Age‐related rhesus macaque models of COVID‐19
Background Since December 2019, an outbreak of the Corona Virus disease 2019 (COVID‐19) caused by severe acute respiratory syndrome coronavirus (SARS‐CoV‐2) in Wuhan, China, has become a public health emergency of international concern. The high fatality of aged cases caused by SARS‐CoV‐2 was a need...
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Published in | Animal models and experimental medicine Vol. 3; no. 1; pp. 93 - 97 |
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Main Authors | , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
United States
John Wiley & Sons, Inc
01.03.2020
John Wiley and Sons Inc Wiley |
Subjects | |
Online Access | Get full text |
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Abstract | Background
Since December 2019, an outbreak of the Corona Virus disease 2019 (COVID‐19) caused by severe acute respiratory syndrome coronavirus (SARS‐CoV‐2) in Wuhan, China, has become a public health emergency of international concern. The high fatality of aged cases caused by SARS‐CoV‐2 was a need to explore the possible age‐related phenomena with non‐human primate models.
Methods
Three 3‐5 years old and two 15 years old rhesus macaques were intratracheally infected with SARS‐CoV‐2, and then analyzed by clinical signs, viral replication, chest X‐ray, histopathological changes and immune response.
Results
Viral replication of nasopharyngeal swabs, anal swabs and lung in old monkeys was more active than that in young monkeys for 14 days after SARS‐CoV‐2 challenge. Monkeys developed typical interstitial pneumonia characterized by thickened alveolar septum accompanied with inflammation and edema, notably, old monkeys exhibited diffuse severe interstitial pneumonia. Viral antigens were detected mainly in alveolar epithelial cells and macrophages.
Conclusion
SARS‐CoV‐2 caused more severe interstitial pneumonia in old monkeys than that in young monkeys. Rhesus macaque models infected with SARS‐CoV‐2 provided insight into the pathogenic mechanism and facilitated the development of vaccines and therapeutics against SARS‐CoV‐2 infection. |
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AbstractList | Since December 2019, an outbreak of the Corona Virus disease 2019 (COVID-19) caused by severe acute respiratory syndrome coronavirus (SARS-CoV-2) in Wuhan, China, has become a public health emergency of international concern. The high fatality of aged cases caused by SARS-CoV-2 was a need to explore the possible age-related phenomena with non-human primate models.
Three 3-5 years old and two 15 years old rhesus macaques were intratracheally infected with SARS-CoV-2, and then analyzed by clinical signs, viral replication, chest X-ray, histopathological changes and immune response.
Viral replication of nasopharyngeal swabs, anal swabs and lung in old monkeys was more active than that in young monkeys for 14 days after SARS-CoV-2 challenge. Monkeys developed typical interstitial pneumonia characterized by thickened alveolar septum accompanied with inflammation and edema, notably, old monkeys exhibited diffuse severe interstitial pneumonia. Viral antigens were detected mainly in alveolar epithelial cells and macrophages.
SARS-CoV-2 caused more severe interstitial pneumonia in old monkeys than that in young monkeys. Rhesus macaque models infected with SARS-CoV-2 provided insight into the pathogenic mechanism and facilitated the development of vaccines and therapeutics against SARS-CoV-2 infection. BackgroundSince December 2019, an outbreak of the Corona Virus disease 2019 (COVID‐19) caused by severe acute respiratory syndrome coronavirus (SARS‐CoV‐2) in Wuhan, China, has become a public health emergency of international concern. The high fatality of aged cases caused by SARS‐CoV‐2 was a need to explore the possible age‐related phenomena with non‐human primate models.MethodsThree 3‐5 years old and two 15 years old rhesus macaques were intratracheally infected with SARS‐CoV‐2, and then analyzed by clinical signs, viral replication, chest X‐ray, histopathological changes and immune response.ResultsViral replication of nasopharyngeal swabs, anal swabs and lung in old monkeys was more active than that in young monkeys for 14 days after SARS‐CoV‐2 challenge. Monkeys developed typical interstitial pneumonia characterized by thickened alveolar septum accompanied with inflammation and edema, notably, old monkeys exhibited diffuse severe interstitial pneumonia. Viral antigens were detected mainly in alveolar epithelial cells and macrophages.ConclusionSARS‐CoV‐2 caused more severe interstitial pneumonia in old monkeys than