Huang Xing-Yao, Chen Qi, Sun Meng-Xu, Zhou Hang-Yu, Ye Qing, Chen Wu, Peng Jin-Yu, Qi Yi-Ni, Zhai Jun-Qiong, Tian Ying, Liu Zi-Xin, Huang Yi-Jiao, Deng Yong-Qiang, Li Xiao-Feng, Wu Aiping, Yang Xiao, Yang Guan, Shen Yongyi, Qin Cheng-Feng
State Key Laboratory of Pathogen and Biosecurity, Beijing Institute of Microbiology and Epidemiology, AMMS, Beijing, China.
Institute of Systems Medicine, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing, China.
Cell Discov. 2023 Jun 17;9(1):59. doi: 10.1038/s41421-023-00557-9.
Virus spillover remains a major challenge to public health. A panel of SARS-CoV-2-related coronaviruses have been identified in pangolins, while the infectivity and pathogenicity of these pangolin-origin coronaviruses (pCoV) in humans remain largely unknown. Herein, we comprehensively characterized the infectivity and pathogenicity of a recent pCoV isolate (pCoV-GD01) in human cells and human tracheal epithelium organoids and established animal models in comparison with SARS-CoV-2. pCoV-GD01 showed similar infectivity to SARS-CoV-2 in human cells and organoids. Remarkably, intranasal inoculation of pCoV-GD01 caused severe lung pathological damage in hACE2 mice and could transmit among cocaged hamsters. Interestingly, in vitro neutralization assays and animal heterologous challenge experiments demonstrated that preexisting immunity induced by SARS-CoV-2 infection or vaccination was sufficient to provide at least partial cross-protection against pCoV-GD01 challenge. Our results provide direct evidence supporting pCoV-GD01 as a potential human pathogen and highlight the potential spillover risk.
病毒溢出仍然是公共卫生面临的一项重大挑战。在穿山甲中已鉴定出一组与严重急性呼吸综合征冠状病毒2(SARS-CoV-2)相关的冠状病毒,然而这些源自穿山甲的冠状病毒(pCoV)对人类的传染性和致病性在很大程度上仍不清楚。在此,我们全面表征了一种近期分离的pCoV(pCoV-GD01)在人细胞和人气管上皮类器官中的传染性和致病性,并与SARS-CoV-2相比建立了动物模型。pCoV-GD01在人细胞和类器官中表现出与SARS-CoV-2相似的传染性。值得注意的是,经鼻接种pCoV-GD01会在人血管紧张素转换酶2(hACE2)小鼠中引起严重肺部病理损伤,并且可以在同笼饲养的仓鼠之间传播。有趣的是,体外中和试验和动物异源攻击实验表明,由SARS-CoV-2感染或疫苗接种诱导的预先存在的免疫力足以提供至少部分针对pCoV-GD01攻击的交叉保护。我们的结果提供了直接证据,支持pCoV-GD01作为一种潜在的人类病原体,并突出了潜在的溢出风险。