AusDiagnostics UK Ltd., Unit 3 Anglo Business Park, Chesham HP5 2QA, UK.
AusDiagnostics Pty Ltd., Mascot, Sydney, NSW 2020, Australia.
Viruses. 2021 Oct 8;13(10):2028. doi: 10.3390/v13102028.
The emergence of variants of SARS-CoV-2 has created challenges for the testing infrastructure. Although large-scale genome sequencing of SARS-CoV-2 has facilitated hospital and public health responses, access to sequencing facilities globally is variable and turnaround times can be significant, so there is a requirement for rapid and cost-effective alternatives. Applying a polymerase chain reaction (PCR)-based single nucleotide polymorphism (SNP) approach enables rapid (<4 h) identification of SARS-CoV-2 lineages from nucleic acid extracts, through the presence or absence of a panel of defined of genomic polymorphisms. For example, the B.1.1.7 lineage ("UK", "Alpha", or "Kent" variant) is characterised by 23 mutations compared to the reference strain, and the most biologically significant of these are found in the S gene. We have developed a SARS-CoV-2 typing assay focused on five positions in the S gene (HV69/70, N501, K417, E484 and P681). This configuration can identify a range of variants, including all the "Variants of Concern" currently designated by national and international public health bodies. The panel has been evaluated using a range of clinical isolates and standardised control materials at four UK hospitals and shows excellent concordance with the known lineage information derived from full sequence analysis. The assay has a turnaround time of about three hours for a set of up to 24 samples and has been utilised to identify emerging variants in a clinical setting.
SARS-CoV-2 变体的出现给检测基础设施带来了挑战。虽然对 SARS-CoV-2 的大规模基因组测序有助于医院和公共卫生部门的应对,但全球范围内获取测序设施的机会各不相同,周转时间可能很长,因此需要快速且具有成本效益的替代方法。应用聚合酶链反应(PCR)为基础的单核苷酸多态性(SNP)方法可以通过存在或不存在一组定义的基因组多态性,快速(<4 小时)从核酸提取物中识别 SARS-CoV-2 谱系。例如,B.1.1.7 谱系(“英国”、“Alpha”或“Kent”变体)与参考株相比有 23 个突变,其中最具生物学意义的突变发生在 S 基因中。我们开发了一种针对 S 基因中五个位置的 SARS-CoV-2 分型检测方法(HV69/70、N501、K417、E484 和 P681)。这种配置可以识别多种变体,包括目前被国家和国际公共卫生机构指定的所有“关注变体”。该面板已在英国四家医院使用一系列临床分离株和标准化对照材料进行了评估,并与从全序列分析得出的已知谱系信息具有极好的一致性。该检测方法的一组最多 24 个样本的周转时间约为三个小时,已用于在临床环境中识别新出现的变体。