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首页> 外文期刊>Molecular Plant-Microbe Interactions >Two-component sensor RhpS promotes induction of Pseudomonas syringae type III secretion system by repressing negative regulator RhpR
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Two-component sensor RhpS promotes induction of Pseudomonas syringae type III secretion system by repressing negative regulator RhpR

机译:两成分传感器RhpS通过抑制负调控因子RhpR促进丁香假单胞菌III型分泌系统的诱导

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The Pseudomonas syringae type III secretion system (T3SS) is induced during interaction with the plant or culture in minimal medium (MM). How the bacterium senses these environments to activate the T3SS is poorly understood. Here, we report the identification of a novel two-component system (TCS), RhpRS, that regulates the induction of P. syringae T3SS genes. The rhpR and rhpS genes are organized in an operon with rhpR encoding a putative TCS response regulator and rhpS encoding a putative biphasic sensor kinase. Transposon insertion in rhpS severely reduced the induction of P. syringae T3SS genes in the plant as well as in MM and significantly compromised the pathogenicity on host plants and hypersensitive response-inducing activity on nonhost plants. However, deletion of the rhpRS locus allowed the induction of T3SS genes to the same level as in the wild-type strain and the recovery of pathogenicity upon infiltration into plants. Overexpression of RhpR in the deltarhpRS deletion strain abolished the induction of T3SS genes. However, overexpression of RhpR in the wild-type strain or overexpression of RhpR(D70A), a mutant of the predicted phosphorylation site of RhpR, in the deltarhpRS deletion strain only slightly reduced the induction of T3SS genes. Based on these results, we propose that the phosphorylated RhpR represses the induction of T3SS genes and that RhpS reverses phosphorylation of RhpR under the T3SS-inducing conditions. Epistasis analysis indicated that rhpS and rhpR act upstream of hrpR to regulate T3SS genes.
机译:在基本培养基(MM)中与植物或培养物相互作用的过程中,诱导了丁香假单胞菌III型分泌系统(T3SS)。细菌如何感知这些环境以激活T3SS的了解很少。在这里,我们报告鉴定一种新型的两组分系统(TCS)RhpRS,该系统调节丁香假单胞菌T3SS基因的诱导。 rhpR和rhpS基因在操纵子中组织,其中rhpR编码假定的TCS反应调节剂,而rhpS编码假定的双相传感器激酶。转座子插入rhpS会严重降低植物和MM中丁香假单胞菌T3SS基因的诱导,并显着损害宿主植物的致病性和对非宿主植物的超敏反应诱导活性。然而,rhpRS基因座的缺失使T3SS基因的诱导水平与野生型菌株相同,并且渗透到植物中后恢复了致病性。 Rhtar在deltarhpRS缺失菌株中的过表达消除了对T3SS基因的诱导。但是,在deltarhpRS缺失菌株中,RhpR在野生型菌株中的过表达或RhpR(D70A)(RhpR的预期磷酸化位点的突变体)的过表达仅略微降低了T3SS基因的诱导。基于这些结果,我们建议磷酸化的RhpR抑制T3SS基因的诱导,并且RhpS在诱导T3SS的条件下逆转RhpR的磷酸化。上位性分析表明,rhpS和rhpR在hrpR的上游起作用以调节T3SS基因。

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