| Literature DB >> 31400550 |
Yiyue Ge1, Ying Chi2, Xiaoyan Min3, Kangchen Zhao2, Bin Wu2, Tao Wu2, Xiaojuan Zhu2, Zhiyang Shi2, Fengcai Zhu2, Lunbiao Cui4.
Abstract
Human infection with H7N9 virus has provoked global public health concern due to the substantial morbidity and mortality. Neuraminidase inhibitors (NAIs) are used as first-line drugs to treat the infection. However, virus quasispecies can evolve rapidly under drug pressure, which may alter various biological characteristics of virus. Using an in vitro evolution platform and next-generation sequencing, we found the presence of peramivir led to changes to the dominant populations of the virus. Two important amino acid substitutions were identified in NA, I222T and H274Y, which caused reduced susceptibilities to oseltamivir or both oseltamivir and peramivir as confirmed by enzyme- and cell-based assays. The NA-H274Y variant showed decreased replicative fitness at the early stage of infection accompanied with impaired NA function. The quasispecies evolution of H7N9 virus and the potential emergence of these two variants should be closely monitored, which may guide the adjustment of antiviral strategies.Entities:
Keywords: Evolution; H7N9; Influenza virus; Mutation; Neuraminidase; Peramivir; Quasispecies; Selective pressure
Mesh:
Substances:
Year: 2019 PMID: 31400550 DOI: 10.1016/j.virol.2019.08.004
Source DB: PubMed Journal: Virology ISSN: 0042-6822 Impact factor: 3.616