Afa/Dr diffusely adhering Escherichia coli infection in T84 cell monolayers induces increased neutrophil transepithelial migration, which in turn promotes cytokine-dependent upregulation of decay-accelerating factor (CD55), the receptor for Afa/Dr adhesins

Infect Immun. 2003 Apr;71(4):1774-83. doi: 10.1128/IAI.71.4.1774-1783.2003.

Abstract

Ulcerative colitis and Crohn's disease are inflammatory bowel diseases thought to involve strains of Escherichia coli. We report here that two wild-type Afa/Dr diffusely adhering E. coli (DAEC) strains, C1845 and IH11128, which harbor the fimbrial F1845 adhesin and the Dr hemagglutinin, respectively, and the E. coli laboratory strain HB101, transformed with the pSSS1 plasmid to produce Afa/Dr F1845 adhesin, all induced interleukin-8 (IL-8) production and transepithelial migration of polymorphonuclear leukocytes (PMNL) in polarized monolayers of the human intestinal cell line T84 grown on semipermeable filters. We observed that after PMNL migration, expression of decay-accelerating factor (DAF, or CD55), the brush border-associated receptor for Afa/Dr adhesins, was strongly enhanced, increasing the adhesion of Afa/Dr DAEC bacteria. When examining the mechanism by which DAF expression was enhanced, we observed that the PMNL transepithelial migration induced epithelial synthesis of tumor necrosis factor alpha and IL-1beta, which in turn promoted the upregulation of DAF.

MeSH terms

  • Adhesins, Escherichia coli / genetics
  • Adhesins, Escherichia coli / metabolism*
  • Adhesins, Escherichia coli / physiology
  • Bacterial Adhesion*
  • CD55 Antigens / metabolism*
  • Cell Polarity
  • Cytokines / metabolism
  • Escherichia coli / genetics
  • Escherichia coli / immunology
  • Escherichia coli / pathogenicity*
  • Escherichia coli / physiology
  • Escherichia coli Proteins / genetics
  • Escherichia coli Proteins / metabolism
  • HeLa Cells
  • Hemagglutinins / genetics
  • Hemagglutinins / metabolism
  • Humans
  • Microscopy, Electron
  • Neutrophil Infiltration*
  • Neutrophils / immunology
  • Tumor Cells, Cultured
  • Up-Regulation*

Substances

  • Adhesins, Escherichia coli
  • CD55 Antigens
  • Cytokines
  • Dr adhesin, E coli
  • Escherichia coli Proteins
  • Hemagglutinins