Orally acquired cyclic dinucleotides drive dSTING-dependent antiviral immunity in enterocytes

Cell Rep. 2021 Dec 28;37(13):110150. doi: 10.1016/j.celrep.2021.110150.

Abstract

Enteric pathogens overcome barrier immunity within the intestinal environment that includes the endogenous flora. The microbiota produces diverse ligands, and the full spectrum of microbial products that are sensed by the epithelium and prime protective immunity is unknown. Using Drosophila, we find that the gut presents a high barrier to infection, which is partially due to signals from the microbiota, as loss of the microbiota enhances oral viral infection. We report cyclic dinucleotide (CDN) feeding is sufficient to protect microbiota-deficient flies from enhanced oral infection, suggesting that bacterial-derived CDNs induce immunity. Mechanistically, we find CDN protection is dSTING- and dTBK1-dependent, leading to NF-kB-dependent gene expression. Furthermore, we identify the apical nucleoside transporter, CNT2, as required for oral CDN protection. Altogether, our studies define a role for bacterial products in priming immune defenses in the gut.

Keywords: Drosophila; NFkB; STING; antiviral; cGAMP; cyclic dinucleotides; immunity; intestine; virus.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alphavirus Infections / drug therapy
  • Alphavirus Infections / immunology*
  • Alphavirus Infections / virology
  • Animals
  • Antiviral Agents / pharmacology*
  • Drosophila melanogaster / drug effects
  • Drosophila melanogaster / genetics
  • Drosophila melanogaster / immunology*
  • Drosophila melanogaster / metabolism
  • Enterocytes / drug effects
  • Enterocytes / immunology*
  • Enterocytes / virology
  • Female
  • Immunity, Innate
  • Membrane Proteins / genetics
  • Membrane Proteins / metabolism*
  • Membrane Transport Proteins / genetics
  • Membrane Transport Proteins / metabolism*
  • NF-kappa B / genetics
  • NF-kappa B / metabolism
  • Nucleotides, Cyclic / administration & dosage*
  • Protein Serine-Threonine Kinases / genetics
  • Protein Serine-Threonine Kinases / metabolism
  • Sindbis Virus / immunology

Substances

  • Antiviral Agents
  • Membrane Proteins
  • Membrane Transport Proteins
  • NF-kappa B
  • Nucleotides, Cyclic
  • cif nucleoside transporter
  • Protein Serine-Threonine Kinases