A SARS-like cluster of circulating bat coronaviruses shows potential for human emergence

被引:595
作者
Menachery, Vineet D. [1 ]
Yount, Boyd L., Jr. [1 ]
Debbink, Kari [1 ]
Agnihothram, Sudhakar [3 ]
Gralinski, Lisa E. [1 ]
Plante, Jessica A. [1 ]
Graham, Rachel L. [1 ]
Scobey, Trevor [1 ]
Ge, Xing-Yi [4 ]
Donaldson, Eric F. [1 ]
Randell, Scott H. [5 ,6 ]
Lanzavecchia, Antonio [7 ]
Marasco, Wayne A. [8 ,9 ]
Shi, Zhengli-Li [4 ]
Baric, Ralph S. [1 ,2 ]
机构
[1] Univ N Carolina, Dept Epidemiol, Chapel Hill, NC 27514 USA
[2] Univ N Carolina, Dept Microbiol & Immunol, Chapel Hill, NC USA
[3] US FDA, Natl Ctr Toxicol Res, Jefferson, AR 72079 USA
[4] Chinese Acad Sci, Wuhan Inst Virol, Key Lab Special Pathogens & Biosafety, Wuhan, Peoples R China
[5] Univ N Carolina, Dept Cell Biol & Physiol, Chapel Hill, NC USA
[6] Univ N Carolina, Cyst Fibrosis Ctr, Marsico Lung Inst, Chapel Hill, NC USA
[7] Bellinzona Inst Microbiol, Inst Res Biomed, Zurich, Switzerland
[8] Harvard Univ, Sch Med, Dana Farber Canc Inst, Dept Canc Immunol & AIDS, Boston, MA 02115 USA
[9] Harvard Univ, Sch Med, Dept Med, Boston, MA USA
基金
美国国家卫生研究院; 中国国家自然科学基金;
关键词
ACUTE RESPIRATORY SYNDROME; RECEPTOR; DISEASE; CELLS; INFECTIONS; MECHANISMS; FITNESS; VACCINE; ESCAPE; MICE;
D O I
10.1038/nm.3985
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 emergence of severe acute respiratory syndrome coronavirus (SARS-CoV) and Middle East respiratory syndrome (MERS)-CoV underscores the threat of cross-species transmission events leading to outbreaks in humans. Here we examine the disease potential of a SARS-like virus, SHC014-CoV, which is currently circulating in Chinese horseshoe bat populations(1). Using the SARS-CoV reverse genetics system(2), we generated and characterized a chimeric virus expressing the spike of bat coronavirus SHC014 in a mouse-adapted SARS-CoV backbone. The results indicate that group 2b viruses encoding the SHC014 spike in a wild-type backbone can efficiently use multiple orthologs of the SARS receptor human angiotensin converting enzyme II (ACE2), replicate efficiently in primary human airway cells and achieve in vitro titers equivalent to epidemic strains of SARS-CoV. Additionally, in vivo experiments demonstrate replication of the chimeric virus in mouse lung with notable pathogenesis. Evaluation of available SARS-based immune-therapeutic and prophylactic modalities revealed poor efficacy; both monoclonal antibody and vaccine approaches failed to neutralize and protect from infection with CoVs using the novel spike protein. On the basis of these findings, we synthetically re-derived an infectious full-length SHC014 recombinant virus and demonstrate robust viral replication both in vitro and in vivo. Our work suggests a potential risk of SARS-CoV re-emergence from viruses currently circulating in bat populations.
引用
收藏
页码:1508 / +
页数:8
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