Complementation of a DnaK-deficient Escherichia coli strain with the dnaK/dnaJ operon of Brucella ovis reduces the rate of initial intracellular killing within the monocytic cell line U937

FEMS Microbiol Lett. 1994 Jul 15;120(3):335-40. doi: 10.1111/j.1574-6968.1994.tb07055.x.

Abstract

Facultatively intracellular bacteria express heat shock proteins after phagocytosis by macrophages. Using non-pathogenic Escherichia coli strains and the human monocytic cell line U937, we showed that deletion of the dnaK gene significantly increased the rate of initial intracellular killing of bacteria. Trans-complementation of the deletion mutant with the dnaK/dnaJ operon of Brucella ovis restored the pattern of intracellular elimination of the control strain expressing dnaK. These differences were not observed using antibody-opsonized bacteria and activated cells. In vitro, strains expressing dnaK resisted hydrogen peroxide better than the deletion mutant; in contrast, the mutant complemented by dnaK/dnaJ of B. ovis tolerated low pH and low H2O2 better than the wild-type strain and the deletion mutant. Our results suggested the participation of DnaK in protection of intracellular bacteria against antimicrobial macrophage factors.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Bacterial Proteins / genetics*
  • Bacterial Proteins / immunology
  • Brucella / genetics*
  • Brucella / immunology
  • Cell Line
  • Escherichia coli / genetics*
  • Escherichia coli / immunology
  • Escherichia coli Proteins*
  • Genetic Complementation Test*
  • HSP70 Heat-Shock Proteins*
  • Heat-Shock Proteins / genetics*
  • Heat-Shock Proteins / immunology
  • Humans
  • Monocytes / immunology*
  • Operon
  • Phagocytosis

Substances

  • Bacterial Proteins
  • Escherichia coli Proteins
  • HSP70 Heat-Shock Proteins
  • Heat-Shock Proteins
  • dnaK protein, E coli