α-Haemolysin of Escherichia coli in IBD: a potentiator of inflammatory activity in the colon

Gut. 2014 Dec;63(12):1893-901. doi: 10.1136/gutjnl-2013-306099. Epub 2014 Feb 17.

Abstract

Objective: α-Haemolysin (HlyA) influences host cell ionic homeostasis and causes concentration-dependent cell lysis. As a consequence, HlyA-producing Escherichia coli is capable of inducing 'focal leaks' in colon epithelia, through which bacteria and antigens translocate. This study addressed the role of HlyA as a virulence factor in the pathogenesis of colitis according to the 'leaky gut' concept.

Design: To study the action of HlyA in the colon, we performed oral administration of HlyA-expressing E coli-536 and its isogenic α-haemolysin-deficient mutant (HDM) in three mouse models: wild type, interleukin-10 knockout mice (IL-10(-/-)) and monoassociated mice. Electrophysiological properties of the colonised colon were characterised in Ussing experiments. Inflammation scores were evaluated and focal leaks in the colon were assessed by confocal laser-scanning microscopy. HlyA quantity in human colon biopsies was measured by quantitative PCR.

Results: All three experimental mouse models infected with HlyA-producing E coli-536 showed an increase in focal leak area compared with HDM. This was associated with a decrease in transepithelial electrical resistance and an increase in macromolecule uptake. As a consequence, inflammatory activity index was increased to a higher degree in inflammation-prone mice. Mucosal samples from human colon were E coli HlyA-positive in 19 of 22 patients with ulcerative colitis, 9 of 9 patients with Crohn's disease and 9 of 12 healthy controls. Moreover, focal leaks were found together with 10-fold increased levels of HlyA in active ulcerative colitis.

Conclusions: E coli HlyA impairs intestinal barrier function via focal leak induction in the epithelium, thereby intensifying antigen uptake and triggering intestinal inflammation in vulnerable mouse models. Therefore, HlyA-expressing E coli strains should be considered as potential cofactors in the pathogenesis of intestinal inflammation.

Keywords: Bacterial Enterotoxins; Bacterial Pathogenesis; Epithelial Barrier; Epithelial Permeability; Ulcerative Colitis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antigens / metabolism*
  • Colitis, Ulcerative* / immunology
  • Colitis, Ulcerative* / microbiology
  • Colitis, Ulcerative* / pathology
  • Crohn Disease* / immunology
  • Crohn Disease* / microbiology
  • Crohn Disease* / pathology
  • Disease Models, Animal
  • Electrophysiological Phenomena
  • Enterocytes* / metabolism
  • Enterocytes* / pathology
  • Escherichia coli Proteins / metabolism*
  • Escherichia coli* / metabolism
  • Escherichia coli* / pathogenicity
  • Hemolysin Proteins / metabolism*
  • Humans
  • Immunity, Mucosal
  • Inflammation / immunology
  • Inflammation / metabolism
  • Mice
  • Mice, Knockout
  • Permeability

Substances

  • Antigens
  • Escherichia coli Proteins
  • Hemolysin Proteins
  • Hlya protein, E coli