Docking and assembly of the type II secretion complex of Vibrio cholerae

J Bacteriol. 2009 May;191(9):3149-61. doi: 10.1128/JB.01701-08. Epub 2009 Feb 27.

Abstract

Secretion of cholera toxin and other virulence factors from Vibrio cholerae is mediated by the type II secretion (T2S) apparatus, a multiprotein complex composed of both inner and outer membrane proteins. To better understand the mechanism by which the T2S complex coordinates translocation of its substrates, we are examining the protein-protein interactions of its components, encoded by the extracellular protein secretion (eps) genes. In this study, we took a cell biological approach, observing the dynamics of fluorescently tagged EpsC and EpsM proteins in vivo. We report that the level and context of fluorescent protein fusion expression can have a bold effect on subcellular location and that chromosomal, intraoperon expression conditions are optimal for determining the intracellular locations of fusion proteins. Fluorescently tagged, chromosomally expressed EpsC and EpsM form discrete foci along the lengths of the cells, different from the polar localization for green fluorescent protein (GFP)-EpsM previously described, as the fusions are balanced with all their interacting partner proteins within the T2S complex. Additionally, we observed that fluorescent foci in both chromosomal GFP-EpsC- and GFP-EpsM-expressing strains disperse upon deletion of epsD, suggesting that EpsD is critical to the localization of EpsC and EpsM and perhaps their assembly into the T2S complex.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Artificial Gene Fusion
  • Bacterial Proteins / genetics
  • Bacterial Proteins / metabolism*
  • Cell Membrane / chemistry
  • Cholera Toxin / genetics
  • Cholera Toxin / metabolism
  • Gene Deletion
  • Genes, Reporter
  • Green Fluorescent Proteins / genetics
  • Green Fluorescent Proteins / metabolism
  • Membrane Proteins / genetics
  • Membrane Proteins / metabolism
  • Membrane Transport Proteins / metabolism*
  • Microscopy, Fluorescence
  • Protein Binding
  • Protein Interaction Mapping
  • Recombinant Fusion Proteins / genetics
  • Recombinant Fusion Proteins / metabolism
  • Vibrio cholerae / physiology*

Substances

  • Bacterial Proteins
  • EpsD protein, Vibrio cholerae
  • EpsM protein, Vibrio cholerae
  • Membrane Proteins
  • Membrane Transport Proteins
  • Recombinant Fusion Proteins
  • Green Fluorescent Proteins
  • Cholera Toxin