Author
Listed:
- Christian K. Holm
(Aarhus University
Aarhus Research Center for Innate Immunity, Aarhus University)
- Stine H. Rahbek
(Aarhus University
Aarhus Research Center for Innate Immunity, Aarhus University)
- Hans Henrik Gad
(Aarhus Research Center for Innate Immunity, Aarhus University
Aarhus University)
- Rasmus O. Bak
(Aarhus University
Aarhus Research Center for Innate Immunity, Aarhus University)
- Martin R. Jakobsen
(Aarhus University
Aarhus Research Center for Innate Immunity, Aarhus University)
- Zhaozaho Jiang
(University of Massachusetts)
- Anne Louise Hansen
(Aarhus University
Aarhus Research Center for Innate Immunity, Aarhus University)
- Simon K. Jensen
(Aarhus University)
- Chenglong Sun
(Aarhus University
Aarhus Research Center for Innate Immunity, Aarhus University)
- Martin K. Thomsen
(Aarhus University
Aarhus Research Center for Innate Immunity, Aarhus University)
- Anders Laustsen
(Aarhus University
Aarhus Research Center for Innate Immunity, Aarhus University)
- Camilla G. Nielsen
(Aarhus University
Aarhus Research Center for Innate Immunity, Aarhus University)
- Kasper Severinsen
(Aarhus University Hospital)
- Yingluo Xiong
(Aarhus University
School of Basic Medical Sciences, Fudan University)
- Dara L. Burdette
(University of California)
- Veit Hornung
(Institute of Molecular Medicine, University Hospital, University of Bonn)
- Robert Jan Lebbink
(University Medical Center)
- Mogens Duch
(Aarhus University
Skauvaccines)
- Katherine A. Fitzgerald
(University of Massachusetts)
- Shervin Bahrami
(Aarhus University
Skauvaccines)
- Jakob Giehm Mikkelsen
(Aarhus University
Aarhus Research Center for Innate Immunity, Aarhus University)
- Rune Hartmann
(Aarhus Research Center for Innate Immunity, Aarhus University
Aarhus University)
- Søren R. Paludan
(Aarhus University
Aarhus Research Center for Innate Immunity, Aarhus University)
Abstract
Stimulator of interferon genes (STING) is known be involved in control of DNA viruses but has an unexplored role in control of RNA viruses. During infection with DNA viruses STING is activated downstream of cGAMP synthase (cGAS) to induce type I interferon. Here we identify a STING-dependent, cGAS-independent pathway important for full interferon production and antiviral control of enveloped RNA viruses, including influenza A virus (IAV). Further, IAV interacts with STING through its conserved hemagglutinin fusion peptide (FP). Interestingly, FP antagonizes interferon production induced by membrane fusion or IAV but not by cGAMP or DNA. Similar to the enveloped RNA viruses, membrane fusion stimulates interferon production in a STING-dependent but cGAS-independent manner. Abolishment of this pathway led to reduced interferon production and impaired control of enveloped RNA viruses. Thus, enveloped RNA viruses stimulate a cGAS-independent STING pathway, which is targeted by IAV.
Suggested Citation
Christian K. Holm & Stine H. Rahbek & Hans Henrik Gad & Rasmus O. Bak & Martin R. Jakobsen & Zhaozaho Jiang & Anne Louise Hansen & Simon K. Jensen & Chenglong Sun & Martin K. Thomsen & Anders Laustsen, 2016.
"Influenza A virus targets a cGAS-independent STING pathway that controls enveloped RNA viruses,"
Nature Communications, Nature, vol. 7(1), pages 1-9, April.
Handle:
RePEc:nat:natcom:v:7:y:2016:i:1:d:10.1038_ncomms10680
DOI: 10.1038/ncomms10680
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