarely seen i...
Effect of back passage of Venezuelan equine encephalomyelitis TC-83 vaccine virus on clinical, virologic, and immune responses in horses.
Journal of the American Veterinary Medical Association    October 1, 1972   Volume 161, Issue 7 824-831 
Luedke AJ, Barber TL, Foster NM, Batalla D, Mercado S.No abstract available
Isolation of an equine adenovirus.
Australian veterinary journal    October 1, 1972   Volume 48, Issue 10 580-581 doi: 10.1111/j.1751-0813.1972.tb08031.x
Wilks CR, Studdert MJ.No abstract available
A review of viral infections of horses.
Australian veterinary journal    September 1, 1972   Volume 48, Issue 9 520-523 doi: 10.1111/j.1751-0813.1972.tb02314.x
Bagust TJ.No abstract available
Central nervous system response of horses to Venezuelan equine encephalomyelitis vaccine (TC-83).
Journal of the American Veterinary Medical Association    August 1, 1972   Volume 161, Issue 3 265-269 
Monlux WS, Luedke AJ, Bowne J.No abstract available
Comparison of methods for diagnosing equine rhinopneumonitis virus abortion.
Veterinary medicine, small animal clinician : VM, SAC    August 1, 1972   Volume 67, Issue 8 895 
Trapp AL, Roberts AW, Carter GR.No abstract available
Isolation of an adenovirus from an Arab foal.
Australian veterinary journal    August 1, 1972   Volume 48, Issue 8 478 doi: 10.1111/j.1751-0813.1972.tb02299.x
Harden TJ, Pascoe RR, Spradbrow PB.No abstract available
Elimination of repeated clot formation in mouse ascitic fluid containing arbovirus antibodies.
Applied microbiology    August 1, 1972   Volume 24, Issue 2 288-289 doi: 10.1128/am.24.2.288-289.1972
Chiewsilp D, McCown JM.Repeated clot formation in mouse ascitic fluids containing antiviral antibody was eliminated by acid precipitation of the fibrinogen.
The role of respiratory viruses in equine disease.
The Veterinary record    July 8, 1972   Volume 91, Issue 2 33-36 doi: 10.1136/vr.91.2.33
Platt H.No abstract available
Japanese encephalitis in horses in Japan.
Equine veterinary journal    July 1, 1972   Volume 4, Issue 3 155-156 doi: 10.1111/j.2042-3306.1972.tb03900.x
Nakamura H.No abstract available
[Excretion of rhinopneumonitis virus in the semen of the stallion]. Thein P, Stolla R.No abstract available
The fluorescent antibody technique in the diagnosis of equine rhinopneumonitis virus abortion. Smith IM, Girard A, Corner AH, Mitchell D.Using two known positive equine viral rhinopneumonitis (EVR) sera, conjugates were prepared with fluorescein isothiocyanate and tested for specificity using EVR infected tissue culture cells. The conjugate was then applied to selected tissues from 32 aborted fetuses and foals submitted during a natural outbreak of EVR. Antigen was detected in various tissues by immunofluorescence in 20 cases (62.5%). In 24 cases bovine fetal kidney cell monolayers were inoculated with a pool of lung and liver and EVR virus was isolated from 15 (62.5%). Histological examination of various tissues from 29 cases ...
Preparation and evaluation of inactivated Venezuelan equine encephalitis vaccines.
Zentralblatt fur Veterinarmedizin. Reihe B. Journal of veterinary medicine. Series B    June 1, 1972   Volume 19, Issue 6 511-517 doi: 10.1111/j.1439-0450.1972.tb00430.x
Mussgay M, Bergold GH, Weiland E, Ueberschär S.No abstract available
Equine abortion (herpes) virus: strain differences in susceptibility to inactivation by dithiothreitol.
Applied microbiology    June 1, 1972   Volume 23, Issue 6 1121-1124 doi: 10.1128/am.23.6.1121-1124.1972
Klingeborn B, Dinter Z.The infectivity of equine abortion (herpes) virus (EAV) was inactivated by treatment with reduced dithiothreitol (DTT). According to their susceptibility to DTT, the EAV strains could be divided into three groups. The vaccine strain RAC-H (419) proved to be more resistant to DTT than all of the other 14 strains tested. The hemagglutinin of EAV was also inactivated by DTT; no strain differences were observed in this respect.
Study of the one-step growth curve of equine infectious anemia virus by immunofluorescence.
Infection and immunity    June 1, 1972   Volume 5, Issue 6 890-895 doi: 10.1128/iai.5.6.890-895.1972
Ushimi C, Henson JB, Gorham JR.Primary horse leukocyte cultures were inoculated with 2 or 10 50% tissue culture infective doses (TCID(50)) of equine infectious anemia (EIA) virus per cell, and the titer of cell-associated and fluid-phase virus was determined from 1 to 72 hr postinoculation (PI). Cover slips were collected from 4 to 72 hr PI and stained for EIA viral antigen by the indirect immunofluorescent (FA) technique. Viral replication was detected after a latent period of approximately 18 to 24 hr and reached peak titers of approximately 10(4.5) to 10(6) TCID(50)/0.5 ml from 48 to 72 hr PI. The fluid phase contained 1...
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