TLR4-dependent activation of inflammatory cytokine response in macrophages by Francisella elongation factor Tu

Cell Immunol. 2011;269(2):69-73. doi: 10.1016/j.cellimm.2011.03.023. Epub 2011 Mar 29.

Abstract

The bacterial determinants of pulmonary Francisella induced inflammatory responses and their interaction with host components are not clearly defined. In this study, proteomic and immunoblot analyses showed presence of a cytoplasmic protein elongation factor Tu (EF-Tu) in the membrane fractions of virulent Francisella novicida, LVS and SchuS4, but not in an attenuated F. novicida mutant. EF-Tu was immunodominant in mice vaccinated and protected from virulent F. novicida. Moreover, recombinant EF-Tu induced macrophages to produce inflammatory cytokines in a TLR4 dependent manner. This study shows immune stimulatory properties of a cytoplasmic protein EF-Tu expressed on the membrane of virulent Francisella strains.

Publication types

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

MeSH terms

  • Animals
  • Bronchoalveolar Lavage Fluid / immunology
  • Cell Membrane / metabolism
  • Cytokines / immunology*
  • Cytokines / metabolism
  • Francisella / immunology*
  • Francisella / metabolism
  • Francisella tularensis / immunology
  • Francisella tularensis / metabolism
  • Immune Sera / immunology
  • Immunity, Humoral / immunology
  • Immunodominant Epitopes / immunology
  • Immunoglobulin A / immunology
  • Immunoglobulin G / blood
  • Immunoglobulin G / immunology
  • Interleukin-6 / metabolism
  • Macrophages / drug effects
  • Macrophages / immunology*
  • Macrophages / metabolism
  • Mice
  • Mice, Inbred C57BL
  • Mice, Knockout
  • Peptide Elongation Factor Tu / genetics
  • Peptide Elongation Factor Tu / immunology*
  • Peptide Elongation Factor Tu / metabolism
  • Peptide Elongation Factor Tu / pharmacology
  • Recombinant Proteins / genetics
  • Recombinant Proteins / immunology
  • Recombinant Proteins / pharmacology
  • Toll-Like Receptor 2 / genetics
  • Toll-Like Receptor 4 / genetics
  • Toll-Like Receptor 4 / immunology*
  • Toll-Like Receptor 4 / metabolism
  • Tumor Necrosis Factor-alpha / metabolism

Substances

  • Cytokines
  • Immune Sera
  • Immunodominant Epitopes
  • Immunoglobulin A
  • Immunoglobulin G
  • Interleukin-6
  • Recombinant Proteins
  • Tlr2 protein, mouse
  • Tlr4 protein, mouse
  • Toll-Like Receptor 2
  • Toll-Like Receptor 4
  • Tumor Necrosis Factor-alpha
  • Peptide Elongation Factor Tu