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Co-regulation of Iron Metabolism and Virulence Associated Functions by Iron and XibR a Novel Iron Binding Transcription Factor in the Plant Pathogen Xanthomonas

机译:铁和Xibb一种新型的铁结合转录因子在植物病原体黄单胞菌中铁代谢和毒力相关功能的共同调节。

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摘要

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.
机译:细菌病原体适应宿主中铁限制的能力对其毒力至关重要。细菌病原体已经进化出多种策略来协调调节铁的代谢和与毒力相关的功能,以响应环境中不断变化的铁利用率来维持铁稳态。在许多细菌中,铁摄取调节剂(Fur)充当转录因子,利用铁的亚铁形式作为辅因子来调节铁代谢和许多细胞功能的转录。然而,除铁和Fur-Fe 2 + 之外的对毒力相关功能的微调和协调调节的机制仍然不确定。在这项研究中,我们显示了NtrC家族的新型转录调节因子XibR(命名为X花色素杆菌铁结合调节剂)对于调节和协同调节植物病原体Xanthomonas中几种铁调节基因的表达和毒力相关功能是必需的。坎普蒂斯里岛campestris(Xcc)。对铁饥饿刺激物和XibR regulon进行基因组广泛表达分析,GUS分析,xibR突变体的遗传和功能研究表明,XibR积极调节铁的存储和吸收,趋化性,运动性,并对铁的产生负响应。此外,染色质免疫沉淀后再进行定量实时PCR表明,铁促进了XibR与参与趋化性和运动性的操纵子上游调控序列的结合。圆二色光谱表明,纯化的XibR结合铁的铁形式。电泳迁移率变动分析表明,铁可积极影响XibR与靶毒力基因上游调控序列的结合,铁螯合剂去铁胺可逆转这种作用。综上所述,这些数据揭示了XibR如何协调Xanthomonads中毒力相关和铁代谢功能以响应铁的有效性。我们的结果提供了对这一重要的植物病原体中铁相关的毒力相关功能进行微调的复杂调节机制的见解。

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