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Combination of multiplex PCR with denaturing high-performance liquid chromatography for rapid detection of Mycobacterium genus and simultaneous identification of the Mycobacterium tuberculosis complex

机译:多重PCR与变性高效液相色谱法相结合可快速检测分枝杆菌属并同时鉴定结核分枝杆菌复合体

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A new assay with the combination of multiplex polymerase chain reaction and denaturing high-performance liquid chromatography analysis was developed for simultaneous detection of Mycobacterium genus and identification of the Mycobacterium tuberculosis complex (MTC). Targeting at genus-specific 16S rRNA sequence of Mycobacterium and specific insertion elements IS6110 and IS1081 of MTC, the assay was validated with 84 strains covering 23 mycobacteria species and 30 strains of non-mycobacteria species. No cross reactivity was observed. Clinical application was carried out on 198 specimens (155 human sputum and 43 bovine tissue samples) and compared with culture. The multiplex assay detected all culture-positive (36 in number) and 35.2% (57/162) culture-negative specimens. The molecular assay was fast that could be completed within 1 h on purified DNA, with the limit of detection as 0.8-1.6 pg per reaction on DNA template. This work provided a useful laboratory tool for rapid identification of Mycobacterium and differentiation of MTC and nontuberculous mycobacteria.
机译:开发了一种结合多重聚合酶链反应和变性高效液相色谱分析相结合的新测定方法,用于同时检测分枝杆菌属和鉴定结核分枝杆菌复合体(MTC)。针对分枝杆菌属的特异性16S rRNA序列和MTC的特定插入元件IS6110和IS1081,该试验已用涵盖23个分枝杆菌物种和30个非分枝杆菌物种的84株菌株进行了验证。没有观察到交叉反应。临床应用了198个标本(155个人体痰液和43个牛组织样品)并与培养物进行了比较。多重分析检测到所有培养阳性样品(数量为36)和35.2%(57/162)培养阴性样品。分子测定速度很快,可以在纯化的DNA上在1小时内完成,在DNA模板上每个反应的检测限为0.8-1.6 pg。这项工作为快速鉴定分枝杆菌以及区分MTC和非结核分枝杆菌提供了有用的实验室工具。

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