基于荧光探针熔融曲线分析的多重实时荧光定量PCR同时检测15种呼吸道病原体。

International journal of molecular epidemiology and genetics Pub Date : 2019-04-15 eCollection Date: 2019-01-01
Shengyun Liao, Lingli Wang, Xiang Ji, Jiandong Chen, Qiang Li, Lan Ma
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摘要

急性呼吸道感染在世界范围内很常见,由多种病原体引起。快速准确的诊断方法对临床及时干预至关重要。本文将荧光熔化曲线分析与多重实时检测相结合,建立了一种可同时检测15种呼吸道病毒的新方法。靶基因的特异性为100%,由47种呼吸道病原体组成的小组进行评估,表明无交叉反应。该方法在核酸水平上的检测限为5拷贝/μL ~ 500拷贝/μL。与常规培养法相比,384份临床标本中各呼吸道病原菌的检测灵敏度均在75%以上,特异性为100%。更重要的是,所有病原体的kappa相关性在0.86到1.00之间。总体而言,该方法具有高通量、低成本、高灵敏度和精密度的特点,适用于呼吸道感染的常规临床检测。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Simultaneous detection of 15 respiratory pathogens with a fluorescence probe melting curve analysis-based multiplex real-time PCR assay.

Acute respiratory tract infections are common worldwide and caused by a great diversity of pathogens. A rapid and accurate diagnosis method of respiratory infection is crucial for timely clinical intervention. Here, by combining fluorescence melting curve analysis and multiplex real-time assay, we developed a novel method which can simultaneously detect 15 respiratory viruses. The specificity for target genes was 100%, as assessed with a panel of 47 respiratory pathogens, which indicated no cross-reactions. The assay's limits of detection at the nucleic acid level ranged from 5 copies/μL to 500 copies/μL nucleic acids. Compared with conventional culture method, our assay showed more than 75% sensitivity and 100% specificity for each respiratory pathogen in 384 clinical samples. Even more, the kappa correlation for all the pathogens ranged from 0.86 to 1.00. Overall, this method has the characteristics of high throughput, low cost and high sensitivity and precision, which demonstrated our method is well suited for routine clinical testing in respiratory infection.

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