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联合世界卫生组织批准的针对包膜和 RNA 依赖的 RNA 聚合酶(RdRp)编码区的两种检测试剂的双 SARS-CoV-2 RT-qPCR 检测试剂的开发和评估。

Development and Evaluation of a duo SARS-CoV-2 RT-qPCR Assay Combining Two Assays Approved by the World Health Organization Targeting the Envelope and the RNA-Dependant RNA Polymerase (RdRp) Coding Regions.

机构信息

UR7310, Laboratoire de Virologie, Université de Corse-Inserm, 20250 Corte, France.

Unité des Virus Émergents (UVE: Aix-Marseille Univ-IRD 190-Inserm 1207-IHU Méditerranée Infection), 13005 Marseille, France.

出版信息

Viruses. 2020 Jun 25;12(6):686. doi: 10.3390/v12060686.

DOI:10.3390/v12060686
PMID:32630601
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7354606/
Abstract

The recent emergence of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) worldwide has highlighted the importance of reliable and rapid diagnostic testing to prevent and control virus circulation. Dozens of monoplex in-house RT-qPCR assays are already available; however, the development of dual-target assays is suited to avoid false-negative results caused by polymorphisms or point mutations, that can compromise the accuracy of diagnostic and screening tests. In this study, two mono-target assays recommended by WHO (E-Sarbeco (enveloppe gene, Charite University, Berlin, Germany) and RdRp-IP4 (RdRp, Institut Pasteur, Paris, France)) were selected and combined in a unique robust test; the resulting duo SARS-CoV-2 RT-qPCR assay was compared to the two parental monoplex tests. The duo SARS-CoV-2 assay performed equally, or better, in terms of sensitivity, specificity, linearity and signal intensity. We demonstrated that combining two single systems into a dual-target assay (with or without an MS2-based internal control) did not impair performances, providing a potent tool adapted for routine molecular diagnosis in clinical microbiology laboratories.

摘要

最近,严重急性呼吸综合征冠状病毒 2(SARS-CoV-2)在全球范围内的出现凸显了可靠和快速诊断测试的重要性,以预防和控制病毒传播。目前已经有数十种单重实时 RT-qPCR 检测方法可用;然而,双靶标检测方法的开发更适合避免由于多态性或点突变引起的假阴性结果,这可能会影响诊断和筛查测试的准确性。在这项研究中,选择了世界卫生组织(E-Sarbeco(包膜基因,柏林 Charite 大学,德国)和 RdRp-IP4(RdRp,巴黎巴斯德研究所,法国))推荐的两种单靶标检测方法,并将其组合在一个独特的稳健测试中;所得的双 SARS-CoV-2 RT-qPCR 检测方法与两种亲本单重检测方法进行了比较。在灵敏度、特异性、线性和信号强度方面,双 SARS-CoV-2 检测方法的性能相等或更好。我们证明,将两种单一系统组合成双靶标检测方法(具有或不具有基于 MS2 的内部对照)不会影响性能,为临床微生物学实验室的常规分子诊断提供了一种有效的工具。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/00f2/7354606/c9f34cef4174/viruses-12-00686-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/00f2/7354606/a2f45e6b3941/viruses-12-00686-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/00f2/7354606/9ab7780d30bf/viruses-12-00686-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/00f2/7354606/c9f34cef4174/viruses-12-00686-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/00f2/7354606/a2f45e6b3941/viruses-12-00686-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/00f2/7354606/9ab7780d30bf/viruses-12-00686-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/00f2/7354606/c9f34cef4174/viruses-12-00686-g003.jpg

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