Morphogenesis and cytopathic effect of SARS-CoV-2 infection in human airway epithelial cells

被引:0
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作者
Na Zhu
Wenling Wang
Zhidong Liu
Chaoyang Liang
Wen Wang
Fei Ye
Baoying Huang
Li Zhao
Huijuan Wang
Weimin Zhou
Yao Deng
Longfei Mao
Chongyu Su
Guangliang Qiang
Taijiao Jiang
Jincun Zhao
Guizhen Wu
Jingdong Song
Wenjie Tan
机构
[1] Chinese Center for Disease Control and Prevention,NHC Key Laboratory of Biosafety, National Institute for Viral Disease Control and Prevention
[2] Capital Medical University (Beijing Tuberculosis and Thoracic Tumor Research Institute),Department of Thoracic Surgery, Beijing Chest Hospital
[3] China–Japan Friendship Hospital,Department of Thoracic Surgery
[4] Suzhou Institute of Systems Medicine,State Key Laboratory of Respiratory Disease, National Clinical Research Center for Respiratory Disease, Guangzhou Institute of Respiratory Health
[5] The First Affiliated Hospital of Guangzhou Medical University,Institute of Infectious Disease
[6] Guangzhou Eighth People’s Hospital of Guangzhou Medical University,State Key Laboratory of Infectious Disease Prevention and Control, National Institute for Viral Disease Control and Prevention
[7] Chinese Center for Disease Control and Prevention,Center for Biosafety Mega
[8] Chinese Academy of Sciences,Science
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摘要
SARS-CoV-2, a β-coronavirus, has rapidly spread across the world, highlighting its high transmissibility, but the underlying morphogenesis and pathogenesis remain poorly understood. Here, we characterize the replication dynamics, cell tropism and morphogenesis of SARS-CoV-2 in organotypic human airway epithelial (HAE) cultures. SARS-CoV-2 replicates efficiently and infects both ciliated and secretory cells in HAE cultures. In comparison, HCoV-NL63 replicates to lower titers and is only detected in ciliated cells. SARS-CoV-2 shows a similar morphogenetic process as other coronaviruses but causes plaque-like cytopathic effects in HAE cultures. Cell fusion, apoptosis, destruction of epithelium integrity, cilium shrinking and beaded changes are observed in the plaque regions. Taken together, our results provide important insights into SARS-CoV-2 cell tropism, replication and morphogenesis.
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