IscR plays a role in oxidative stress resistance and pathogenicity of a plant pathogen, Xanthomonas campestris

Abstract Iron–sulfur ([Fe–S]) cluster is an essential cofactor of proteins involved in various physiological processes including cellular defense against oxidative stress. In Xanthomonas campestris pv. campestris (Xcc), IscR plays a negative role in regulation of the transcription of [Fe–S] assembly genes, iscR-sufBCDS . The expression level of sufBCDS was up-regulated in an Xcc iscR mutant. In addition, the iscR promoter activity in an Xcc iscR mutant was also higher than the wild-type strain, indicating an autoregulatory circuit. Purified IscR was shown to bind at the iscR promoter region and three putative IscR binding sites were identified. The expression of iscR-suf operon was highly induced by oxidant treatments and iron limited conditions. The iscR mutant showed increased sensitivity toward hydrogen peroxide phenotype but, surprisingly, had hyper-resistant phenotype toward plumbagin compared to the wild-type strain. Most importantly, the iscR mutant was impaired in its ability to cause lesion on leaves of a compatible host plant, Chinese radish ( Raphanus sativus ). These results demonstrate that a transcription regulator gene, iscR , negatively regulates genes involved in [Fe–S] biosynthesis and plays a role in oxidative stress response and pathogenesis of Xcc.