新型多重实时RT-PCR检测MERS-CoV感染方法的建立

Peihua Niu, Roujian Lu, Jiaming Lan, Gaoshan Liu, Wenling Wang, Wenjie Tan
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摘要

以中东呼吸综合征冠状病毒(MERS-CoV)的upE、ORF1带n2基因为靶点,建立了几种新型多重实时RT-PCR检测方法;将新检测方法与之前的单组分实时RT-PCR检测方法进行比较。为了验证,我们检测了一株MERS- cov毒株(hCoVEMC)、上海发热患者的临床标本和中国首例输入性MERS病例的标本。新型多重实时RT-PCR检测限为10 PFU / ml,与基于upE或N2的单一实时RT-PCR检测限相同。该检测对MERS-CoV具有特异性。在临床样本验证中,上海患者咽拭子检测为阴性,而中国首例输入性MERS病例咽拭子检测为阳性。利用1例MERS病例全血样本,以N2为靶点的检测结果优于upE。我们认为本研究建立的所有新检测方法均可用于MERS-CoV的检测;与基于upE的单组分实时RT-PCR相比,它们显示出改进的潜力。
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[Development of Novel Multiplex Real-time RT-PCR Assays for Detection of MERS-CoV Infection].

We aimed to develop a novel laboratory assay for the detection of Middle East respiratory syndrome coronavirus (MERS-CoV) infection .Several novel multiplex real-time RT-PCR assays were developed using the upE,ORF1 band N2genes of MERS-CoV as targets; the novel assays were compared with previous monoplex real-time RT-PCR assays. For validation, we tested a MERS-CoV strain (hCoVEMC), clinical specimens from patients with fever in Shanghai, and specimens from the first imported MERS case in China. The detection limit of the novel multiplex real-time RT-PCR assays was 10 PFU of MERS-CoV per ml, the same as that in monoplex real-time RT-PCR assays based on upE or N2. The detection was specific for MERS-CoV. In validation using clinical samples, pharyngeal swabs from Shanghai patients were detected as negative, while swabs from the first imported MERS case in China were detected as positive. Using whole blood samples from a MERS case, better detection results were obtained with N2 as the target than upE. We conclude that all the novel assays established in this study could be used for the detection of MERS-CoV; they show potential for improvement compared with monoplex real-time RT-PCR assay based on upE.

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