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Complement mediated Klebsiella pneumoniae capsule changes
Affiliation:1. Department of Life Sciences, University of Trieste, via L. Giorgieri 1, Bdg C11, 34127 Trieste, Italy;2. Department of Chemistry, University of Cape Town, Rondebosch 7701, South Africa;3. Department of Medical Biotechnologies, University of Siena, Siena, Italy;4. Department of Biology, University of Rome “Tor Vergata”, Rome, Italy;5. Department of Experimental and Clinical Medicine, University of Florence, Florence, Italy;6. Microbiology and Virology Unit, Florence Careggi University Hospital, Florence, Italy
Abstract:The Gram-negative bacterium Klebsiella pneumoniae is an opportunistic pathogen, which can cause life-threatening infections such as sepsis. Worldwide, emerging multidrug resistant K. pneumoniae infections are challenging to treat, hence leading to increased mortality. Therefore, understanding the interactions between K. pneumoniae and the immune system is important to develop new treatment options.We characterized ten clinical K. pneumoniae isolates obtained from blood of bacteremia patients. The interaction of the isolates with human serum was investigated to elucidate how K. pneumoniae escapes the host immune system, and how complement activation by K. pneumoniae changed the capsule structure. All K. pneumoniae isolates activated the alternative complement pathway despite serum resistance of seven isolates. One serum sensitive isolate activated two or all three pathways, and this isolate was lysed and had numerous membrane attack complexes in the outer membrane. However, we also found deposition of complement components in the capsule of serum resistant isolates resulting in morphological capsule changes and capsule shedding. These bacteria did not lyse, and no membrane attack complex was observed despite deposition of C5b-9 within the capsule, indicating that the capsule of serum resistant K. pneumoniae isolates is a defense mechanism against complement-mediated lysis.
Keywords:Bacterial capsules  Complement system  Membrane attack complex  Serum resistance
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