Nitric oxide contributes to induction of innate immune responses to gram-negative bacteria in Drosophila

Genes Dev. 2003 Jan 1;17(1):115-25. doi: 10.1101/gad.1018503.

Abstract

Studies in mammals uncovered important signaling roles of nitric oxide (NO), and contributions to innate immunity. Suggestions of conservation led us to explore the involvement of NO in Drosophila innate immunity. Inhibition of nitric oxide synthase (NOS) increased larval sensitivity to gram-negative bacterial infection, and abrogated induction of the antimicrobial peptide Diptericin. NOS was up-regulated after infection. Antimicrobial peptide reporters revealed that NO triggered an immune response in uninfected larvae. NO induction of Diptericin reporters in the fat body required immune deficiency (imd) and domino. These findings show that NOS activity is required for a robust innate immune response to gram-negative bacteria, NOS is induced by infection, and NO is sufficient to trigger response in the absence of infection. We propose that NO mediates an early step of the signal transduction pathway, inducing the innate immune response upon natural infection with gram-negative bacteria.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Amino Acid Sequence
  • Animals
  • Drosophila Proteins / antagonists & inhibitors
  • Drosophila Proteins / genetics
  • Drosophila Proteins / physiology*
  • Drosophila melanogaster / growth & development
  • Drosophila melanogaster / immunology*
  • Enzyme Inhibitors / pharmacology
  • Epistasis, Genetic
  • Escherichia coli / immunology*
  • Fat Body / physiology
  • Genes, Reporter
  • Immunity, Innate
  • Insect Proteins / genetics
  • Insect Proteins / physiology
  • Larva
  • Molecular Sequence Data
  • NG-Nitroarginine Methyl Ester / pharmacology
  • Nitric Oxide / physiology*
  • Nitric Oxide Synthase / antagonists & inhibitors
  • Pectobacterium carotovorum / immunology*
  • Receptors, Cell Surface / physiology
  • Recombinant Fusion Proteins / biosynthesis
  • Toll-Like Receptors
  • Trans-Activators / genetics
  • Trans-Activators / physiology
  • Transcription Factors / genetics
  • Transcription Factors / physiology

Substances

  • DptA protein, Drosophila
  • Drosophila Proteins
  • Enzyme Inhibitors
  • Insect Proteins
  • Receptors, Cell Surface
  • Recombinant Fusion Proteins
  • Rel protein, Drosophila
  • Tl protein, Drosophila
  • Toll-Like Receptors
  • Trans-Activators
  • Transcription Factors
  • imd protein, Drosophila
  • Nitric Oxide
  • Nitric Oxide Synthase
  • NG-Nitroarginine Methyl Ester