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新型冠状病毒实时逆转录聚合酶链反应检测中的分析前问题及循环阈值:检测结果应包含这些吗?

Preanalytical Issues and Cycle Threshold Values in SARS-CoV-2 Real-Time RT-PCR Testing: Should Test Results Include These?

作者信息

Engelmann Ilka, Alidjinou Enagnon Kazali, Ogiez Judith, Pagneux Quentin, Miloudi Sana, Benhalima Ilyes, Ouafi Mahdi, Sane Famara, Hober Didier, Roussel Alain, Cambillau Christian, Devos David, Boukherroub Rabah, Szunerits Sabine

机构信息

Univ. Lille, CHU Lille, Laboratoire de Virologie ULR3610, F-59000 Lille, France.

Univ. Lille, CNRS, Centrale Lille, University Polytechnique Hauts-de-France, UMR 8520-IEMN, F-59000 Lille, France.

出版信息

ACS Omega. 2021 Mar 6;6(10):6528-6536. doi: 10.1021/acsomega.1c00166. eCollection 2021 Mar 16.

Abstract

Since the emergence of SARS-CoV-2 pandemic, clinical laboratories worldwide are overwhelmed with SARS-CoV-2 testing using the current gold standard: real-time reverse-transcription polymerase chain reaction (RT-PCR) assays. The large numbers of suspected cases led to shortages in numerous reagents such as specimen transport and RNA extraction buffers. We try to provide some answers on how strongly preanalytical issues affect RT-PCR results by reviewing the utility of different transport buffer media and virus inactivation procedures and comparing the literature data with our own recent findings. We show that various viral inactivation procedures and transport buffers are available and are less of a bottleneck for PCR-based methods. However, efficient alternative lysis buffers remain more difficult to find, and several fast RT-PCR assays are not compatible with guanidine-containing media, making this aspect more of a challenge in the current crisis. Furthermore, the availability of different SARS-CoV-2-specific RT-PCR kits with different sensitivities makes the definition of a general cutoff level for the cycle threshold (Ct) value challenging. Only a few studies have considered how Ct values relate to viral infectivity and how preanalytical issues might affect viral infectivity and RNA detection. We review the current data on the correlation between Ct values and viral infectivity. The presence of the SARS-CoV-2 viral genome in its own is not sufficient proof of infectivity and caution is needed in evaluation of the infectivity of samples. The correlation between Ct values and viral infectivity revealed an RT-PCR cutoff value of 34 cycles for SARS-CoV-2 infectivity using a laboratory-developed RT-PCR assay targeting the RdRp gene. While ideally each clinical laboratory should perform its own correlation, we believe this perspective article could be a reference point for others, in particular medical doctors and researchers interested in COVID-19 diagnostics, and a first step toward harmonization.

摘要

自新冠病毒大流行出现以来,全球临床实验室都因使用当前金标准——实时逆转录聚合酶链反应(RT-PCR)检测法进行新冠病毒检测而不堪重负。大量疑似病例导致许多试剂短缺,如样本运输和RNA提取缓冲液。我们试图通过回顾不同运输缓冲液介质和病毒灭活程序的效用,并将文献数据与我们自己最近的发现进行比较,来回答分析前问题对RT-PCR结果的影响程度。我们表明,有多种病毒灭活程序和运输缓冲液可供使用,对于基于PCR的方法来说,它们不再是瓶颈。然而,高效的替代裂解缓冲液仍然更难找到,并且几种快速RT-PCR检测法与含胍介质不兼容,这使得在当前危机中这方面更具挑战性。此外,不同灵敏度的新冠病毒特异性RT-PCR试剂盒的可用性使得定义循环阈值(Ct)值的通用截止水平具有挑战性。只有少数研究考虑了Ct值与病毒传染性的关系,以及分析前问题可能如何影响病毒传染性和RNA检测。我们回顾了关于Ct值与病毒传染性之间相关性的当前数据。新冠病毒基因组本身的存在不足以证明其具有传染性,在评估样本传染性时需要谨慎。使用针对RdRp基因的实验室开发的RT-PCR检测法,Ct值与病毒传染性之间的相关性显示,新冠病毒传染性的RT-PCR截止值为34个循环。虽然理想情况下每个临床实验室都应该进行自己的相关性研究,但我们相信这篇观点文章可以为其他人,特别是对新冠病毒诊断感兴趣的医生和研究人员提供一个参考点,并朝着统一迈出第一步。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/13f1/7970463/931b5f1b964a/ao1c00166_0002.jpg

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