Identification of a novel coronavirus causing severe pneumonia in human: a descriptive study

Human infections with zoonotic coronaviruses (CoVs), including severe acute respiratory syndrome (SARS)-CoV and Middle East respiratory syndrome (MERS)-CoV, have raised great public health concern globally. Here, we report a novel bat-origin CoV causing severe and fatal pneumonia in humans. We colle...

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Published inChinese medical journal Vol. 133; no. 9; pp. 1015 - 1024
Main Authors Ren, Li-Li, Wang, Ye-Ming, Wu, Zhi-Qiang, Xiang, Zi-Chun, Guo, Li, Xu, Teng, Jiang, Yong-Zhong, Xiong, Yan, Li, Yong-Jun, Li, Xing-Wang, Li, Hui, Fan, Guo-Hui, Gu, Xiao-Ying, Xiao, Yan, Gao, Hong, Xu, Jiu-Yang, Yang, Fan, Wang, Xin-Ming, Wu, Chao, Chen, Lan, Liu, Yi-Wei, Liu, Bo, Yang, Jian, Wang, Xiao-Rui, Dong, Jie, Li, Li, Huang, Chao-Lin, Zhao, Jian-Ping, Hu, Yi, Cheng, Zhen-Shun, Liu, Lin-Lin, Qian, Zhao-Hui, Qin, Chuan, Jin, Qi, Cao, Bin, Wang, Jian-Wei
Format Journal Article
LanguageEnglish
Published China The Chinese Medical Association, produced by Wolters Kluwer, Inc. under the CC-BY-NC-ND license 05.05.2020
Lippincott Williams & Wilkins Ovid Technologies
Institute of Respiratory Medicine, Chinese Academy of Medical Sciences, Peking Union Medical College, Beijing 100029, China%National Health Commission of the People’s Republic of China Key Laboratory of Systems Biology of Pathogens, Institute of Pathogen Biology, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing 100730, China%Vision Medicals Co., Ltd, Guangzhou, Guangdong 510000, China%Hubei Provincial Center for Disease Control and Prevention, Wuhan, Hubei 430079, China%Wuhan Center for Disease Control and Prevention, Wuhan, Hubei 430022, China%Clinical and Research Center of Infectious Diseases, Beijing Ditan Hospital, Capital Medical University, Beijing 100015, China%Institute of Clinical Medical Sciences, China-Japan Friendship Hospital, Beijing 100029, China%Department of Pulmonary and Critical Care Medicine, Center of Respiratory Medicine, National Clinical Research Center for Respiratory Diseases, China-Japan Friendship Hospital, Beijing 100029, China
Institute of Respiratory Medicine, Chinese Academy of Medical Sciences, Peking Union Medical College, Beijing 100029, China
National Health Commission of the People’s Republic of China Key Laboratory of Systems Biology of Pathogens and Christophe Mérieux Laboratory, Institute of Pathogen Biology, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing 100730, China%Department of Pulmonary and Critical Care Medicine, Center of Respiratory Medicine, National Clinical Research Center for Respiratory Diseases, China-Japan Friendship Hospital, Beijing 100029, China
Institute of Clinical Medical Sciences, China-Japan Friendship Hospital, Beijing 100029, China%Institute of Laboratory Animal Science, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing 100021, China%Department of Basic Medical Sciences, Tsinghua University School of Medicine, Beijing 100084, China%Wuhan Jinyintan Hospital, Wuhan, Hubei 430022, China%Department of Pulmonary and Critical Care Medicine, Tongji Hospital, Tongji Medical College, Huazhong University of Sciences and Technology, Wuhan, Hubei 430030, China%Department of Pulmonary and Critical Care Medicine, The Central Hospital of Wuhan, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, Hubei 430014, China%Department of Respiratory Medicine, Zhongnan Hospital of Wuhan University, Wuhan, Hubei 430071, China
Wolters Kluwer Health
Wolters Kluwer
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ISSN0366-6999
2542-5641
2542-5641
DOI10.1097/CM9.0000000000000722

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Abstract Human infections with zoonotic coronaviruses (CoVs), including severe acute respiratory syndrome (SARS)-CoV and Middle East respiratory syndrome (MERS)-CoV, have raised great public health concern globally. Here, we report a novel bat-origin CoV causing severe and fatal pneumonia in humans. We collected clinical data and bronchoalveolar lavage (BAL) specimens from five patients with severe pneumonia from Wuhan Jinyintan Hospital, Hubei province, China. Nucleic acids of the BAL were extracted and subjected to next-generation sequencing. Virus isolation was carried out, and maximum-likelihood phylogenetic trees were constructed. Five patients hospitalized from December 18 to December 29, 2019 presented with fever, cough, and dyspnea accompanied by complications of acute respiratory distress syndrome. Chest