Gu Haogao, Quadeer Ahmed Abdul, Krishnan Pavithra, Ng Daisy Y M, Chang Lydia D J, Liu Gigi Y Z, Cheng Samuel S M, Lam Tommy T Y, Peiris Malik, McKay Matthew R, Poon Leo L M
School of Public Health, LKS Faculty of Medicine, The University of Hong Kong, Hong Kong, China.
Department of Electronic and Computer Engineering, The Hong Kong University of Science and Technology, Hong Kong SAR, China.
Res Sq. 2022 Aug 11:rs.3.rs-1927944. doi: 10.21203/rs.3.rs-1927944/v1.
Viral and host factors can shape SARS-CoV-2 within-host viral diversity and virus evolution. However, little is known about lineage-specific and vaccination-specific mutations that occur within individuals. Here we analysed deep sequencing data from 2,146 SARS-CoV-2 samples with different viral lineages to describe the patterns of within-host diversity in different conditions, including vaccine-breakthrough infections. Variant of Concern (VOC) Alpha, Delta, and Omicron samples were found to have higher within-host nucleotide diversity while being under weaker purifying selection at full genome level compared to non-VOC SARS-CoV-2 viruses. Breakthrough Delta and Omicron infections in Comirnaty and CoronaVac vaccinated individuals appeared to have higher within-host purifying selection at the full-genome and/or Spike gene levels. Vaccine-induced antibody or T cell responses did not appear to have significant impact on within-host SARS-CoV-2 evolution. Our findings suggest that vaccination does not increase SARS-CoV-2 protein sequence space and may not facilitate emergence of more viral variants.
病毒和宿主因素可塑造严重急性呼吸综合征冠状病毒2(SARS-CoV-2)在宿主体内的病毒多样性和病毒进化。然而,对于个体内发生的谱系特异性和疫苗特异性突变,我们知之甚少。在此,我们分析了来自2146份具有不同病毒谱系的SARS-CoV-2样本的深度测序数据,以描述不同条件下(包括疫苗突破性感染)宿主体内的多样性模式。与非关注变异株(VOC)的SARS-CoV-2病毒相比,关注变异株(VOC)阿尔法、德尔塔和奥密克戎样本在全基因组水平上的纯化选择较弱,但宿主体内核苷酸多样性更高。在接种了辉瑞/BioNTech新冠疫苗(Comirnaty)和科兴新冠疫苗(CoronaVac)的个体中,德尔塔和奥密克戎突破性感染在全基因组和/或刺突基因水平上似乎具有更强的宿主体内纯化选择。疫苗诱导的抗体或T细胞反应似乎对宿主体内的SARS-CoV-2进化没有显著影响。我们的研究结果表明,接种疫苗不会增加SARS-CoV-2蛋白序列空间,可能也不会促进更多病毒变体的出现。