School of Pathology, Faculty of Health Sciences, University of the Witwatersrand, Johannesburg 2193, South Africa.
Department of Virology, National Health Laboratory Service, Charlotte Maxeke Johannesburg Academic Hospital, Johannesburg 2193, South Africa.
Viruses. 2023 May 18;15(5):1194. doi: 10.3390/v15051194.
SARS-CoV-2 lineages and variants of concern (VOC) have gained more efficient transmission and immune evasion properties with time. We describe the circulation of VOCs in South Africa and the potential role of low-frequency lineages on the emergence of future lineages. Whole genome sequencing was performed on SARS-CoV-2 samples from South Africa. Sequences were analysed with Nextstrain pangolin tools and Stanford University Coronavirus Antiviral & Resistance Database. In 2020, 24 lineages were detected, with B.1 (3%; 8/278), B.1.1 (16%; 45/278), B.1.1.348 (3%; 8/278), B.1.1.52 (5%; 13/278), C.1 (13%; 37/278) and C.2 (2%; 6/278) circulating during the first wave. Beta emerged late in 2020, dominating the second wave of infection. B.1 and B.1.1 continued to circulate at low frequencies in 2021 and B.1.1 re-emerged in 2022. Beta was outcompeted by Delta in 2021, which was thereafter outcompeted by Omicron sub-lineages during the 4th and 5th waves in 2022. Several significant mutations identified in VOCs were also detected in low-frequency lineages, including S68F (E protein); I82T (M protein); P13L, R203K and G204R/K (N protein); R126S (ORF3a); P323L (RdRp); and N501Y, E484K, D614G, H655Y and N679K (S protein). Low-frequency variants, together with VOCs circulating, may lead to convergence and the emergence of future lineages that may increase transmissibility, infectivity and escape vaccine-induced or natural host immunity.
SARS-CoV-2 谱系和关注变异株(VOC)随着时间的推移获得了更高的传播效率和免疫逃逸特性。我们描述了南非 VOC 的传播情况,以及低频谱系在未来谱系出现中的潜在作用。对南非的 SARS-CoV-2 样本进行了全基因组测序。使用 Nextstrain pangolin 工具和斯坦福大学冠状病毒抗病毒和耐药性数据库对序列进行了分析。2020 年,检测到 24 个谱系,其中 B.1(3%;278 例中的 8 例)、B.1.1(16%;278 例中的 45 例)、B.1.1.348(3%;278 例中的 8 例)、B.1.1.52(5%;278 例中的 13 例)、C.1(13%;278 例中的 37 例)和 C.2(2%;278 例中的 6 例)在第一波期间传播。贝塔在 2020 年末出现,主导了第二波感染。B.1 和 B.1.1 在 2021 年继续以低频传播,B.1.1 在 2022 年再次出现。贝塔在 2021 年被德尔塔取代,随后在 2022 年的第四波和第五波中被奥密克戎亚谱系取代。在 VOC 中发现的几个重要突变也在低频谱系中检测到,包括 S68F(E 蛋白);I82T(M 蛋白);P13L、R203K 和 G204R/K(N 蛋白);R126S(ORF3a);P323L(RdRp);以及 N501Y、E484K、D614G、H655Y 和 N679K(S 蛋白)。低频变体与循环的 VOC 一起,可能导致未来谱系的趋同和出现,从而增加传染性、感染力,并逃避疫苗诱导或自然宿主免疫。