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Topic:Infectious Disease

Infectious diseases in horses encompass a range of illnesses caused by bacteria, viruses, fungi, or parasites. These diseases can affect various systems within the equine body, leading to symptoms that range from mild discomfort to severe systemic illness. Common infectious diseases in horses include equine influenza, strangles, equine herpesvirus, and West Nile virus. These diseases can be transmitted through direct contact with infected animals, contaminated surfaces, or vectors such as insects. Understanding the mechanisms of transmission, pathogenesis, and immune response is essential for effective prevention and control. This page compiles peer-reviewed research studies and scholarly articles that explore the epidemiology, diagnosis, treatment, and management of infectious diseases in horses.
Treatment of equine piroplasmosis (B caballi) with imidocarb dipropionate.
The Veterinary record    August 31, 1974   Volume 95, Issue 9 188-189 doi: 10.1136/vr.95.9.188
Frerichs WM, Holbrook AA.No abstract available
Mastitis in a mare caused by C ovis.
The Veterinary record    August 31, 1974   Volume 95, Issue 9 193 doi: 10.1136/vr.95.9.193
Addo PB, Wilcox GE, Taussig R.No abstract available
[Equine rhinovirus infection].
Berliner und Munchener tierarztliche Wochenschrift    August 15, 1974   Volume 87, Issue 16 305-308 
Becker W, Heller H, Teufel P.No abstract available
Experimental transmission of equine adenovirus in Arabian and non-Arabian foals.
American journal of veterinary research    August 1, 1974   Volume 35, Issue 8 1015-1023 
McChesney AE, England JJ, Whiteman CE, Adcock JL, Rich LJ, Chow TL.No abstract available
Isolation, cultivation and characterization of a poxvirus from some horses in Kenya.
Zentralblatt fur Veterinarmedizin. Reihe B. Journal of veterinary medicine. Series B    August 1, 1974   Volume 21, Issue 8 592-601 doi: 10.1111/j.1439-0450.1974.tb00534.x
Kaminjolo JS, Nyaga PN, Gicho JN.No abstract available
Equine infection with Micronema deletrix.
Journal of the American Veterinary Medical Association    August 1, 1974   Volume 165, Issue 3 256-258 
Rubin HL, Woodard JC.No abstract available
Chlamydial polyarthritis in a foal.
Journal of the American Veterinary Medical Association    August 1, 1974   Volume 165, Issue 3 259-261 
McChesney AE, Becerra V, England JJ.No abstract available
Equine encephalomyelitis due to a protozoan parasite resembling Toxoplasma gondii.
Journal of the American Veterinary Medical Association    August 1, 1974   Volume 165, Issue 3 249-255 
Dubey JP, Davis GW, Koestner A, Kiryu K.No abstract available
Recall of immunity in horses previously immunised with an aluminium based tetanus toxoid.
The Veterinary record    July 20, 1974   Volume 95, Issue 3 62-63 doi: 10.1136/vr.95.3.62
Scarnell J.No abstract available
Strongylus vulgaris infection in the horse.
The Veterinary record    July 13, 1974   Volume 95, Issue 2 34-37 doi: 10.1136/vr.95.2.34
Duncan JL.No abstract available
Diagnosis and prophylaxis of the most important infectious diseases of the respiratory tract in the horse (author’s transl).
Folia veterinaria Latina    July 1, 1974   Volume 4, Issue 3 455-485 
Thein P.No abstract available
[Clinical observations on virus-induced respiratory tract diseases in young trotting horses].
Berliner und Munchener tierarztliche Wochenschrift    July 1, 1974   Volume 87, Issue 13 251-253 
Keller H.No abstract available
Letter: The isolation of Leptospira pomona from a sick foal.
Australian veterinary journal    July 1, 1974   Volume 50, Issue 7 326 doi: 10.1111/j.1751-0813.1974.tb05336.x
Hogg GG.No abstract available
The diagnosis of rabies in a horse by brain neutralization test. Tabel H, Charlton KM.A horse showing clinical signs of a neurological disorder was killed and various diagnostic tests for rabies were carried out. Histopathlogy revealed a nonsuppurative encephalitis. Fluorescent antibody test and mouse inoculation test were negative. A positive diagnosis of rabies was based on a high antibody titer (1:10,000) to rabies virus in brain tissue.
[Natural antidiphtheria immunity in horses. Its relationship to decrease of diphtheria morbidity in Romania].
Archives roumaines de pathologie experimentales et de microbiologie    July 1, 1974   Volume 33, Issue 3-4 357-361 
Stănică E, Stoian C, Potorac E, Oprişan R, Cuşa E.No abstract available
Diagnosis, epidemiology and prophylaxis of equine infectious anaemia (author’s transl).
