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The Citrobacter rodentium Mouse Model: Studying Pathogen and Host Contributions to Infectious Colitis
Published on: February 19, 2013
Identification and regulation of a novel Citrobacter rodentium gut colonization fimbria (Gcf)
Gustavo G Caballero-Flores1, Matthew A Croxen2, Verónica I Martínez-Santos1
1Departamento de Microbiología Molecular, Instituto de Biotecnología, Universidad Nacional Autónoma de México, Cuernavaca, Morelos, Mexico.
Unlabelled:
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 gut colonization fimbria (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 Δhns1 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.
Insights
Researchers discovered a new fimbria in Citrobacter rodentium, called gut colonization fimbria (Gcf), crucial for early mouse infection. This novel Gcf fimbria is regulated by the histone-like nucleoid structuring protein (H-NS) and offers insights into bacterial colonization factors.
Area of Science:
- Microbiology
- Bacterial Pathogenesis
- Molecular Biology
Background:
- Fimbriae are critical surface structures for bacterial adhesion and colonization.
- Citrobacter rodentium serves as a model for studying human enteric pathogens like E. coli.
- The specific roles and regulation of many fimbrial operons in C. rodentium remain uncharacterized.
Purpose of the Study:
- To identify and characterize novel colonization factors in Citrobacter rodentium.
- To investigate the function and regulation of a newly discovered fimbria, gut colonization fimbria (Gcf).
- To elucidate the role of histone-like nucleoid structuring protein (H-NS) in controlling Gcf expression.
Main Methods:
- Genetic manipulation to create gcfA mutants.
- In vitro and in vivo colonization assays.
- Reporter assays to assess promoter activity.
- Electrophoretic mobility shift assays (EMSAs) to study protein-DNA interactions.
Main Results:
- A novel fimbria, gut colonization fimbria (Gcf), was identified in C. rodentium.
- A gcfA mutant exhibited a significant defect in early colonization of mice.
- Gcf expression is repressed by H-NS, with promoter activity observed in a Δhns1 mutant.
- H-NS directly binds to the gcf promoter region.
Conclusions:
- Gut colonization fimbria (Gcf) is a novel and essential factor for early C. rodentium colonization in mice.
- Histone-like nucleoid structuring protein (H-NS) acts as a direct repressor of the gcf operon.
- This study expands our understanding of fimbrial gene regulation and function in bacterial pathogenesis.
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