Institute of Infectious Diseases and Molecular Medicine, Division Of Computational Biology, Department of Integrative Biomedical Sciences, University of Cape Town, Cape Town 7701, South Africa.
Institute for Genomics and Evolutionary Medicine, Department of Biology, Temple University, Philadelphia, PA 19122, USA.
Cell. 2021 Sep 30;184(20):5189-5200.e7. doi: 10.1016/j.cell.2021.09.003. Epub 2021 Sep 7.
The independent emergence late in 2020 of the B.1.1.7, B.1.351, and P.1 lineages of SARS-CoV-2 prompted renewed concerns about the evolutionary capacity of this virus to overcome public health interventions and rising population immunity. Here, by examining patterns of synonymous and non-synonymous mutations that have accumulated in SARS-CoV-2 genomes since the pandemic began, we find that the emergence of these three "501Y lineages" coincided with a major global shift in the selective forces acting on various SARS-CoV-2 genes. Following their emergence, the adaptive evolution of 501Y lineage viruses has involved repeated selectively favored convergent mutations at 35 genome sites, mutations we refer to as the 501Y meta-signature. The ongoing convergence of viruses in many other lineages on this meta-signature suggests that it includes multiple mutation combinations capable of promoting the persistence of diverse SARS-CoV-2 lineages in the face of mounting host immune recognition.
2020 年末,B.1.1.7、B.1.351 和 P.1 三种 SARS-CoV-2 谱系的独立出现,再次引发了人们对该病毒克服公共卫生干预措施和不断上升的人群免疫力的进化能力的担忧。在这里,通过检查自大流行开始以来在 SARS-CoV-2 基因组中积累的同义和非同义突变模式,我们发现这三种“501Y 谱系”的出现与作用于各种 SARS-CoV-2 基因的选择压力的重大全球转变同时发生。在它们出现后,501Y 谱系病毒的适应性进化涉及在 35 个基因组位点上反复出现有利的趋同突变,我们称之为 501Y 元特征。许多其他谱系中的病毒持续趋同于该元特征,表明它包含多种能够促进不同 SARS-CoV-2 谱系在面对宿主免疫识别时持续存在的突变组合。