Drosophila Toll is activated by Gram-positive bacteria through a circulating peptidoglycan recognition protein

Nature. 2001 Dec 13;414(6865):756-9. doi: 10.1038/414756a.

Abstract

Microbial infection activates two distinct intracellular signalling cascades in the immune-responsive fat body of Drosophila. Gram-positive bacteria and fungi predominantly induce the Toll signalling pathway, whereas Gram-negative bacteria activate the Imd pathway. Loss-of-function mutants in either pathway reduce the resistance to corresponding infections. Genetic screens have identified a range of genes involved in these intracellular signalling cascades, but how they are activated by microbial infection is largely unknown. Activation of the transmembrane receptor Toll requires a proteolytically cleaved form of an extracellular cytokine-like polypeptide, Spätzle, suggesting that Toll does not itself function as a bona fide recognition receptor of microbial patterns. This is in apparent contrast with the mammalian Toll-like receptors and raises the question of which host molecules actually recognize microbial patterns to activate Toll through Spätzle. Here we present a mutation that blocks Toll activation by Gram-positive bacteria and significantly decreases resistance to this type of infection. The mutation semmelweis (seml) inactivates the gene encoding a peptidoglycan recognition protein (PGRP-SA). Interestingly, seml does not affect Toll activation by fungal infection, indicating the existence of a distinct recognition system for fungi to activate the Toll pathway.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Sequence
  • Animals
  • Anti-Bacterial Agents
  • Anti-Infective Agents / metabolism
  • Bacillus thuringiensis
  • Carrier Proteins / blood
  • Carrier Proteins / genetics*
  • Carrier Proteins / metabolism
  • Chromosome Mapping
  • Drosophila / genetics
  • Drosophila / immunology
  • Drosophila / metabolism
  • Drosophila / microbiology*
  • Drosophila Proteins / genetics
  • Drosophila Proteins / metabolism*
  • Enterococcus faecalis
  • Fungi / immunology
  • Fungi / metabolism
  • Genes, Insect
  • Gram-Positive Bacteria / immunology
  • Gram-Positive Bacteria / metabolism*
  • Hemolymph
  • Humans
  • Insect Proteins / genetics
  • Insect Proteins / physiology
  • Membrane Glycoproteins / genetics
  • Membrane Glycoproteins / metabolism*
  • Micrococcus luteus
  • Molecular Sequence Data
  • Mutation
  • Receptors, Cell Surface
  • Sequence Homology, Amino Acid
  • Toll-Like Receptors

Substances

  • Anti-Bacterial Agents
  • Anti-Infective Agents
  • Carrier Proteins
  • Drosophila Proteins
  • Insect Proteins
  • Membrane Glycoproteins
  • Receptors, Cell Surface
  • Tl protein, Drosophila
  • Toll-Like Receptors
  • peptidoglycan recognition protein
  • DRS protein, Drosophila