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牛分枝杆菌环介导等温扩增检测方法的建立。

Development of a loop-mediated isothermal amplification assay for the detection of Mycobacterium bovis.

机构信息

College of Veterinary Medicine, South China Agricultural University, 483 Wushan Street, Guangzhou 510642, People's Republic of China.

出版信息

Vet J. 2011 Mar;187(3):393-6. doi: 10.1016/j.tvjl.2010.01.001. Epub 2010 Feb 7.

Abstract

Bovine tuberculosis caused by Mycobacterium bovis is an important zoonosis. In this study, a simple, rapid method for detecting this organism was developed based on loop-mediated isothermal amplification of the mpt83 gene. The technique will be of value in the clinical and field-based diagnosis of M. bovis and can differentiate it from other bacteria such as Corynebacterium diphtheriae, Streptococcus pneumoniae, β-haemolytic streptococci, Pseudomonas aeruginosa, Yersinia pseudotuberculosis, Staphylococcus aureus, and Klebsiella pneumoniae. The limit of detection was 10 copies/μL and the results were corroborated by PCR. The method was highly specific and more sensitive than PCR.

摘要

牛分枝杆菌引起的牛结核病是一种重要的人畜共患病。本研究基于 mpt83 基因环介导等温扩增,建立了一种简单、快速的检测该病原体的方法。该技术将有助于牛分枝杆菌的临床和现场诊断,并可将其与白喉棒状杆菌、肺炎链球菌、β-溶血性链球菌、铜绿假单胞菌、假结核耶尔森菌、金黄色葡萄球菌和肺炎克雷伯菌等其他细菌区分开来。检测限为 10 拷贝/μL,结果与 PCR 相符。该方法具有高度特异性,比 PCR 更灵敏。

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