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首页> 外文期刊>Annals of Clinical and Laboratory Science: Official Journal of the Association of Clinical Scientists >Comparison between a Broad-Range Real-Time and a Broad-Range End-Point PCR Assays for the Detection of Bacterial 16S rRNA in Clinical Samples
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Comparison between a Broad-Range Real-Time and a Broad-Range End-Point PCR Assays for the Detection of Bacterial 16S rRNA in Clinical Samples

机译:在临床样品中检测细菌16S rRNA的大范围实时和大范围终点PCR检测方法的比较

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摘要

Broad range PCR targeting the 16S rRNA gene is widely used to test clinical samples for the presence of bacterial DNA. End-point 16S PCR is both time-consuming and at high risk of cross-contamination. Prior to the replacement of the 16S end-point PCR assay routinely used in our clinical laboratory by a new 16S real-time PCR assay, we aimed to compare the performances of both techniques for the direct diagnosis of bacterial infections in clinical samples. In this prospective study, 129 clinical samples were included for direct comparison of both techniques. The sensitivity of 16S real-time PCR assay (76%) was significantly higher than that of end-point 16S PCR assay (41%) (p<0.01). Specificities of both PCR assays did not differ significantly (p=0.43). The 16S real-time PCR assay yielded an etiological diagnosis in 19% of culture-negative samples. It constitutes a reliable and complementary diagnostic tool to the bacterial culture.
机译:靶向16S rRNA基因的大范围PCR被广泛用于测试临床样品中细菌DNA的存在。终点16S PCR既费时又有交叉污染的高风险。在用新的16S实时PCR检测方法代替我们临床实验室中常规使用的16S终点PCR检测方法之前,我们旨在比较这两种技术在临床样品中直接诊断细菌感染的性能。在这项前瞻性研究中,包括129个临床样本以直接比较这两种技术。 16S实时PCR分析的灵敏度(76%)显着高于终点16S PCR分析的灵敏度(41%)(p <0.01)。两种PCR分析的特异性均无显着差异(p = 0.43)。 16S实时PCR检测可在19%的培养阴性样品中进行病因诊断。它构成了细菌培养的可靠且互补的诊断工具。

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