posted on 2020-11-12, 14:41authored byRui Wang, Jiahui Chen, Yuta Hozumi, Changchuan Yin, Guo-Wei Wei
One of the major challenges in controlling
the coronavirus disease
2019 (COVID-19) outbreak is its asymptomatic transmission. The pathogenicity
and virulence of asymptomatic COVID-19 remain mysterious. On the basis
of the genotyping of 75775 SARS-CoV-2 genome isolates, we reveal that
asymptomatic infection is linked to SARS-CoV-2 11083G>T mutation
(i.e.,
L37F at nonstructure protein 6 (NSP6)). By analyzing the distribution
of 11083G>T in various countries, we unveil that 11083G>T may
correlate
with the hypotoxicity of SARS-CoV-2. Moreover, we show a global decaying
tendency of the 11083G>T mutation ratio indicating that 11083G>T
hinders
the SARS-CoV-2 transmission capacity. Artificial intelligence, sequence
alignment, and network analysis are applied to show that NSP6 mutation
L37F may have compromised the virus’s ability to undermine
the innate cellular defense against viral infection via autophagy
regulation. This assessment is in good agreement with our genotyping
of the SARS-CoV-2 evolution and transmission across various countries
and regions over the past few months.