The evolution and characterization of influenza A(H7N9) virus under the selective pressure of peramivir

被引:1
|
作者
Ge, Yiyue [1 ]
Chi, Ying [1 ]
Min, Xiaoyan [2 ]
Zhao, Kangchen [1 ]
Wu, Bin [1 ]
Wu, Tao [1 ]
Zhu, Xiaojuan [1 ]
Shi, Zhiyang [1 ]
Zhu, Fengcai [1 ]
Cui, Lunbiao [1 ]
机构
[1] Jiangsu Prov Ctr Dis Control & Prevent, NHC Key Labs Enter Pathogen Microbiol, Inst Pathogen Microbiol, Nanjing 210009, Jiangsu, Peoples R China
[2] Nanjing Med Univ, Affiliated Hosp 1, Dept Geriatr Cardiol, Nanjing 210029, Jiangsu, Peoples R China
基金
中国国家自然科学基金;
关键词
H7N9; Influenza virus; Quasispecies; Evolution; Selective pressure; Neuraminidase; Peramivir; Mutation; A H7N9; NEURAMINIDASE; OSELTAMIVIR; I222T;
D O I
10.1016/j.virol.2019.08.004
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
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.
引用
收藏
页码:58 / 67
页数:10
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