Chen Jinkun, Hilt Evann E, Li Fan, Wu Huan, Jiang Zhuojing, Zhang Qinchao, Wang Jiling, Wang Yifang, Li Ziqin, Tang Jialiang, Yang Shangxin
Shaoxing Center for Disease Control and Prevention, Shaoxing, China.
Department of Pathology and Laboratory Medicine, University of California, Los Angeles, Los Angeles, CA, United States.
Front Public Health. 2020 Sep 18;8:567621. doi: 10.3389/fpubh.2020.567621. eCollection 2020.
A novel coronavirus known as severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is the cause of the ongoing Coronavirus Disease 2019 (COVID-19) pandemic. In this study, we performed a comprehensive epidemiological and genomic analysis of SARS-CoV-2 genomes from 10 patients in Shaoxing (Zhejiang Province), a mid-sized city outside of the epicenter Hubei province, China, during the early stage of the outbreak (late January to early February, 2020). We obtained viral genomes with >99% coverage and a mean depth of 296X demonstrating that viral genomic analysis is feasible via metagenomics sequencing directly on nasopharyngeal samples with SARS-CoV-2 Real-time PCR C values <28. We found that a cluster of four patients with travel history to Hubei shared the exact same virus with patients from Wuhan, Taiwan, Belgium, and Australia, highlighting how quickly this virus spread to the globe. The virus from another cluster of two family members living together without travel history but with a sick contact of a confirmed case from another city outside of Hubei accumulated significantly more mutations (9 SNPs vs. average 4 SNPs), suggesting a complex and dynamic nature of this outbreak. Our findings add to the growing knowledge of the epidemiological and genomic characteristics of SARS-CoV-2 and offers a glimpse into the early phase of this viral infection outside of Hubei, China.
一种名为严重急性呼吸综合征冠状病毒2(SARS-CoV-2)的新型冠状病毒是正在肆虐的2019冠状病毒病(COVID-19)大流行的病原体。在本研究中,我们对中国湖北省以外的中型城市绍兴市10例患者的SARS-CoV-2基因组进行了全面的流行病学和基因组分析,这些分析数据来自疫情暴发早期(2020年1月下旬至2月上旬)。我们获得了覆盖度>99%且平均深度为296X的病毒基因组,这表明通过宏基因组测序直接对SARS-CoV-2实时PCR C值<28的鼻咽样本进行病毒基因组分析是可行的。我们发现,有4名有湖北旅行史的患者与来自武汉、台湾、比利时和澳大利亚的患者共享完全相同的病毒,这凸显了这种病毒在全球传播的速度之快。另一个由两名居住在一起且无旅行史但与湖北省以外另一个城市的确诊病例有过接触的家庭成员组成的集群中的病毒积累了明显更多的突变(9个单核苷酸多态性,而平均为4个单核苷酸多态性),这表明此次疫情具有复杂和动态的性质。我们调查结果丰富了人们对SARS-CoV-2流行病学和基因组特征的认识,并让我们得以一窥中国湖北省以外地区这种病毒感染的早期情况。