DEAD-box RNA helicase DDX3X inhibits DENV replication via regulating type one interferon pathway.

Guanghao Li, Tingting Feng, Wen Pan, Xiaohong Shi, Jianfeng Dai

Biochemical and biophysical research communications 2015 Jan 2

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Dengue virus (DENV) is a mosquito-borne virus that threatens approximately 2.5 billion people worldwide. Vaccines against DENV are currently unavailable. DEAD-box RNA helicases (DDXs) have been reported to participate in viral replication and host innate immune response. In the present study, we analyzed the role of 40 DDX proteins during DENV replication. Among these proteins, DDX3X showed antiviral effect against DENV infection. Viral replication significantly increased in DDX3X-silenced cells compared with the controls. The interferon (IFN)-β transcription level decreased during the early stage of DENV infection in DDX3X-silenced cells compared with that in the controls. DDX3X could stimulate IFN-β transcription through the IRF3 and the NFκB branches in DENV-infected cells. Our data imply that DDX3X, a member of DEAD-box RNA helicase, is necessary for IFN production and could inhibit DENV replication. Copyright © 2014 Elsevier Inc. All rights reserved.

Citation

Guanghao Li, Tingting Feng, Wen Pan, Xiaohong Shi, Jianfeng Dai. DEAD-box RNA helicase DDX3X inhibits DENV replication via regulating type one interferon pathway. Biochemical and biophysical research communications. 2015 Jan 2;456(1):327-32