that in young monkeys. Rhesus macaque models infected with SARS‐CoV‐2 provided insight into the pathogenic mechanism and facilitated the development of vaccines and therapeutics against SARS‐CoV‐2 infection. Since December 2019, an outbreak of the Corona Virus disease 2019 (COVID-19) caused by severe acute respiratory syndrome coronavirus (SARS-CoV-2) in Wuhan, China, has become a public health emergency of international concern. The high fatality of aged cases caused by SARS-CoV-2 was a need to explore the possible age-related phenomena with non-human primate models.BACKGROUNDSince December 2019, an outbreak of the Corona Virus disease 2019 (COVID-19) caused by severe acute respiratory syndrome coronavirus (SARS-CoV-2) in Wuhan, China, has become a public health emergency of international concern. The high fatality of aged cases caused by SARS-CoV-2 was a need to explore the possible age-related phenomena with non-human primate models.Three 3-5 years old and two 15 years old rhesus macaques were intratracheally infected with SARS-CoV-2, and then analyzed by clinical signs, viral replication, chest X-ray, histopathological changes and immune response.METHODSThree 3-5 years old and two 15 years old rhesus macaques were intratracheally infected with SARS-CoV-2, and then analyzed by clinical signs, viral replication, chest X-ray, histopathological changes and immune response.Viral replication of nasopharyngeal swabs, anal swabs and lung in old monkeys was more active than that in young monkeys for 14 days after SARS-CoV-2 challenge. Monkeys developed typical interstitial pneumonia characterized by thickened alveolar septum accompanied with inflammation and edema, notably, old monkeys exhibited diffuse severe interstitial pneumonia. Viral antigens were detected mainly in alveolar epithelial cells and macrophages.RESULTSViral replication of nasopharyngeal swabs, anal swabs and lung in old monkeys was more active than that in young monkeys for 14 days after SARS-CoV-2 challenge. Monkeys developed typical interstitial pneumonia characterized by thickened alveolar septum accompanied with inflammation and edema, notably, old monkeys exhibited diffuse severe interstitial pneumonia. Viral antigens were detected mainly in alveolar epithelial cells and macrophages.SARS-CoV-2 caused more severe interstitial pneumonia in old monkeys than that in young monkeys. Rhesus macaque models infected with SARS-CoV-2 provided insight into the pathogenic mechanism and facilitated the development of vaccines and therapeutics against SARS-CoV-2 infection.CONCLUSIONSARS-CoV-2 caused more severe interstitial pneumonia in old monkeys than that in young monkeys. Rhesus macaque models infected with SARS-CoV-2 provided insight into the pathogenic mechanism and facilitated the development of vaccines and therapeutics against SARS-CoV-2 infection. Abstract Background Since December 2019, an outbreak of the Corona Virus disease 2019 (COVID‐19) caused by severe acute respiratory syndrome coronavirus (SARS‐CoV‐2) in Wuhan, China, has become a public health emergency of international concern. The high fatality of aged cases caused by SARS‐CoV‐2 was a need to explore the possible age‐related phenomena with non‐human primate models. Methods Three 3‐5 years old and two 15 years old rhesus macaques were intratracheally infected with SARS‐CoV‐2, and then analyzed by clinical signs, viral replication, chest X‐ray, histopathological changes and immune response. Results Viral replication of nasopharyngeal swabs, anal swabs and lung in old monkeys was more active than that in young monkeys for 14 days after SARS‐CoV‐2 challenge. Monkeys developed typical interstitial pneumonia characterized by thickened alveolar septum accompanied with inflammation and edema, notably, old monkeys exhibited diffuse severe interstitial pneumonia. Viral antigens were detected mainly in alveolar epithelial cells and macrophages. Conclusion SARS‐CoV‐2 caused more severe interstitial pneumonia in old monkeys than that in young monkeys. Rhesus macaque models infected with SARS‐CoV‐2 provided insight into the pathogenic mechanism and facilitated the development of vaccines and therapeutics against SARS‐CoV‐2 infection. Background Since December 2019, an outbreak of the Corona Virus disease 2019 (COVID‐19) caused by severe acute respiratory syndrome coronavirus (SARS‐CoV‐2) in Wuhan, China, has become a public health emergency of international concern. The high fatality of aged cases caused by SARS‐CoV‐2 was a need to explore the possible age‐related phenomena with non‐human primate models. Methods Three 3‐5 years old and two 15 years old rhesus macaques were