radiography revealed diffuse opacities and consolidation. One of these patients died. Sequence results revealed the presence of a previously unknown β-CoV strain in all five patients, with 99.8% to 99.9% nucleotide identities among the isolates. These isolates showed 79.0% nucleotide identity with the sequence of SARS-CoV (GenBank NC_004718) and 51.8% identity with the sequence of MERS-CoV (GenBank NC_019843). The virus is phylogenetically closest to a bat SARS-like CoV (SL-ZC45, GenBank MG772933) with 87.6% to 87.7% nucleotide identity, but is in a separate clade. Moreover, these viruses have a single intact open reading frame gene 8, as a further indicator of bat-origin CoVs. However, the amino acid sequence of the tentative receptor-binding domain resembles that of SARS-CoV, indicating that these viruses might use the same receptor. A novel bat-borne CoV was identified that is associated with severe and fatal respiratory disease in humans.
AbstractList BackgroundHuman infections with zoonotic coronaviruses (CoVs), including severe acute respiratory syndrome (SARS)-CoV and Middle East respiratory syndrome (MERS)-CoV, have raised great public health concern globally. Here, we report a novel bat-origin CoV causing severe and fatal pneumonia in humans.MethodsWe collected clinical data and bronchoalveolar lavage (BAL) specimens from five patients with severe pneumonia from Wuhan Jinyintan Hospital, Hubei province, China. Nucleic acids of the BAL were extracted and subjected to next-generation sequencing. Virus isolation was carried out, and maximum-likelihood phylogenetic trees were constructed.ResultsFive patients hospitalized from December 18 to December 29, 2019 presented with fever, cough, and dyspnea accompanied by complications of acute respiratory distress syndrome. Chest radiography revealed diffuse opacities and consolidation. One of these patients died. Sequence results revealed the presence of a previously unknown β-CoV strain in all five patients, with 99.8% to 99.9% nucleotide identities among the isolates. These isolates showed 79.0% nucleotide identity with the sequence of SARS-CoV (GenBank NC_004718) and 51.8% identity with the sequence of MERS-CoV (GenBank NC_019843). The virus is phylogenetically closest to a bat SARS-like CoV (SL-ZC45, GenBank MG772933) with 87.6% to 87.7% nucleotide identity, but is in a separate clade. Moreover, these viruses have a single intact open reading frame gene 8, as a further indicator of bat-origin CoVs. However, the amino acid sequence of the tentative receptor-binding domain resembles that of SARS-CoV, indicating that these viruses might use the same receptor.ConclusionA novel bat-borne CoV was identified that is associated with severe and fatal respiratory disease in humans.
Background::Human infections with zoonotic coronaviruses (CoVs), including severe acute respiratory syndrome (SARS)-CoV and Middle East respiratory syndrome (MERS)-CoV, have raised great public health concern globally. Here, we report a novel batorigin CoV causing severe and fatal pneumonia in humans.Methods::We collected clinical data and bronchoalveolar lavage (BAL) specimens from five patients with severe pneumonia from Wuhan Jinyintan Hospital, Hubei province, China. Nucleic acids of the BAL were extracted and subjected to next-generation sequencing. Virus isolation was carried out, and maximum-likelihood phylogenetic trees were constructed.Results::Five patients hospitalized from December 18 to December 29, 2019 presented with fever, cough, and dyspnea accompanied by complications of acute respiratory distress syndrome. Chest radiography revealed diffuse opacities and consolidation. One of these patients died. Sequence results revealed the presence of a previously unknown β-CoV strain in all five patients, with 99.8% to 99.9% nucleotide identities among the isolates. These isolates showed 79.0% nucleotide identity with the sequence of SARS-CoV (GenBank NC_004718) and 51.8% identity with the sequence of MERS-CoV (GenBank NC_019843). The virus is phylogenetically closest to a bat SARS-like CoV (SL-ZC45, GenBank MG772933) with 87.6% to 87.7% nucleotide identity, but is in a separate clade. Moreover, these viruses have a single intact open reading frame gene 8, as a further indicator of bat-origin CoVs. However, the amino acid sequence of the tentative receptor-binding domain resembles that of SARS-CoV, indicating that these viruses might use the same receptor.Conclusion::A novel bat-borne CoV was identified that is associated with severe and fatal respiratory disease in humans.
