• Media type: E-Article
  • Title: Identification of a Conserved Chromosomal Region Encoding Klebsiella pneumoniae Type 1 and Type 3 Fimbriae and Assessment of the Role of Fimbriae in Pathogenicity
  • Contributor: Struve, Carsten; Bojer, Martin; Krogfelt, Karen Angeliki
  • imprint: American Society for Microbiology, 2009
  • Published in: Infection and Immunity
  • Language: English
  • DOI: 10.1128/iai.00585-09
  • ISSN: 0019-9567; 1098-5522
  • Keywords: Infectious Diseases ; Immunology ; Microbiology ; Parasitology
  • Origination:
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  • Description: <jats:title>ABSTRACT</jats:title> <jats:p> Type 3 fimbriae are expressed by most clinical <jats:italic>Klebsiella pneumoniae</jats:italic> isolates and mediate adhesion to host structures in vitro. However, the role of type 3 fimbriae in <jats:italic>K. pneumoniae</jats:italic> virulence has not been evaluated by use of in vivo infection models. In this study, the type 3 fimbrial gene cluster ( <jats:italic>mrk</jats:italic> ) of the clinical isolate C3091 is described in detail. The <jats:italic>mrk</jats:italic> gene cluster was revealed to be localized in close proximity to the type 1 fimbrial gene cluster. Thus, a 20.4-kb fimbria-encoding region was identified and found to be highly conserved among different <jats:italic>K. pneumoniae</jats:italic> isolates. Interestingly, a homologue to PecS, known as a global regulator of virulence in <jats:italic>Erwinia chrysanthemi</jats:italic> , was identified in the fimbria-encoding region. Comparison to the previously characterized plasmid encoded <jats:italic>mrk</jats:italic> gene cluster revealed significant differences, and it is established here that the putative regulatory gene <jats:italic>mrkE</jats:italic> is not a part of the chromosomally encoded type 3 fimbrial gene cluster. To evaluate the role of type 3 fimbriae in virulence, a type 3 fimbria mutant and a type 1 and type 3 fimbria double mutant was constructed. Type 3 fimbria expression was found to strongly promote biofilm formation. However, the fimbria mutants were as effective at colonizing the intestine as the wild type, and their virulence was not attenuated in a lung infection model. Also, in a urinary tract infection model, type 3 fimbriae did not influence the virulence, whereas type 1 fimbriae were verified as an essential virulence factor. Thus, type 3 fimbriae were established not to be a virulence factor in uncomplicated <jats:italic>K. pneumoniae</jats:italic> infections. However, since type 3 fimbriae promote biofilm formation, their role in development of infections in catheterized patients needs to be elucidated. </jats:p>
  • Access State: Open Access