Vaccinia E5 is a major inhibitor of the DNA sensor cGAS

Author:

Yang NingORCID,Wang YiORCID,Dai Peihong,Li TuoORCID,Zierhut ChristianORCID,Tan Adrian,Zhang TuoORCID,Xiang Jenny Zhaoying,Ordureau AlbanORCID,Funabiki HironoriORCID,Chen ZhijianORCID,Deng LiangORCID

Abstract

AbstractThe DNA sensor cyclic GMP-AMP synthase (cGAS) is critical in host antiviral immunity. Vaccinia virus (VACV) is a large cytoplasmic DNA virus that belongs to the poxvirus family. How vaccinia virus antagonizes the cGAS-mediated cytosolic DNA-sensing pathway is not well understood. In this study, we screened 80 vaccinia genes to identify potential viral inhibitors of the cGAS/Stimulator of interferon gene (STING) pathway. We discovered that vaccinia E5 is a virulence factor and a major inhibitor of cGAS. E5 is responsible for abolishing cGAMP production during vaccinia virus (Western Reserve strain) infection of dendritic cells. E5 localizes to the cytoplasm and nucleus of infected cells. Cytosolic E5 triggers ubiquitination of cGAS and proteasome-dependent degradation via interacting with cGAS. Deleting the E5R gene from the Modified vaccinia virus Ankara (MVA) genome strongly induces type I IFN production by dendritic cells (DCs) and promotes DC maturation, and thereby improves antigen-specific T cell responses.

Funder

Cancer Prevention and Research Institute of Texas

IMVAQ Therapeutics (L.D.) MSK Technology Development fund (L.D) American Skin Association Research Scholar Award

Publisher

Springer Science and Business Media LLC

Subject

General Physics and Astronomy,General Biochemistry, Genetics and Molecular Biology,General Chemistry,Multidisciplinary

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