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评价两种实时 RT-PCR 检测方法在真实医院环境下对关注的 SARS-CoV-2 变异株的分析和临床性能及实用性。

Evaluation of Analytical and Clinical Performance and Usefulness in a Real-Life Hospital Setting of Two in-House Real-Time RT-PCR Assays to Track SARS-CoV-2 Variants of Concern.

机构信息

Univ Rouen Normandie, UNICAEN, INSERM, DYNAMICURE UMR 1311, CHU Rouen, Department of Virology, F-76000 Rouen, France.

Department of Genetics and Reference Center for Developmental Disorders, FHU G4 Génomique, Normandie University, UNIROUEN, CHU Rouen, INSERM U1245, 76000 Rouen, France.

出版信息

Viruses. 2023 May 4;15(5):1115. doi: 10.3390/v15051115.

Abstract

Since the end of 2020, multiple severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) variants of concern (VOCs) have emerged and spread worldwide. Tracking their evolution has been a challenge due to the huge number of positive samples and limited capacities of whole-genome sequencing. Two in-house variant-screening RT-PCR assays were successively designed in our laboratory in order to detect specific known mutations in the spike region and to rapidly detect successively emerging VOCs. The first one (RT-PCR#1) targeted the 69-70 deletion and the N501Y substitution simultaneously, whereas the second one (RT-PCR#2) targeted the E484K, E484Q, and L452R substitutions simultaneously. To evaluate the analytical performance of these two RT-PCRs, 90 negative and 30 positive thawed nasopharyngeal swabs were retrospectively analyzed, and no discordant results were observed. Concerning the sensitivity, for RT-PCR#1, serial dilutions of the WHO international standard SARS-CoV-2 RNA, corresponding to the genome of an Alpha variant, were all detected up to 500 IU/mL. For RT-PCR#2, dilutions of a sample harboring the E484K substitution and of a sample harboring the L452R and E484Q substitutions were all detected up to 1000 IU/mL and 2000 IU/mL, respectively. To evaluate the performance in a real-life hospital setting, 1308 and 915 profiles of mutations, obtained with RT-PCR#1 and RT-PCR#2, respectively, were prospectively compared to next-generation sequencing (NGS) data. The two RT-PCR assays showed an excellent concordance with the NGS data, with 99.8% for RT-PCR#1 and 99.2% for RT-PCR#2. Finally, for each mutation targeted, the clinical sensitivity, the clinical specificity and the positive and negative predictive values showed excellent clinical performance. Since the beginning of the SARS-CoV-2 pandemic, the emergence of variants-impacting the disease's severity and the efficacy of vaccines and therapies-has forced medical analysis laboratories to constantly adapt to the strong demand for screening them. Our data showed that in-house RT-PCRs are useful and adaptable tools for monitoring such rapid evolution and spread of SARS-CoV-2 VOCs.

摘要

自 2020 年底以来,多种严重急性呼吸综合征冠状病毒 2(SARS-CoV-2)变异株(VOC)已经出现并在全球范围内传播。由于阳性样本数量巨大,全基因组测序能力有限,对其进化的跟踪一直是一个挑战。为了检测刺突区的特定已知突变并快速检测相继出现的 VOC,我们实验室先后设计了两种内部变异筛选 RT-PCR 检测方法。第一种(RT-PCR#1)同时针对 69-70 缺失和 N501Y 取代,而第二种(RT-PCR#2)同时针对 E484K、E484Q 和 L452R 取代。为了评估这两种 RT-PCR 的分析性能,对 90 份阴性和 30 份阳性解冻鼻咽拭子进行了回顾性分析,未观察到不一致的结果。关于敏感性,对于 RT-PCR#1,世界卫生组织(WHO)国际标准 SARS-CoV-2 RNA 的连续稀释液,对应于 Alpha 变异株的基因组,均可检测到 500 IU/mL。对于 RT-PCR#2,携带 E484K 取代的样本和携带 L452R 和 E484Q 取代的样本的稀释液均分别可检测到 1000 IU/mL 和 2000 IU/mL。为了评估在现实医院环境中的性能,分别用 RT-PCR#1 和 RT-PCR#2 前瞻性地比较了 1308 例和 915 例突变谱与下一代测序(NGS)数据。两种 RT-PCR 检测方法与 NGS 数据具有极好的一致性,RT-PCR#1 为 99.8%,RT-PCR#2 为 99.2%。最后,对于每个靶向突变,临床灵敏度、临床特异性以及阳性和阴性预测值均表现出极好的临床性能。自 SARS-CoV-2 大流行开始以来,影响疾病严重程度以及疫苗和治疗效果的变异株的出现迫使医学分析实验室不断适应对其进行筛选的强烈需求。我们的数据表明,内部 RT-PCR 是监测 SARS-CoV-2 VOC 如此快速进化和传播的有用且适应性强的工具。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b4fd/10221153/28a5967171b3/viruses-15-01115-g001.jpg

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