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七种用于 COVID-19 的商业 RT-PCR 诊断试剂盒的比较。

Comparison of seven commercial RT-PCR diagnostic kits for COVID-19.

机构信息

National Institute for Public Health and the Environment, Center for Infectious Disease Control, A. van Leeuwenhoeklaan 9, 3721 MA, Bilthoven, the Netherlands.

Erasmus Medical Center, Viroscience Department, 's Gravendijkwal 230, 3015 CE, Rotterdam, the Netherlands.

出版信息

J Clin Virol. 2020 Jul;128:104412. doi: 10.1016/j.jcv.2020.104412. Epub 2020 May 8.

Abstract

The final months of 2019 witnessed the emergence of a novel coronavirus in the human population. Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) has since spread across the globe and is posing a major burden on society. Measures taken to reduce its spread critically depend on timely and accurate identification of virus-infected individuals by the most sensitive and specific method available, i.e. real-time reverse transcriptase PCR (RT-PCR). Many commercial kits have recently become available, but their performance has not yet been independently assessed. The aim of this study was to compare basic analytical and clinical performance of selected RT-PCR kits from seven different manufacturers (Altona Diagnostics, BGI, CerTest Biotec, KH Medical, PrimerDesign, R-Biopharm AG, and Seegene). We used serial dilutions of viral RNA to establish PCR efficiency and estimate the 95 % limit of detection (LOD95). Furthermore, we ran a panel of SARS-CoV-2-positive clinical samples (n = 13) for a preliminary evaluation of clinical sensitivity. Finally, we used clinical samples positive for non-coronavirus respiratory viral infections (n = 6) and a panel of RNA from related human coronaviruses to evaluate assay specificity. PCR efficiency was ≥96 % for all assays and the estimated LOD95 varied within a 6-fold range. Using clinical samples, we observed some variations in detection rate between kits. Importantly, none of the assays showed cross-reactivity with other respiratory (corona)viruses, except as expected for the SARS-CoV-1 E-gene. We conclude that all RT-PCR kits assessed in this study may be used for routine diagnostics of COVID-19 in patients by experienced molecular diagnostic laboratories.

摘要

2019 年最后几个月,新型冠状病毒在人群中出现。严重急性呼吸系统综合征冠状病毒 2(SARS-CoV-2)已在全球范围内传播,给社会带来了重大负担。为了减少其传播,所采取的措施严重依赖于通过最敏感和最特异的方法,即实时逆转录聚合酶链反应(RT-PCR),及时、准确地识别病毒感染个体。最近出现了许多商业试剂盒,但它们的性能尚未得到独立评估。本研究旨在比较来自 7 家不同制造商(Altona Diagnostics、BGI、CerTest Biotec、KH Medical、PrimerDesign、R-Biopharm AG 和 Seegene)的选定 RT-PCR 试剂盒的基本分析和临床性能。我们使用病毒 RNA 的系列稀释液来建立 PCR 效率并估计 95%检测限(LOD95)。此外,我们对 SARS-CoV-2 阳性临床样本(n=13)进行了初步临床敏感性评估。最后,我们使用非冠状病毒呼吸道病毒感染的临床阳性样本(n=6)和一组相关人类冠状病毒的 RNA 来评估测定的特异性。所有检测的 PCR 效率均≥96%,估计的 LOD95 范围在 6 倍以内。使用临床样本,我们观察到试剂盒之间的检测率存在一些差异。重要的是,除了 SARS-CoV-1 E 基因的预期情况外,没有一种检测方法显示与其他呼吸道(冠状病毒)病毒交叉反应。我们得出结论,经验丰富的分子诊断实验室可以使用本研究中评估的所有 RT-PCR 试剂盒对患者进行 COVID-19 的常规诊断。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/735f/7206434/323ad0dc0a9d/gr1_lrg.jpg

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