Alpha to JN.1 variants: SARS-CoV-2 genomic analysis unfolding its various lineages/sublineages evolved in Chhattisgarh, India from 2020 to 2024.

Pushpendra Singh, Ruchi Khare, Kuldeep Sharma, Anudita Bhargava, Sanjay Singh Negi
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引用次数: 0

Abstract

Background: The evolutionary mutational changes of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) since its emergence in Chhattisgarh, India in 2020 have warranted the need for the characterization of every lineage/sublineage that has evolved until February 2024.

Aim: To unravel the evolutionary pathway of SARS-CoV-2 in Chhattisgarh from 2020 to February 2024.

Methods: A total of 635 coronavirus disease 2019 cases obtained between 2020 and February 2024 were investigated by whole genome sequencing.

Results: Whole genome sequencing analysis identified the evolution of SARS-CoV-2 into seventeen lineages from 2020 to 2024. SARS-CoV-2 initially emerged in Chhattisgarh in its Alpha (B.1.1.7) variant in 2020. Thereafter, it continuously underwent periodical mutational changes in the spike gene to further differentiate into various lineages/sublineages, viz., Kappa, Delta, BA.1, and BA.2 in 2021; the Omicron lineage (BA.5, BA.2.12.1, BA.2.75, BQ.1, and XBB) in 2022; the new Omicron lineage (XBB.1.5, XBB.1.16, XBB.1.9.1, and XBB.2.3) in 2023; and finally to JN.1 in January and February 2024. The predominant lineages over these 4 years were BA.1.1.7 (Alpha) in 2020, B.1.617.2 (Delta) in the period between 2021 and mid-2022, B.1.1.529 (Omicron) in late 2022 to 2023, and Omicron-JN.1 in early 2024. The presently circulating JN.1 lineage was observed harboring exclusive predominant mutations of E4554K, A570V, P621A, and P1143 L with 99% prevalence.

Conclusion: SARS-CoV-2 from 2020 to 2024 has evolved into 17 lineages/sublineages in Chhattisgarh. The presently circulating JN.1 harbored 40 mutations, especially E554K, A570V, P621S, and P1143 L, capacitating the virus with features of host cell entry, stability, replication, rapid transmissibility, and crucial immune evasion. Therefore, earlier immunity from either vaccination or prior infection may not protect against the current lineage and increases the possibility of future outbreaks. Thus, the periodical genomic surveillance of SARS-CoV-2 is essential for the genomic blueprint of the circulating virus, which may help in updating the vaccine strain and various basic research for developing appropriate therapeutics and diagnostics.

α到JN.1变体:SARS-CoV-2基因组分析揭示了其2020年至2024年在印度恰蒂斯加尔邦进化的各种谱系/亚谱系。
背景:自2020年在印度恰蒂斯加尔邦出现以来,严重急性呼吸综合征冠状病毒2 (SARS-CoV-2)的进化突变变化证明有必要对截至2024年2月进化的每个谱系/亚谱系进行表征。目的:揭示2020年至2024年2月恰蒂斯加尔邦SARS-CoV-2的进化路径。方法:对2020年至2024年2月收集的635例2019冠状病毒病病例进行全基因组测序。结果:全基因组测序分析确定了2020 - 2024年SARS-CoV-2进化为17个谱系。SARS-CoV-2最初于2020年在恰蒂斯加尔邦以其Alpha (B.1.1.7)变体出现。此后,其穗基因不断发生周期性突变变化,在2021年进一步分化为Kappa、Delta、BA.1、BA.2等多个系/亚系;2022年的Omicron谱系(BA.5, BA.2.12.1, BA.2.75, BQ.1和XBB);2023年新的Omicron谱系(XBB.1.5, XBB.1.16, XBB.1.9.1和XBB.2.3);最后在2024年1月和2月到达JN.1。这4年的主要血统是2020年的BA.1.1.7 (Alpha), 2021年至2022年中期的B.1.617.2 (Delta), 2022年底至2023年的B.1.1.529 (Omicron)和Omicron- jn。2024年初。目前流行的JN.1谱系具有E4554K、A570V、P621A和p1143l的独家优势突变,患病率为99%。结论:2020 - 2024年在恰蒂斯加尔邦,SARS-CoV-2已演变成17个谱系/亚谱系。目前流行的JN.1含有40个突变,特别是E554K、A570V、P621S和p1143l,使病毒具有进入宿主细胞、稳定、复制、快速传播和关键免疫逃避的特点。因此,接种疫苗或先前感染的早期免疫可能不能保护免受当前谱系的侵害,并增加未来暴发的可能性。因此,对SARS-CoV-2进行周期性基因组监测对于绘制该循环病毒的基因组蓝图至关重要,这可能有助于更新疫苗株和开展各种基础研究,以开发适当的治疗和诊断方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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