Human infections with zoonotic coronaviruses (CoVs), including severe acute respiratory syndrome (SARS)-CoV and Middle East respiratory syndrome (MERS)-CoV, have raised great public health concern globally. Here, we report a novel bat-origin CoV causing severe and fatal pneumonia in humans. We collected clinical data and bronchoalveolar lavage (BAL) specimens from five patients with severe pneumonia from Wuhan Jinyintan Hospital, Hubei province, China. Nucleic acids of the BAL were extracted and subjected to next-generation sequencing. Virus isolation was carried out, and maximum-likelihood phylogenetic trees were constructed. Five patients hospitalized from December 18 to December 29, 2019 presented with fever, cough, and dyspnea accompanied by complications of acute respiratory distress syndrome. Chest radiography revealed diffuse opacities and consolidation. One of these patients died. Sequence results revealed the presence of a previously unknown β-CoV strain in all five patients, with 99.8% to 99.9% nucleotide identities among the isolates. These isolates showed 79.0% nucleotide identity with the sequence of SARS-CoV (GenBank NC_004718) and 51.8% identity with the sequence of MERS-CoV (GenBank NC_019843). The virus is phylogenetically closest to a bat SARS-like CoV (SL-ZC45, GenBank MG772933) with 87.6% to 87.7% nucleotide identity, but is in a separate clade. Moreover, these viruses have a single intact open reading frame gene 8, as a further indicator of bat-origin CoVs. However, the amino acid sequence of the tentative receptor-binding domain resembles that of SARS-CoV, indicating that these viruses might use the same receptor. A novel bat-borne CoV was identified that is associated with severe and fatal respiratory disease in humans.
Background. Human infections with zoonotic coronaviruses (CoVs), including severe acute respiratory syndrome (SARS)-CoV and Middle East respiratory syndrome (MERS)-CoV, have raised great public health concern globally. Here, we report a novel bat-origin CoV causing severe and fatal pneumonia in humans. Methods. We collected clinical data and bronchoalveolar lavage (BAL) specimens from five patients with severe pneumonia from Wuhan Jinyintan Hospital, Hubei province, China. Nucleic acids of the BAL were extracted and subjected to next-generation sequencing. Virus isolation was carried out, and maximum-likelihood phylogenetic trees were constructed. Results. Five patients hospitalized from December 18 to December 29, 2019 presented with fever, cough, and dyspnea accompanied by complications of acute respiratory distress syndrome. Chest radiography revealed diffuse opacities and consolidation. One of these patients died. Sequence results revealed the presence of a previously unknown β-CoV strain in all five patients, with 99.8% to 99.9% nucleotide identities among the isolates. These isolates showed 79.0% nucleotide identity with the sequence of SARS-CoV (GenBank NC_004718) and 51.8% identity with the sequence of MERS-CoV (GenBank NC_019843). The virus is phylogenetically closest to a bat SARS-like CoV (SL-ZC45, GenBank MG772933) with 87.6% to 87.7% nucleotide identity, but is in a separate clade. Moreover, these viruses have a single intact open reading frame gene 8, as a further indicator of bat-origin CoVs. However, the amino acid sequence of the tentative receptor-binding domain resembles that of SARS-CoV, indicating that these viruses might use the same receptor. Conclusion. A novel bat-borne CoV was identified that is associated with severe and fatal respiratory disease in humans.
