Centre for Epidemic Response and Innovation (CERI), School of Data Science and Computational Thinking, Stellenbosch University, Stellenbosch, South Africa.
KwaZulu-Natal Research Innovation and Sequencing Platform (KRISP), Nelson R. Mandela School of Medicine, University of KwaZulu-Natal, Durban, South Africa.
Nat Med. 2022 Sep;28(9):1785-1790. doi: 10.1038/s41591-022-01911-2. Epub 2022 Jun 27.
Three lineages (BA.1, BA.2 and BA.3) of the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) Omicron variant of concern predominantly drove South Africa's fourth Coronavirus Disease 2019 (COVID-19) wave. We have now identified two new lineages, BA.4 and BA.5, responsible for a fifth wave of infections. The spike proteins of BA.4 and BA.5 are identical, and similar to BA.2 except for the addition of 69-70 deletion (present in the Alpha variant and the BA.1 lineage), L452R (present in the Delta variant), F486V and the wild-type amino acid at Q493. The two lineages differ only outside of the spike region. The 69-70 deletion in spike allows these lineages to be identified by the proxy marker of S-gene target failure, on the background of variants not possessing this feature. BA.4 and BA.5 have rapidly replaced BA.2, reaching more than 50% of sequenced cases in South Africa by the first week of April 2022. Using a multinomial logistic regression model, we estimated growth advantages for BA.4 and BA.5 of 0.08 (95% confidence interval (CI): 0.08-0.09) and 0.10 (95% CI: 0.09-0.11) per day, respectively, over BA.2 in South Africa. The continued discovery of genetically diverse Omicron lineages points to the hypothesis that a discrete reservoir, such as human chronic infections and/or animal hosts, is potentially contributing to further evolution and dispersal of the virus.
三种谱系(BA.1、BA.2 和 BA.3)的严重急性呼吸综合征冠状病毒 2(SARS-CoV-2)奥密克戎变异株是南非第四波 2019 年冠状病毒病(COVID-19)的主要驱动因素。我们现在已经确定了两种新的谱系,BA.4 和 BA.5,它们导致了第五波感染。BA.4 和 BA.5 的刺突蛋白相同,与 BA.2 相似,除了增加 69-70 缺失(存在于 Alpha 变体和 BA.1 谱系中)、L452R(存在于 Delta 变体中)、F486V 和 Q493 野生型氨基酸。这两个谱系仅在刺突区以外存在差异。刺突中的 69-70 缺失使这些谱系能够通过 S 基因靶标失败的替代标记来识别,背景是变体不具有此特征。BA.4 和 BA.5 迅速取代了 BA.2,到 2022 年 4 月的第一周,它们在南非的测序病例中达到了 50%以上。使用多项逻辑回归模型,我们估计 BA.4 和 BA.5 在南非相对于 BA.2 的日增长率优势分别为 0.08(95%置信区间(CI):0.08-0.09)和 0.10(95% CI:0.09-0.11)。奥密克戎谱系的不断发现表明,一个离散的储层,如人类慢性感染和/或动物宿主,可能有助于病毒的进一步进化和传播。