Liu Zhi-Yang, Zou Li-Fang, Xue Xiao-Bo, Cai Lu-Lu, Ma Wen-Xiu, Xiong Li, Ji Zhi-Yuan, Chen Gong-You
School of Agriculture and Biology/State Key Laboratory of Microbial Metabolism, Shanghai Jiao Tong University, Shanghai, China.
School of Agriculture and Biology/State Key Laboratory of Microbial Metabolism, Shanghai Jiao Tong University, Shanghai, China
Appl Environ Microbiol. 2014 Jul;80(13):3908-19. doi: 10.1128/AEM.00308-14. Epub 2014 Apr 18.
The type III secretion system (T3SS), encoded by hrp (hypersensitive response and pathogenicity) genes in Gram-negative phytopathogenic bacteria, delivers repertoires of T3SS effectors (T3SEs) into plant cells to trigger the hypersensitive response (HR) in nonhost or resistant-host plants and promote pathogenicity in susceptible plants. The expression of hrp genes in Xanthomonas is regulated by two key regulatory proteins, HrpG and HrpX. However, the interactions between hrp gene products in directing T3SE secretion are largely unknown. Here we demonstrated that HrcT of X. oryzae pv. oryzicola functions as a T3SS component and positively regulates the expression of hrpX. Transcription of hrcT occurs via two distinct promoters; one (T1) is with the hrpB operon and the second (T3) within hrpB7 Via either promoter T1 or T3, the defect in Hrp phenotype by hrcT deletion was corrected in the presence of hrcT only from Xanthomonas species but not from other phytopathogenic bacteria. An N-terminally truncated HrcT was able to bind the hrpX promoter and activate the expression of hrpX, supporting that HrcT is a positive regulator of hrpX. A revised model showing the regulatory interactions between HrcT, HrpX, and HrpG is proposed.
III型分泌系统(T3SS)由革兰氏阴性植物病原菌中的hrp(过敏反应和致病性)基因编码,将T3SS效应子(T3SEs)转运到植物细胞中,以触发非寄主或抗性寄主植物中的过敏反应(HR),并促进感病植物中的致病性。黄单胞菌中hrp基因的表达受两个关键调节蛋白HrpG和HrpX调控。然而,hrp基因产物在指导T3SE分泌过程中的相互作用在很大程度上尚不清楚。在此,我们证明了水稻白叶枯病菌的HrcT作为T3SS的一个组分,并正向调控hrpX的表达。hrcT的转录通过两个不同的启动子进行;一个(T1)与hrpB操纵子在一起,另一个(T3)在hrpB7内。通过启动子T1或T3,只有来自黄单胞菌属的hrcT才能纠正因hrcT缺失导致的Hrp表型缺陷,而来自其他植物病原菌的hrcT则不能。一个N端截短的HrcT能够结合hrpX启动子并激活hrpX的表达,这支持了HrcT是hrpX的正向调节因子这一观点。我们提出了一个显示HrcT、HrpX和HrpG之间调节相互作用的修正模型。