Human infections with zoonotic coronaviruses (CoVs), including severe acute respiratory syndrome (SARS)-CoV and Middle East respiratory syndrome (MERS)-CoV, have raised great public health concern globally. Here, we report a novel bat-origin CoV causing severe and fatal pneumonia in humans.BACKGROUNDHuman infections with zoonotic coronaviruses (CoVs), including severe acute respiratory syndrome (SARS)-CoV and Middle East respiratory syndrome (MERS)-CoV, have raised great public health concern globally. Here, we report a novel bat-origin CoV causing severe and fatal pneumonia in humans.We collected clinical data and bronchoalveolar lavage (BAL) specimens from five patients with severe pneumonia from Wuhan Jinyintan Hospital, Hubei province, China. Nucleic acids of the BAL were extracted and subjected to next-generation sequencing. Virus isolation was carried out, and maximum-likelihood phylogenetic trees were constructed.METHODSWe collected clinical data and bronchoalveolar lavage (BAL) specimens from five patients with severe pneumonia from Wuhan Jinyintan Hospital, Hubei province, China. Nucleic acids of the BAL were extracted and subjected to next-generation sequencing. Virus isolation was carried out, and maximum-likelihood phylogenetic trees were constructed.Five patients hospitalized from December 18 to December 29, 2019 presented with fever, cough, and dyspnea accompanied by complications of acute respiratory distress syndrome. Chest radiography revealed diffuse opacities and consolidation. One of these patients died. Sequence results revealed the presence of a previously unknown β-CoV strain in all five patients, with 99.8% to 99.9% nucleotide identities among the isolates. These isolates showed 79.0% nucleotide identity with the sequence of SARS-CoV (GenBank NC_004718) and 51.8% identity with the sequence of MERS-CoV (GenBank NC_019843). The virus is phylogenetically closest to a bat SARS-like CoV (SL-ZC45, GenBank MG772933) with 87.6% to 87.7% nucleotide identity, but is in a separate clade. Moreover, these viruses have a single intact open reading frame gene 8, as a further indicator of bat-origin CoVs. However, the amino acid sequence of the tentative receptor-binding domain resembles that of SARS-CoV, indicating that these viruses might use the same receptor.RESULTSFive patients hospitalized from December 18 to December 29, 2019 presented with fever, cough, and dyspnea accompanied by complications of acute respiratory distress syndrome. Chest radiography revealed diffuse opacities and consolidation. One of these patients died. Sequence results revealed the presence of a previously unknown β-CoV strain in all five patients, with 99.8% to 99.9% nucleotide identities among the isolates. These isolates showed 79.0% nucleotide identity with the sequence of SARS-CoV (GenBank NC_004718) and 51.8% identity with the sequence of MERS-CoV (GenBank NC_019843). The virus is phylogenetically closest to a bat SARS-like CoV (SL-ZC45, GenBank MG772933) with 87.6% to 87.7% nucleotide identity, but is in a separate clade. Moreover, these viruses have a single intact open reading frame gene 8, as a further indicator of bat-origin CoVs. However, the amino acid sequence of the tentative receptor-binding domain resembles that of SARS-CoV, indicating that these viruses might use the same receptor.A novel bat-borne CoV was identified that is associated with severe and fatal respiratory disease in humans.CONCLUSIONA novel bat-borne CoV was identified that is associated with severe and fatal respiratory disease in humans.
Abstract_FL Background::Human infections with zoonotic coronaviruses (CoVs), including severe acute respiratory syndrome (SARS)-CoV and Middle East respiratory syndrome (MERS)-CoV, have raised great public health concern globally. Here, we report a novel batorigin CoV causing severe and fatal pneumonia in humans.Methods::We collected clinical data and bronchoalveolar lavage (BAL) specimens from five patients with severe pneumonia from Wuhan Jinyintan Hospital, Hubei province, China. Nucleic acids of the BAL were extracted and subjected to next-generation sequencing. Virus isolation was carried out, and maximum-likelihood phylogenetic trees were constructed.Results::Five patients hospitalized from December 18 to December 29, 2019 presented with fever, cough, and dyspnea accompanied by complications of acute respiratory distress syndrome. Chest radiography revealed diffuse opacities and consolidation. One of these patients died. Sequence results revealed the presence of a previously unknown β-CoV strain in all five patients, with 99.8% to 99.9% nucleotide identities among the isolates. These isolates showed 79.0% nucleotide identity with the sequence of SARS-CoV (GenBank NC_004718) and 51.8% identity with the sequence of MERS-CoV (GenBank NC_019843). The virus is phylogenetically closest to a bat SARS-like CoV (SL-ZC45, GenBank MG772933) with 87.6% to 87.7% nucleotide identity, but is in a separate clade. Moreover, these viruses have a single intact open reading frame gene 8, as a further indicator of bat-origin CoVs. However, the amino acid sequence of the tentative receptor-binding domain resembles that of SARS-CoV, indicating that these viruses might use the same receptor.Conclusion::A novel bat-borne CoV was identified that is associated with severe and fatal respiratory disease in humans.
