Abstract
Severe acute respiratory syndrome coronavirus 2 (SARS-CoV) and 2019
novel coronavirus (2019-nCoV) pose a serious threat to human health. To
determine the genetic relationships between the two clades and the
genetic mechanism of origin of 2019-nCoV, we compared the whole genomic
sequences of SARS-CoV and 2019-nCoV and dissected their phylogenetic
histories. Surprisingly, we found that the two clades have frequently
exchanged genetic material through homologous recombination in recent
decades. Nearly 2/3 of the genetic material of CoVZC45 comes from
2019-nCoV lineage, while the other 1/3 descends from SARS-CoV clade. In
particular, the 2019-nCoV lineage might have acquired its
receptor-binding domain from the SARS-CoV clade, enabling 2019-nCoV to
bind to human angiotensin-converting enzyme 2 receptor and helping it to
spread rapidly in humans. Our findings suggest the role of a virus of
the SARS-CoV clade in causing COVID-19 and warn of the possible
emergence of more mosaic CoVs capable of causing severe epidemics.