Suppression of NF-kappaB-mediated beta-defensin gene expression in the mammalian airway by the Bordetella type III secretion system

Cell Microbiol. 2005 Apr;7(4):489-97. doi: 10.1111/j.1462-5822.2004.00473.x.

Abstract

Expression of innate immune genes such as beta-defensins is induced in airway epithelium by bacterial components via activation of NF-kappaB. We show here that live Gram-negative bacteria can similarly stimulate this pathway, resulting in upregulation of the beta-defensin tracheal antimicrobial peptide (TAP) in primary cultures of bovine tracheal epithelial cells (TECs), by a Toll-like receptor 4 (TLR4)-mediated pathway. The Gram-negative airway pathogen Bordetella bronchiseptica possesses a type III secretion system previously suggested to inhibit the nuclear translocation of NF-kappaB in a cell line by immunohistochemistry. We therefore hypothesized that this pathogen might interfere in the innate immune response of the epithelium. Exposure of TECs to wild-type B. bronchiseptica suppressed the activation of NF-kappaB and the subsequent induction of TAP mRNA levels, whereas a type III secretion-defective strain did not. These results suggest a mechanism for bacterial evasion of the innate immune response in the airway, which could allow for the observed persistent colonization of this pathogen.

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
  • Antimicrobial Cationic Peptides / genetics
  • Antimicrobial Cationic Peptides / metabolism*
  • Bordetella bronchiseptica / pathogenicity*
  • Cattle
  • Cells, Cultured
  • Epithelial Cells / microbiology
  • Gene Expression Regulation*
  • Membrane Glycoproteins / metabolism
  • NF-kappa B / metabolism*
  • Receptors, Cell Surface / metabolism
  • Toll-Like Receptor 4
  • Toll-Like Receptors
  • Trachea / cytology
  • Trachea / microbiology*
  • Up-Regulation
  • beta-Defensins / genetics
  • beta-Defensins / metabolism*

Substances

  • Antimicrobial Cationic Peptides
  • Membrane Glycoproteins
  • NF-kappa B
  • Receptors, Cell Surface
  • Toll-Like Receptor 4
  • Toll-Like Receptors
  • beta-Defensins
  • tracheal antimicrobial peptide, bovine