The DEAD-Box RNA Helicase DDX1 Interacts with the Viral Protein 3D and Inhibits Foot-and-Mouth Disease Virus Replication

被引:21
|
作者
Xue, Qiao [1 ]
Liu, Huisheng [1 ]
Zeng, Qiaoying [1 ]
Zheng, Haixue [2 ]
Xue, Qinghong [3 ]
Cai, Xuepeng [3 ]
机构
[1] Gansu Agr Univ, Coll Vet Med, Lab Vet Microbiol, Lanzhou 730070, Peoples R China
[2] Chinese Acad Agr Sci, Lanzhou Vet Res Inst, State Key Lab Vet Etiol Biol, Natl Foot & Mouth Dis Reference Lab,Key Lab Anim, Lanzhou 730046, Peoples R China
[3] China Inst Vet Drug Control, Beijing 100081, Peoples R China
基金
中国国家自然科学基金;
关键词
Foot-and-mouth disease virus (FMDV); Interaction; DEAD-box RNA helicase 1 (DDX1); Antiviral function; Interferon; DEGRADATION; POLYMERASE; ACTS; 3A;
D O I
10.1007/s12250-019-00148-7
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Foot-and-mouth disease virus (FMDV) can infect domestic and wild cloven-hoofed animals. The non-structural protein 3D plays an important role in FMDV replication and pathogenesis. However, the interaction partners of 3D, and the effects of those interactions on FMDV replication, remain incompletely elucidated. In the present study, using the yeast two-hybrid system, we identified a porcine cell protein, DEAD-box RNA helicase 1 (DDX1), which interacted with FMDV 3D. The DDX1-3D interaction was further confirmed by co-immunoprecipitation experiments and an indirect immunofluorescence assay (IFA) in porcine kidney 15 (PK-15) cells. DDX1 was reported to either inhibit or facilitate viral replication and regulate host innate immune responses. However, the roles of DDX1 during FMDV infection remain unclear. Our results revealed that DDX1 inhibited FMDV replication in an ATPase/helicase activity-dependent manner. In addition, DDX1 stimulated IFN-beta activation in FMDV-infected cells. Together, our results expand the body of knowledge regarding the role of DDX1 in FMDV infection.
引用
收藏
页码:610 / 617
页数:8
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