Author Guo, Li
Liu, Lin-Lin
Gu, Xiao-Ying
Jin, Qi
Liu, Yi-Wei
Fan, Guo-Hui
Qin, Chuan
Gao, Hong
Wu, Chao
Liu, Bo
Zhao, Jian-Ping
Li, Yong-Jun
Cheng, Zhen-Shun
Li, Xing-Wang
Wu, Zhi-Qiang
Li, Li
Xiang, Zi-Chun
Xiong, Yan
Wang, Xin-Ming
Li, Hui
Wang, Jian-Wei
Wang, Ye-Ming
Ren, Li-Li
Jiang, Yong-Zhong
Xiao, Yan
Qian, Zhao-Hui
Dong, Jie
Cao, Bin
Hu, Yi
Yang, Jian
Huang, Chao-Lin
Yang, Fan
Wang, Xiao-Rui
Xu, Teng
Xu, Jiu-Yang
Chen, Lan
AuthorAffiliation Institute of Clinical Medical Sciences, China-Japan Friendship Hospital, Beijing 100029, China
National Health Commission of the People's Republic of China Key Laboratory of Systems Biology of Pathogens, Institute of Pathogen Biology, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing 100730, China
Department of Pulmonary and Critical Care Medicine, The Central Hospital of Wuhan, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, Hubei 430014, China
Hubei Provincial Center for Disease Control and Prevention, Wuhan, Hubei 430079, China
Wuhan Jinyintan Hospital, Wuhan, Hubei 430022, China
Department of Basic Medical Sciences, Tsinghua University School of Medicine, Beijing 100084, China
National Health Commission of the People's Republic of China Key Laboratory of Systems Biology of Pathogens and Christophe Mérieux Laboratory, Institute of Pathogen Biology, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing 100730, Ch
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Yang Jian
Qian Zhao-Hui
Xu Teng
Wu Chao
Li Hui
Fan Guo-Hui
Li Li
Xiao Yan
Xiang Zi-Chun
Chen Lan
Huang Chao-Lin
Li Xing-Wang
Hu Yi
Wang Jian-Wei
Jiang Yong-Zhong
Wu Zhi-Qiang
Wang Xiao-Rui
Guo Li
Xu Jiu-Yang
Liu Lin-Lin
Xiong Yan
Liu Bo
Dong Jie
Wang Xin-Ming
Wang Ye-Ming
Qin Chuan
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  surname: Xu
  fullname: Xu, Jiu-Yang
  organization: Department of Basic Medical Sciences, Tsinghua University School of Medicine, Beijing 100084, China
– sequence: 17
  givenname: Fan
  surname: Yang
  fullname: Yang, Fan
  organization: National Health Commission of the People's Republic of China Key Laboratory of Systems Biology of Pathogens, Institute of Pathogen Biology, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing 100730, China
– sequence: 18
  givenname: Xin-Ming
  surname: Wang
  fullname: Wang, Xin-Ming
  organization: National Health Commission of the People's Republic of China Key Laboratory of Systems Biology of Pathogens and Christophe Mérieux Laboratory, Institute of Pathogen Biology, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing 100730, China
– sequence: 19
  givenname: Chao
  surname: Wu
  fullname: Wu, Chao
  organization: National Health Commission of the People's Republic of China Key Laboratory of Systems Biology of Pathogens and Christophe Mérieux Laboratory, Institute of Pathogen Biology, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing 100730, China
– sequence: 20
  givenname: Lan
  surname: Chen
  fullname: Chen, Lan
  organization: National Health Commission of the People's Republic of China Key Laboratory of Systems Biology of Pathogens and Christophe Mérieux Laboratory, Institute of Pathogen Biology, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing 100730, China
– sequence: 21
  givenname: Yi-Wei
  surname: Liu
  fullname: Liu, Yi-Wei
  organization: National Health Commission of the People's Republic of China Key Laboratory of Systems Biology of Pathogens and Christophe Mérieux Laboratory, Institute of Pathogen Biology, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing 100730, China
– sequence: 22
  givenname: Bo
  surname: Liu
  fullname: Liu, Bo
  organization: National Health Commission of the People's Republic of China Key Laboratory of Systems Biology of Pathogens, Institute of Pathogen Biology, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing 100730, China
– sequence: 23
  givenname: Jian
  surname: Yang
  fullname: Yang, Jian
