LIU Xiuliang, LI Yanjiao, CHEN Weijie, WANG Yuxi, GAO Qile, HU Jingjing, ZHANG Zhijie, XIONG Chenglong. Polymorphisms of host tropism relating amino acid sites in influenza A virus[J]. Shanghai Journal of Preventive Medicine, 2023, 35(7): 626-633. DOI: 10.19428/j.cnki.sjpm.2023.22776
Citation: LIU Xiuliang, LI Yanjiao, CHEN Weijie, WANG Yuxi, GAO Qile, HU Jingjing, ZHANG Zhijie, XIONG Chenglong. Polymorphisms of host tropism relating amino acid sites in influenza A virus[J]. Shanghai Journal of Preventive Medicine, 2023, 35(7): 626-633. DOI: 10.19428/j.cnki.sjpm.2023.22776

Polymorphisms of host tropism relating amino acid sites in influenza A virus

  • Objective To discover and analyze single or several correlative key amino acid sites that influence the host tropism during the influenza A virus (IAV) infection based on complete internal protein gene segments of IAV strains, and to provide evidence for the study of human host-adaptive mutations of IAV.
    Methods The full-length nucleotide sequences of 43 671 IAV strains containing 6 complete internal gene segments were downloaded from the GISAID EpiFluTM database, and 698 human-tropic (HU) and 1 266 avian-tropic (AV) representative strains were included. The consensus coding sequences of the representative strains from the amphitropic category were compared by R script, and the differential amino acid sites and their polymorphisms were then obtained. The multi-site combination analysis of differential sites was conducted with R script.
    Results A total of 49 and 57 conserved differential sites were obtained from the consensus sequence comparison between AV and H1N1 (subtype from HU), and comparison between AV and H3N2 (another subtype from HU), separately. 79 and 65 multi-site combinations were found between HU and AV strains through 3 and 4 sites combination analysis, respectively, and a total of 11 conserved sites were involved: site 271 and 684 in PB2; site 336, 486, 581 and 621 in PB1; site 204 and 356 in PA; site 33, 305 and 357 in NP. No eligible differential sites were found in M1 and NS1.
    Conclusion Several conserved amino acid differential sites, between HU and AV strains of IAV, are found in PB2, PB1, PA and NP proteins. Instead of working as single units, these sites may have interactions, forming specific amino acid combinations that determine the host tropism of IAV collectively.
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