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.
The Journal of hygieneJune 1, 1971
Volume 69, Issue 2 201-207 doi: 10.1017/s0022172400021434
Sinclair IS, McCormick JS, Clark JG.The three heterologous anti-sera currently provided for tetanus prophylaxis have been compared with reference to the production of untoward reactions in 498 patients, and to the blood antitoxin concentrations produced in 76 patients. Equine serum, although giving rise to more reactions, was the only effective agent in terms of the levels and duration of serum antitoxin concentration produced. The local response to a test dose of any of the three sera is not a reliable guide to immediate or late general reactions.
Lawrence WC.Autoradiographic analyses of deoxyribonucleic acid (DNA) synthesis in randomly growing KB cell cultures infected with equine abortion virus (EAV) suggested that viral DNA synthesis was initiated only at times that coincided with the entry of noninfected control cells into the S phase of the cell cycle. Synchronized cultures of KB cells were infected at different stages of the cell cycle, and rates of synthesis of cellular and viral DNA were measured. When cells were infected at different times within the S phase, viral DNA synthesis was initiated 2 to 3 hr after infection. However, when cells ...
DeMeio JL, DeSanctis AN.Normal and immune sera were obtained from horses immunized with either aqueous, alum, or adjuvant bivalent vaccines containing Milford equine 2 virus. Upon heating at 56 C for 30 min, a factor, required for hemagglutination-inhibition but not complement fixation or neutralization testing, was destroyed. This factor which is present in normal sera does not appear to be complement.
Heydrick FP, Comer JF, Wachter RF.Phospholipid analyses of Venezuelan equine encephalitis virus showed that virus propagated in L-cell monolayers had a higher sphingomyelin content and a lower phosphatidylcholine content than virus grown in chick fibroblast monolayers. Virus of L-cell origin also was found to possess greater thermal stability than virus derived from the chick fibroblast cell.
Gruber J.Purified and concentrated Venezuelan equine encephalitis (VEE) virus derived from tissue cultures, rendered noninfectious by ionizing radiation with retention of in vitro serological activity, also retained a high level of immunogenicity. In mice, fluid vaccines afforded excellent protection against lethal challenge with homologous Trinidad strain VEE virus. A direct relationship was observed between concentration of vaccine or number of injections and survival. One intraperitoneal inoculation of undiluted vaccine protected essentially all mice challenged 21 days later with 100,000 mouse intra...
Henderson BE, Chappell WA, Johnston JG, Sudia WD.Henderson, B. E., W. A. Chappell, J. G. Johnston, Jr. and W. D. Sudia (CDC, Atlanta, Ga. 30333). Experimental Infection of horses with three strains of Venezuelan equine encephalomyelitis virus. I. Clinical and virological studies. Amer J Epidem 93: 194–205, 1971.—Clinical effect, viremias and antibody responses were compared in horses inoculated with the following strains of Venezuelan equine encephalomyelitis (VEE) virus: Fe3-7C, isolated from Culex (Melano-conion) spp. mosquitoes collected In 1963 in the Florida Everglades; TC-83, the Fort Detrick live, attenuated vaccine strain; and GJ...
Sturm RT, Lang GH, Mitchell WR.The sera of 2596 thoroughbred and standardbred racehorses from Ontario were examined by hemagglutination-inhibition for antibodies to reovirus types 1, 2 and 3. The prevalence of antibodies differed between the standardbred and thoroughbred horses and varied with the age groups within the two populations. While reovirus 1 was the principal virus type infecting thoroughbreds, all three types seemed to infect standardbred horses. Differences of these findings with data from similar studies in Europe are mentioned and the epizootiological and pathological significance of these findings are discus...
Balasuriya UBR.The primary goals of this chapter are to discuss common viral RNA isolation and purification methods that are routinely used by various diagnostic laboratories and to highlight the advantages and drawbacks of each method and to identify the most suitable and reliable method to increase the sensitivity and specificity of RT-PCR assays for the detection of equine influenza virus (EIV) in clinical specimens. Our experiences and review of literature show that magnetic bead-based nucleic extraction methods (manual and automatic) work well for isolation and purification of EIV RNA from nasal swab sp...
Orsini JA.The multiple topics summarized in this article and discussed in detail in this issue of VCNA are comprehensive and in-depth, exploring concepts and clinical experiences for state-of-the-art care of the equine foot. The research on the equine foot will translate to the clinical setting and with this the compassionate care of the horse.