ANXA2 Facilitates Enterovirus 71 Infection by Interacting with 3D Polymerase and PI4KB to Assist the Assembly of Replication Organelles

被引:1
|
作者
Qiuhan Zhang [1 ,2 ]
Siliang Li [1 ]
Ping Lei [1 ]
Zixian Li [1 ]
Feifei Chen [1 ]
Qi Chen [1 ]
Yulu Wang [1 ]
Jiami Gong [1 ]
Qi Tang [1 ]
Xinjin Liu [1 ]
Ke Lan [1 ,2 ,3 ]
Shuwen Wu [1 ]
机构
[1] State Key Laboratory of Virology, College of Life Sciences,Wuhan University
[2] Medical Research Institute, Wuhan University
[3] Frontier Science Center for Immunology and Metabolism,Wuhan University
基金
美国国家科学基金会;
关键词
D O I
暂无
中图分类号
R373.2 [肠道病毒与肝炎病毒];
学科分类号
100103 ; 100705 ;
摘要
Similar to that of other enteroviruses, the replication of enterovirus 71(EV71) occurs on rearranged membranous structures called replication organelles(ROs). Phosphatidylinositol 4-kinase Ⅲ(PI4KB), which is required by enteroviruses for RO formation, yields phosphatidylinositol-4-phosphate(PI4P) on ROs. PI4P then binds and induces conformational changes in the RNA-dependent RNA polymerase(Rd Rp) to modulate Rd Rp activity. Here, we targeted 3D polymerase, the core enzyme of EV71 ROs, and found that the host factor Annexin A2(ANXA2) can interact with 3 D polymerase and promote the replication of EV71. Then, an experiment showed that the annexin domain of ANXA2, which possesses membranebinding capacity, mediates the interaction of ANXA2 with EV71 3 D polymerase. Further research showed that ANXA2 is localized on ROs and interacts with PI4KB. Overexpression of ANXA2 stimulated the formation of PI4P, and the level of PI4P was decreased in ANXA2-knockout cells. Furthermore, ANXA2, PI4KB, and 3D were shown to be localized to the viral RNA replication site, where they form a higher-order protein complex, and the presence of ANXA2 promoted the PI4 KB-3D interaction. Altogether, our data provide new insight into the role of ANXA2 in facilitating formation of the EV71 RNA replication complex.
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收藏
页码:1387 / 1399
页数:13
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