intratracheally infected with SARS‐CoV‐2, and then analyzed by clinical signs, viral replication, chest X‐ray, histopathological changes and immune response. Results Viral replication of nasopharyngeal swabs, anal swabs and lung in old monkeys was more active than that in young monkeys for 14 days after SARS‐CoV‐2 challenge. Monkeys developed typical interstitial pneumonia characterized by thickened alveolar septum accompanied with inflammation and edema, notably, old monkeys exhibited diffuse severe interstitial pneumonia. Viral antigens were detected mainly in alveolar epithelial cells and macrophages. Conclusion SARS‐CoV‐2 caused more severe interstitial pneumonia in old monkeys than that in young monkeys. Rhesus macaque models infected with SARS‐CoV‐2 provided insight into the pathogenic mechanism and facilitated the development of vaccines and therapeutics against SARS‐CoV‐2 infection. BACKGROUND: Since December 2019, an outbreak of the Corona Virus disease 2019 (COVID‐19) caused by severe acute respiratory syndrome coronavirus (SARS‐CoV‐2) in Wuhan, China, has become a public health emergency of international concern. The high fatality of aged cases caused by SARS‐CoV‐2 was a need to explore the possible age‐related phenomena with non‐human primate models. METHODS: Three 3‐5 years old and two 15 years old rhesus macaques were intratracheally infected with SARS‐CoV‐2, and then analyzed by clinical signs, viral replication, chest X‐ray, histopathological changes and immune response. RESULTS: Viral replication of nasopharyngeal swabs, anal swabs and lung in old monkeys was more active than that in young monkeys for 14 days after SARS‐CoV‐2 challenge. Monkeys developed typical interstitial pneumonia characterized by thickened alveolar septum accompanied with inflammation and edema, notably, old monkeys exhibited diffuse severe interstitial pneumonia. Viral antigens were detected mainly in alveolar epithelial cells and macrophages. CONCLUSION: SARS‐CoV‐2 caused more severe interstitial pneumonia in old monkeys than that in young monkeys. Rhesus macaque models infected with SARS‐CoV‐2 provided insight into the pathogenic mechanism and facilitated the development of vaccines and therapeutics against SARS‐CoV‐2 infection. |
Author | Wang, Guanpeng Tan, Wenjie Liu, Peipei Jin, Qi Wang, Jianwei Qin, Chuan Liu, Mingya Yu, Haisheng Liu, Xing Gao, Hong Liu, Jiangning Lv, Qi Ye, Fei Wang, Wenling Huang, Baoying Han, Jun Deng, Wei Xiang, Zhiguang Wang, Shunyi Zhao, Li Gong, Shuran Yu, Pin Xu, Yanfeng Xiao, Chong Wang, Huijuan Qi, Feifei Zhou, Weimin Xue, Jing Wu, Guizhen Wei, Qiang Bao, Linlin Song, Zhiqi Li, Fengdi Qu, Yajin Liu, Jiayi Zhen, Wei |
AuthorAffiliation | 2 MHC Key Laboratory of Biosafety National Institute for Viral Disease Control and Prevention China CDC Beijing China 3 Department of Radiology Bejing Anzhen Hospital Capital Medical University Beijing China 4 Institute of Pathogen Biology Chinese Academy of Medical Sciences Beijing China 1 Key Laboratory of Human Disease Comparative Medicine Chinese Ministry of Health Beijing Key Laboratory for Animal Models of Emerging and Remerging Infectious Diseases Institute of Laboratory Animal Science Chinese Academy of Medical Sciences and Comparative Medicine Center Peking Union Medical College Beijing China 5 Chinese Academy of Medical Sciences and Peking Union Medical College Beijing China |
AuthorAffiliation_xml | – name: 2 MHC Key Laboratory of Biosafety National Institute for Viral Disease Control and Prevention China CDC Beijing China – name: 5 Chinese Academy of Medical Sciences and Peking Union Medical College Beijing China – name: 1 Key Laboratory of Human Disease Comparative Medicine Chinese Ministry of Health Beijing Key Laboratory for Animal Models of Emerging and Remerging Infectious Diseases Institute of Laboratory Animal Science Chinese Academy of Medical Sciences and Comparative Medicine Center Peking Union Medical College Beijing China – name: 4 Institute of Pathogen Biology Chinese Academy of Medical Sciences Beijing China – name: 3 Department of Radiology Bejing Anzhen Hospital Capital Medical University Beijing China |
