Centre for Health System Strengthening (CfHSS), Kumasi, Ghana.
Department of Microbiology, School of Medical Sciences, Kwame Nkrumah University of Science and Technology (KNUST), Kumasi, Ghana.
PLoS Negl Trop Dis. 2021 Apr 26;15(4):e0009335. doi: 10.1371/journal.pntd.0009335. eCollection 2021 Apr.
Since late 2019, the coronavirus disease 2019 (COVID-19) outbreak, caused by SARS-CoV-2, has rapidly evolved to become a global pandemic. Each country was affected but with a varying number of infected cases and mortality rates. Africa was hit late by the pandemic but the number of cases rose sharply. In this study, we investigated 224 SARS-CoV-2 genome sequences from the Global Initiative on Sharing Avian Influenza Data (GISAID) in the early part of the outbreak, of which 69 were from Africa. We analyzed a total of 550 mutations by comparing them with the reference SARS-CoV-2 sequence from Wuhan. We classified the mutations observed based on country and region, and afterwards analyzed common and unique mutations on the African continent as a whole. Correlation analyses showed that the duo variants ORF1ab/RdRp 4715L and S protein 614G variants, which are strongly linked to fatality rate, were not significantly and positively correlated with fatality rates (r = -0.03757, P = 0.5331 and r = -0.2876, P = 0.6389, respectively), although increased number of cases correlated with number of deaths (r = 0.997, P = 0.0002). Furthermore, most cases in Africa were mainly imported from American and European countries, except one isolate with no mutation and was similar to the original isolate from Wuhan. Moreover, unique mutations specific to countries were identified in the early phase of the outbreak but these mutations were not regional-specific. There were common mutations in all isolates across the continent as well as similar isolate-specific mutations in different regions. Our findings suggest that mutation is rapid in SARS-CoV-2 in Africa and although these mutations spread across the continent, the duo variants could not possibly be the sole cause of COVID-19 deaths in Africa in the early phase of the outbreak.
自 2019 年末以来,由 SARS-CoV-2 引起的 2019 年冠状病毒病(COVID-19)疫情迅速蔓延,成为全球大流行。每个国家都受到了影响,但感染病例和死亡率各不相同。非洲受到疫情的影响较晚,但病例数量急剧上升。在本研究中,我们调查了疫情早期全球共享流感数据倡议组织(GISAID)中 224 个 SARS-CoV-2 基因组序列,其中 69 个来自非洲。我们通过将它们与来自武汉的参考 SARS-CoV-2 序列进行比较,总共分析了 550 个突变。我们根据国家和地区对突变进行分类,然后分析整个非洲大陆的常见和独特突变。相关性分析表明,与死亡率密切相关的 ORF1ab/RdRp 4715L 和 S 蛋白 614G 变体,与死亡率没有显著正相关(r=-0.03757,P=0.5331 和 r=-0.2876,P=0.6389),尽管病例数增加与死亡人数相关(r=0.997,P=0.0002)。此外,非洲的大多数病例主要是从美洲和欧洲国家输入的,除了一个没有突变的分离株,与武汉的原始分离株相似。此外,在疫情早期阶段确定了针对个别国家的独特突变,但这些突变不是区域性的。在整个非洲大陆的所有分离株中都存在共同突变,并且在不同地区也存在类似的分离株特异性突变。我们的研究结果表明,SARS-CoV-2 在非洲的突变速度很快,尽管这些突变在整个非洲大陆传播,但这两种变体不太可能是疫情早期非洲 COVID-19 死亡的唯一原因。