Nuclear-resident RIG-I senses viral replication inducing antiviral immunity

被引:77
|
作者
Liu, GuanQun [1 ,2 ]
Lu, Yao [1 ,3 ]
Raman, Sathya N. Thulasi [1 ]
Xu, Fang [1 ]
Wu, Qi [1 ,3 ]
Li, Zhubing [1 ,2 ]
Brownlie, Robert [1 ]
Liu, Qiang [1 ,2 ,3 ]
Zhou, Yan [1 ,2 ,3 ]
机构
[1] Univ Saskatchewan, Vaccine & Infect Dis Org Int Vaccine Ctr VIDO Int, Saskatoon, SK S7N 5E3, Canada
[2] Univ Saskatchewan, Sch Publ Hlth, Vaccinol & Immunotherapeut Program, Saskatoon, SK S7N 5E3, Canada
[3] Univ Saskatchewan, Dept Vet Microbiol, Western Coll Vet Med, Saskatoon, SK S7N 5E3, Canada
来源
NATURE COMMUNICATIONS | 2018年 / 9卷
基金
加拿大自然科学与工程研究理事会;
关键词
INFLUENZA-A VIRUS; DOUBLE-STRANDED-RNA; N-TERMINAL REGION; HEPATITIS-B-VIRUS; INTERFERON INDUCTION; PATHOGEN SENSOR; INNATE IMMUNITY; PA SUBUNIT; PROTEIN; ACTIVATION;
D O I
10.1038/s41467-018-05745-w
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The nucleus represents a cellular compartment where the discrimination of self from non-self nucleic acids is vital. While emerging evidence establishes a nuclear non-self DNA sensing paradigm, the nuclear sensing of non-self RNA, such as that from nuclear-replicating RNA viruses, remains unexplored. Here, we report the identification of nuclear-resident RIG-I actively involved in nuclear viral RNA sensing. The nuclear RIG-I, along with its cytoplasmic counterpart, senses influenza A virus (IAV) nuclear replication leading to a cooperative induction of type I interferon response. Its activation signals through the canonical signaling axis and establishes an effective antiviral state restricting IAV replication. The exclusive signaling specificity conferred by nuclear RIG-I is reinforced by its inability to sense cytoplasmic-replicating Sendai virus and appreciable sensing of hepatitis B virus pregenomic RNA in the nucleus. These results refine the RNA sensing paradigm for nuclear-replicating viruses and reveal a previously unrecognized subcellular milieu for RIG-I-like receptor sensing.
引用
收藏
页数:14
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