Disease outbreaks in horses refer to the occurrence and spread of infectious diseases within equine populations. These outbreaks can be caused by various pathogens, including bacteria, viruses, and parasites, and can lead to significant health issues in affected horses. Common diseases that may result in outbreaks include equine influenza, equine herpesvirus, strangles, and equine infectious anemia. The transmission of these diseases can occur through direct contact, environmental exposure, or vectors such as insects. Disease outbreaks can have substantial impacts on horse health, welfare, and the equine industry as a whole. This page compiles peer-reviewed research studies and scholarly articles that explore the epidemiology, transmission dynamics, and management strategies associated with disease outbreaks in equine populations.
Pocurull DW, Gaines SA, Mercer HD.Salmonella cultures were obtained from outbreaks of animal disease from 37 states and 1 territory. They were screened for resistance to 11 antimicrobial drugs. Of the 1,251 strains studied, 935 were resistant to one or more of these agents. The three most common resistance patterns were ampicillin, dihydrostreptomycin, sulfamethoxypyridazine, tetracycline; ampicillin, dihydrostreptomycin, sulfamethoxypyridazine; dihydrostreptomycin, sulfamethoxypyridazine, tetracycline. Resistance transfer was demonstrated on 267 multiply resistant cultures, of which 181 were able to transfer all or part of th...
Scott GR.Twelve DNA viruses and forty‐three RNA viruses are known to infect horses. In addition, there are three unclassified viruses and, at least, three alleged viruses infecting horses. Differential diagnosis is difficult. At least twenty‐eight of the fifty‐eight viruses induce clinical disease but the range of syndromes is limited; eleven provoke respiratory symptoms and eleven cause encephalitis. Thirty‐four equine viruses with a limited geographical distribution are transmitted by arthropod vectors. Twenty viruses are spread by contact and their distribution, in general, is global. The ve...
McClure JJ.Diagnostic criteria should be carefully defined and described in disease association studies to allow (1) comparison among studies from different laboratories evaluating the same disease, (2) critical evaluation of selection procedures of patients, and (3) to strengthen genuine associations with any genetic marker system. Factors to consider include age at onset of disease, specialized diagnostic methods necessary to diagnose or eliminate patients with a selected disease, ranges of affectedness and differences in sex expression.
Andersson-Eklund L, Andersson L, Sandberg K.A study was carried out to attempt to explain the basis of the association between the Es locus and starting proportion in Swedish Trotters which had been observed previously. The effect of Es genotype on starting proportion has diminished among horses born in the late 1970s. There are indications that the incidence of leg lesions varies between Es genotypes. If this is true, it is possible that the decreasing effect of the Es locus on starting proportion is due to the environmental changes which have been made at race tracks in the early 1980s to reduce the strain on the legs of the trotters....
de Almeida Campos AC, Cicolo S, de Oliveira CM, Molina CV, Navas-Suárez PE, Dos Santos TP, da Silveira VB, Barbosa CM, Baccarin RYA, Durigon EL....No abstract available
Wichtel JJ, Whitlock RH.Botulism was believed to be the cause of progressive symmetric myasthenia in 8 horses on a farm in North Carolina. One horse was found dead, 6 were euthanatized after becoming recumbent, and 1 affected horse recovered. Cecal and colonic contents of 2 horses were determined to contain Clostridium botulinum spores. Alfalfa hay that was fed to the horses contained spores and toxin.
Heitmann J, Kirchhoff H, Chercheletzi C, Jonas E, Deegen E.Acholeplasmas were detected in five of 96 feces samples from clinically normal horses. Three of the five strains isolated were identified as A. equifetale, one as A. hippikon, and one was serologically identical with the Acholeplasma strain 881.