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Characterization of the Yersinia pestis Yfu ABC inorganic iron transport system
S Gong1, S W Bearden, V A Geoffroy
1Department of Microbiology and Immunology, University of Kentucky, Lexington, Kentucky 40536-0298, USA.
Abstract:
In Yersinia pestis, the causative agent of plague, two inorganic iron transport systems have been partially characterized. The yersiniabactin (Ybt) system is a siderophore-dependent transport system required for full virulence. Yfe is an ABC transport system that accumulates both iron and manganese. We have identified and cloned a Y. pestis yfuABC operon. The YfuABC system is a member of the cluster of bacterial ABC iron transporters that include Sfu of Serratia, Hit of Haemophilus, and Yfu of Yersinia enterocolitica. The Y. pestis KIM6+ system is most homologous to that in Y. enterocolitica, showing identities of 84% for YfuA (periplasmic binding protein), 87% for YfuB (inner membrane permease), and 75% for YfuC (ATP hydrolase). We constructed a yfuABC promoter-lacZ fusion to examine regulation of transcription. This promoter contains a potential Fur binding sequence and is iron and Fur regulated. Significant expression from the yfuABC promoter occurred during iron-deficient growth conditions. In vitro transcription and translation of a recombinant plasmid encoding yfuABC indicates that YfuABC proteins are expressed. Escherichia coli 1017 (an enterobactin-deficient mutant) carrying this plasmid was able to grow in an iron-restrictive complex medium. We constructed a deletion encompassing the yfuABC promoter and most of yfuA. This mutation was introduced into strains with mutations in Ybt, Yfe, or both systems to examine the role of Yfu in iron acquisition in Y. pestis. Growth of the yfu mutants in a deferrated, defined medium (PMH2) at 26 and 37 degrees C failed to identify a growth or iron transport defect due to the yfu mutation. Fifty percent lethal dose studies in mice did not demonstrate a role for the Yfu system in mammalian virulence.
Insights
The Yersinia pestis yfuABC operon, involved in iron transport, is iron-regulated but does not appear essential for bacterial growth or virulence in mice. Further studies are needed to fully understand its role.
Area of Science:
- Microbiology
- Molecular Biology
- Bacterial Pathogenesis
Background:
- Yersinia pestis, the plague pathogen, possesses known iron transport systems like yersiniabactin (Ybt) and Yfe.
- Understanding iron acquisition is crucial for Y. pestis virulence and survival.
Purpose of the Study:
- To identify and characterize a novel iron transport system, yfuABC, in Yersinia pestis.
- To investigate the regulation and function of the YfuABC system in iron acquisition and virulence.
Main Methods:
- Cloning and characterization of the yfuABC operon.
- Construction of a yfuABC promoter-lacZ fusion to study transcriptional regulation.
- Gene deletion mutagenesis to assess the role of YfuABC in iron transport and virulence.
- Growth assays in iron-restricted media and murine LD50 studies.
Main Results:
- The Y. pestis yfuABC operon was identified and cloned, showing homology to other bacterial ABC iron transporters.
- The yfuABC promoter is iron- and Fur-regulated, with expression increasing under iron-deficient conditions.
- yfuABC mutants did not exhibit growth defects in iron-restricted media, and the Yfu system was not essential for virulence in a murine model.
Conclusions:
- The YfuABC system in Y. pestis is expressed and regulated by iron availability but does not seem to play a critical role in iron acquisition or virulence.
- The Ybt and Yfe systems likely fulfill the primary iron transport needs for Y. pestis under the tested conditions.
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