Related Experiment Video
Updated: Oct 9, 2025

Dissecting Host-virus Interaction in Lytic Replication of a Model Herpesvirus
Published on: October 7, 2011
DEAD/H-box helicases:Anti-viral and pro-viral roles during infections
Rizwan Ullah1, Jia Li1, Puxian Fang1
1State Key Laboratory of Agricultural Microbiology, Huazhong Agricultural University, Wuhan, Hubei 430070, China; College of Animal Science and Technology/Veterinary Medicine, Huazhong Agricultural University, Wuhan, Hubei 430070, China; The Cooperative Innovation Center for Sustainable Pig Production, Huazhong Agricultural University, Wuhan, Hubei 430070, China.
Abstract:
DEAD/H-box RNA helicases make the prominent family of helicases super family-2 which take part in almost all RNA-related processes, from initiation of transcription to RNA decay pathways. In addition to these RNA-related activities, in recent years a certain number of these helicases are reported to play important roles in anti-viral immunity through various ways. Along with RLHs, endosomal TLRs, and cytosolic DNA receptors, many RNA helicases including DDX3, DHX9, DDX6, DDX41, DHX33, DDX60, DHX36 and DDX1-DDX21-DHX36 complex act as viral nucleic acid sensors or co-sensors. These helicases mostly follow RLHs-MAVS and STING mediated signaling cascades to trigger induction of type-I interferons and pro-inflammatory cytokines. Many of them also function as downstream adaptor molecules (DDX3), segments of stress and processing bodies (DDX3 and DDX6) or negative regulators (DDX19, DDX24, DDX25, DDX39A and DDX46). On the contrary, many studies indicated that several DEAD/H-box helicases such as DDX1, DDX3, DDX6, DDX24, and DHX9 could be exploited by viruses to evade innate immune responses, suggesting that these helicases seem to have a dual function as anti-viral innate immune mediators and viral replication cofactors. In this review, we summarized the current knowledge on several representative DEAD/H-box helicases, with an emphasis on their functions in innate immunity responses, involved in their anti-viral and pro-viral roles.
Insights
DEAD/H-box RNA helicases are crucial for RNA processes and antiviral immunity, acting as sensors or co-sensors. Some DEAD/H-box helicases exhibit dual roles, mediating antiviral responses while also aiding viral replication.
Area of Science:
- Molecular Biology
- Immunology
- Virology
Background:
- DEAD/H-box RNA helicases are vital for numerous RNA-related cellular processes.
- These helicases are increasingly recognized for their significant roles in antiviral immunity.
- They function alongside other pattern recognition receptors in detecting viral nucleic acids.
Purpose of the Study:
- To review the multifaceted roles of DEAD/H-box RNA helicases in innate immunity.
- To highlight their involvement in both antiviral defense and viral replication.
- To summarize current knowledge on representative DEAD/H-box helicases.
Main Methods:
- Literature review of studies on DEAD/H-box RNA helicases and their immune functions.
- Analysis of their roles as viral nucleic acid sensors and in signaling pathways.
- Examination of their involvement in cellular structures like stress and processing bodies.
Main Results:
- Several DEAD/H-box helicases (e.g., DDX3, DHX9) act as viral nucleic acid sensors, activating interferon and cytokine production via MAVS and STING pathways.
- These helicases can function as adaptor molecules, components of cellular bodies, or negative regulators of immune responses.
- A subset of these helicases, including DDX1 and DHX9, can be exploited by viruses to suppress innate immunity, indicating a dual role.
Conclusions:
- DEAD/H-box RNA helicases possess critical and often dual functions in the innate immune response to viral infections.
- Understanding these roles is essential for developing novel antiviral strategies.
- Further research is needed to fully elucidate the complex interplay between these helicases and viral pathogenesis.
Related Concept Videos
DNA Helicases
Viruses with RNA Genomes
Size and Structure of Viral Genomes
Retrovirus Life Cycles
Mechanisms of Retrovirus-induced Cancers
Retroviruses

