Preliminary investigation of a mice model of Klebsiella pneumoniae subsp. ozaenae induced pneumonia

Microbes Infect. 2011 Nov;13(12-13):1045-51. doi: 10.1016/j.micinf.2011.05.013. Epub 2011 Jun 30.

Abstract

In the present study, we comparatively assessed the pathophysiological mechanisms developed during lung infection of BALB/C female mice infected by an original wild type Klebsiella pneumoniae subsp. ozaenae strain (CH137) or by a referent subspecies K. pneumoniae. subsp. pneumoniae strain (ATCC10031). The mice infected with 2.10⁶ CFU K. p. subsp. pneumoniae (n = 10) showed transient signs of infection and all of them recovered. All of those infected with 1.10⁶ CFU K. p. subsp. ozaenae (n = 10) developed pneumonia within 24 h and died between 48 and 72 h. Few macrophages, numerous polymorphonuclear cells and lymphocytes were observed in their lungs in opposite to K. p. subsp. pneumoniae. In bronchoalveolar lavage, a significant increase in MIP-2, IL-6, KC and MCP-1 levels was only observed in K. p. subsp. ozaenae infected mice whereas high levels of TNF-α were evidenced with the two subspecies. Our findings indicated a lethal effect of a wild type K. p. subsp. ozaenae strain by acute pneumonia reflecting an insufficient alveolar macrophage response. This model might be of a major interest to comparatively explore the pathogenicity of K. p. subsp ozaenae strains and to further explore the physiopathological mechanisms of gram-negative bacteria induced human pneumonia.

Publication types

  • Comparative Study

MeSH terms

  • Animals
  • Bronchoalveolar Lavage Fluid / cytology
  • Colony Count, Microbial
  • Cytokines / analysis*
  • Cytokines / metabolism
  • Disease Models, Animal
  • Female
  • Humans
  • Immunity, Innate
  • Klebsiella Infections / immunology
  • Klebsiella Infections / microbiology
  • Klebsiella Infections / mortality
  • Klebsiella Infections / pathology*
  • Klebsiella pneumoniae / classification
  • Klebsiella pneumoniae / immunology
  • Klebsiella pneumoniae / pathogenicity*
  • Lung / immunology
  • Lung / microbiology
  • Lung / pathology
  • Macrophages, Alveolar / immunology
  • Macrophages, Alveolar / microbiology
  • Mice
  • Mice, Inbred BALB C
  • Pneumonia, Bacterial / immunology
  • Pneumonia, Bacterial / microbiology
  • Pneumonia, Bacterial / mortality
  • Pneumonia, Bacterial / pathology*
  • Spleen / immunology
  • Spleen / microbiology
  • Spleen / pathology
  • Time Factors

Substances

  • Cytokines