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基因组流行病学揭示了严重急性呼吸综合征冠状病毒2(SARS-CoV-2)在单源社区暴发中的变异和传播特性。

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

作者信息

Zhao Ning, He Min, Wang HengXue, Zhu LiGuo, Wang Nan, Yong Wei, Fan HuaFeng, Ding SongNing, Ma Tao, Zhang Zhong, Dong XiaoXiao, Wang ZiYu, Dong XiaoQing, Min XiaoYu, Zhang HongBo, Ding Jie

机构信息

Microbiology Laboratory, Nanjing Medical University Affiliated Nanjing Municipal Center for Disease Control and Prevention, 2 Zizhulin Road, Nanjing, Jiangsu 210003, China.

School of Public Health, Nanjing Medical University, 101 Longmian Avenue, Nanjing, Jiangsu 211166, China.

出版信息

Virus Evol. 2024 Oct 17;10(1):veae085. doi: 10.1093/ve/veae085. eCollection 2024.

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.

摘要

严重急性呼吸综合征冠状病毒2(SARS-CoV-2)引发了2019冠状病毒病(COVID-19)大流行,这仍是一个全球公共卫生问题。2022年3月期间,在南京市的一个社区发现了一起快速且局限的SARS-CoV-2单源暴发。总体而言,95人实验室确诊感染SARS-CoV-2。获得了61份病毒样本的全基因组,这些样本均为BA.2.2谱系成员,清楚显示存在一个大分支,所有感染都可追溯到最初的索引病例。与索引病例距离最远的序列有4个单核苷酸多态性(SNP)差异,在74个基因组位点鉴定出118个宿主内单核苷酸变异(iSNV)。一些次要的iSNV能够传播并随后在病毒群体中迅速固定下来。次要iSNV的传播导致在此次暴发中鉴定出的所有7个SNP中至少有两个核苷酸替换,产生了基因多样化的群体。我们使用11对可信的供体-受体传播配对估计总体传播瓶颈大小为3。我们的研究为基因组流行病学和病毒传播提供了新见解,揭示了iSNV如何在局部聚集簇中固定下来,随后在社区中传播,这促成了群体多样性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3682/11529616/9c7bed3d2b20/veae085f1.jpg

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