The RNA receptor RIG-I binding synthetic oligodeoxynucleotide promotes pneumonia survival

JCI Insight. 2024 Nov 8;9(21):e180584. doi: 10.1172/jci.insight.180584.

Abstract

Pneumonia is a worldwide threat to public health, demanding novel preventative and therapeutic strategies. The lung epithelium is a critical environmental interface that functions as a physical barrier to pathogen invasion while also actively sensing and responding to pathogens. We have reported that stimulating lung epithelial cells with a combination therapeutic consisting of a diacylated lipopeptide and a synthetic CpG oligodeoxynucleotide (ODN) induces synergistic pneumonia protection against a wide range of pathogens. We report here that mice deficient in TLR9, the previously described receptor for ODN, still displayed partial ODN-induced protection. This prompted us to seek an alternate ODN receptor, and we discovered by mass spectroscopy that the RNA sensor RIG-I could also bind DNA-like ODN. ODN binding by RIG-I resulted in MAVS-dependent pneumonia-protective signaling events. While RIG-I is essential to native defenses against viral infections, we report that therapeutic RIG-I activation with ODN promoted pathogen killing and host survival following both viral and bacterial challenges. These data indicate that maximal ODN-induced pneumonia protection requires activation of both the TLR9/MyD88 and RIG-I/MAVS signaling pathways. These findings not only identify what we believe to be a novel pattern recognition receptor for DNA-like molecules, but reveal a potential therapeutic strategy to protect susceptible individuals against lethal pneumonias during periods of peak vulnerability.

Keywords: Bacterial infections; Cell biology; Immunology; Influenza; Innate immunity.

MeSH terms

  • Adaptor Proteins, Signal Transducing / genetics
  • Adaptor Proteins, Signal Transducing / metabolism
  • Animals
  • DEAD Box Protein 58* / metabolism
  • Female
  • Lung / metabolism
  • Lung / microbiology
  • Lung / pathology
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Mice, Knockout
  • Myeloid Differentiation Factor 88 / metabolism
  • Oligodeoxyribonucleotides* / pharmacology
  • Pneumonia / metabolism
  • Signal Transduction*
  • Toll-Like Receptor 9* / metabolism

Substances

  • Oligodeoxyribonucleotides
  • DEAD Box Protein 58
  • Toll-Like Receptor 9
  • Ddx58 protein, mouse
  • Tlr9 protein, mouse
  • CPG-oligonucleotide
  • Adaptor Proteins, Signal Transducing
  • IPS-1 protein, mouse
  • Myeloid Differentiation Factor 88