๐ Isolation and characterization of a bat SARS-like coronavirus that uses the ACE2 receptor
The 2002-3 pandemic caused by severe acute respiratory syndrome coronavirus (SARS-CoV) was one of the most significant public health events in recent history. An ongoing outbreak of Middle East respiratory syndrome coronavirus suggests that this group of viruses remains a key threat and that their distribution is wider than previously recognized. Although bats have been suggested to be the natural reservoirs of both viruses, attempts to isolate the progenitor virus of SARS-CoV from bats have been unsuccessful. Diverse SARS-like coronaviruses (SL-Co. Vs) have now been reported from bats in China, Europe and Africa, but none is considered a direct progenitor of SARS-CoV because of their phylogenetic disparity from this virus and the inability of their spike proteins to use the SARS-CoV cellular receptor molecule, the human angiotensin converting enzyme II (ACE2). Here we report whole-genome sequences of two novel bat coronaviruses from Chinese horseshoe bats (family: Rhinolophidae) in Yunnan, China: RsSHC014 and Rs3367. These viruses are far more closely related to SARS-CoV than any previously identified bat coronaviruses, particularly in the receptor binding domain of the spike protein. Most importantly, we report the first recorded isolation of a live SL-CoV (bat SL-CoV-WIV1) from bat faecal samples in Vero E6 cells, which has typical coronavirus morphology, 99.9% sequence identity to Rs3367 and uses ACE2 from humans, civets and Chinese horseshoe bats for cell entry. Preliminary in vitro testing indicates that WIV1 also has a broad species tropism. Our results provide the strongest evidence to date that Chinese horseshoe bats are natural reservoirs of SARS-CoV, and that intermediate hosts may not be necessary for direct human infection by some bat SL-Co. Vs. They also highlight the importance of pathogen-discovery programs targeting high-risk wildlife groups in emerging disease hotspots as a strategy for pandemic preparedness. ยฉ 2013 Macmillan Publishers Limited.
keywords
๐ severe acute (1373)
๐ syndrome coronavirus (1074)
๐ closely related (222)
๐ spike protein (353)
๐ public health (392)
๐ angiotensin converting (23)
๐ genome sequence (133)
๐ converting enzyme (162)
๐ intermediate hosts (17)
๐ faecal samples (44)
๐ receptor binding (86)
๐ respiratory syndrome (2004)
๐ acute respiratory (1734)
๐ genome sequences (60)
author
๐ค Ge, Xing Yi
๐ค Li, Jia Lu
๐ค Yang, Xing Lou
๐ค Chmura, Aleksei A.
๐ค Zhu, Guangjian
๐ค Epstein, Jonathan H.
๐ค Mazet, Jonna K.
๐ค Hu, Ben
๐ค Zhang, Wei
๐ค Peng, Cheng
๐ค Zhang, Yu Ji
๐ค Luo, Chu Ming
๐ค Tan, Bing
๐ค Wang, Ning
๐ค Zhu, Yan
๐ค Crameri, Gary
๐ค Zhang, Shu Yi
๐ค Wang, Lin Fa
๐ค Daszak, Peter
๐ค Shi, Zheng Li
year
โฐ 2013
journal
๐ Nature
issn
๐ 00280836 14764687
volume
503
number
7477
page
535-538
citedbycount
307
download
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