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利用扩增子熔解温度通过ORF 8基因中的G28048T突变检测严重急性呼吸综合征冠状病毒2(SARS-CoV-2)B.1.1.7谱系变体。

Use of amplicon melt temperature to detect SARS-CoV-2 Lineage B.1.1.7 variant through the G28048T mutation in the ORF 8 gene.

作者信息

Hale Richard S, Green Ashleigh, Cunningham Emma, Paul Joel

机构信息

AusDiagnostics UK Limited, Unit 3 Anglo Business Park, Asheridge Road, Chesham, Bucks, HP5 2QA, United Kingdom.

Viapath, Infection Sciences - Virology, St. Thomas' Hospital, Westminster Bridge Road, London, SE1 7EH, United Kingdom.

出版信息

J Clin Virol Plus. 2021 Sep;1(3):100025. doi: 10.1016/j.jcvp.2021.100025. Epub 2021 Jun 6.

Abstract

A new variant of SARS-CoV-2 (Lineage B.1.1.7) was identified in the UK in December 2020 which was associated with higher transmissibility of COVID-19. The AusDiagnostics SARS-CoV-2, Influenza and RSV 8-well assay is used at sixteen UK hospitals and detects part of the ORF8 gene (together with a segment from the ORF1a gene). The objective of this study was to determine if the recently identified mutation in ORF8 (G28048T) in the B.1.1.7. lineage could be used to identify the new variant quickly in clinical cases with PCR positive results. The melt data from SARS-CoV-2 positives from two hospitals (October through December 2020) were reviewed, and distribution over time and location was evaluated. A low melt variant of the ORF8 amplicon started to appear in samples from Guy's and St. Thomas' NHS Trust, London, at the start of November, and grew as a proportion of the total positives during the subsequent two months. These low melt variants were very rare during the same period at the Northern Care Alliance, Greater Manchester, North West of UK. It was confirmed that these carried the G28048T mutation. The geographic and temporal distribution of the low melt amplicons makes it very likely that these are lineage B.1.1.7 strains. The melt temperature of this amplicon could be used to discriminate between the original and new variants in advance of the full sequencing of the isolate. However, the appearance of other mutations in the same amplicon means that this approach would be of diminishing value over time.

摘要

2020年12月在英国发现了一种新型严重急性呼吸综合征冠状病毒2(SARS-CoV-2,谱系B.1.1.7),它与新冠病毒病(COVID-19)的更高传播性有关。英国16家医院使用AusDiagnostics SARS-CoV-2、流感和呼吸道合胞病毒8孔检测法,该方法可检测开放阅读框8(ORF8)基因的一部分(以及来自ORF1a基因的一个片段)。本研究的目的是确定在B.1.1.7谱系中最近发现的ORF8基因中的突变(G28048T)是否可用于在聚合酶链反应(PCR)结果呈阳性的临床病例中快速识别新变种。对两家医院(2020年10月至12月)SARS-CoV-2阳性样本的熔解数据进行了回顾,并评估了其随时间和地点的分布情况。11月初,伦敦盖伊和圣托马斯国民保健服务信托基金样本中开始出现ORF8扩增子的低熔解变种,在随后的两个月中,其在总阳性样本中的比例不断增加。在英国西北部大曼彻斯特北部护理联盟的同一时期,这些低熔解变种非常罕见。经确认,这些变种携带G28048T突变。低熔解扩增子的地理和时间分布极有可能表明这些是B.1.1.7谱系毒株。在对分离株进行全序列测序之前,该扩增子的熔解温度可用于区分原始变种和新变种。然而,同一扩增子中出现其他突变意味着这种方法的价值会随着时间的推移而逐渐降低。

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