与伊朗SARS-COV-2基因组n基因靶失败相关的新突变,病例系列

Ali Maleki, Zahra Fereydouni, Mahsa Tavakoli, Akram Ezani, Mirshamsedin Hosseini, Amir Hesam Nemati, Parastoo Yektay Sanat, T. Jalali, M. Pouriayevali, Mostafa Salehi-Vaziri
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引用次数: 0

摘要

在COVID-19等病毒大流行期间,精确跟踪和监测病毒基因组突变至关重要。随着用于诊断多种感染因子的分子分析方法的开发,RT-PCR仍然是检测SARS-CoV-2的金标准。尽管具有校对能力,但与其他RNA病毒一样,SARS-CoV-2的基因组也发生了一些变化。如果这些突变,特别是缺失,发生在引物和探针的靶区,它们将阻碍分子检测方法识别给定基因。作者描述了尽管缺乏N基因检测,但发现ORF1ab基因具有相对较低的阈值周期(Ct)的病例。测序后,在SARS-CoV-2检测试剂盒中使用的正、反向引物和探针的退火区发现了变化。其中最重要的突变是N基因中15个核苷酸的大量缺失,这在以前的变异中从未见过。这凸显了在COVID-19大流行期间通过测序和更新分子检测试剂盒持续监测SARS-CoV-2基因组高变区域的重要性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Novel Mutations Associated with N-Gene Target Failure in SARS-COV-2 Genome in Iran, Case Series
Precision tracking and monitoring viral genome mutations are critical during a viral pandemic such as COVID-19. As molecular assays for diagnosing numerous infectious agents are being developed, RT-PCR is still deployed as the gold standard for detecting SARS-CoV-2. Despite its proofreading capability, SARS-CoV-2, like other RNA viruses, adopts several changes in its genome. If these mutations, especially deletions, occur in the target areas of primers and probes, they will hinder molecular detection methods from identifying the given gene. The authors describe the cases in which, despite the lack of the N gene detection, the ORF1ab gene was discovered with a relatively low cycle of threshold (Ct). Following sequencing, changes were discovered in the annealing region of the forward and reverse primers and probes used in the SARS-CoV-2 detection kit. Among the most significant mutations is a large deletion of 15 nucleotides in the N gene, which has never been seen in prior variants. This highlights the importance of persistent monitoring of hypervariable regions in the SARS-CoV-2 genome through sequencing and updating the molecular detection kits during the COVID-19 pandemic.
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