首页> 美国卫生研究院文献>Journal of Clinical Microbiology >Performance of an IS6110-Based PCR Assay and the COBAS AMPLICOR MTB PCR System for Detection of Mycobacterium tuberculosis Complex DNA in Human Lymph Node Samples
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Performance of an IS6110-Based PCR Assay and the COBAS AMPLICOR MTB PCR System for Detection of Mycobacterium tuberculosis Complex DNA in Human Lymph Node Samples

机译:基于IS6110的PCR检测和COBAS AMPLICOR MTB PCR系统检测人淋巴结样本中结核分枝杆菌复合物DNA的性能

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摘要

We compared the performance of two PCR assays, an IS6110-based in-house protocol and the COBAS AMPLICOR MTB PCR (COBAS MTB) system, for the detection of Mycobacterium tuberculosis complex in 43 human lymph node samples from 40 patients. For the in-house PCR and the COBAS MTB assays, respectively, sensitivities were 87.5% versus 45.5% (P < 0.05), specificities were 100.0% versus 91.3% (P > 0.05), and inhibition rates were 4.8% versus 19.5% (P < 0.05). For the COBAS MTB system, additional N-acetyl-l-cysteine-NaOH pretreatment of the samples changed neither the inhibition rate nor the sensitivity significantly.
机译:我们比较了两种PCR检测(基于IS6110的内部协议)和COBAS AMPLICOR MTB PCR(COBAS MTB)系统的性能,以检测40例患者的43例人类淋巴结样本中的结核分枝杆菌复合体。对于内部PCR和COBAS MTB检测,灵敏度分别为87.5%和45.5%(P <0.05),特异性分别为100.0%和91.3%(P> 0.05),抑制率分别为4.8%和19.5%( P <0.05)。对于COBAS MTB系统,对样品进行额外的N-乙酰基-1-半胱氨酸-NaOH预处理不会显着改变抑制率或灵敏度。

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