Sustained applicability of SARS-CoV-2 variants identification by Sanger Sequencing Strategy on emerging various SARS-CoV-2 Omicron variants in Hiroshima, Japan.

IF 3.5 2区 生物学 Q2 BIOTECHNOLOGY & APPLIED MICROBIOLOGY BMC Genomics Pub Date : 2024-11-11 DOI:10.1186/s12864-024-10973-0
Chanroth Chhoung, Ko Ko, Serge Ouoba, Zayar Phyo, Golda Ataa Akuffo, Aya Sugiyama, Tomoyuki Akita, Hiroshi Sasaki, Tadashi Yamamoto, Kazuaki Takahashi, Junko Tanaka
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Abstract

Background: The evolution of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) persists, giving rise to new variants characterized by mutations in the spike protein. However, public data regarding the virus's evolutionary trend is not widely available after the downgrade of coronavirus disease 2019(COVID-19). Therefore, this study aimed to investigate the applicability of an in-house Sanger-based method for identifying SARS-CoV-2 variants, particularly focusing on newly emerged Omicron variants, and updating the epidemiology of COVID-19 during the 8th wave in Hiroshima Prefecture.

Results: A total of 639 saliva samples of individuals who had tested positive for COVID-19, received from Hiroshima City Medical Association Clinical Laboratory Center between February 01, 2023, and March 12, 2024, were included in the study. SARS-CoV-2 variants were identified in 69.3% (443/639) with the mean viral titer 2 × 106 copies/mL, and high viral titer in Omicron variant XBC.1.6* (5 × 108 copies/mL) using RT-qPCR. By partial Spike gene-based sequencing using the Sanger Sequencing strategy, Omicron sub-lineages XXB.1, BA.5, and EG.1 were identified during different periods. A comprehensive phylogenetic analysis of 7383 SARS-CoV-2 strains retrieved from GISAID, collected in Hiroshima from the onset of the COVID-19 pandemic in early 2020 until July 2024, revealed the dynamic evolution of SARS-CoV-2 variants over time. The study found a similar pattern of variant distribution between the full genomes from GISAID, and the partial genomes obtained from our screening strategy during the same period.

Conclusions: Our study revealed that all SARS-CoV-2 viruses circulated in Hiroshima were Omicron variants and their sub-lineages during the 8th wave outbreak in Hiroshima. Persistent molecular surveillance of SARS-CoV-2 is needed for the decision-making and strategic planning of the public promptly. Our study added evidence for the usefulness of SARS-CoV-2 spike gene partial sequencing-based SARS-CoV-2 variant identification strategy for mass screening and molecular surveillance even though the evolution of newly emerged various SARS-CoV-2 Omicron variants.

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针对日本广岛出现的各种 SARS-CoV-2 Omicron 变异株,采用 Sanger 测序策略持续鉴定 SARS-CoV-2 变异株。
背景:严重急性呼吸系统综合征冠状病毒2(SARS-CoV-2)持续进化,产生了以尖峰蛋白突变为特征的新变种。然而,在冠状病毒病 2019(COVID-19)降级后,有关该病毒进化趋势的公开数据并不广泛。因此,本研究旨在调查一种基于 Sanger 的内部方法是否适用于识别 SARS-CoV-2 变异体,特别是新出现的 Omicron 变异体,并更新广岛县第 8 次流行期间 COVID-19 的流行病学:研究共纳入了广岛市医学会临床检验中心在 2023 年 2 月 1 日至 2024 年 3 月 12 日期间采集的 639 份 COVID-19 检测呈阳性者的唾液样本。通过 RT-qPCR,在 69.3%(443/639)的患者中发现了 SARS-CoV-2 变异株,平均病毒滴度为 2 × 106 copies/mL,其中 Omicron 变异株 XBC.1.6* 的病毒滴度较高(5 × 108 copies/mL)。通过使用桑格测序策略进行基于 Spike 基因的部分测序,确定了不同时期的 Omicron 亚系 XXB.1、BA.5 和 EG.1。对从 GISAID 中检索到的 7383 株 SARS-CoV-2 株系进行了全面的系统发育分析,这些株系是从 2020 年初 COVID-19 大流行开始到 2024 年 7 月在广岛收集的,分析结果显示了 SARS-CoV-2 变体随时间的动态演变。研究发现,在同一时期,来自 GISAID 的全基因组和通过我们的筛选策略获得的部分基因组之间存在相似的变异分布模式:我们的研究表明,在广岛第 8 次疫情爆发期间,广岛流行的所有 SARS-CoV-2 病毒都是 Omicron 变种及其亚系。需要对 SARS-CoV-2 进行持续的分子监测,以便及时做出公共决策和战略规划。我们的研究为基于 SARS-CoV-2 棘波基因部分测序的 SARS-CoV-2 变异识别策略在大规模筛查和分子监测中的实用性提供了证据,即使新出现的各种 SARS-CoV-2 Omicron 变异也是如此。
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来源期刊
BMC Genomics
BMC Genomics 生物-生物工程与应用微生物
CiteScore
7.40
自引率
4.50%
发文量
769
审稿时长
6.4 months
期刊介绍: BMC Genomics is an open access, peer-reviewed journal that considers articles on all aspects of genome-scale analysis, functional genomics, and proteomics. BMC Genomics is part of the BMC series which publishes subject-specific journals focused on the needs of individual research communities across all areas of biology and medicine. We offer an efficient, fair and friendly peer review service, and are committed to publishing all sound science, provided that there is some advance in knowledge presented by the work.
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