[HTML][HTML] A pneumonia outbreak associated with a new coronavirus of probable bat origin

P Zhou, XL Yang, XG Wang, B Hu, L Zhang, W Zhang… - nature, 2020 - nature.com
P Zhou, XL Yang, XG Wang, B Hu, L Zhang, W Zhang, HR Si, Y Zhu, B Li, CL Huang…
nature, 2020nature.com
Since the outbreak of severe acute respiratory syndrome (SARS) 18 years ago, a large
number of SARS-related coronaviruses (SARSr-CoVs) have been discovered in their natural
reservoir host, bats 1, 2, 3, 4. Previous studies have shown that some bat SARSr-CoVs have
the potential to infect humans 5, 6, 7. Here we report the identification and characterization
of a new coronavirus (2019-nCoV), which caused an epidemic of acute respiratory
syndrome in humans in Wuhan, China. The epidemic, which started on 12 December 2019 …
Abstract
Since the outbreak of severe acute respiratory syndrome (SARS) 18 years ago, a large number of SARS-related coronaviruses (SARSr-CoVs) have been discovered in their natural reservoir host, bats 1, 2, 3, 4. Previous studies have shown that some bat SARSr-CoVs have the potential to infect humans 5, 6, 7. Here we report the identification and characterization of a new coronavirus (2019-nCoV), which caused an epidemic of acute respiratory syndrome in humans in Wuhan, China. The epidemic, which started on 12 December 2019, had caused 2,794 laboratory-confirmed infections including 80 deaths by 26 January 2020. Full-length genome sequences were obtained from five patients at an early stage of the outbreak. The sequences are almost identical and share 79.6% sequence identity to SARS-CoV. Furthermore, we show that 2019-nCoV is 96% identical at the whole-genome level to a bat coronavirus. Pairwise protein sequence analysis of seven conserved non-structural proteins domains show that this virus belongs to the species of SARSr-CoV. In addition, 2019-nCoV virus isolated from the bronchoalveolar lavage fluid of a critically ill patient could be neutralized by sera from several patients. Notably, we confirmed that 2019-nCoV uses the same cell entry receptor—angiotensin converting enzyme II (ACE2)—as SARS-CoV.
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