Human heat shock protein (Hsp) 90 interferes with Neisseria meningitidis adhesin A (NadA)-mediated adhesion and invasion

Cell Microbiol. 2012 Mar;14(3):368-85. doi: 10.1111/j.1462-5822.2011.01722.x. Epub 2011 Dec 8.

Abstract

NadA (N eisseria meningitidisadhesin A), a meningococcal surface protein, mediates adhesion to and invasion of human cells, an activity in which host membrane proteins have been implicated. While investigating these host factors in human epithelial cells by affinity chromatography, we discovered an unanticipated interaction of NadA with heat shock protein (Hsp) 90, a molecular chaperone. The specific in vitro interaction of recombinant soluble NadA and Hsp90 was confirmed by co-immunoprecipitations, dot and far-Western blot. Intriguingly, ADP, but not ATP, was required for this association, and the Hsp90 inhibitor 17-AAG promoted complex formation. Hsp90 binding to an Escherichia coli strain used as carrier to express surface exposed NadA confirmed these results in live bacteria. We also examined RNA interference, plasmid-driven overexpression, addition of exogenous rHsp90 and 17-AAG inhibition in human epithelial cells to further elucidate the involvement of Hsp90 in NadA-mediated adhesion and invasion. Together, these data suggest an inverse correlation between the amount of host Hsp90 and the NadA adhesive/invasive phenotype. Confocal microscopy also demonstrated that meningococci interact with cellular Hsp90, a completely novel finding. Altogether our results show that variation of host Hsp90 expression or activity interferes with adhesive and invasive events driven by NadA.

MeSH terms

  • Adhesins, Bacterial / metabolism*
  • Amino Acid Sequence
  • Bacterial Adhesion*
  • Benzoquinones / pharmacology
  • Cells, Cultured
  • Escherichia coli / genetics
  • Escherichia coli / physiology
  • HSP90 Heat-Shock Proteins / antagonists & inhibitors
  • HSP90 Heat-Shock Proteins / metabolism*
  • Host-Pathogen Interactions
  • Humans
  • Lactams, Macrocyclic / pharmacology
  • Meningococcal Infections / metabolism
  • Meningococcal Infections / microbiology
  • Molecular Sequence Data
  • Neisseria meningitidis / physiology*
  • Protein Binding
  • Recombinant Proteins / metabolism

Substances

  • Adhesins, Bacterial
  • Benzoquinones
  • HSP90 Heat-Shock Proteins
  • Lactams, Macrocyclic
  • Recombinant Proteins
  • tanespimycin