Author_xml | – sequence: 1 givenname: Pin surname: Yu fullname: Yu, Pin organization: Peking Union Medical College – sequence: 2 givenname: Feifei surname: Qi fullname: Qi, Feifei organization: Peking Union Medical College – sequence: 3 givenname: Yanfeng surname: Xu fullname: Xu, Yanfeng organization: Peking Union Medical College – sequence: 4 givenname: Fengdi surname: Li fullname: Li, Fengdi organization: Peking Union Medical College – sequence: 5 givenname: Peipei surname: Liu fullname: Liu, Peipei organization: China CDC – sequence: 6 givenname: Jiayi surname: Liu fullname: Liu, Jiayi organization: Capital Medical University – sequence: 7 givenname: Linlin surname: Bao fullname: Bao, Linlin organization: Peking Union Medical College – sequence: 8 givenname: Wei surname: Deng fullname: Deng, Wei organization: Peking Union Medical College – sequence: 9 givenname: Hong surname: Gao fullname: Gao, Hong organization: Peking Union Medical College – sequence: 10 givenname: Zhiguang surname: Xiang fullname: Xiang, Zhiguang organization: Peking Union Medical College – sequence: 11 givenname: Chong surname: Xiao fullname: Xiao, Chong organization: Peking Union Medical College – sequence: 12 givenname: Qi surname: Lv fullname: Lv, Qi organization: Peking Union Medical College – sequence: 13 givenname: Shuran surname: Gong fullname: Gong, Shuran organization: Peking Union Medical College – sequence: 14 givenname: Jiangning surname: Liu fullname: Liu, Jiangning organization: Peking Union Medical College – sequence: 15 givenname: Zhiqi surname: Song fullname: Song, Zhiqi organization: Peking Union Medical College – sequence: 16 givenname: Yajin surname: Qu fullname: Qu, Yajin organization: Peking Union Medical College – sequence: 17 givenname: Jing surname: Xue fullname: Xue, Jing organization: Peking Union Medical College – sequence: 18 givenname: Qiang surname: Wei fullname: Wei, Qiang organization: Peking Union Medical College – sequence: 19 givenname: Mingya surname: Liu fullname: Liu, Mingya organization: Peking Union Medical College – sequence: 20 givenname: Guanpeng surname: Wang fullname: Wang, Guanpeng organization: Peking Union Medical College – sequence: 21 givenname: Shunyi surname: Wang fullname: Wang, Shunyi organization: Peking Union Medical College – sequence: 22 givenname: Haisheng surname: Yu fullname: Yu, Haisheng organization: Peking Union Medical College – sequence: 23 givenname: Xing surname: Liu fullname: Liu, Xing organization: Peking Union Medical College – sequence: 24 givenname: Baoying surname: Huang fullname: Huang, Baoying organization: China CDC – sequence: 25 givenname: Wenling surname: Wang fullname: Wang, Wenling organization: China CDC – sequence: 26 givenname: Li surname: Zhao fullname: Zhao, Li organization: China CDC – sequence: 27 givenname: Huijuan surname: Wang fullname: Wang, Huijuan organization: China CDC – sequence: 28 givenname: Fei surname: Ye fullname: Ye, Fei organization: China CDC – sequence: 29 givenname: Weimin surname: Zhou fullname: Zhou, Weimin organization: China CDC – sequence: 30 givenname: Wei surname: Zhen fullname: Zhen, Wei organization: China CDC – sequence: 31 givenname: Jun surname: Han fullname: Han, Jun organization: China CDC – sequence: 32 givenname: Guizhen surname: Wu fullname: Wu, Guizhen organization: China CDC – sequence: 33 givenname: Qi surname: Jin fullname: Jin, Qi organization: Chinese Academy of Medical Sciences – sequence: 34 givenname: Jianwei surname: Wang fullname: Wang, Jianwei organization: Chinese Academy of Medical Sciences and Peking Union Medical College – sequence: 35 givenname: Wenjie surname: Tan fullname: Tan, Wenjie email: tanwj@ivdc.chinacdc.cn organization: China CDC – sequence: 36 givenname: Chuan orcidid: 0000-0002-6261-1232 surname: Qin fullname: Qin, Chuan email: qinchuan@pumc.edu.cn organization: Peking Union Medical College |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/32318665$$D View this record in MEDLINE/PubMed |
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References | 2005; 206 2020; 382 2020; 63 2020 2020; 395 e_1_2_7_11_1 e_1_2_7_10_1 e_1_2_7_4_1 e_1_2_7_3_1 Letko M (e_1_2_7_6_1) 2020 e_1_2_7_9_1 e_1_2_7_8_1 e_1_2_7_7_1 Bao L (e_1_2_7_12_1) 2020 Yang Y (e_1_2_7_5_1) 2020 e_1_2_7_2_1 |
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Since December 2019, an outbreak of the Corona Virus disease 2019 (COVID‐19) caused by severe acute respiratory syndrome coronavirus (SARS‐CoV‐2) in... Since December 2019, an outbreak of the Corona Virus disease 2019 (COVID-19) caused by severe acute respiratory syndrome coronavirus (SARS-CoV-2) in Wuhan,... BackgroundSince December 2019, an outbreak of the Corona Virus disease 2019 (COVID‐19) caused by severe acute respiratory syndrome coronavirus (SARS‐CoV‐2) in... BACKGROUND: Since December 2019, an outbreak of the Corona Virus disease 2019 (COVID‐19) caused by severe acute respiratory syndrome coronavirus (SARS‐CoV‐2)... Abstract Background Since December 2019, an outbreak of the Corona Virus disease 2019 (COVID‐19) caused by severe acute respiratory syndrome coronavirus... |
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