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甲型流感病毒A/WSN/1933(H1N1)的NS1蛋白C末端可调节受感染的人类巨噬细胞和小鼠的抗病毒反应。

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

作者信息

Anastasina Maria, Schepens Bert, Söderholm Sandra, Nyman Tuula A, Matikainen Sampsa, Saksela Kalle, Saelens Xavier, Kainov Denis E

机构信息

Institute for Molecular Medicine Finland (FIMM), University of Helsinki, Helsinki 00290, Finland.

Inflammation Research Center, VIB, Ghent 9000, Belgium.

出版信息

J Gen Virol. 2015 Aug;96(8):2086-2091. doi: 10.1099/vir.0.000171. Epub 2015 May 1.

Abstract

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.

摘要

甲型流感病毒的非结构蛋白NS1通过其N端RNA结合结构域、中间效应结构域和C端非结构化结构域与细胞因子相互作用。NS1可减弱受感染细胞中的抗病毒反应,从而确保病毒高效复制。由于NS1基因中的无义突变,一些流感毒株表达C端截短的NS1蛋白。为了解NS1 C端区域在抗病毒反应调节中的作用,我们利用A/WSN/33(H1N1)反向遗传学技术构建了表达C端截短NS1蛋白的流感病毒,并在人类巨噬细胞和小鼠中进行了测试。我们发现,一种表达C端缺失28个氨基酸的NS1的WSN病毒在体外比表达全长NS1的病毒或NS1截短10个氨基酸的病毒更能有效诱导抗病毒反应。因此,我们的研究结果表明,NS1的C端区域对于抗病毒反应的调节至关重要。此外,表达截短NS1蛋白的病毒可能是良好的疫苗候选物。

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