The C terminus of NS1 protein of influenza A/WSN/1933(H1N1) virus modulates antiviral responses in infected human macrophages and mice

被引:17
作者
Anastasina, Maria [1 ]
Schepens, Bert [2 ,3 ]
Soderholm, Sandra [4 ,5 ]
Nyman, Tuula A. [5 ]
Matikainen, Sampsa [4 ]
Saksela, Kalle [6 ]
Saelens, Xavier [2 ,3 ]
Kainov, Denis E. [1 ]
机构
[1] Univ Helsinki, Inst Mol Med Finland FIMM, FIN-00290 Helsinki, Finland
[2] VIB, Inflammat Res Ctr, B-9000 Ghent, Belgium
[3] Univ Ghent, Dept Biomed Mol Biol, B-9000 Ghent, Belgium
[4] Finnish Inst Occupat Hlth, Unit Syst Toxicol, Helsinki 00250, Finland
[5] Univ Helsinki, Inst Biotechnol, FI-00014 Helsinki, Finland
[6] Univ Helsinki, Haartman Inst, Dept Virol, FIN-00290 Helsinki, Finland
基金
芬兰科学院;
关键词
A VIRUS; CELLS;
D O I
10.1099/vir.0.000171
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 [微生物学]; 090105 [作物生产系统与生态工程];
摘要
Non-structural protein NS1 of influenza A viruses interacts with cellular factors through its N-terminal RNA-binding, middle effector and C-terminal non-structured domains. NS1 attenuates antiviral responses in infected cells and thereby secures efficient virus replication. Some influenza strains express C-terminally truncated NS1 proteins due to nonsense mutations in the NS1 gene. To understand the role of the NS1 C-terminal region in regulation of antiviral responses, we engineered influenza viruses expressing C-terminally truncated NS1 proteins using A/WSN/33(H1N1) reverse genetics and tested them in human macrophages and in mice. We showed that a WSN virus expressing NS1 with a 28 aa deletion from its C terminus is a more powerful inducer of antiviral responses than the virus expressing full-length NS1, or one with a 10 aa truncation of NS1 in vitro. Thus, our findings suggest that the C-terminal region of NS1 is essential for regulation of antiviral responses. Moreover, viruses expressing truncated NS1 proteins could be good vaccine candidates.
引用
收藏
页码:2086 / 2091
页数:6
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