In silico analysis of usher encoding genes in Klebsiella pneumoniae and characterization of their role in adhesion and colonization.

Chaperone/usher (CU) assembly pathway is used by a wide range of Enterobacteriaceae to assemble adhesive surface structures called pili or fimbriae that play a role in bacteria-host cell interactions. In silico analysis revealed that the genome of Klebsiella pneumoniae LM21 harbors eight chromosomal...

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Main Authors: Fida Khater, Damien Balestrino, Nicolas Charbonnel, Jean François Dufayard, Sylvain Brisse, Christiane Forestier
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2015-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC4353729?pdf=render
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spelling doaj-2208da1fa1824286990fb5bdfde1695a2020-11-25T00:24:21ZengPublic Library of Science (PLoS)PLoS ONE1932-62032015-01-01103e011621510.1371/journal.pone.0116215In silico analysis of usher encoding genes in Klebsiella pneumoniae and characterization of their role in adhesion and colonization.Fida KhaterDamien BalestrinoNicolas CharbonnelJean François DufayardSylvain BrisseChristiane ForestierChaperone/usher (CU) assembly pathway is used by a wide range of Enterobacteriaceae to assemble adhesive surface structures called pili or fimbriae that play a role in bacteria-host cell interactions. In silico analysis revealed that the genome of Klebsiella pneumoniae LM21 harbors eight chromosomal CU loci belonging to γκп and ϭ clusters. Of these, only two correspond to previously described operons, namely type 1 and type 3-encoding operons. Isogenic usher deletion mutants of K. pneumoniae LM21 were constructed for each locus and their role in adhesion to animal (Intestine 407) and plant (Arabidopsis thaliana) cells, biofilm formation and murine intestinal colonization was investigated. Type 3 pili usher deleted mutant was impaired in all assays, whereas type 1 pili usher deleted mutant only showed attenuation in adhesion to plant cells and in intestinal colonization. The LM21ΔkpjC mutant was impaired in its capacity to adhere to Arabidopsis cells and to colonize the murine intestine, either alone or in co-inoculation experiments. Deletion of LM21kpgC induced a significant decrease in biofilm formation, in adhesion to animal cells and in colonization of the mice intestine. The LM21∆kpaC and LM21∆kpeC mutants were only attenuated in biofilm formation and the adhesion abilities to Arabidopsis cells, respectively. No clear in vitro or in vivo effect was observed for LM21∆kpbC and LM21∆kpdC mutants. The multiplicity of CU loci in K. pneumoniae genome and their specific adhesion pattern probably reflect the ability of the bacteria to adhere to different substrates in its diverse ecological niches.http://europepmc.org/articles/PMC4353729?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Fida Khater
Damien Balestrino
Nicolas Charbonnel
Jean François Dufayard
Sylvain Brisse
Christiane Forestier
spellingShingle Fida Khater
Damien Balestrino
Nicolas Charbonnel
Jean François Dufayard
Sylvain Brisse
Christiane Forestier
In silico analysis of usher encoding genes in Klebsiella pneumoniae and characterization of their role in adhesion and colonization.
PLoS ONE
author_facet Fida Khater
Damien Balestrino
Nicolas Charbonnel
Jean François Dufayard
Sylvain Brisse
Christiane Forestier
author_sort Fida Khater
title In silico analysis of usher encoding genes in Klebsiella pneumoniae and characterization of their role in adhesion and colonization.
title_short In silico analysis of usher encoding genes in Klebsiella pneumoniae and characterization of their role in adhesion and colonization.
title_full In silico analysis of usher encoding genes in Klebsiella pneumoniae and characterization of their role in adhesion and colonization.
title_fullStr In silico analysis of usher encoding genes in Klebsiella pneumoniae and characterization of their role in adhesion and colonization.
title_full_unstemmed In silico analysis of usher encoding genes in Klebsiella pneumoniae and characterization of their role in adhesion and colonization.
title_sort in silico analysis of usher encoding genes in klebsiella pneumoniae and characterization of their role in adhesion and colonization.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2015-01-01
description Chaperone/usher (CU) assembly pathway is used by a wide range of Enterobacteriaceae to assemble adhesive surface structures called pili or fimbriae that play a role in bacteria-host cell interactions. In silico analysis revealed that the genome of Klebsiella pneumoniae LM21 harbors eight chromosomal CU loci belonging to γκп and ϭ clusters. Of these, only two correspond to previously described operons, namely type 1 and type 3-encoding operons. Isogenic usher deletion mutants of K. pneumoniae LM21 were constructed for each locus and their role in adhesion to animal (Intestine 407) and plant (Arabidopsis thaliana) cells, biofilm formation and murine intestinal colonization was investigated. Type 3 pili usher deleted mutant was impaired in all assays, whereas type 1 pili usher deleted mutant only showed attenuation in adhesion to plant cells and in intestinal colonization. The LM21ΔkpjC mutant was impaired in its capacity to adhere to Arabidopsis cells and to colonize the murine intestine, either alone or in co-inoculation experiments. Deletion of LM21kpgC induced a significant decrease in biofilm formation, in adhesion to animal cells and in colonization of the mice intestine. The LM21∆kpaC and LM21∆kpeC mutants were only attenuated in biofilm formation and the adhesion abilities to Arabidopsis cells, respectively. No clear in vitro or in vivo effect was observed for LM21∆kpbC and LM21∆kpdC mutants. The multiplicity of CU loci in K. pneumoniae genome and their specific adhesion pattern probably reflect the ability of the bacteria to adhere to different substrates in its diverse ecological niches.
url http://europepmc.org/articles/PMC4353729?pdf=render
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