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一步法实时 RT-PCR 检测试剂盒,含装甲 RNA 对照,用于 SARS-CoV-2 的检测。

One-step quantitative RT-PCR assay with armored RNA controls for detection of SARS-CoV-2.

机构信息

Department of Epidemiology, Pasteur Institute, Federal Service on Consumers' Rights Protection and Human Well-Being Surveillance, Saint Petersburg, Russia.

Martsinovsky Institute of Medical Parasitology, Tropical and Vector Borne Diseases, Sechenov First Moscow State Medical University, Moscow, Russia.

出版信息

J Med Virol. 2021 Mar;93(3):1694-1701. doi: 10.1002/jmv.26540. Epub 2020 Oct 5.

Abstract

Coronavirus disease 2019 (COVID-19) has become pandemic since March 11, 2020. Thus, development and integration in clinics of fast and sensitive diagnostic tools are essential. The aim of the study is a development and evaluation of a one-step quantitative reverse transcription-polymerase chain reaction (RT-qPCR) assay (COVID-19 Amp) for severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) detection with an armored positive control and internal controls constructed from synthetic MS2-phage-based RNA particles. The COVID-19 Amp assay limit of detection was 10  copies/ml, the analytical specificity was 100%. A total of 109 biological samples were examined using COVID-19 Amp and World Health Organization (WHO)-based assay. Discordance in nine samples was observed (negative by the WHO-based assay) and discordant samples were retested as positive according to the results obtained from the Vector-PCRrv-2019-nCoV-RG assay. The developed COVID-19 Amp assay has high sensitivity and specificity, includes virus particles-based controls, provides the direct definition of the SARS-CoV-2 RdRp gene partial sequence, and is suitable for any hospital and laboratory equipped for RT-qPCR.

摘要

自 2020 年 3 月 11 日以来,2019 年冠状病毒病(COVID-19)已成为大流行疾病。因此,快速灵敏的诊断工具的开发和整合在临床上至关重要。本研究旨在开发和评估一种一步式定量逆转录聚合酶链反应(RT-qPCR)检测试剂盒(COVID-19 Amp),用于检测严重急性呼吸综合征冠状病毒 2(SARS-CoV-2),该试剂盒具有装甲阳性对照和内部对照,由合成的基于 MS2 噬菌体的 RNA 颗粒构建。COVID-19 Amp 检测试剂盒的检测限为 10 拷贝/ml,分析特异性为 100%。使用 COVID-19 Amp 和世界卫生组织(WHO)检测试剂盒共检测了 109 个生物样本。在 9 个样本中观察到不一致(WHO 检测试剂盒为阴性),根据 Vector-PCRrv-2019-nCoV-RG 检测试剂盒的结果,对不一致的样本进行了重新检测,结果为阳性。开发的 COVID-19 Amp 检测试剂盒具有高灵敏度和特异性,包含基于病毒颗粒的对照,可直接定义 SARS-CoV-2 RdRp 基因的部分序列,适用于任何配备 RT-qPCR 的医院和实验室。

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