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Combined rpoB duplex PCR and hsp65 PCR restriction fragment length polymorphism with capillary electrophoresis as an effective algorithm for identification of Mycobacterial species from clinical isolates

机译:结合rpoB双工PCR和hsp65 PCR限制性片段长度多态性与毛细管电泳的结合作为鉴定临床分离株中分枝杆菌种类的有效算法

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Background Mycobacteria can be quickly and simply identified by PCR restriction-enzyme analysis (PRA), but misidentification can occur because of similarities in band sizes that are critical for discriminating among species. Capillary electrophoresis can provide computer-aided band discrimination. The aim of this research was to develop an algorithm for identifying mycobacteria by combined rpoB duplex PRA (DPRA) and hsp65 PRA with capillary electrophoresis. Results Three hundred and seventy-six acid-fast bacillus smear-positive BACTEC cultures, including 200 Mycobacterium tuberculosis complexes (MTC) and 176 non-tuberculous mycobacteria (NTM) were analyzed. With combined hsp65 and rpoB DPRA, the accuracy rate was 100% (200 isolates) for the MTC and 91.4% (161 isolates) for the NTM. Among the discordant results (8.6%) for the NTM, one isolate of Mycobacterial species and an isolate of M. flavescens were found as new sub-types in hsp65 PRA. Conclusions This effective and novel identification algorithm using combined rpoB DPRA and hsp65 PRA with capillary electrophoresis can rapidly identify mycobacteria and find new sub-types in hsp65 PRA. In addition, it is complementary to 16 S rDNA sequencing.
机译:背景分枝杆菌可以通过PCR限制性酶切分析(PRA)来快速,简单地识别,但是由于条带大小的相似对于区分物种至关重要,因此可能会发生错误识别。毛细管电泳可以提供计算机辅助的波段判别。这项研究的目的是开发一种通过毛细管电泳结合rpoB双工PRA(DPRA)和hsp65 PRA来鉴定分枝杆菌的算法。结果共分析了367株抗酸杆菌涂片阳性的BACTEC培养物,其中包括200株结核分枝杆菌复合物(MTC)和176株非结核分枝杆菌(NTM)。结合使用hsp65和rpoB DPRA,MTC的准确率为100%(200个分离株),NTM的准确率为91.4%(161个分离株)。在NTM的不一致结果中(8.6%),在hsp65 PRA中发现了一种分离的分枝杆菌属和一种苦参分支杆菌作为新的亚型。结论结合rpoB DPRA和hsp65 PRA结合毛细管电泳的这种有效新颖的鉴定算法可以快速鉴定分枝杆菌并在hsp65 PRA中发现新的亚型。另外,它与16 S rDNA测序互补。

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