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A novel bat coronavirus reveals natural insertions at the S1/S2 cleavage site of the Spike protein and a possible recombinant origin of HCoV-19
Hong Zhou; Xing Chen; Tao Hu; Juan Li; Hao Song; Yanran Liu; Peihan Wang; Di Liu; Jing Yang; Edward C. Holmes; Alice C. Hughes; Yuhai Bi; Weifeng Shi.
Affiliation
  • Hong Zhou; Shandong First Medical University & Shandong Academy of Medical Sciences
  • Xing Chen; Xishuangbanna Tropical Botanical Garden, Chinese Academy of Sciences
  • Tao Hu; Shandong First Medical University & Shandong Academy of Medical Sciences
  • Juan Li; Shandong First Medical University & Shandong Academy of Medical Sciences
  • Hao Song; Beijing Institutes of Life Science, Chinese Academy of Sciences
  • Yanran Liu; Shandong First Medical University & Shandong Academy of Medical Sciences
  • Peihan Wang; Shandong First Medical University & Shandong Academy of Medical Sciences
  • Di Liu; Wuhan Institute of Virology, Chinese Academy of Sciences
  • Jing Yang; Institute of Microbiology, Chinese Academy of Sciences
  • Edward C. Holmes; The University of Sydney
  • Alice C. Hughes; Xishuangbanna Tropical Botanical Garden, Chinese Academy of Sciences
  • Yuhai Bi; Institute of Microbiology, Chinese Academy of Sciences
  • Weifeng Shi; Shandong First Medical University & Shandong Academy of Medical Sciences
Preprint in English | bioRxiv | ID: ppbiorxiv-974139
ABSTRACT
The unprecedented epidemic of pneumonia caused by a novel coronavirus, HCoV-19, in China and beyond has caused public health concern at a global scale. Although bats are regarded as the most likely natural hosts for HCoV-191,2, the origins of the virus remain unclear. Here, we report a novel bat-derived coronavirus, denoted RmYN02, identified from a metagenomics analysis of samples from 227 bats collected from Yunnan Province in China between May and October, 2019. RmYN02 shared 93.3% nucleotide identity with HCoV-19 at the scale of the complete virus genome and 97.2% identity in the 1ab gene in which it was the closest relative of HCoV-19. In contrast, RmYN02 showed low sequence identity (61.3%) to HCoV-19 in the receptor binding domain (RBD) and might not bind to angiotensin-converting enzyme 2 (ACE2). Critically, however, and in a similar manner to HCoV-19, RmYN02 was characterized by the insertion of multiple amino acids at the junction site of the S1 and S2 subunits of the Spike (S) protein. This provides strong evidence that such insertion events can occur in nature. Together, these data suggest that HCoV-19 originated from multiple naturally occurring recombination events among those viruses present in bats and other wildlife species.
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Full text: Available Collection: Preprints Database: bioRxiv Language: English Year: 2020 Document type: Preprint
Full text: Available Collection: Preprints Database: bioRxiv Language: English Year: 2020 Document type: Preprint
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