Abstract
A novel bat coronavirus (2019-nCoV) caused an outbreak of infectious
pneumonia termed COVID-19 in the world. This reminds us of another
notorious bat coronavirus, SARS-CoV, which mysteriously broke out in
China 17 years ago and killed nearly 800 people worldwide. A key to its
efficient human attack is adopting angiotensin-converting enzyme 2
(ACE2) as the receptor. The relationship between 2019-nCoV and SARS-CoV
has aroused much public concern. To our surprise, we found that the two
CoV lineages may frequently exchange their genetic materials through
homologous recombination. Particularly 2019-nCoV might thereby acquire
the receptor-binding domain from the SARS-CoV clade, enabling it to make
use of ACE2 as well and thus spread rapidly in humans. Our findings
suggest the accomplice role of a virus of SARS-CoV clade in COVID-19 and
warn of the possible emergence of more mosaic CoVs capable of launching
severe epidemic.