Genomic epidemiology reveals the variation and transmission properties of SARS-CoV-2 in a single-source community outbreak.

IF 5.5 2区 医学 Q1 VIROLOGY
Virus Evolution Pub Date : 2024-10-17 eCollection Date: 2024-01-01 DOI:10.1093/ve/veae085
Ning Zhao, Min He, HengXue Wang, LiGuo Zhu, Nan Wang, Wei Yong, HuaFeng Fan, SongNing Ding, Tao Ma, Zhong Zhang, XiaoXiao Dong, ZiYu Wang, XiaoQing Dong, XiaoYu Min, HongBo Zhang, Jie Ding
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引用次数: 0

Abstract

Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) has caused the coronavirus disease 2019 (COVID-19) pandemic, which is still a global public health concern. During March 2022, a rapid and confined single-source outbreak of SARS-CoV-2 was identified in a community in Nanjing municipal city. Overall, 95 individuals had laboratory-confirmed SARS-CoV-2 infection. The whole genomes of 61 viral samples were obtained, which were all members of the BA.2.2 lineage and clearly demonstrated the presence of one large clade, and all the infections could be traced back to the original index case. The most distant sequence from the index case presented a difference of 4 SNPs, and 118 intrahost single-nucleotide variants (iSNVs) at 74 genomic sites were identified. Some minor iSNVs can be transmitted and subsequently rapidly fixed in the viral population. The minor iSNVs transmission resulted in at least two nucleotide substitutions among all seven SNPs identified in the outbreak, generating genetically diverse populations. We estimated the overall transmission bottleneck size to be 3 using 11 convincing donor-recipient transmission pairs. Our study provides new insights into genomic epidemiology and viral transmission, revealing how iSNVs become fixed in local clusters, followed by viral transmission across the community, which contributes to population diversity.

基因组流行病学揭示了单一来源社区疫情中 SARS-CoV-2 的变异和传播特性。
严重急性呼吸系统综合征冠状病毒2型(SARS-CoV-2)引发了2019年冠状病毒病(COVID-19)大流行,至今仍是全球公共卫生关注的问题。2022 年 3 月,南京市某社区发现了一起快速、局限的 SARS-CoV-2 单源疫情。共有 95 人经实验室确诊感染了 SARS-CoV-2。我们获得了 61 份病毒样本的全基因组,它们都是 BA.2.2 系的成员,清楚地表明存在一个大的支系,所有感染者都可以追溯到最初的疫点病例。与索引病例最远的序列出现了 4 个 SNPs 差异,在 74 个基因组位点上发现了 118 个宿主内单核苷酸变异(iSNVs)。一些次要的 iSNVs 可以传播,随后迅速固定在病毒种群中。小的 iSNVs 传播导致疫情中发现的所有 7 个 SNPs 中至少有两个核苷酸发生了置换,从而产生了基因多样化的种群。我们利用 11 对令人信服的供体-受体传播对,估计总体传播瓶颈规模为 3。我们的研究为基因组流行病学和病毒传播提供了新的见解,揭示了 iSNV 如何在局部集群中固定下来,然后在整个群落中传播,从而导致种群多样性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Virus Evolution
Virus Evolution Immunology and Microbiology-Microbiology
CiteScore
10.50
自引率
5.70%
发文量
108
审稿时长
14 weeks
期刊介绍: Virus Evolution is a new Open Access journal focusing on the long-term evolution of viruses, viruses as a model system for studying evolutionary processes, viral molecular epidemiology and environmental virology. The aim of the journal is to provide a forum for original research papers, reviews, commentaries and a venue for in-depth discussion on the topics relevant to virus evolution.
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