Mycobacterial Esx-3 is required for mycobactin-mediated iron acquisition

Proc Natl Acad Sci U S A. 2009 Nov 3;106(44):18792-7. doi: 10.1073/pnas.0900589106. Epub 2009 Oct 21.

Abstract

The Esx secretion pathway is conserved across Gram-positive bacteria. Esx-1, the best-characterized system, is required for virulence of Mycobacterium tuberculosis, although its precise function during infection remains unclear. Esx-3, a paralogous system present in all mycobacterial species, is required for growth in vitro. Here, we demonstrate that mycobacteria lacking Esx-3 are defective in acquiring iron. To compete for the limited iron available in the host and the environment, these organisms use mycobactin, high-affinity iron-binding molecules. In the absence of Esx-3, mycobacteria synthesize mycobactin but are unable to use the bound iron and are impaired severely for growth during macrophage infection. Mycobacteria thus require a specialized secretion system for acquiring iron from siderophores.

Publication types

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

MeSH terms

  • Animals
  • Bacterial Proteins / genetics
  • Bacterial Proteins / metabolism*
  • Genome, Bacterial / genetics
  • Iron / metabolism*
  • Iron / pharmacology
  • Macrophages / drug effects
  • Macrophages / microbiology
  • Mice
  • Mutation / genetics
  • Mycobacterium / genetics
  • Mycobacterium / growth & development
  • Mycobacterium / metabolism*
  • Mycobacterium Infections / microbiology
  • Oxazoles / chemistry
  • Oxazoles / metabolism*
  • Protein Binding / drug effects
  • Secretory Pathway / drug effects
  • Siderophores / biosynthesis
  • Transcription, Genetic / drug effects
  • Up-Regulation / drug effects

Substances

  • Bacterial Proteins
  • Oxazoles
  • Siderophores
  • mycobactins
  • Iron