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首页> 外文期刊>Journal of Clinical Microbiology >Rapid Identification of Mycobacterium tuberculosis and Nontuberculous Mycobacteria by Multiplex, Real-Time PCR
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Rapid Identification of Mycobacterium tuberculosis and Nontuberculous Mycobacteria by Multiplex, Real-Time PCR

机译:多重实时PCR快速鉴定结核分枝杆菌和非结核分枝杆菌

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The rapid identification of mycobacteria from culture is of primary importance for the administration of empirical antibiotic therapy and for the implementation of public health measures, yet there are few commercially available assays that can easily and accurately identify the mycobacteria in culture in a timely manner. Here we report on the development of a multiplex, real-time PCR assay that can identify 93% of the pathogenic mycobacteria in our laboratory in two parallel reactions. The mycobacteria identified by this assay include the Mycobacterium tuberculosis complex (MTC), the M. avium complex (MAC), the M. chelonae-M. abscessus group (MCAG), the M. fortuitum group (MFG), and M. mucogenicum. The primer targets included the 16S rRNA gene and the internal transcribed spacer. The assay was initially validated with a repository of reference strains and was subsequently tested with 314 clinical cultures identified by the AccuProbe assay or high-performance liquid chromatography. Of the 314 cultures tested, multiplex, real-time PCR produced congruent results for 99.8% of the 1,559 targets evaluated. The sensitivity and the specificity were each 99% or greater for MTC (n = 96), MAC (n = 97), MCAG (n = 68), and M. mucogenicum (n = 9) and 95% and 100%, respectively, for MFG (n = 19). We conclude that this multiplex, real-time PCR assay is a useful diagnostic tool for the rapid and accurate identification of MTC and clinically relevant nontuberculous mycobacteria.
机译:从培养中快速鉴定分枝杆菌对于经验性抗生素治疗的实施和公共卫生措施的实施至关重要,但是很少有商业化的检测方法可以轻松,准确地及时鉴定培养物中的分枝杆菌。在这里,我们报告了一种实时多重PCR检测方法的开发情况,该方法可以在两个平行反应中鉴定出我们实验室中93%的致病性分枝杆菌。通过该测定法鉴定的分枝杆菌包括结核分枝杆菌复合物(MTC), M。鸟笼(em)复合物(MAC),即 M。 chelonae - M 脓肿组(MCAG), M。 组(MFG)和 M。 mucogenicum 。引物的靶标包括16S rRNA基因和内部转录的间隔区。该方法最初使用参考菌株库进行了验证,随后使用AccuProbe分析或高效液相色谱法鉴定的314种临床培养物进行了测试。在测试的314种培养物中,多重实时PCR产生的结果与评估的1559个靶标中的99.8%一致。 MTC( n = 96),MAC( n = 97),MCAG( n )的敏感性和特异性均达到99%或更高= 68)和 M。 mucogenicum n = 9)和MFG( n = 19)分别为95%和100%。我们得出的结论是,这种多重实时PCR分析是快速,准确地鉴定MTC和临床相关的非结核分枝杆菌的有用诊断工具。

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