Specificity of immunomodulator secretion in urinary samples in response to infection by alpha-hemolysin and CNF1 bearing uropathogenic Escherichia coli

Cytokine. 2007 Jan;37(1):22-5. doi: 10.1016/j.cyto.2007.02.016. Epub 2007 Mar 26.

Abstract

Escherichia coli are the most common etiological agents of urinary tract infections (UTIs). Uropathogenic E. coli (UPECs) produce specific toxins including the cytotoxic necrotizing factor-1 (CNF1) and the alpha-hemolysin (alpha-Hly). CNF1 triggers, through Rho protein activation, a specific gene response of host cells, which results in the production for instance of interleukin-8 (IL-8), monocyte chemoattractant protein-1 (MCP-1) and the macrophage inflammatory protein-3alpha (MIP-3alpha). The alpha hemolysin alpha-Hly also triggers the production of inflammatory mediators. Cnf1 is always associated with alpha-hly in a pathogenicity island conserved among UPECs. Using two complementary approaches we have investigated whether alpha-hly and cnf1 bearing UPECs are associated with a specific type of UTI both in term of pathology and host response. Here we report that UPECs bearing alpha-hly/cnf1 have a prevalence of 50% in UPECs isolated from hemorrhagic UTIs, as compared to 30% in the overall UPEC population. In addition, we observed that MCP-1, and IL-8 to a lower extent, is produced in urine at higher concentrations in UTIs caused by UPECs carrying alpha-hly/cnf1.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Bacterial Toxins / genetics
  • Bacterial Toxins / metabolism*
  • Chemokine CCL2 / metabolism
  • Chemokine CCL2 / urine*
  • Chemokine CCL20
  • Chemokines, CC / metabolism
  • Chemokines, CC / urine*
  • Escherichia coli / immunology*
  • Escherichia coli / pathogenicity*
  • Escherichia coli Infections / genetics
  • Escherichia coli Infections / immunology
  • Escherichia coli Infections / microbiology*
  • Escherichia coli Infections / urine*
  • Escherichia coli Proteins / genetics
  • Escherichia coli Proteins / metabolism*
  • Health
  • Hemolysin Proteins / metabolism*
  • Hemorrhage / genetics
  • Hemorrhage / microbiology
  • Hemorrhage / pathology
  • Humans
  • Interleukin-8 / metabolism
  • Interleukin-8 / urine*
  • Macrophage Inflammatory Proteins / metabolism
  • Macrophage Inflammatory Proteins / urine*

Substances

  • Bacterial Toxins
  • CCL2 protein, human
  • CCL20 protein, human
  • Chemokine CCL2
  • Chemokine CCL20
  • Chemokines, CC
  • Escherichia coli Proteins
  • Hemolysin Proteins
  • Hlya protein, E coli
  • Interleukin-8
  • Macrophage Inflammatory Proteins
  • cytotoxic necrotizing factor type 1