Two-step fitness selection for intra-host variations in SARS-CoV-2

Jiarui Li(Capital Medical University), Pengcheng Du(Capital Medical University), Lijiang Yang(Peking University), Ju Zhang(Capital Medical University), Chuan Song(Capital Medical University), Danying Chen(Capital Medical University), Yangzi Song(Capital Medical University), Nan Ding(Capital Medical University), Mingxi Hua(Capital Medical University), Kai Han(Capital Medical University), Rui Song(Capital Medical University), Wen Xie(Capital Medical University), Zhihai Chen(Capital Medical University), Xianbo Wang(Capital Medical University), Jingyuan Liu(Capital Medical University), Yanli Xu(Capital Medical University), Guiju Gao(Capital Medical University), Qi Wang(Capital Medical University), Lin Pu(Capital Medical University), Lin Di(Peking University), Jie Li(Beijing Ditan Hospital), Jinglin Yue(Peking University), Junyan Han(Capital Medical University), Xuesen Zhao(Capital Medical University), Yonghong Yan(Capital Medical University), Fengting Yu(Capital Medical University), Angela Ruohao Wu(Hong Kong University of Science and Technology), Fujie Zhang(Capital Medical University), Yi Qin Gao(Peking University), Yanyi Huang(Peking University), Jianbin Wang(Chinese Institute for Brain Research), Hui Zeng(Capital Medical University), Chen Chen(Capital Medical University)
Cell Reports
December 16, 2021
Cited by 101Open Access
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Abstract

Spontaneous mutations introduce uncertainty into coronavirus disease 2019 (COVID-19) control procedures and vaccine development. Here, we perform a spatiotemporal analysis on intra-host single-nucleotide variants (iSNVs) in 402 clinical samples from 170 affected individuals, which reveals an increase in genetic diversity over time after symptom onset in individuals. Nonsynonymous mutations are overrepresented in the pool of iSNVs but underrepresented at the single-nucleotide polymorphism (SNP) level, suggesting a two-step fitness selection process: a large number of nonsynonymous substitutions are generated in the host (positive selection), and these substitutions tend to be unfixed as SNPs in the population (negative selection). Dynamic iSNV changes in subpopulations with different gender, age, illness severity, and viral shedding time displayed a varied fitness selection process among populations. Our study highlights that iSNVs provide a mutational pool shaping the rapid global evolution of the virus.


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