Rodrigues Grazielle Motta, Volpato Fabiana Caroline Zempulski, Wink Priscila Lamb, Paiva Rodrigo Minuto, Barth Afonso Luís, de-Paris Fernanda
Residência Multiprofissional em Saúde e em Área Profissional da Saúde do Hospital de Clínicas de Porto Alegre, Porto Alegre 90035-903, Rio Grande do Sul, Brazil.
Serviço de Diagnóstico Laboratorial, Hospital de Clínicas de Porto Alegre, Porto Alegre 90035-903, Rio Grande do Sul, Brazil.
Diagnostics (Basel). 2023 Mar 27;13(7):1256. doi: 10.3390/diagnostics13071256.
Variants of concern (VOCs) of SARS-CoV-2 are viral strains that have mutations associated with increased transmissibility and/or increased virulence, and their main mutations are in the receptor binding domain (RBD) region of the viral spike. This study aimed to characterize SARS-CoV-2 VOCs via Sanger sequencing of the RBD region and compare the results with data obtained via whole genome sequencing (WGS). Clinical samples (oro/nasopharyngeal) with positive RT-qPCR results for SARS-CoV-2 were used in this study. The viral RNA from SARS-CoV-2 was extracted and a PCR fragment of 1006 base pairs was submitted for Sanger sequencing. The results of the Sanger sequencing were compared to the lineage assigned by WGS using next-generation sequencing (NGS) techniques. A total of 37 specimens were sequenced via WGS, and classified as: VOC gamma (8); delta (7); omicron (10), with 3 omicron specimens classified as the BQ.1 subvariant and 12 specimens classified as non-VOC variants. The results of the partial Sanger sequencing presented as 100% in agreement with the WGS. The Sanger protocol made it possible to characterize the main SARS-CoV-2 VOCs currently circulating in Brazil through partial Sanger sequencing of the RBD region of the viral spike. Therefore, the sequencing of the RBD region is a fast and cost-effective laboratory tool for clinical and epidemiological use in the genomic surveillance of SARS-CoV-2.
严重急性呼吸综合征冠状病毒2(SARS-CoV-2)的关注变异株(VOCs)是具有与传播性增加和/或毒力增加相关突变的病毒株,其主要突变位于病毒刺突的受体结合域(RBD)区域。本研究旨在通过对RBD区域进行桑格测序来鉴定SARS-CoV-2 VOCs,并将结果与通过全基因组测序(WGS)获得的数据进行比较。本研究使用了SARS-CoV-2逆转录定量聚合酶链反应(RT-qPCR)结果呈阳性的临床样本(口咽/鼻咽)。提取SARS-CoV-2的病毒RNA,并提交一个1006个碱基对的PCR片段进行桑格测序。将桑格测序结果与使用下一代测序(NGS)技术通过WGS确定的谱系进行比较。通过WGS对总共37个样本进行了测序,并分类如下:VOCγ(8个);δ(7个);奥密克戎(10个),其中3个奥密克戎样本被分类为BQ.1亚变体,12个样本被分类为非VOC变体。部分桑格测序结果与WGS结果100%一致。桑格方案使得通过对病毒刺突RBD区域进行部分桑格测序来鉴定目前在巴西流行的主要SARS-CoV-2 VOCs成为可能。因此,RBD区域测序是一种快速且经济高效的实验室工具,可用于SARS-CoV-2基因组监测的临床和流行病学用途。