| Literature DB >> 31747596 |
Ying Xu1, Ruchao Peng2, Wei Zhang2, Jianxun Qi2, Hao Song3, Sheng Liu1, Haiyuan Wang4, Min Wang2, Haixia Xiao5, Lifeng Fu6, Zheng Fan2, Yuhai Bi6, Jinghua Yan7, Yi Shi8, George F Gao9.
Abstract
Since 2013, H7N9 avian influenza viruses (AIVs) have caused more than 1,600 human infections, posing a threat to public health. An emerging concern is whether H7N9 AIVs will cause pandemics among humans. Molecular analysis of hemagglutinin (HA), which is a critical determinant of interspecies transmission, shows that the current H7N9 AIVs are still dual-receptor tropic, indicating limited human-to-human transmission potency. Mutagenesis and structural studies reveal that a G186V substitution is sufficient for H7N9 AIVs to acquire human receptor-binding capacity, and a Q226L substitution would favor binding to both avian and human receptors only when paired with A138/V186/P221 hydrophobic residues. These data suggest a different evolutionary route of H7N9 viruses compared to other AIV-subtype HAs.Entities:
Keywords: H7N9; hemagglutinin; influenza A virus; interspecies transmission; receptor-binding property; structural basis
Year: 2019 PMID: 31747596 DOI: 10.1016/j.celrep.2019.10.047
Source DB: PubMed Journal: Cell Rep Impact factor: 9.423