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首页> 外文期刊>Journal of Veterinary Diagnostic Investigation >Quantification of Malassezia pachydermatis by real-time PCR in swabs from the external ear canal of dogs
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Quantification of Malassezia pachydermatis by real-time PCR in swabs from the external ear canal of dogs

机译:从狗外耳运河的拭子实时PCR定量Malassezia pachydermatis

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Malassezia pachydermatis is part of the normal microbiota of canine skin and external ear canal, and is also associated with otitis externa in dogs. Laboratory detection of Malassezia otitis relies on the presence of elevated numbers of the yeast on cytologic examination of otic exudate. Although cytology has high specificity, it has low sensitivity, resulting in false-negatives and posing a challenge for clinicians to accurately diagnose Malassezia otitis. We developed a quantitative PCR (qPCR) to detect and quantify M. pachydermatis yeasts and validate the method with swabs from external ear canals of dogs. Our qPCR uses the -tubulin gene, a single-copy gene, as a target. The limit of quantification was established as 0.18ng/reaction, equivalent to 2.0 x 10(4) genome equivalents (gEq). Swabs from healthy dogs yielded quantification values of 2.7 x 10(4)gEq in the qPCR, whereas swabs from dogs with otitis yielded quantification values of 2.5 x 10(5)gEq. Our qPCR assay provides accurate quantification of M. pachydermatis yeasts from swab samples from dogs, is more sensitive than cytology, and could be used to monitor response to treatment. Our assay could also be valuable in a research setting to better understand the pathogenesis of M. pachydermatis.
机译:Malassezia pachydermatis是犬皮肤和外耳道正常微生物群的一部分,也与狗中的耳炎有关。实验室检测malassezia耳炎依赖于酵母数量升高的酵母渗透物渗出物的情况。虽然细胞学具有很高的特异性,但敏感性低,导致虚假否定,对临床医生构成挑战,以准确诊断Malassezia耳炎。我们开发了定量的PCR(QPCR),以检测和定量M. pachydermatis酵母,并验证狗的外耳道拭子的拭子。我们的QPCR使用-Tubulin基因,单拷贝基因作为目标。定量限定为0.18ng /反应,相当于2.0×10(4)个基因组当量(GEQ)。来自健康狗的拭子在QPCR中产生了2.7×10(4)个GEQ的定量值,而来自耳儿炎的狗的拭子会产生2.5×10(5)GEQ的定量值。我们的QPCR测定提供了从狗的棉签样本的M. pachydermatis酵母的准确定量,比细胞学更敏感,可用于监测对治疗的反应。我们的测定在研究环境中也可能是有价值的,以更好地了解M. Pachydermatis的发病机制。

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