2019
DOI: 10.1016/j.tvjl.2019.02.003
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Long term silent carriers of Streptococcus equi ssp. equi following strangles; carrier detection related to sampling site of collection and culture versus qPCR

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Cited by 22 publications
(27 citation statements)
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“…In this study J. Pringle and colleagues in Sweden and Germany reported on long‐term silent carriers of Streptococcus equi ssp . equi ( S. equi ) following strangles .…”
Section: Silent Carriers Of S Equi Ssp Equi After Stranglesmentioning
confidence: 90%
“…In this study J. Pringle and colleagues in Sweden and Germany reported on long‐term silent carriers of Streptococcus equi ssp . equi ( S. equi ) following strangles .…”
Section: Silent Carriers Of S Equi Ssp Equi After Stranglesmentioning
confidence: 90%
“…Two horses were euthanized at the onset of the outbreak because of the development of clinical signs of strangles in combination with advanced age and poor dentition. The remaining 41 horses (mean age, 16.0 ± SD 6.6 years), including 32 geldings and 9 mares, were followed prospectively clinically, serologically and by upper respiratory microbiology from acute illness through clinical recovery as part of a larger study on the development of silent carriers . All horses were S. equi positive by culture, qPCR positive, or both during the acute phase (first 7 weeks after the index case) and all but 1 horse had an episode of fever during that time.…”
Section: Methodsmentioning
confidence: 99%
“…Visual appearance of the guttural pouches was graded by experienced endoscopists blinded to carrier status. 5 Scoring was based on summation of grades from both guttural pouches, with 0 for no abnormalities, 1 if there was any trace of cloudy mucous in either guttural pouch, and 2 for presence of moderate to marked purulence, chondroid formation or visible remnants of scarring in the ventral aspect of the guttural pouch, providing a theoretical maximal grade of 6 ( Table 1). Table 1.…”
Section: Timing Of Carrier State Examinationmentioning
confidence: 99%
“…Guidelines for detection of S. equi in carriers, either by culture or detection of bacterial DNA by qPCR, have been described 2 consisting of either nasopharyngeal washes and/ or guttural pouch endoscopy and lavage. 5 Ideally, in unvaccinated populations incorporation of the recently developed combined iELISA to identify animals that have been exposed to S. equi, followed with targeted testing by qPCR for those animals which may still harbor S. equi is advised to optimize within herd biosecurity measures. 2 However, for many countries such early intervention is not applied widely, with uniform diagnostic testing lacking in most strangles outbreaks.…”
mentioning
confidence: 99%