Infection with novel coronavirus (SARS-CoV-2) causes pneumonia in Rhesus macaques

Chao Shan(Chinese Academy of Sciences), Yanfeng Yao(Chinese Academy of Sciences), Xing‐Lou Yang(Chinese Academy of Sciences), Yiwu Zhou(Huazhong University of Science and Technology), Ge Gao(Chinese Academy of Sciences), Yun Peng(Chinese Academy of Sciences), Lian Yang(Union Hospital), Xue Hu(Chinese Academy of Sciences), Jin Xiong(Chinese Academy of Sciences), Ren-Di Jiang(Chinese Academy of Sciences), Huajun Zhang(Chinese Academy of Sciences), Xiaoxiao Gao(Chinese Academy of Sciences), Cheng Peng(Chinese Academy of Sciences), Juan Min(Chinese Academy of Sciences), Ying Chen(Chinese Academy of Sciences), Hao-Rui Si(Chinese Academy of Sciences), Jia Wu(Chinese Academy of Sciences), Peng Zhou(Chinese Academy of Sciences), Yan‐Yi Wang(Chinese Academy of Sciences), Hongping Wei(Chinese Academy of Sciences), Wei Pang(Kunming Institute of Zoology), Zhengfei Hu(Kunming Institute of Zoology), Longbao Lv(Kunming Institute of Zoology), Yong‐Tang Zheng(Kunming Institute of Zoology), Zheng‐Li Shi(Chinese Academy of Sciences), Zhiming Yuan(Chinese Academy of Sciences)
Cell Research
July 7, 2020
Cited by 250Open Access
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Abstract

The 2019 novel coronavirus (SARS-CoV-2) outbreak is a major challenge for public health. SARS-CoV-2 infection in human has a broad clinical spectrum ranging from mild to severe cases, with a mortality rate of ~6.4% worldwide (based on World Health Organization daily situation report). However, the dynamics of viral infection, replication and shedding are poorly understood. Here, we show that Rhesus macaques are susceptible to the infection by SARS-CoV-2. After intratracheal inoculation, the first peak of viral RNA was observed in oropharyngeal swabs one day post infection (1 d.p.i.), mainly from the input of the inoculation, while the second peak occurred at 5 d.p.i., which reflected on-site replication in the respiratory tract. Histopathological observation shows that SARS-CoV-2 infection can cause interstitial pneumonia in animals, characterized by hyperemia and edema, and infiltration of monocytes and lymphocytes in alveoli. We also identified SARS-CoV-2 RNA in respiratory tract tissues, including trachea, bronchus and lung; and viruses were also re-isolated from oropharyngeal swabs, bronchus and lung, respectively. Furthermore, we demonstrated that neutralizing antibodies generated from the primary infection could protect the Rhesus macaques from a second-round challenge by SARS-CoV-2. The non-human primate model that we established here provides a valuable platform to study SARS-CoV-2 pathogenesis and to evaluate candidate vaccines and therapeutics.


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