Folia veterinaria Latina    July 1, 1974   Volume 4, Issue 3 486-510 
Toma B.No abstract available
Purification and antigenicity of an M-like protein of Streptococcus equi.
Infection and immunity    July 1, 1974   Volume 10, Issue 1 116-122 doi: 10.1128/iai.10.1.116-122.1974
Woolcock JB.A cell wall component of Streptococcus equi analogous to the M protein of group A streptococci has been identified and purified. A highly purified product has been obtained from cells by hot acid extraction, followed by acid precipitation, ammonium sulfate fractionation, and column chromatography. This product reacts with S. equi antiserum. The existence of this fraction in S. equi has been confirmed by the failure of trypsin-treated cells and their extracts to remove the long-chaining capacity of S. equi antiserum. The antigenicity of this M-like protein when incorporated in adjuvant has been...
Antimicrobial sensitivity patterns in Staphylococcus aureus from animals.
Journal of the American Veterinary Medical Association    June 15, 1974   Volume 164, Issue 12 1183-1186 
Biberstein EL, Franti CE, Jang SS, Ruby A.No abstract available
Isolation of Mycoplasma bovigenitalium from an aborted equine foetus.
The Veterinary record    June 8, 1974   Volume 94, Issue 23 528 doi: 10.1136/vr.94.23.528
Langford EV.No abstract available
Letter: Experimental infection of a horse with an equine adenovirus.
Australian veterinary journal    June 1, 1974   Volume 50, Issue 6 278-279 doi: 10.1111/j.1751-0813.1974.tb05306.x
Pascoe RR, Harden TJ, Spradbrow PB.No abstract available
Isolation of haemolytic Actinobacilli from horses.
Acta pathologica et microbiologica Scandinavica. Section B: Microbiology and immunology    June 1, 1974   Volume 82, Issue 3 453-454 doi: 10.1111/j.1699-0463.1974.tb02351.x
Larsen JL.No abstract available
Equine infectious anemia.
Modern veterinary practice    June 1, 1974   Volume 55, Issue 6 471-472 
Vernon DF, Cox T.No abstract available
[Production of an antigen and antiserum for the serodiagnosis of equine infectious anemia].
Veterinariia    June 1, 1974   Issue 7 42-43 
Tokarik BI, Nikitin EE, Bondarenko NE, Shlygin AN, Belousov FF.No abstract available
Acute epistaxis associated with guttural pouch mycosis in two horses.
Journal of the American Veterinary Medical Association    May 15, 1974   Volume 164, Issue 10 1038-1040 
Lingard DR, Gosser HS, Monfort TN.No abstract available
A survey for Toxoplasma antibodies in northern California livestock and dogs.
Journal of the American Veterinary Medical Association    May 15, 1974   Volume 164, Issue 10 1034-1037 
Vanderwagen LC, Behymer DE, Riemann HP, Franti CE.No abstract available
[Outbreak of equine infectious anemia in the area of Kassel].
DTW. Deutsche tierarztliche Wochenschrift    May 15, 1974   Volume 81, Issue 10 237 
Feiling O, Heun E, Primus K, Zettl K.No abstract available
[Outbreak of equine infectious anemia in the area of Kassel].
DTW. Deutsche tierarztliche Wochenschrift    May 1, 1974   Volume 81, Issue 9 201 
Feiling O, Heun E, Primus K, Zettl K.No abstract available
[Experimental genital and nasal infection of horses with the equine coital exanthema virus]. Bürki F, Lorin D, Sibalin M, Ruttner O, Arbeiter K.No abstract available
Antigenic comparisons and serologic survey of equine adenoviruses.
American journal of veterinary research    May 1, 1974   Volume 35, Issue 5 693-699 
Studdert MJ, Wilks CR, Coggins L.No abstract available
Pancreatic involvement by Venezuelan equine encephalomyelitis virus in the hamster.
The American journal of pathology    May 1, 1974   Volume 75, Issue 2 349-362 
Gorelkin L, Jahrling PB.Pancreatic tissue from hamsters inoculated with a virulent strain of Venezuelan equine encephalomyelitis virus (VEE) was studied sequentially with fluorescent antibody, light and electron microscopic technics. Progressive viral growth and cellular necrosis in the pancreas were demonstrated. Pancreatic infection resulted from both viremia and direct extension from the spleen across contaminated serosal planes. Mature viruses traversed the endothelium within endothelial vesicles and were associated with acinar as well as islet cells.