Regulation of Mycobacterium tuberculosis cell envelope composition and virulence by intramembrane proteolysis

Nature. 2005 Jul 21;436(7049):406-9. doi: 10.1038/nature03713.

Abstract

Mycobacterium tuberculosis infection is a continuing global health crisis that kills 2 million people each year. Although the structurally diverse lipids of the M. tuberculosis cell envelope each have non-redundant roles in virulence or persistence, the molecular mechanisms regulating cell envelope composition in M. tuberculosis are undefined. In higher eukaryotes, membrane composition is controlled by site two protease (S2P)-mediated cleavage of sterol regulatory element binding proteins, membrane-bound transcription factors that control lipid biosynthesis. S2P is the founding member of a widely distributed family of membrane metalloproteases that cleave substrate proteins within transmembrane segments. Here we show that a previously uncharacterized M. tuberculosis S2P homologue (Rv2869c) regulates M. tuberculosis cell envelope composition, growth in vivo and persistence in vivo. These results establish that regulated intramembrane proteolysis is a conserved mechanism controlling membrane composition in prokaryotes and show that this proteolysis is a proximal regulator of cell envelope virulence determinants in M. tuberculosis.

Publication types

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

MeSH terms

  • Animals
  • Cell Division
  • Cell Membrane / chemistry*
  • Cell Membrane / metabolism*
  • Mice
  • Mycobacterium tuberculosis / classification
  • Mycobacterium tuberculosis / cytology*
  • Mycobacterium tuberculosis / growth & development
  • Mycobacterium tuberculosis / pathogenicity*
  • Mycolic Acids / analysis
  • Mycolic Acids / metabolism
  • Oligonucleotide Array Sequence Analysis
  • Peptide Hydrolases / metabolism*
  • Protein Processing, Post-Translational
  • Tuberculosis / virology
  • Virulence / physiology

Substances

  • Mycolic Acids
  • Peptide Hydrolases