Choga Wonderful T, Gustani-Buss Emanuele, Tegally Houriiyah, Maruapula Dorcas, Yu Xiaoyu, Moir Monika, Zuze Boitumelo J L, James San Emmanuel, Ndlovu Nokuthula S, Seru Kedumetse, Motshosi Patience, Blenkinsop Alexandra, Gobe Irene, Baxter Cheryl, Manasa Justen, Lockman Shahin, Shapiro Roger, Makhema Joseph, Wilkinson Eduan, Blackard Jason T, Lemey Phillipe, Lessells Richard J, Martin Darren P, de Oliveira Tulio, Gaseitsiwe Simani, Moyo Sikhulile
Research Laboratory, Botswana Harvard Health Partnership, Gaborone, Private Bag BO 320, Botswana.
Faculty of Health Sciences, School of Allied Health Sciences, Gaborone, Private Bag UB 0022, Botswana.
Virus Evol. 2024 Nov 22;10(1):veae095. doi: 10.1093/ve/veae095. eCollection 2024.
Botswana, like the rest of the world, has been significantly impacted by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). In December 2022, we detected a monophyletic cluster of genomes comprising a sublineage of the Omicron variant of concern (VOC) designated as B.1.1.529.5.3.1.1.1.1.1.1.74.1 (alias FN.1, clade 22E). These genomes were sourced from both epidemiologically linked and unlinked samples collected in three close locations within the district of Greater Gaborone. In this study, we assessed the worldwide prevalence of the FN.1 lineage, evaluated its mutational profile, and conducted a phylogeographic analysis to reveal its global dispersal dynamics. Among approximately 16 million publicly available SARS-CoV-2 sequences generated by 30 September 2023, only 87 were of the FN.1 lineage, including 22 from Botswana, 6 from South Africa, and 59 from the UK. The estimated time to the most recent common ancestor of the 87 FN.1 sequences was 22 October 2022 [95% highest posterior density: 2 September 2022-24 November 2022], with the earliest of the 22 Botswana sequences having been sampled on 7 December 2022. Discrete trait reconstruction of FN.1 identified Botswana as the most probable place of origin. The FN.1 lineage is derived from the BQ.1.1 lineage and carries two missense variants in the spike protein, S:K182E in NTD and S:T478R in RDB. Among the over 90 SARS-CoV-2 lineages circulating in Botswana between September 2020 and July 2023, FN.1 was most closely related to BQ.1.1.74 based on maximum likelihood phylogenetic inference, differing only by the S:K182E mutation found in FN.1. Given the early detection of numerous novel variants from Botswana and its neighbouring countries, our study underscores the necessity of continuous surveillance to monitor the emergence of potential VOCs, integrating molecular and spatial data to identify dissemination patterns enhancing preparedness efforts.
与世界其他地区一样,博茨瓦纳也受到了严重急性呼吸综合征冠状病毒2(SARS-CoV-2)的重大影响。2022年12月,我们检测到一个单系基因组簇,它包含一个被指定为B.1.1.529.5.3.1.1.1.1.1.1.74.1(别名FN.1,进化枝22E)的奥密克戎变异株(VOC)亚系。这些基因组来自在哈博罗内大区三个相邻地点收集的有流行病学关联和无关联的样本。在本研究中,我们评估了FN.1谱系在全球的流行情况,评估了其突变特征,并进行了系统地理学分析以揭示其全球传播动态。在截至2023年9月30日生成的约1600万条公开可用的SARS-CoV-2序列中,只有87条属于FN.1谱系,其中22条来自博茨瓦纳,6条来自南非,59条来自英国。这87条FN.1序列的最近共同祖先的估计时间为2022年10月22日[95%最高后验密度:2022年9月2日至2022年11月24日],22条博茨瓦纳序列中最早的样本采集于2022年12月7日。对FN.1的离散性状重建确定博茨瓦纳是最有可能的起源地。FN.1谱系源自BQ.1.1谱系,在刺突蛋白中携带两个错义变异,NTD中的S:K182E和RDB中的S:T478R。在2020年9月至2023年7月期间在博茨瓦纳传播的9多株SARS-CoV-2谱系中,根据最大似然系统发育推断,FN.1与BQ.1.1.74关系最为密切,仅在FN.1中发现的S:K182E突变有所不同。鉴于在博茨瓦纳及其邻国早期检测到众多新型变异株,我们的研究强调了持续监测以监测潜在VOC出现的必要性,整合分子和空间数据以识别传播模式,加强防范措施。