Functional Insights into ANP32A-Dependent Influenza A Virus Polymerase Host Restriction

被引:54
作者
Domingues, Patricia [1 ]
Hale, Benjamin G. [1 ]
机构
[1] Univ Zurich, Inst Med Virol, Winterthurerstr 190, CH-8057 Zurich, Switzerland
来源
CELL REPORTS | 2017年 / 20卷 / 11期
基金
欧洲研究理事会;
关键词
AMINO-ACID; RIG-I; SUMOYLATION; ADAPTATION; COMPLEX; MANNER; RANGE;
D O I
10.1016/j.celrep.2017.08.061
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Host restriction of influenza A virus limits pandemic emergence. The viral RNA polymerase (vPol) is an essential enzyme that must adapt for avian viruses to replicate in humans. Species differences in host ANP32A dictate adaptation: human ANP32A lacks an uncharacterized 33 amino-acid insertion that is present in avian ANP32A. Here, we uncover important contributions of host SUMOylation to vPol activity, including avANP32A function. We also identify a hydrophobic SUMO interaction motif (SIM)-like sequence unique to avANP32A that critically supports avian-signature vPol. Unrelated SIM sequences partially recapitulate this function when introduced into huANP32A. By investigating ANP32A-vPol interactions, we find that huANP32A interacts weakly with both human-and avian-signature vPols, while the hydrophobic motif of avANP32A promotes stronger interactions. Furthermore, we identify a highly acidic stretch in avANP32A that constitutes a major site of vPol interaction. Our data suggest compensatory mechanisms underlying vPol adaptation to host ANP32A independent of species-specific interactions.
引用
收藏
页码:2538 / 2546
页数:9
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