  organization: National Health Commission of the People's Republic of China Key Laboratory of Systems Biology of Pathogens, Institute of Pathogen Biology, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing 100730, China
– sequence: 24
  givenname: Xiao-Rui
  surname: Wang
  fullname: Wang, Xiao-Rui
  organization: Vision Medicals Co., Ltd, Guangzhou, Guangdong 510000, China
– sequence: 25
  givenname: Jie
  surname: Dong
  fullname: Dong, Jie
  organization: National Health Commission of the People's Republic of China Key Laboratory of Systems Biology of Pathogens, Institute of Pathogen Biology, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing 100730, China
– sequence: 26
  givenname: Li
  surname: Li
  fullname: Li, Li
  organization: National Health Commission of the People's Republic of China Key Laboratory of Systems Biology of Pathogens, Institute of Pathogen Biology, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing 100730, China
– sequence: 27
  givenname: Chao-Lin
  surname: Huang
  fullname: Huang, Chao-Lin
  organization: Wuhan Jinyintan Hospital, Wuhan, Hubei 430022, China
– sequence: 28
  givenname: Jian-Ping
  surname: Zhao
  fullname: Zhao, Jian-Ping
  organization: Department of Pulmonary and Critical Care Medicine, Tongji Hospital, Tongji Medical College, Huazhong University of Sciences and Technology, Wuhan, Hubei 430030, China
– sequence: 29
  givenname: Yi
  surname: Hu
  fullname: Hu, Yi
  organization: Department of Pulmonary and Critical Care Medicine, The Central Hospital of Wuhan, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, Hubei 430014, China
– sequence: 30
  givenname: Zhen-Shun
  surname: Cheng
  fullname: Cheng, Zhen-Shun
  organization: Department of Respiratory Medicine, Zhongnan Hospital of Wuhan University, Wuhan, Hubei 430071, China
– sequence: 31
  givenname: Lin-Lin
  surname: Liu
  fullname: Liu, Lin-Lin
  organization: Hubei Provincial Center for Disease Control and Prevention, Wuhan, Hubei 430079, China
– sequence: 32
  givenname: Zhao-Hui
  surname: Qian
  fullname: Qian, Zhao-Hui
  organization: National Health Commission of the People's Republic of China Key Laboratory of Systems Biology of Pathogens, Institute of Pathogen Biology, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing 100730, China
– sequence: 33
  givenname: Chuan
  surname: Qin
  fullname: Qin, Chuan
  organization: Institute of Laboratory Animal Science, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing 100021, China
– sequence: 34
  givenname: Qi
  surname: Jin
  fullname: Jin, Qi
  organization: National Health Commission of the People's Republic of China Key Laboratory of Systems Biology of Pathogens, Institute of Pathogen Biology, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing 100730, China
– sequence: 35
  givenname: Bin
  surname: Cao
  fullname: Cao, Bin
  organization: Department of Pulmonary and Critical Care Medicine, Center of Respiratory Medicine, National Clinical Research Center for Respiratory Diseases, China-Japan Friendship Hospital, Beijing 100029, China
– sequence: 36
  givenname: Jian-Wei
  surname: Wang
  fullname: Wang, Jian-Wei
  organization: National Health Commission of the People's Republic of China Key Laboratory of Systems Biology of Pathogens and Christophe Mérieux Laboratory, Institute of Pathogen Biology, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing 100730, China
BackLink https://www.ncbi.nlm.nih.gov/pubmed/32004165$$D View this record in MEDLINE/PubMed
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ContentType Journal Article
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Keywords Bat-origin
Pneumonia
Coronavirus
Next-generation sequencing
Zoonotic transmission
Etiology
Language English
