巢式PCR检测环境样品中的牛分枝杆菌

Tae-woon Kim, Yunho Jang, M. K. Jeong, Jae-Myung Kim, Y. J. Lee, Seung-Bum Kim, Soon-Seek Yoon, Jeong-Soo Choi
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引用次数: 0

摘要

在环境样本中精确检测牛分枝杆菌(M. bovis)对于在牛群水平上控制牛结核病(bTB)感染至关重要,因为残留的牛分枝杆菌仍然是反复感染的主要原因之一。本研究采用巢式PCR方法检测环境样品中的牛分枝杆菌,以确定该细菌的潜在环境宿主。采用巢式PCR检测残留牛支原体的方法,对来自39个有bTB暴发史的畜群的200份环境样本(167份粪便样本和33份水样)进行分析。利用已建立的两组引物从牛分枝杆菌DNA中扩增出IS6110靶基因片段的扩增文库。69.5%的粪便和66.7%的水样巢式PCR阳性,表明btb阳性畜群的环境样品中存在较高比例的牛分枝杆菌残留。这项研究首次证明了环境样本中存在高水平的牛支原体DNA,并表明这种病原体的环境宿主有助于结核分枝杆菌的反复暴发。对发生bTB暴发的畜群进行高灵敏度和特异性的环境监测,有望有助于预防潜在的bTB疾病复发并改善畜群环境。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Detection of Mycobacterium bovis in environmental samples using nested PCR
The detection of Mycobacterium bovis (M. bovis) in environmental samples with precision is imperative to control bovine tuberculosis (bTB) infections at the herd level, as residual M. bovis remains one of the major causes of recurring infections. In this study, a nested PCR method for the detection of M. bovis in environmental samples was applied to identify potential environmental reservoirs of the bacterium. A set of 200 environmental samples (167 fecal samples and 33 water samples) from 39 herds with a history of bTB outbreak was analyzed using a nested PCR method to detect residual M. bovis. Amplicon libraries of the IS6110 target gene fragment were amplified from M. bovis DNA using two established primer sets. A positive nested PCR result was observed in 69.5% of fecal samples and 66.7% of water samples, thus showing that residual M. bovis was present in the environmental samples of bTB-positive herds in a high proportion. This study is the first to demonstrate high levels of M. bovis DNA in environmental samples and to show that environmental reservoirs of this pathogen contribute to recurring outbreaks of bTB. Environmental monitoring of herds in which bTB outbreaks have occurred with high sensitivity and specificity is expected to help prevent the recurrence of potential bTB disease and improve the herd environment.
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