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Regulation of the Expression of Iron-acquisition System Genes in Pathogenic Vibrio Species
1Laboratory of Hygienic Chemistry, College of Pharmaceutical Sciences, Matsuyama University.
Abstract:
The genus Vibrio includes >70 species, of which roughly a dozen cause vibriosis such as gastroenteritis, wound infections, and septicemia. Most bacteria, including Vibrio species, require iron for survival and growth. However, the bioavailability of iron is extremely low because it is usually present as an insoluble ferric complex in an aerobic environment or is bound to iron-binding proteins in mammalian hosts. Therefore many bacteria have developed iron acquisition systems, including biosynthesis and secretion of low-molecular-mass iron-chelating compounds called siderophores, and uptake of iron-bound siderophores into bacterial cells through specific active transport systems. Vibrio parahaemolyticus, a major pathogenic Vibrio species, contains multiple iron-acquisition systems mediated by its own siderophore vibrioferrin and several xenosiderophores produced by other microorganisms. In this review, I have focused on the transcriptional and posttranscriptional regulation of genes encoding iron acquisition systems in V. parahaemolyticus. All genes involved in its iron acquisition systems are repressed by Fur, which acts as a ferrous-dependent transcriptional repressor. Furthermore, the stability of polycistronic mRNA involved in vibrioferrin biosynthesis is positively regulated by a small RNA, RyhB, which is repressed by Fur. Expression of PeuA receptor required for utilization of a xenosiderophore, enterobactin, occurs under iron-limiting conditions at alkaline pH. PeuA expression is induced by a two-component regulatory system, PeuRS, which enhances expression of an alternative peuA transcript without an intrinsic translation-inhibitory structure in response to changes in alkaline pH.
Insights
Vibrio parahaemolyticus employs complex iron acquisition systems regulated by Fur and RyhB. Alkaline pH triggers PeuRS to induce PeuA receptor expression for xenosiderophore utilization.
Area of Science:
- Microbiology
- Bacterial Pathogenesis
- Gene Regulation
Background:
- The genus Vibrio contains over 70 species, with several causing significant human diseases like vibriosis.
- Iron is essential for bacterial survival, but its low bioavailability in hosts necessitates sophisticated acquisition systems.
- Vibrio parahaemolyticus, a key pathogen, utilizes multiple iron uptake mechanisms, including its own siderophore, vibrioferrin, and external siderophores.
Purpose of the Study:
- To review the transcriptional and posttranscriptional regulation of iron acquisition systems in Vibrio parahaemolyticus.
- To elucidate the roles of Fur, RyhB, and PeuRS in controlling iron uptake gene expression.
Main Methods:
- Review of existing literature on Vibrio iron acquisition and regulation.
- Analysis of regulatory mechanisms involving transcriptional repressors (Fur) and small RNAs (RyhB).
- Examination of two-component systems (PeuRS) controlling outer membrane receptor expression (PeuA).
Main Results:
- Iron acquisition genes in V. parahaemolyticus are repressed by the ferrous-dependent regulator Fur.
- The stability of vibrioferrin biosynthesis mRNA is positively regulated by RyhB, which is itself repressed by Fur.
- PeuA receptor expression, crucial for enterobactin utilization, is induced by the PeuRS system under alkaline pH and iron-limiting conditions.
Conclusions:
- Vibrio parahaemolyticus exhibits intricate regulatory networks for iron acquisition, involving both global repressors and specific environmental responses.
- Small RNAs like RyhB play a critical role in posttranscriptional control of iron homeostasis.
- The PeuRS two-component system provides a mechanism for adapting iron uptake strategies to host environmental conditions, such as alkaline pH.
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