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Published on: October 13, 2015
The pesticin receptor of Yersinia enterocolitica: a novel virulence factor with dual function
Abstract:
The iron-repressible outer membrane protein FyuA of Yersinia enterocolitica operates as a receptor with dual function: (i) as a receptor for the Y. pestis bacteriocin pesticin, and (ii) as a receptor for yersiniabactin, a siderophore that is produced by mouse-virulent Y. enterocolitica strains of biogroup IB. Cloning of the FyuA-encoding gene was achieved by mobilization of a genomic cosmid library of the pesticin-sensitive and mouse-virulent Y. enterocolitica O:8 strain WA into the pesticin-resistant WA fyuA mutant and subsequent in vivo selection of transconjugants for the ability to survive and multiply in mice (phenotype mouse virulence). The reisolated transconjugants which survived in mice for 3 d harboured a unique cosmid and phenotypically were pesticin sensitive. From this cosmid a 2650 bp SalI-PstI fragment conferring pesticin sensitivity was subcloned. Sequencing of this DNA fragment revealed a single open reading frame of 2022 bp, which encodes a deduced polypeptide of 673 amino acids with a predicted molecular mass of 73,677 Da. Cleavage of a putative signal sequence composed of 22 amino acids should lead to a mature protein of 651 amino acids with a molecular mass of 71,368 Da. The open reading frame is preceded by a sequence which shares homology with the postulated consensus Fur iron-repressor protein-binding site. FyuA shows homology to other iron-regulated TonB-dependent outer membrane proteins with receptor functions (e.g. BtuB, CirA, FepA, IutA, FhuA, FoxA, FcuA). On the basis of multiple alignment of amino acid sequences of FyuA and other TonB-dependent receptors, a phylogenetic tree was constructed, demonstrating that FyuA probably belongs to the citrate subfamily or represents a new subfamily of TonB-dependent receptors. Moreover, by complementation of the WA fyuA mutant by the cloned fyuA gene, yersiniabactin uptake and mouse virulence were restored. These studies demonstrate that the cloned pesticin/yersiniabactin receptor FyuA of Y. enterocolitica has the typical features of iron-regulated TonB-dependent outer membrane receptors for siderophores and bacteriocins and is required for mouse virulence.
Insights
The FyuA outer membrane protein in Yersinia enterocolitica acts as a dual receptor for pesticin and yersiniabactin. This protein is crucial for mouse virulence and shares characteristics with iron-regulated TonB-dependent receptors.
Area of Science:
- Microbiology
- Molecular Biology
- Protein Structure and Function
Background:
- Yersinia enterocolitica is a pathogen that causes disease in mice.
- Outer membrane proteins play vital roles in bacterial interactions and virulence.
- Iron availability regulates bacterial gene expression, impacting virulence factors.
Purpose of the Study:
- To clone and characterize the FyuA gene, an iron-repressible outer membrane protein in Yersinia enterocolitica.
- To investigate the dual function of FyuA as a receptor for pesticin and yersiniabactin.
- To determine the role of FyuA in mouse virulence.
Main Methods:
- Genomic cosmid library screening and in vivo selection in a mouse model.
- Subcloning and DNA sequencing of the FyuA gene.
- Bioinformatic analysis including homology searches and phylogenetic tree construction.
- Complementation assays to restore FyuA function.
Main Results:
- The FyuA gene was successfully cloned and sequenced, revealing an open reading frame encoding a 651-amino acid mature protein.
- FyuA functions as a receptor for both the bacteriocin pesticin and the siderophore yersiniabactin.
- FyuA exhibits homology to other iron-regulated TonB-dependent outer membrane receptors.
- Expression of FyuA restored pesticin sensitivity, yersiniabactin uptake, and mouse virulence in a fyuA mutant.
Conclusions:
- The cloned FyuA protein is an iron-regulated TonB-dependent outer membrane receptor.
- FyuA is essential for Yersinia enterocolitica's virulence in mice, mediating uptake of yersiniabactin.
- FyuA represents a potential target for therapeutic interventions against Yersinia infections.
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