Delivery of cardiolipins to the Salmonella outer membrane is necessary for survival within host tissues and virulence

Cell Host Microbe. 2015 Apr 8;17(4):441-51. doi: 10.1016/j.chom.2015.03.003.

Abstract

The outer membrane (OM) of Gram-negative bacteria is an asymmetric lipid bilayer that serves as a barrier to the environment. During infection, Gram-negative bacteria remodel their OM to promote survival and replication within host tissues. Salmonella rely on the PhoPQ two-component regulators to coordinate OM remodeling in response to environmental cues. In a screen for mediators of PhoPQ-regulated OM remodeling in Salmonella Typhimurium, we identified PbgA, a periplasmic domain-containing transmembrane protein, which binds cardiolipin glycerophospholipids near the inner membrane and promotes their PhoPQ-regulated trafficking to the OM. Purified-PbgA oligomers are tetrameric, and the periplasmic domain contains a globular region that binds to the OM in a PhoPQ-dependent manner. Thus, PbgA forms a complex that may bridge the envelope for regulated cardiolipin delivery. PbgA globular region-deleted mutant bacteria are severely attenuated for pathogenesis, suggesting that increased cardiolipin trafficking to the OM is necessary for Salmonella to survive within host tissues that activate PhoPQ.

Publication types

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

MeSH terms

  • Bacterial Proteins / genetics
  • Bacterial Proteins / metabolism*
  • Cardiolipins / metabolism*
  • Cell Membrane / metabolism*
  • Host-Pathogen Interactions*
  • Membrane Proteins / genetics
  • Membrane Proteins / metabolism*
  • Protein Multimerization
  • Salmonella typhimurium / growth & development
  • Salmonella typhimurium / metabolism
  • Salmonella typhimurium / physiology*
  • Virulence

Substances

  • Bacterial Proteins
  • Cardiolipins
  • Membrane Proteins