Escherichia coli cytotoxic necrotizing factor-1 (CNF-1) increases the adherence to epithelia and the oxidative burst of human polymorphonuclear leukocytes but decreases bacteria phagocytosis

J Leukoc Biol. 2000 Oct;68(4):522-8.

Abstract

Recruitment of polymorphonuclear leukocytes (PMNL) is a hallmark of both urinary and digestive infections caused by Escherichia coli. Cytotoxic necrotizing factor 1 (CNF-1) is a toxin produced by uropathogenic E. coli strains that mediates its effects via the activation of small GTP-binding proteins. However, the role and the consequences of CNF-1 on PMNL physiology remain largely unknown. In this study, we provide evidence that CNF-1 dramatically affects the PMNL cytoskeleton architecture by inducing an increased content of F-actin. Furthermore, we demonstrate that CNF-1 increases functional features of PMNL, such as superoxide generation and adherence on epithelial T84 monolayers, but significantly decreases their phagocytic function. Our results suggest that CNF-1 may behave as a virulence factor in urinary or digestive infection by stimulating PMNL cytotoxicity as a result of its enhancing effect on their adherence to epithelial cells as well as the production of radical oxygen products. Moreover, the decreased phagocytosis of PMNL induced by CNF-1 likely facilitates growth of bacteria. In these conditions, CNF-1 would intervene in the initiation and in the perpetuation of the inflammatory process.

MeSH terms

  • Actins / metabolism
  • Bacterial Toxins / pharmacology*
  • Cell Adhesion / drug effects
  • Cells, Cultured
  • Cytoskeleton / drug effects
  • Cytotoxins / pharmacology*
  • Epithelial Cells / cytology
  • Escherichia coli / pathogenicity*
  • Escherichia coli Proteins*
  • Humans
  • Inflammation / chemically induced
  • Intestinal Mucosa / cytology
  • Macrophage-1 Antigen / metabolism
  • Neutrophils / drug effects*
  • Neutrophils / microbiology
  • Neutrophils / physiology
  • Neutrophils / ultrastructure
  • Opsonin Proteins / pharmacology
  • Phagocytosis / drug effects*
  • Reactive Oxygen Species / metabolism
  • Respiratory Burst / drug effects*
  • Superoxides / metabolism
  • Virulence
  • Zymosan / pharmacology
  • rho GTP-Binding Proteins / antagonists & inhibitors
  • rho GTP-Binding Proteins / physiology

Substances

  • Actins
  • Bacterial Toxins
  • Cytotoxins
  • Escherichia coli Proteins
  • Macrophage-1 Antigen
  • Opsonin Proteins
  • Reactive Oxygen Species
  • cytotoxic necrotizing factor type 1
  • Superoxides
  • Zymosan
  • rho GTP-Binding Proteins