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热失活降低了 COVID-19 中高循环阈值临床样本的实时 RT-PCR 定性检测率。

Heat inactivation decreases the qualitative real-time RT-PCR detection rates of clinical samples with high cycle threshold values in COVID-19.

机构信息

Yongchuan District Center for Disease Control and Prevention of Chongqing, Changjiang Road, Yuzhong District, Chongqing, China.

Chongqing University Central Hospital, Chongqing Emergency Medical Center, Jiankang Road, Yuzhong District, Chongqing, China.

出版信息

Diagn Microbiol Infect Dis. 2020 Sep;98(1):115109. doi: 10.1016/j.diagmicrobio.2020.115109. Epub 2020 Jun 11.

Abstract

SARS-CoV-2 has caused COVID-19 pandemic globally in the beginning of 2020, and qualitative real-time RT-PCR has become the gold standard in diagnosis. As SARSCoV-2 with strong transmissibility and pathogenicity, it has become a professional consensus that clinical samples from suspected patients should be heat inactivated at 56°C for 30 min before further processing. However, previous studies on the effect of inactivation on qualitative real-time RT-PCR were conducted with diluted samples rather than clinical samples. The aim of this study was to investigate whether heat inactivation on clinical samples before detection will affect the accuracy of qualitative real-time RT-PCR detection. All 46 throat swab samples from 46 confirmed inpatients were detected by qualitative real-time RT-PCR directly, as well as after heat inactivation. Heat-Inactivation has significantly influenced the qualitative detection results on clinical samples, especially weakly positive samples. The results indicate the urgency to establish a more suitable protocol for COVID-19 clinical sample's inactivation.

摘要

2020 年初,SARS-CoV-2 引发了全球 COVID-19 大流行,定性实时 RT-PCR 已成为诊断的金标准。由于 SARS-CoV-2 具有很强的传染性和致病性,临床医生普遍认为疑似患者的临床样本在进一步处理之前应在 56°C 加热 30 分钟灭活。然而,之前关于灭活对定性实时 RT-PCR 影响的研究是用稀释样本而不是临床样本进行的。本研究旨在探讨检测前对临床样本进行灭活是否会影响定性实时 RT-PCR 检测的准确性。对 46 例确诊住院患者的 46 份咽拭子样本直接进行定性实时 RT-PCR 检测,以及灭活后进行检测。热灭活对临床样本的定性检测结果有显著影响,尤其是弱阳性样本。结果表明,迫切需要为 COVID-19 临床样本的灭活建立更合适的方案。

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