Hu Renjian, Zhao Fu, Asif Muhammad, Gu Jiaoyan, Liang Shuang, Fan Rong, Long Youhua, Wang Yong, Tian Fenghua, Zhao Zhibo
Department of Plant Pathology, College of Agriculture, Guizhou University, Guiyang, China.
Research Center for Engineering Technology of Kiwifruit, Institute of Crop Protection, College of Agriculture, Guizhou University, Guiyang, China.
Appl Environ Microbiol. 2025 Jul 23;91(7):e0049425. doi: 10.1128/aem.00494-25. Epub 2025 Jun 10.
Kiwifruit bacterial canker, caused by pv. (Psa), is an emerging global concern in kiwifruit production. Successful Psa infection in kiwifruit relies on the type III secretion system (T3SS), which is governed by the HrpR/S-HrpL regulatory pathway. However, the mechanisms by which certain transcriptional factors regulate this pathway remain poorly understood. In this study, we identified the TetR/AcrR family transcription factors () and (hybrid histidine kinase; ) in the pv. (biovar 3) strain S26 using transposon libraries and a DNA pull-down strategy. Both the mutant strains and exhibited significantly reduced pathogenicity in kiwifruit leaf discs and a diminished ability to induce , , and expression and showed a reduced hypersensitive response in . Moreover, transcriptomic studies showed considerable overlap in downregulated genes between the and two-component system (TCS) mutant, highlighting the intertwined regulatory roles of both genes. This overlap suggests a tightly coordinated regulatory system, where serves as the response regulator of the hybrid histidine kinase to regulate T3SS and virulence. The electrophoretic mobility shift assays and luciferase-based promoter activity detection further revealed that TetR1 positively regulates the T3SS by directly binding to the promoter regions of / and . This study identifies the gene as the first TetR-family transcription factor directly linking the hybrid TCS to HrpR/S-HrpL-mediated T3SS regulatory pathway activation in Psa for regulation.
This study uncovers the critical roles of two regulatory genes, () and (), in pv. (Psa) virulence via the type III secretion system (T3SS). Through genetic knockouts, complementation, and transcriptomic analyses, we establish , a TetR/AcrR family transcription factor, as a pivotal activator of T3SS-related genes essential for Psa's virulence in kiwifruit. We further demonstrate that , a hybrid histidine kinase two-component system regulator, acts upstream by enhancing expression, forming a hierarchical network that drives the T3SS cascade during infection. serves as the response regulator of the hybrid histidine kinase RetS to regulate T3SS and virulence in Psa. These insights reveal how Psa orchestrates virulence to colonize kiwifruit tissues, advancing our understanding of bacterial plant interactions. Moreover, this regulatory framework offers promising targets for developing precise strategies to combat bacterial canker, mitigating its devastating economic toll on global kiwifruit production.
由丁香假单胞菌猕猴桃致病变种(Psa)引起的猕猴桃细菌性溃疡病是猕猴桃生产中一个新出现的全球关注问题。Psa在猕猴桃中的成功感染依赖于III型分泌系统(T3SS),该系统由HrpR/S - HrpL调控途径控制。然而,某些转录因子调控该途径的机制仍知之甚少。在本研究中,我们利用转座子文库和DNA下拉策略,在丁香假单胞菌猕猴桃致病变种(生物变种3)菌株S26中鉴定出TetR/AcrR家族转录因子TetR1和RetS(杂合组氨酸激酶)。突变菌株ΔtetR1和Δrets在猕猴桃叶片圆片中均表现出致病性显著降低,诱导hrpA、hrpL和hpaR表达的能力减弱,并且在烟草中显示过敏反应降低。此外,转录组学研究表明,ΔtetR1和双组分系统(TCS)Δrets突变体之间下调基因有相当大的重叠,突出了这两个基因相互交织的调控作用。这种重叠表明存在一个紧密协调的调控系统,其中RetS作为杂合组氨酸激酶TetR1的响应调节因子来调控T3SS和毒力。电泳迁移率变动分析和基于荧光素酶的启动子活性检测进一步表明,TetR1通过直接结合hrpA/hrpL和hpaR的启动子区域来正向调控T3SS。本研究确定tetR1基因是第一个将杂合TCS RetS与Psa中HrpR/S - HrpL介导的T3SS调控途径激活直接联系起来进行调控的TetR家族转录因子。
本研究揭示了两个调控基因tetR1和rets在丁香假单胞菌猕猴桃致病变种(Psa)通过III型分泌系统(T3SS)发挥毒力方面的关键作用。通过基因敲除、互补和转录组分析,我们确定TetR1,一个TetR/AcrR家族转录因子,是T3SS相关基因的关键激活因子,对Psa在猕猴桃中的毒力至关重要。我们进一步证明,RetS,一个杂合组氨酸激酶双组分系统调节因子,通过增强tetR1表达在其上游起作用,形成一个层次网络,在感染期间驱动T3SS级联反应。RetS作为杂合组氨酸激酶RetS的响应调节因子来调控Psa中的T3SS和毒力。这些见解揭示了Psa如何协调毒力以定殖猕猴桃组织,增进了我们对细菌与植物相互作用的理解。此外,这个调控框架为制定精确策略对抗细菌性溃疡病提供了有前景的靶点,减轻其对全球猕猴桃生产造成的毁灭性经济损失。