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首页> 外文期刊>Journal of Clinical Microbiology >Rapid Determination of Rifampin Resistance in Clinical Isolates of Mycobacterium tuberculosis by Real-Time PCR
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Rapid Determination of Rifampin Resistance in Clinical Isolates of Mycobacterium tuberculosis by Real-Time PCR

机译:实时荧光定量PCR快速测定结核分枝杆菌临床分离株对利福平的耐药性

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Real-time PCR was used to determine rifampin resistance in clinical isolates of Mycobacterium tuberculosis. Ninety-six rifampin-resistant isolates and 23 rifampin-susceptible isolates were included in the study. A 305-bp region covering the 81-bp “rifampin resistance-determining region” of rpoB was amplified. Two hybridization probe pairs that covered the most frequent mutation sites in rpoB, codon regions 526 to 531 and 513 to 516, were used. The results obtained by real-time PCR were compared to those obtained by the proportion method. For detection of rifampin resistance, the real-time PCR assay yielded a sensitivity of 92.7% and a specificity of 100%. Real-time PCR is a very rapid method, and it can be especially helpful for the reporting of resistant clinical isolates in a very short period of time.
机译:实时荧光定量PCR检测结核分枝杆菌的临床分离株对利福平的耐药性。该研究包括96种耐利福平的分离株和23种对利福平敏感的分离株。扩增了一个305 bp的区域,该区域覆盖了 rpoB 的81 bp的“利福平抗性决定区域”。使用覆盖 rpoB 中最频繁的突变位点的两个杂交探针对,密码子区域526至531和513至516。将通过实时PCR获得的结果与通过比例法获得的结果进行比较。对于利福平耐药性的检测,实时荧光定量PCR的灵敏度为92.7%,特异性为100%。实时PCR是一种非常快速的方法,对于在很短的时间内报告耐药性临床分离株尤其有用。

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