The Afa/Dr adhesins of diffusely adhering Escherichia coli stimulate interleukin-8 secretion, activate mitogen-activated protein kinases, and promote polymorphonuclear transepithelial migration in T84 polarized epithelial cells

Infect Immun. 2003 Mar;71(3):1068-74. doi: 10.1128/IAI.71.3.1068-1074.2003.

Abstract

Afa/Dr diffusely adhering Escherichia coli (Afa/Dr DAEC) strains cause symptomatic urinary tract and intestinal infections. The proinflammatory effects of Afa/Dr DAEC strains in vitro have been not investigated to date. In the present study, we used confluent polarized monolayers of intestinal cell line T84 to evaluate the consequences of epithelial infection by Afa/Dr DAEC strains in terms of proinflammatory response. Polymorphonuclear leukocyte (PMNL) migration across the epithelial barrier was induced after incubation of the T84 monolayers with the wild-type Afa/Dr DAEC strain C1845 harboring the fimbrial F1845 adhesin and strain IH11128 harboring the Dr hemagglutinin, and the E. coli laboratory strain HB101 was transformed with the pSSS1 plasmid, producing Afa/Dr F1845 adhesin. PMNL migrations were correlated with a basolateral secretion of interleukin-8 by T84 cells and were abolished after incubation of epithelial cells with an anti-decay accelerating factor (DAF) antibody that recognized the short consensus repeat 3 domain of DAF (monoclonal antibody 1H4). Moreover, Afa/Dr DAEC strains induced tyrosine phosphorylation of several T84 proteins and activated the mitogen-activated protein kinases (ERK1/2 mitogen-activated protein, P38, and Jun-C kinases). These data demonstrated for the first time that, in vitro, Afa/Dr DAEC strains exert a proinflammatory signal in intestinal epithelial cells.

MeSH terms

  • Adhesins, Escherichia coli / physiology*
  • Bacterial Adhesion*
  • Cell Movement
  • Cell Polarity
  • Cells, Cultured
  • Enzyme Activation
  • Escherichia coli / physiology*
  • Humans
  • Interleukin-8 / biosynthesis*
  • Intestinal Mucosa / microbiology
  • Mitogen-Activated Protein Kinases / metabolism*
  • Neutrophils / physiology*
  • Phosphorylation
  • Signal Transduction
  • Tyrosine / metabolism

Substances

  • Adhesins, Escherichia coli
  • Interleukin-8
  • Tyrosine
  • Mitogen-Activated Protein Kinases