Klebsiella pneumoniae secretes outer membrane vesicles that induce the innate immune response

FEMS Microbiol Lett. 2012 Jun;331(1):17-24. doi: 10.1111/j.1574-6968.2012.02549.x. Epub 2012 Apr 13.

Abstract

Outer membrane vesicles (OMVs) derived from pathogenic Gram-negative bacteria are an important vehicle for delivery of effector molecules to host cells, but the production of OMVs from Klebsiella pneumoniae, an opportunistic pathogen of both nosocomial and community-acquired infections, and their role in bacterial pathogenesis have not yet been determined. In the present study, we examined the production of OMVs from K. pneumoniae and determined the induction of the innate immune response against K. pneumoniae OMVs. Klebsiella pneumoniae ATCC 13883 produced and secreted OMVs during in vitro culture. Proteomic analysis revealed that 159 different proteins were associated with K. pneumoniae OMVs. Klebsiella pneumoniae OMVs did not inhibit cell growth or induce cell death. However, these vesicles induced expression of proinflammatory cytokine genes such as interleukin (IL)-1β and IL-8 in epithelial cells. An intratracheal challenge of K. pneumoniae OMVs in neutropenic mice resulted in severe lung pathology similar to K. pneumoniae infection. In conclusion, K. pneumoniae produces OMVs like other pathogenic Gram-negative bacteria and K. pneumoniae OMVs are a molecular complex that induces the innate immune response.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Bacterial Proteins / analysis
  • Cytokines / biosynthesis
  • Epithelial Cells / immunology
  • Exosomes / chemistry
  • Exosomes / immunology*
  • Exosomes / metabolism*
  • Female
  • Gene Expression Profiling
  • Histocytochemistry
  • Immunity, Innate*
  • Klebsiella pneumoniae / immunology*
  • Klebsiella pneumoniae / metabolism*
  • Lung / pathology
  • Mice
  • Mice, Inbred BALB C
  • Microscopy
  • Pneumonia / chemically induced
  • Pneumonia / pathology
  • Proteome / analysis

Substances

  • Bacterial Proteins
  • Cytokines
  • Proteome