Basic Sciences Division and Computational Biology Program, Fred Hutchinson Cancer Center, Seattle, WA.
Department of Genome Sciences, University of Washington, Seattle, WA.
Mol Biol Evol. 2023 Apr 4;40(4). doi: 10.1093/molbev/msad085.
SARS-CoV-2 evolves rapidly in part because of its high mutation rate. Here, we examine whether this mutational process itself has changed during viral evolution. To do this, we quantify the relative rates of different types of single-nucleotide mutations at 4-fold degenerate sites in the viral genome across millions of human SARS-CoV-2 sequences. We find clear shifts in the relative rates of several types of mutations during SARS-CoV-2 evolution. The most striking trend is a roughly 2-fold decrease in the relative rate of G→T mutations in Omicron versus early clades, as was recently noted by Ruis et al. (2022. Mutational spectra distinguish SARS-CoV-2 replication niches. bioRxiv, doi:10.1101/2022.09.27.509649). There is also a decrease in the relative rate of C→T mutations in Delta, and other subtle changes in the mutation spectrum along the phylogeny. We speculate that these changes in the mutation spectrum could arise from viral mutations that affect genome replication, packaging, and antagonization of host innate-immune factors, although environmental factors could also play a role. Interestingly, the mutation spectrum of Omicron is more similar than that of earlier SARS-CoV-2 clades to the spectrum that shaped the long-term evolution of sarbecoviruses. Overall, our work shows that the mutation process is itself a dynamic variable during SARS-CoV-2 evolution and suggests that human SARS-CoV-2 may be trending toward a mutation spectrum more similar to that of other animal sarbecoviruses.
SARS-CoV-2 在进化过程中迅速变异,部分原因是其具有较高的突变率。在这里,我们研究了病毒进化过程中突变过程本身是否发生了变化。为此,我们在病毒基因组的 4 倍简并位点上,对 SARS-CoV-2 的数百万个人类序列进行分析,以定量研究不同类型单核苷酸突变的相对速率。我们发现,在 SARS-CoV-2 进化过程中,几种类型突变的相对速率发生了明显变化。最显著的趋势是,与早期分支相比,奥密克戎(Omicron)中 G→T 突变的相对速率大约降低了 2 倍,正如 Ruis 等人(2022. 突变谱区分了 SARS-CoV-2 的复制生态位。bioRxiv,doi:10.1101/2022.09.27.509649)最近所指出的那样。Delta 中 C→T 突变的相对速率也有所下降,沿系统发育树,突变谱还有其他细微变化。我们推测,这种突变谱的变化可能源于影响基因组复制、包装和拮抗宿主先天免疫因子的病毒突变,尽管环境因素也可能发挥作用。有趣的是,奥密克戎的突变谱与早期 SARS-CoV-2 分支的突变谱比与长期进化的沙贝病毒科(sarbecovirus)的突变谱更为相似。总的来说,我们的工作表明,突变过程本身是 SARS-CoV-2 进化过程中的一个动态变量,并表明人类 SARS-CoV-2 可能正在朝着与其他动物沙贝病毒科更为相似的突变谱方向发展。