Department of Infectious, Respiratory and Digestive Medicine, Graduate School of Medicine, University of the Ryukyus. 207 Uehara, Nishihara, Okinawa 903-0215, Japan.
Department of Infectious, Respiratory and Digestive Medicine, Graduate School of Medicine, University of the Ryukyus. 207 Uehara, Nishihara, Okinawa 903-0215, Japan.
J Clin Virol. 2021 Aug;141:104877. doi: 10.1016/j.jcv.2021.104877. Epub 2021 May 29.
. The emergence of SARS-CoV-2 variants has caused an unexpected rebound globally. The World Health Organization has listed three variants (B.1.1.7, B.1.351, and P.1) as variants of concern. To understand the epidemiology and thereby plan appropriate safety measures, differential identification of the variants is indeed critical.
. Although whole-genome sequencing is the gold standard for variant identification, it is time-consuming and relatively expensive. Therefore, a rapid, easy, and cost-effective platform targeting multiple regions of the genome is required. Here, we assessed the usefulness of the Novaplex™ SARS-CoV-2 Variants I Assay kit in identifying mutations in the variants.
. We retrospectively examined 30 stored nasal swabs from COVID-19-positive patients tested between November 2020 and March 2021. RNA extracted from these swabs was subjected to the commercial kit and real-time reverse transcription-PCR was performed. To determine the genome sequences of SARS-CoV-2 in the collected samples and deduce the consensus sequences among the identified variants, genome sequencing libraries were prepared and mapped to the reference genome.
. Four of the tested samples were determined as variants. Of them, two harbored both H69/V70 deletion and N501Y substitution, whereas two harbored E484K substitution alone.
. The variant with E484K substitution alone ("R.1") has been now categorized as a variant of interest in Japan. Additionally, the kit-based assay was found to be feasible, convenient, and user-friendly in identifying the abovementioned mutations with a turnaround time of only 2 h.
SARS-CoV-2 变体的出现导致了全球范围内的意外反弹。世界卫生组织已将三种变体(B.1.1.7、B.1.351 和 P.1)列为关注变体。为了了解流行病学,从而制定适当的安全措施,对变体进行差异化识别确实至关重要。
虽然全基因组测序是变体识别的金标准,但它既耗时又相对昂贵。因此,需要一种针对基因组多个区域的快速、简便且具有成本效益的平台。在这里,我们评估了 Novaplex™ SARS-CoV-2 Variants I 检测试剂盒在识别变体中的突变方面的有用性。
我们回顾性地检查了 30 个储存在 COVID-19 阳性患者的鼻腔拭子,这些拭子是在 2020 年 11 月至 2021 年 3 月期间检测的。从这些拭子中提取的 RNA 进行了商业试剂盒检测,并进行了实时逆转录-PCR。为了确定收集样本中 SARS-CoV-2 的基因组序列并推断出鉴定变体之间的共识序列,制备了基因组测序文库并将其映射到参考基因组上。
测试的四个样本被确定为变体。其中,两个样本同时携带 H69/V70 缺失和 N501Y 取代,而两个样本则单独携带 E484K 取代。
单独携带 E484K 取代的变体(“R.1”)现在已被归类为日本的关注变体。此外,该试剂盒检测法被发现是可行的、方便的和用户友好的,仅需 2 小时即可识别上述突变。