| Literature DB >> 24993557 |
D Wang1, L Yang, R Gao, X Zhang, Y Tan, A Wu, W Zhu, J Zhou, S Zou, Xiyan Li, Y Sun, Y Zhang, Y Liu, T Liu, Y Xiong, J Xu, L Chen, Y Weng, X Qi, J Guo, Xiaodan Li, J Dong, W Huang, Y Zhang, L Dong, X Zhao, L Liu, J Lu, Y Lan, H Wei, L Xin, Y Chen, C Xu, T Chen, Y Zhu, T Jiang, Z Feng, W Yang, Y Wang, H Zhu, Y Guan, G F Gao, D Li, J Han, S Wang, G Wu, Y Shu.
Abstract
A novel avian influenza A(H7N9) virus causing human infection emerged in February 2013 in China. To elucidate the mechanism of interspecies transmission, we compared the signature amino acids of avian influenza A(H7N9) viruses from human and non-human hosts and analysed the reassortants of 146 influenza A(H7N9) viruses with full genome sequences. We propose a genetic tuning procedure with continuous amino acid substitutions and reassorting that mediates host adaptation and interspecies transmission. When the early influenza A(H7N9) virus, containing ancestor haemagglutinin (HA) and neuraminidase (NA) genes similar to A/Shanghai/05 virus, circulated in waterfowl and transmitted to terrestrial poultry, it acquired an NA stalk deletion at amino acid positions 69 to 73. Then, receptor binding preference was tuned to increase the affinity to human-like receptors through HA G186V and Q226L mutations in terrestrial poultry. Additional mammalian adaptations such as PB2 E627K were selected in humans. The continual reassortation between H7N9 and H9N2 viruses resulted in multiple genotypes for further host adaptation. When we analysed a potential association of mutations and reassortants with clinical outcome, only the PB2 E627K mutation slightly increased the case fatality rate. Genetic tuning may create opportunities for further adaptation of influenza A(H7N9) and its potential to cause a pandemic.Entities:
Mesh：
Substances：
Year: 2014 PMID： 24993557 DOI： 10.2807/1560-7917.es2014.19.25.20836
Source DB: PubMed Journal: Euro Surveill ISSN： 1025-496X