A Mouse-Adapted SARS-CoV-2 Induces Acute Lung Injury and Mortality in Standard Laboratory Mice

被引:427
作者
Leist, Sarah R. [1 ]
Dinnon, Kenneth H. [2 ]
Schafer, Alexandra [1 ]
Tse, Longping, V [1 ]
Okuda, Kenichi [3 ]
Hou, Yixuan J. [1 ]
West, Ande [1 ]
Edwards, Caitlin E. [1 ]
Sanders, Wes [2 ,3 ]
Fritch, Ethan J. [2 ]
Gully, Kendra L. [1 ]
Scobey, Trevor [1 ]
Brown, Ariane J. [1 ]
Sheahan, Timothy P. [1 ]
Moorman, Nathaniel J. [2 ,4 ,6 ]
Boucher, Richard C. [3 ]
Gralinski, Lisa E. [1 ]
Montgomery, Stephanie A. [4 ,5 ]
Baric, Ralph S. [1 ,2 ,6 ]
机构
[1] Univ North Carolina, Dept Epidemiol, Chapel Hill, NC 27515 USA
[2] Univ North Carolina, Dept Microbiol & Immunol, Chapel Hill, NC 27515 USA
[3] Univ North Carolina, Mars Lung Inst, Chapel Hill, NC 27515 USA
[4] Univ North Carolina, Lineberger Comprehens Canc Ctr, Chapel Hill, NC 27515 USA
[5] Univ North Carolina, Dept Pathol & Lab Med, Chapel Hill, NC 27515 USA
[6] Univ North Carolina, Rapidly Emerging Antiviral Drug Discovery Initiat, Chapel Hill, NC 27515 USA
关键词
HUMAN CORONAVIRUS; PATHOGENESIS; SARS; INFECTION; RESPONSES; COVID-19;
D O I
10.1016/j.cell.2020.09.050
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The SARS-CoV-2 pandemic has caused extreme human suffering and economic harm. We generated and characterized a new mouse-adapted SARS-CoV-2 virus that captures multiple aspects of severe COVID-19 disease in standard laboratory mice. This SARS-CoV-2 model exhibits the spectrum of morbidity and mortality of COVID-19 disease as well as aspects of host genetics, age, cellular tropisms, elevated Th1 cytokines, and loss of surfactant expression and pulmonary function linked to pathological features of acute lung injury (ALI) and acute respiratory distress syndrome (ARDS). This model can rapidly access existing mouse resources to elucidate the role of host genetics, underlying molecular mechanisms governing SARS-CoV-2 pathogenesis, and the protective or pathogenic immune responses related to disease severity. The model promises to provide a robust platform for studies of ALI and ARDS to evaluate vaccine and antiviral drug performance, including in the most vulnerable populations (i.e., the aged) using standard laboratory mice.
引用
收藏
页码:1070 / +
页数:28
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