Intoxication strategy of Helicobacter pylori VacA toxin

Trends Microbiol. 2012 Apr;20(4):165-74. doi: 10.1016/j.tim.2012.01.008. Epub 2012 Feb 23.

Abstract

VacA toxin from the cancer-inducing bacterium Helicobacter pylori is currently classified as a pore-forming toxin but is also considered a multifunctional toxin, apparently causing many pleiotropic cell effects. However, an increasing body of evidence suggests that VacA could be the prototype of a new class of monofunctional A-B toxins in which the A subunit exhibits pore-forming instead of enzymatic activity. Thus, VacA may use a peculiar mechanism of action, allowing it to intoxicate the human stomach. By combining the action of a cell-binding domain, a specific intracellular trafficking pathway and a novel mitochondrion-targeting sequence, the VacA pore-forming domain is selectively delivered to the inner mitochondrial membrane to efficiently kill target epithelial cells by apoptosis.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Bacterial Proteins / metabolism
  • Bacterial Proteins / toxicity*
  • Cell Death
  • Epithelial Cells / microbiology*
  • Helicobacter pylori / pathogenicity*
  • Humans
  • Mitochondria / drug effects
  • Mitochondria / metabolism
  • Mitochondrial Membranes / drug effects
  • Mitochondrial Membranes / physiology
  • Protein Binding
  • Protein Transport

Substances

  • Bacterial Proteins
  • VacA protein, Helicobacter pylori