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用于研究猪肺炎支原体菌株间遗传多样性的实时聚合酶链反应检测

Real-time PCR assays to address genetic diversity among strains of Mycoplasma hyopneumoniae.

作者信息

Strait Erin L, Madsen Melissa L, Minion F Chris, Christopher-Hennings Jane, Dammen Matthew, Jones Katherine R, Thacker Eileen L

机构信息

Department of Veterinary Microbiology and Preventive Medicine, Iowa State University, Ames, IA 50011, USA.

出版信息

J Clin Microbiol. 2008 Aug;46(8):2491-8. doi: 10.1128/JCM.02366-07. Epub 2008 Jun 4.

Abstract

Mycoplasma hyopneumoniae is an important cause of pneumonia in pigs around the world, but confirming its presence in (or absence from) pigs can be difficult. Culture for diagnosis is impractical, and seroconversion is often delayed after natural infection, limiting the use of serology. Numerous PCR assays for the detection of M. hyopneumoniae have been developed, targeting several different genes. Recently, genetic diversity among strains of M. hyopneumoniae was demonstrated. The effect of this diversity on the accuracy and sensitivity of the M. hyopneumoniae PCR assays could result in false-negative results in current PCR tests. In this study, a panel of isolates of M. hyopneumoniae, M. flocculare, M. hyorhinis, and M. hyosynoviae were tested with a number of M. hyopneumoniae-specific PCR assays. Some M. hyopneumoniae PCR assays tested did not detect all isolates of M. hyopneumoniae. To increase the efficiency of PCR testing, two new real-time PCR assays that are specific and capable of detecting all of the M. hyopneumoniae isolates used in this study were developed.

摘要

猪肺炎支原体是全球猪肺炎的重要病因,但要确定其在猪体内的存在(或不存在)可能很困难。用于诊断的培养方法不切实际,而且自然感染后血清转化通常会延迟,这限制了血清学的应用。已经开发了许多用于检测猪肺炎支原体的PCR检测方法,针对几个不同的基因。最近,已证明猪肺炎支原体菌株之间存在遗传多样性。这种多样性对猪肺炎支原体PCR检测方法的准确性和敏感性的影响可能导致当前PCR检测出现假阴性结果。在本研究中,使用多种猪肺炎支原体特异性PCR检测方法对一组猪肺炎支原体、絮状支原体、猪鼻支原体和猪滑膜支原体分离株进行了检测。所测试的一些猪肺炎支原体PCR检测方法未能检测到所有猪肺炎支原体分离株。为了提高PCR检测效率,开发了两种新的实时PCR检测方法,它们具有特异性,能够检测本研究中使用的所有猪肺炎支原体分离株。

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