Human SARS CoV-2 spike protein mutations in West Africa

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引用次数: 1

Abstract

Background: The COVID-19 pandemic was caused by the severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2), first detected in Wuhan, Hubei province, China in December 2019. The virus rapidly spread worldwide, with mutations in various parts of its genetic material affecting its transmissibility and infectivity. Objective: This study addressed some of the mutations present in the human SARS-CoV-2 spike proteins relative to Wuhan-Hu-1 reference sequence from China, according to different countries from West Africa. Methods: The SARS-CoV-2 spike protein sequences were obtained from the National Center for Biotechnology Information virus database in the FASTA format on November12,2021. The multiple sequence alignment of the proteins was carried out by MAFFT version 7 online. The human SARS-CoV-2 spike protein sequences from selected West African countries were analyzed by comparing them with the reference SARS-CoV-2 protein sequence from Wuhan-Hu-1, China. Results: Out of 148 spike protein sequences analyzed, 137 proteins had one or more mutations. A total of 486 mutations were observed corresponding to 47 distinct mutation sites. In the analysis of the spike proteins in the study, it was observed that the Receptor Binding Domain which is involved in the interactions with human angiotensin-converting enzyme-2 (ACE-2) receptor causing infection leading to the COVID-19 disease had 8 distinct mutation sites. The D614G mutation is the most common in the SARS-CoV-2 spike protein observed so far among all the West African countries examined in this study and thus the most predominant. In this study, we examined spike proteins not associated with mutations, the distribution of mutations in spike proteins, mutation density in different regions of the spike protein sequence, spike protein sequences with multiple mutations and the Human SARS-CoV-2 spike protein mutation in West Africa and implications for vaccination and drug development purposes. Conclusion: The identified mutations in SARS-CoV-2 are significant for infection prevention, control, and public health interventions. Further studies are imperative to understand the mutations in the virus's spike proteins to guide vaccine development and antiviral drug designs. Investigations should also be conducted to determine the infectivity of emerging variants in West Africa and their response to vaccines and available drugs to address public health concerns on vaccination and drug design goals
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西非人类SARS冠状病毒-2刺突蛋白突变
背景:2019冠状病毒病大流行是由2019年12月在中国湖北省武汉市首次发现的严重急性呼吸综合征冠状病毒-2 (SARS-CoV-2)引起的。该病毒在世界范围内迅速传播,其遗传物质的各个部分发生突变,影响其传播性和传染性。目的:本研究针对西非不同国家的SARS-CoV-2人类刺突蛋白中与中国武汉-胡-1参考序列相关的一些突变进行了研究。方法:于2021年11月12日以FASTA格式从国家生物技术信息中心病毒数据库中获取SARS-CoV-2刺突蛋白序列。蛋白的多序列比对采用MAFFT version 7进行在线比对。选择来自西非国家的人SARS-CoV-2刺突蛋白序列与来自中国武汉-湖-1的参考SARS-CoV-2蛋白序列进行比较分析。结果:148个刺突蛋白序列中,137个蛋白有一个或多个突变。总共观察到486个突变,对应于47个不同的突变位点。在对研究中刺突蛋白的分析中,观察到与人血管紧张素转换酶-2 (ACE-2)受体相互作用导致COVID-19疾病的受体结合域有8个不同的突变位点。在本研究调查的所有西非国家中,D614G突变是迄今为止观察到的SARS-CoV-2刺突蛋白中最常见的,因此也是最主要的。在这项研究中,我们研究了与突变无关的刺突蛋白、刺突蛋白中的突变分布、刺突蛋白序列不同区域的突变密度、多突变刺突蛋白序列和西非人类SARS-CoV-2刺突蛋白突变,以及对疫苗接种和药物开发目的的影响。结论:发现的SARS-CoV-2突变对预防、控制感染和公共卫生干预具有重要意义。进一步的研究必须了解病毒刺突蛋白的突变,以指导疫苗的开发和抗病毒药物的设计。还应开展调查,以确定西非新出现变种的传染性及其对疫苗和现有药物的反应,以解决有关疫苗接种和药物设计目标的公共卫生关切
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