Viral priming of cell intrinsic innate antiviral signaling by the unfolded protein response

被引:46
作者
Carletti, Tea [1 ]
Zakaria, Mohammad Khalid [1 ,3 ]
Faoro, Valentina [1 ]
Reale, Laura [1 ]
Kazungu, Yvette [1 ]
Licastro, Danilo [2 ]
Marcello, Alessandro [1 ]
机构
[1] ICGEB, Lab Mol Virol, Trieste, Italy
[2] CBM Scrl, Trieste, Italy
[3] Pirbright Inst, Ash Rd, Woking GU24 0NF, Surrey, England
关键词
ENDOPLASMIC-RETICULUM STRESS; NILE-VIRUS-INFECTION; IFN-BETA INDUCTION; RIG-I; REPLICATION; ATF6; INHIBITION; PATHWAY; GENES; RNA;
D O I
10.1038/s41467-019-11663-2
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 innate response to a pathogen is critical in determining the outcome of the infection. However, the interplay of different cellular responses that are activated following viral infection and their contribution to innate antiviral signalling has not been clearly established. This work shows that flaviviruses, including Dengue, Zika, West Nile and Tick-borne encephalitis viruses, activate the unfolded protein response before transcription of interferon regulatory factor 3 induced genes. Infection in conditions of unfolded protein response priming leads to early activation of innate antiviral responses and cell intrinsic inhibition of viral replication, which is interferon regulatory factor 3 dependent. These results demonstrate that the unfolded protein response is not only a physiological reaction of the cell to viral infection, but also synergizes with pattern recognition sensing to mount a potent antiviral response.
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页数:9
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