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Institute of Respiratory Medicine, Chinese Academy of Medical Sciences, Peking Union Medical College, Beijing 100029, China%National Health Commission of the People’s Republic of China Key Laboratory of Systems Biology of Pathogens, Institute of Pathogen Biology, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing 100730, China%Vision Medicals Co., Ltd, Guangzhou, Guangdong 510000, China%Hubei Provincial Center for Disease Control and Prevention, Wuhan, Hubei 430079, China%Wuhan Center for Disease Control and Prevention, Wuhan, Hubei 430022, China%Clinical and Research Center of Infectious Diseases, Beijing Ditan Hospital, Capital Medical University, Beijing 100015, China%Institute of Clinical Medical Sciences, China-Japan Friendship Hospital, Beijing 100029, China%Department of Pulmonary and Critical Care Medicine, Center of Respiratory Medicine, National Clinical Research Center for Respiratory Diseases, China-Japan Friendship Hospital, Beijing 100029, China
Institute of Respiratory Medicine, Chinese Academy of Medical Sciences, Peking Union Medical College, Beijing 100029, China
National Health Commission of the People’s Republic of China Key Laboratory of Systems Biology of Pathogens and Christophe Mérieux Laboratory, Institute of Pathogen Biology, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing 100730, China%Department of Pulmonary and Critical Care Medicine, Center of Respiratory Medicine, National Clinical Research Center for Respiratory Diseases, China-Japan Friendship Hospital, Beijing 100029, China
Institute of Clinical Medical Sciences, China-Japan Friendship Hospital, Beijing 100029, China%Institute of Laboratory Animal Science, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing 100021, China%Department of Basic Medical Sciences, Tsinghua University School of Medicine, Beijing 100084, China%Wuhan Jinyintan Hospital, Wuhan, Hubei 430022, China%Department of Pulmonary and Critical Care Medicine, Tongji Hospital, Tongji Medical College, Huazhong University of Sciences and Technology, Wuhan, Hubei 430030, China%Department of Pulmonary and Critical Care Medicine, The Central Hospital of Wuhan, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, Hubei 430014, China%Department of Respiratory Medicine, Zhongnan Hospital of Wuhan University, Wuhan, Hubei 430071, China
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Snippet Human infections with zoonotic coronaviruses (CoVs), including severe acute respiratory syndrome (SARS)-CoV and Middle East respiratory syndrome (MERS)-CoV,...
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Background. Human infections with zoonotic coronaviruses (CoVs), including severe acute respiratory syndrome (SARS)-CoV and Middle East respiratory syndrome...
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SubjectTerms Adult
Aged
Betacoronavirus - genetics
Betacoronavirus - isolation & purification
Coronavirus Infections - diagnostic imaging
Coronavirus Infections - therapy
Coronavirus Infections - virology
Coronaviruses
COVID-19
Dyspnea
Epidemics
Female
Fever
Genomes
Genomics
Hospitals
Humans
Laboratories
Lavage
Male
Microscopy
Middle Aged
Middle East respiratory syndrome
Original
Pandemics
Patients
Phylogenetics
Pneumonia
Pneumonia, Viral - diagnostic imaging
Pneumonia, Viral - therapy
Pneumonia, Viral - virology
Proteins
Public health
Respiratory diseases
SARS-CoV-2
Seafood
Software
Tomography, X-Ray
Treatment Outcome
Viruses
Zoonoses
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Title Identification of a novel coronavirus causing severe pneumonia in human: a descriptive study
URI https://ovidsp.ovid.com/ovidweb.cgi?T=JS&NEWS=n&CSC=Y&PAGE=fulltext&D=ovft&AN=00029330-202005050-00003
https://www.ncbi.nlm.nih.gov/pubmed/32004165
https://www.proquest.com/docview/2459358844
https://www.proquest.com/docview/2350097450
https://d.wanfangdata.com.cn/periodical/zhcmj202009014
https://pubmed.ncbi.nlm.nih.gov/PMC7147275
https://doaj.org/article/1544192251664517b8fa7316d750a8bb
Volume 133
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