Identification and Regulation of a Novel Citrobacter rodentium Gut Colonization Fimbria (Gcf)

The Gram-negative enteric bacterium Citrobacter rodentium is a natural mouse pathogen that has been extensively used as a surrogate model for studying the human pathogens enteropathogenic and enterohemorrhagic Escherichia coli . All three pathogens produce similar attaching and effacing (A/E) lesion...

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Veröffentlicht in:Journal of bacteriology 2015-04, Vol.197 (8), p.1478-1491
Hauptverfasser: Caballero-Flores, Gustavo G, Croxen, Matthew A, Martóínez-Santos, Verónica I, Finlay, B. Brett, Puente, Josóíé L
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container_issue 8
container_start_page 1478
container_title Journal of bacteriology
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creator Caballero-Flores, Gustavo G
Croxen, Matthew A
Martóínez-Santos, Verónica I
Finlay, B. Brett
Puente, Josóíé L
description The Gram-negative enteric bacterium Citrobacter rodentium is a natural mouse pathogen that has been extensively used as a surrogate model for studying the human pathogens enteropathogenic and enterohemorrhagic Escherichia coli . All three pathogens produce similar attaching and effacing (A/E) lesions in the intestinal epithelium. During infection, these bacteria employ surface structures called fimbriae to adhere and colonize the host intestinal epithelium. For C. rodentium , the roles of only a small number of its genome-carried fimbrial operons have been evaluated. Here, we report the identification of a novel C. rodentium colonization factor, called g ut c olonization f imbria (Gcf), which is encoded by a chaperone-usher fimbrial operon. A gcfA mutant shows a severe colonization defect within the first 10 days of infection. The gcf promoter is not active in C. rodentium under several in vitro growth conditions; however, it is readily expressed in a C. rodentium Δ hns1 mutant lacking the closest ortholog of the Escherichia coli histone-like nucleoid structuring protein (H-NS) but not in mutants with deletion of the other four genes encoding H-NS homologs. H-NS binds to the regulatory region of gcf , further supporting its direct role as a repressor of the gcf promoter that starts transcription 158 bp upstream of the start codon of its first open reading frame. The gcf operon possesses interesting novel traits that open future opportunities to expand our knowledge of the structure, regulation, and function during infection of these important bacterial structures. IMPORTANCE Fimbriae are surface bacterial structures implicated in a variety of biological processes. Some have been shown to play a critical role during host colonization and thus in disease. Pathogenic bacteria possess the genetic information for an assortment of fimbriae, but their function and regulation and the interplay between them have not been studied in detail. This work provides new insights into the function and regulation of a novel fimbria called Gcf that is important for early establishment of a successful infection by C. rodentium in mice, despite being poorly expressed under in vitro growth conditions. This discovery offers an opportunity to better understand the individual role and the regulatory mechanisms controlling the expression of specific fimbrial operons that are critical during infection.
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Here, we report the identification of a novel C. rodentium colonization factor, called g ut c olonization f imbria (Gcf), which is encoded by a chaperone-usher fimbrial operon. A gcfA mutant shows a severe colonization defect within the first 10 days of infection. The gcf promoter is not active in C. rodentium under several in vitro growth conditions; however, it is readily expressed in a C. rodentium Δ hns1 mutant lacking the closest ortholog of the Escherichia coli histone-like nucleoid structuring protein (H-NS) but not in mutants with deletion of the other four genes encoding H-NS homologs. H-NS binds to the regulatory region of gcf , further supporting its direct role as a repressor of the gcf promoter that starts transcription 158 bp upstream of the start codon of its first open reading frame. The gcf operon possesses interesting novel traits that open future opportunities to expand our knowledge of the structure, regulation, and function during infection of these important bacterial structures. IMPORTANCE Fimbriae are surface bacterial structures implicated in a variety of biological processes. Some have been shown to play a critical role during host colonization and thus in disease. Pathogenic bacteria possess the genetic information for an assortment of fimbriae, but their function and regulation and the interplay between them have not been studied in detail. This work provides new insights into the function and regulation of a novel fimbria called Gcf that is important for early establishment of a successful infection by C. rodentium in mice, despite being poorly expressed under in vitro growth conditions. 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All Rights Reserved.</rights><rights>Copyright American Society for Microbiology Apr 2015</rights><rights>Copyright © 2015, American Society for Microbiology. 