Taking stock of the mutations in human SARS-CoV-2 spike proteins: From early days to nearly the end of COVID-19 pandemic

IF 2.7 Q3 BIOCHEMISTRY & MOLECULAR BIOLOGY Current Research in Structural Biology Pub Date : 2023-01-01 DOI:10.1016/j.crstbi.2023.100107
Lalitha Guruprasad, Gatta KRS. Naresh, Ganesh Boggarapu
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Abstract

The severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2), causative agent of the coronavirus disease-2019 (COVID-19) has resulted in several deaths and severe economic losses throughout the world. The spike protein in the virus binds to the human ACE-2 receptor in order to mediate virus-host interactions required for the viral transmission. Since first report of the SARS-CoV-2 sequence during December 2019 from patient infected with the virus in Wuhan, China, the virus has undergone rapid changes leading to mutations comprising substitutions, deletions and insertions in the sequence resulting in several variants of the virus that were more virulent and transmissible or less virulent but highly transmissible. The timely intervention with COVID-19 vaccines proved to be effective in controlling the number of infections. However, rapid mutations in the virus led to the lowering of vaccine efficacies being administered to people. In May 2023, the World Health Organization declared COVID-19 was not a public health emergency of international concern anymore. In order to take stock of mutations in the virus from early days to nearly end of COVID-19 pandemic, sequence analyses of the SARS-CoV-2 spike proteins available in the NCBI Virus database was carried out. The mutations and invariant residues in the SARS-CoV-2 spike protein sequences relative to the reference sequence were analysed. The location of the invariant residues and residues at interface of the protein chains in the spike protein trimer complex structure were examined. A total of 111,298 non-redundant SARS-CoV-2 spike protein sequences representing 2,345,585 spike proteins in the NCBI Virus database showed mutations at 1252 of the 1273 positions in the amino acid sequence. The mutations represented 6129 different mutation types in the sequences analysed. Besides, some sequences also contained insertion mutations. The SARS-CoV-2 spike protein sequences represented 1435 lineages. In addition, several spike protein sequences with mutations whose lineages were either ‘not classified’ or were ‘unclassifiable’ indicated the virus could still be evolving.

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评估人类SARS-CoV-2刺突蛋白的突变:从新冠肺炎大流行的早期到几乎结束。
2019冠状病毒病(新冠肺炎)的病原体严重急性呼吸综合征冠状病毒2型(SARS-CoV-2)已在世界各地造成数人死亡和严重经济损失。病毒中的刺突蛋白与人类ACE-2受体结合,以介导病毒传播所需的病毒-宿主相互作用。自2019年12月中国武汉感染该病毒的患者首次报告严重急性呼吸系统综合征冠状病毒2型序列以来,该病毒发生了快速变化,导致序列发生了包括替换、缺失和插入在内的突变,导致病毒的几种变体更具毒力和传播性,或毒性较低但具有高度传播性。新冠肺炎疫苗的及时干预被证明在控制感染人数方面是有效的。然而,病毒的快速突变导致人们接种疫苗的效力降低。2023年5月,世界卫生组织宣布新冠肺炎不再是国际关注的突发公共卫生事件。为了评估从新冠肺炎大流行早期到接近尾声的病毒突变,对NCBI病毒数据库中可用的SARS-CoV-2刺突蛋白进行了序列分析。分析了严重急性呼吸系统综合征冠状病毒2型刺突蛋白序列相对于参考序列的突变和不变残基。检测了刺突蛋白三聚体复合物结构中不变残基和蛋白链界面残基的位置。NCBI病毒数据库中共有111298个非冗余严重急性呼吸系统综合征冠状病毒2型刺突蛋白序列,代表2345585个刺突蛋白,在氨基酸序列的1273个位置中的1252个位置显示突变。在所分析的序列中,这些突变代表了6129种不同的突变类型。此外,一些序列还含有插入突变。严重急性呼吸系统综合征冠状病毒2型刺突蛋白序列代表1435个谱系。此外,一些具有突变的刺突蛋白序列的谱系要么“未分类”,要么“无法分类”,这表明病毒可能仍在进化。
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来源期刊
CiteScore
4.60
自引率
0.00%
发文量
33
审稿时长
104 days
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