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基于实时等位基因特异性 PCR 策略的 SARS-CoV-2 及其变体联合检测评估:对临床实践的优势。

Evaluation of a combined detection of SARS-CoV-2 and its variants using real-time allele-specific PCR strategy: an advantage for clinical practice.

机构信息

Servicio de Microbiología, Hospital Universitario Clínico San Cecilio, Granada, Spain.

Instituto de Investigación Biosanitaria Ibs.Granada, Granada, Spain.

出版信息

Epidemiol Infect. 2023 Nov 24;151:e201. doi: 10.1017/S095026882300184X.

Abstract

This study aimed to assess the ability of a real-time reverse transcription polymerase chain reaction (RT-PCR) with multiple targets to detect SARS-CoV-2 and its variants in a single test. Nasopharyngeal specimens were collected from patients in Granada, Spain, between January 2021 and December 2022. Five allele-specific RT-PCR kits were used sequentially, with each kit designed to detect a predominant variant at the time. When the Alpha variant was dominant, the kit included the HV69/70 deletion, E and N genes. When Delta replaced Alpha, the kit incorporated the L452R mutation in addition to E and N genes. When Omicron became dominant, L452R was replaced with the N679K mutation. Before incorporating each variant kit, a comparative analysis was carried out with SARS-CoV-2 whole genome sequencing (WGS). The results demonstrated that RT-PCR with multiple targets can provide rapid and effective detection of SARS-CoV-2 and its variants in a single test. A very high degree of agreement (96.2%) was obtained between the comparison of RT-PCR and WGS. Allele-specific RT-PCR assays make it easier to implement epidemiological surveillance systems for effective public health decision making.

摘要

本研究旨在评估一种实时多重靶标逆转录聚合酶链反应(RT-PCR)在单次检测中检测 SARS-CoV-2 及其变体的能力。从 2021 年 1 月至 2022 年 12 月,西班牙格拉纳达的患者采集了鼻咽标本。使用了五个等位基因特异性 RT-PCR 试剂盒,每个试剂盒均针对当时的主要变体进行设计。当 Alpha 变体占主导地位时,试剂盒包括 HV69/70 缺失、E 和 N 基因。当 Delta 取代 Alpha 时,试剂盒除了 E 和 N 基因外,还包括 L452R 突变。当 Omicron 占主导地位时,L452R 被 N679K 突变取代。在引入每个变体试剂盒之前,与 SARS-CoV-2 全基因组测序(WGS)进行了比较分析。结果表明,多重靶标 RT-PCR 可在单次检测中快速有效地检测 SARS-CoV-2 及其变体。RT-PCR 与 WGS 的比较结果高度一致(96.2%)。等位基因特异性 RT-PCR 检测法使实施有效的公共卫生决策的流行病学监测系统变得更加容易。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/83b0/10753446/1297b94ce01b/S095026882300184X_fig1.jpg

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