Suppr超能文献

基于 RT-PCR/MALDI-TOF 多重靶向方法的 SARS-CoV-2 变异株的稳健临床检测。

Robust clinical detection of SARS-CoV-2 variants by RT-PCR/MALDI-TOF multitarget approach.

机构信息

Department of Pathology, Molecular, and Cell-Based Medicine, Icahn School of Medicine at Mount Sinai, New York, New York, USA.

Department of Genetics and Genomic Sciences, Icahn School of Medicine at Mount Sinai, New York, New York, USA.

出版信息

J Med Virol. 2022 Apr;94(4):1606-1616. doi: 10.1002/jmv.27510. Epub 2021 Dec 16.

Abstract

The coronavirus disease 2019 (COVID-19) pandemic has sparked the rapid development of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) diagnostics. However, emerging variants pose the risk for target dropout and false-negative results secondary to primer/probe binding site (PBS) mismatches. The Agena MassARRAY® SARS-CoV-2 Panel combines reverse-transcription polymerase chain reaction and matrix-assisted laser desorption/ionization time-of-flight mass-spectrometry to probe for five targets across N and ORF1ab genes, which provides a robust platform to accommodate PBS mismatches in divergent viruses. Herein, we utilize a deidentified data set of 1262 SARS-CoV-2-positive specimens from Mount Sinai Health System (New York City) from December 2020 to April 2021 to evaluate target results and corresponding sequencing data. Overall, the level of PBS mismatches was greater in specimens with target dropout. Of specimens with N3 target dropout, 57% harbored an A28095T substitution that is highly specific for the Alpha (B.1.1.7) variant of concern. These data highlight the benefit of redundancy in target design and the potential for target performance to illuminate the dynamics of circulating SARS-CoV-2 variants.

摘要

2019 年冠状病毒病(COVID-19)大流行促使严重急性呼吸综合征冠状病毒 2(SARS-CoV-2)诊断技术迅速发展。然而,新出现的变异株存在靶标缺失和假阴性结果的风险,这是由于引物/探针结合位点(PBS)不匹配所致。Agena MassARRAY® SARS-CoV-2 检测面板结合逆转录聚合酶链反应和基质辅助激光解吸/电离飞行时间质谱法,检测 N 和 ORF1ab 基因中的 5 个靶标,为应对不同病毒中的 PBS 不匹配提供了稳健的平台。在此,我们利用 2020 年 12 月至 2021 年 4 月期间来自西奈山卫生系统(纽约市)的 1262 份 SARS-CoV-2 阳性样本的匿名数据集,评估靶标结果和相应的测序数据。总体而言,靶标缺失的样本中 PBS 不匹配的程度更大。在 N3 靶标缺失的样本中,57%存在高度特异性针对 Alpha(B.1.1.7)变体的 A28095T 取代。这些数据突出了靶标设计冗余的优势,以及靶标性能揭示循环 SARS-CoV-2 变体动态的潜力。

相似文献

引用本文的文献

本文引用的文献

6
Testing at scale during the COVID-19 pandemic.大流行期间的大规模检测。
Nat Rev Genet. 2021 Jul;22(7):415-426. doi: 10.1038/s41576-021-00360-w. Epub 2021 May 4.

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验