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J.</contributor><creatorcontrib>Caballero-Flores, Gustavo G</creatorcontrib><creatorcontrib>Croxen, Matthew A</creatorcontrib><creatorcontrib>Martóínez-Santos, Verónica I</creatorcontrib><creatorcontrib>Finlay, B. Brett</creatorcontrib><creatorcontrib>Puente, Josóíé L</creatorcontrib><title>Identification and Regulation of a Novel Citrobacter rodentium Gut Colonization Fimbria (Gcf)</title><title>Journal of bacteriology</title><addtitle>J Bacteriol</addtitle><description>The Gram-negative enteric bacterium Citrobacter rodentium is a natural mouse pathogen that has been extensively used as a surrogate model for studying the human pathogens enteropathogenic and enterohemorrhagic Escherichia coli . All three pathogens produce similar attaching and effacing (A/E) lesions in the intestinal epithelium. During infection, these bacteria employ surface structures called fimbriae to adhere and colonize the host intestinal epithelium. For C. rodentium , the roles of only a small number of its genome-carried fimbrial operons have been evaluated. Here, we report the identification of a novel C. rodentium colonization factor, called g ut c olonization f imbria (Gcf), which is encoded by a chaperone-usher fimbrial operon. A gcfA mutant shows a severe colonization defect within the first 10 days of infection. The gcf promoter is not active in C. rodentium under several in vitro growth conditions; however, it is readily expressed in a C. rodentium Δ hns1 mutant lacking the closest ortholog of the Escherichia coli histone-like nucleoid structuring protein (H-NS) but not in mutants with deletion of the other four genes encoding H-NS homologs. H-NS binds to the regulatory region of gcf , further supporting its direct role as a repressor of the gcf promoter that starts transcription 158 bp upstream of the start codon of its first open reading frame. 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For C. rodentium , the roles of only a small number of its genome-carried fimbrial operons have been evaluated. Here, we report the identification of a novel C. rodentium colonization factor, called g ut c olonization f imbria (Gcf), which is encoded by a chaperone-usher fimbrial operon. A gcfA mutant shows a severe colonization defect within the first 10 days of infection. The gcf promoter is not active in C. rodentium under several in vitro growth conditions; however, it is readily expressed in a C. rodentium Δ hns1 mutant lacking the closest ortholog of the Escherichia coli histone-like nucleoid structuring protein (H-NS) but not in mutants with deletion of the other four genes encoding H-NS homologs. H-NS binds to the regulatory region of gcf , further supporting its direct role as a repressor of the gcf promoter that starts transcription 158 bp upstream of the start codon of its first open reading frame. The gcf operon possesses interesting novel traits that open future opportunities to expand our knowledge of the structure, regulation, and function during infection of these important bacterial structures. IMPORTANCE Fimbriae are surface bacterial structures implicated in a variety of biological processes. Some have been shown to play a critical role during host colonization and thus in disease. Pathogenic bacteria possess the genetic information for an assortment of fimbriae, but their function and regulation and the interplay between them have not been studied in detail. This work provides new insights into the function and regulation of a novel fimbria called Gcf that is important for early establishment of a successful infection by C. rodentium in mice, despite being poorly expressed under in vitro growth conditions. This discovery offers an opportunity to better understand the individual role and the regulatory mechanisms controlling the expression of specific fimbrial operons that are critical during infection.</abstract><cop>United States</cop><pub>American Society for Microbiology</pub><pmid>25666139</pmid><doi>10.1128/JB.02486-14</doi><tpages>14</tpages><oa>free_for_read</oa></addata></record>
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ispartof Journal of bacteriology, 2015-04, Vol.197 (8), p.1478-1491
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subjects Animals
bacteria
Bacterial infections
Bacterial Proteins - genetics
Bacterial Proteins - metabolism
Bacteriology
Citrobacter rodentium
Citrobacter rodentium - genetics
Citrobacter rodentium - metabolism
Colonization
E coli
enterohemorrhagic Escherichia coli
Escherichia coli
Fimbria
fimbriae
Fimbriae, Bacterial - genetics
Fimbriae, Bacterial - metabolism
Gastrointestinal Tract - microbiology
Gene expression
Gene Expression Regulation, Bacterial - physiology
Gram-negative bacteria
Growth conditions
humans
intestinal mucosa
Mice
Multigene Family
mutants
Mutation
open reading frames
Operon
Pathogens
RNA, Bacterial - genetics
RNA, Bacterial - metabolism
start codon
Virulence Factors - genetics
Virulence Factors - metabolism
title Identification and Regulation of a Novel Citrobacter rodentium Gut Colonization Fimbria (Gcf)
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