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Modulation of surface antigen expression by Klebsiella pneumoniae in response to growth environment

S Camprubi1, M A Smith, J M Tomas

  • 1Department of Microbiology, Faculty of Biology, University of Barcelona, Spain.

Microbial Pathogenesis
|August 1, 1992
PubMed

Insights

Klebsiella pneumoniae adapts its cell envelope antigens, including outer membrane proteins and lipopolysaccharide, when grown in human body fluids. This phenotype flexibility highlights the O-antigen

Area of Science:

  • Microbiology
  • Immunology
  • Pathogen Adaptation

Background:

  • Klebsiella pneumoniae is an opportunistic pathogen.
  • Cell envelope antigens play a role in bacterial virulence and host immune response.
  • Understanding bacterial adaptation to host environments is crucial for developing effective treatments.

Purpose of the Study:

  • To investigate how Klebsiella pneumoniae modulates its cell envelope antigen expression when grown in human body fluids.
  • To compare the effects of different human body fluids (urine, serum, peritoneal dialysate) on antigen expression in virulent and avirulent strains.
  • To determine the role of O-antigen and K-antigen in bacterial survival in serum.

Main Methods:

  • Culturing virulent (O1:K1) and avirulent (O1:K66) Klebsiella pneumoniae strains in pooled human body fluids (urine, serum, peritoneal dialysate) and standard broth.
  • Analyzing outer membrane protein (OMP) and lipopolysaccharide (LPS) profiles using gel electrophoresis.
  • Assessing the reversion of O- and K-antigen deficient mutants to the O+ and K+ phenotypes after growth in different media.
  • Evaluating bacterial survival in serum after growth in body fluids.

Main Results:

  • Growth in human body fluids significantly altered OMP and LPS profiles compared to broth cultures.
  • Specific iron-regulated OMPs were expressed in a medium-dependent manner in the O1:K1 strain.
  • LPS core polysaccharide migration patterns changed in the O1:K1 strain but not in the O1:K66 strain.
  • O-antigen deficient mutants reverted to O+ phenotype after growth in fresh serum, but not in heat-inactivated serum, urine, or HPD.
  • K-antigen production and surface LPS exposure were unaffected by body fluid growth.
  • No reversion of K- mutants to K+ phenotype was observed.

Conclusions:

  • Klebsiella pneumoniae exhibits significant phenotype flexibility in response to growth in human body fluids.
  • The O-antigen, rather than the K-antigen, is critical for protecting Klebsiella pneumoniae from complement-mediated killing in serum.
  • These findings have implications for understanding K. pneumoniae pathogenesis and host-pathogen interactions.

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