The Kinase IKKβ Regulates a STING- and NF-κB-Dependent Antiviral Response Pathway in Drosophila

Akira Gotō(Centre National de la Recherche Scientifique), Kiyoshi Okado(Centre National de la Recherche Scientifique), Nelson Martins(Centre National de la Recherche Scientifique), Hua Cai(Centre National de la Recherche Scientifique), Vincent Barbier(Centre National de la Recherche Scientifique), Olivier Lamiable(Centre National de la Recherche Scientifique), Laurent Troxler(Centre National de la Recherche Scientifique), Estelle Santiago(Centre National de la Recherche Scientifique), Lauriane Kühn(Centre National de la Recherche Scientifique), Donggi Paik(University of Massachusetts Chan Medical School), Neal Silverman(University of Massachusetts Chan Medical School), Andreas Holleufer(Aarhus University), Rune Hartmann(Aarhus University), Jiyong Liu(Guangzhou Medical University), Tao Peng(Guangzhou Medical University), Jules A. Hoffmann(Centre National de la Recherche Scientifique), Carine Meignin(Centre National de la Recherche Scientifique), Laurent Daeffler(Centre National de la Recherche Scientifique), Jean‐Luc Imler(Centre National de la Recherche Scientifique)
Immunity
August 1, 2018
Cited by 168Open Access
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Abstract

Antiviral immunity in Drosophila involves RNA interference and poorly characterized inducible responses. Here, we showed that two components of the IMD pathway, the kinase dIKKβ and the transcription factor Relish, were required to control infection by two picorna-like viruses. We identified a set of genes induced by viral infection and regulated by dIKKβ and Relish, which included an ortholog of STING. We showed that dSTING participated in the control of infection by picorna-like viruses, acting upstream of dIKKβ to regulate expression of Nazo, an antiviral factor. Our data reveal an antiviral function for STING in an animal model devoid of interferons and suggest an evolutionarily ancient role for this molecule in antiviral immunity.


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