Abstract

Abilities of bacterial pathogens to adapt to the iron limitation present in hosts is critical to their virulence. Bacterial pathogens have evolved diverse strategies to coordinately regulate iron metabolism and virulence associated functions to maintain iron homeostasis in response to changing iron availability in the environment. In many bacteria the ferric uptake regulator (Fur) functions as transcription factor that utilize ferrous form of iron as cofactor to regulate transcription of iron metabolism and many cellular functions. However, mechanisms of fine-tuning and coordinated regulation of virulence associated function beyond iron and Fur-Fe2+ remain undefined. In this study, we show that a novel transcriptional regulator XibR (named X anthomonas iron binding regulator) of the NtrC family, is required for fine-tuning and co-coordinately regulating the expression of several iron regulated genes and virulence associated functions in phytopathogen Xanthomonas campestris pv. campestris (Xcc). Genome wide expression analysis of iron-starvation stimulon and XibR regulon, GUS assays, genetic and functional studies of xibR mutant revealed that XibR positively regulates functions involved in iron storage and uptake, chemotaxis, motility and negatively regulates siderophore production, in response to iron. Furthermore, chromatin immunoprecipitation followed by quantitative real-time PCR indicated that iron promoted binding of the XibR to the upstream regulatory sequence of operon’s involved in chemotaxis and motility. Circular dichroism spectroscopy showed that purified XibR bound ferric form of iron. Electrophoretic mobility shift assay revealed that iron positively affected the binding of XibR to the upstream regulatory sequences of the target virulence genes, an effect that was reversed by ferric iron chelator deferoxamine. Taken together, these data revealed that how XibR coordinately regulates virulence associated and iron metabolism functions in Xanthomonads in response to iron availability. Our results provide insight of the complex regulatory mechanism of fine-tuning of virulence associated functions with iron availability in this important group of phytopathogen.

Highlights

  • Iron homeostasis is vital for survival and cellular metabolism in many organisms

  • The ferric uptake regulator (Fur) regulates the expression of genes involved in iron metabolism in response to change in iron availability in several bacteria

  • We show that a novel ferric iron binding transcription factor, XibR, is required for optimum virulence in phytopathogen Xanthomonas campestris pv. campestris (Xcc) by coordinately regulating expression of genes involved in iron metabolism and several virulence associated function such as chemotaxis and motility

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Summary

Introduction

Iron homeostasis is vital for survival and cellular metabolism in many organisms. Bacteria maintain cellular iron homeostasis by coordinately regulating iron uptake, metabolism and storage, to achieve sufficient iron under iron-replete condition, and to store intracellular iron surplus for utilization under condition of iron limitation [1]. Iron is required for virulence of several animal and plant pathogenic bacteria [1,2,3]. The availability of iron within the host plays a critical role in the growth and survival of the pathogens. Iron-withholding strategies are employed to limit iron availability to infecting pathogens [1]. In plants, several studies have shown that iron availability is likely to be a limiting factor for pathogen growth within host [2,3]

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