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两种DNA提取方法与巢式PCR、实时荧光定量PCR、一种新型商业PCR检测方法以及细菌培养法用于检测牛粪便中副结核分枝杆菌的比较

Comparison of two DNA extractions and nested PCR, real-time PCR, a new commercial PCR assay, and bacterial culture for detection of Mycobacterium avium subsp. paratuberculosis in bovine feces.

作者信息

Christopher-Hennings Jane, Dammen Matthew A, Weeks Shelleen R, Epperson William B, Singh Shri N, Steinlicht Gina L, Fang Ying, Skaare Jessica L, Larsen Jill L, Payeur Janet B, Nelson Eric A

机构信息

Animal Disease Research and Diagnostic Laboratory, South Dakota State University, Brookings, SD 57007, USA.

出版信息

J Vet Diagn Invest. 2003 Mar;15(2):87-93. doi: 10.1177/104063870301500201.

Abstract

In this study, 5 combinations of 2 DNA extractions and 3 polymerase chain reaction (PCR) techniques were compared with culture for the detection of Mycobacterium paratuberculosis directly from bovine feces. These combinations included a new commercial extraction technique combined with a commercial PCR/Southern blot technique, nested PCR (nPCR), or real-time PCR, and a university-developed extraction combined with nPCR or real-time PCR. Four of the 5 combinations had statistically similar sensitivities between 93% and 100% and specificity between 95% and 100%, when compared with culture results from 63 bovine fecal samples. These results indicated that using a commercial extraction with a commercial PCR/Southern blot, nPCR, or real-time PCR, or a university-developed extraction with real-time PCR would result in similar sensitivities to culture for the identification of M. paratuberculosis from bovine feces and are valid alternatives to culture.

摘要

在本研究中,对2种DNA提取方法和3种聚合酶链反应(PCR)技术的5种组合与培养法进行了比较,以直接从牛粪便中检测副结核分枝杆菌。这些组合包括一种新的商业提取技术与一种商业PCR/ Southern印迹技术、巢式PCR(nPCR)或实时PCR相结合,以及一种大学研发的提取方法与nPCR或实时PCR相结合。与63份牛粪便样本的培养结果相比,5种组合中的4种在敏感性方面具有统计学上的相似性,介于93%至100%之间,特异性介于95%至100%之间。这些结果表明,使用商业提取方法与商业PCR/ Southern印迹、nPCR或实时PCR相结合,或使用大学研发的提取方法与实时PCR相结合,在从牛粪便中鉴定副结核分枝杆菌时,其敏感性与培养法相似,是培养法的有效替代方法。

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