Liu Yuhan, Li Xiao, He Qiguang, Zuo Minghao, Guo Yinjie, Liu Lijuan, Yin Jinyao, He Lijuan, Li Xiaoli, Shan Jiaxin, Liu Wenbo, Lin Chunhua, Miao Weiguo
Sanya Nanfan Research Institute, Key Laboratory of Green Prevention and Control of Tropical Plant Diseases and Pest (Ministry of Education)/School of Tropical Agriculture and Forestry, Hainan University, Haikou, China.
School of Life and Health Science, Hainan University, Haikou, China.
mBio. 2025 Apr 9;16(4):e0395924. doi: 10.1128/mbio.03959-24. Epub 2025 Mar 17.
Powdery mildew is a global threat to crops and economically valuable plants. Salicylic acid (SA) signaling plays a significant role in plant resistance to biotrophic parasites; however, the mechanisms behind how powdery mildew fungi circumvent SA-mediated resistance remain unclear. Many phytopathogenic microbes deliver effectors into the host to sustain infection. In this study, we showed that the rubber tree powdery mildew fungus inhibits host SA biosynthesis by employing two effector proteins, EqCmu and EqPdt. These effector proteins can be delivered into plant cells to hydrolyze chorismate, the main precursor of SA, through their enzymatic activities. Notably, EqCmu and EqPdt can interact with each other, providing mutual protection against protein degradation mediated by the plant ubiquitin-proteasome system. This interaction enhances their activities in the hydrolysis of chorismate. Our study reveals a new pathogenic strategy by which two powdery mildew effector proteins cooperate to evade recognition by dampening the host immune system.
Powdery mildew fungi may develop diverse strategies to disturb salicylic acid (SA) signaling in plants, which plays an important role in activating immunity, and little is known about these strategies. Our results suggest that the effector protein EqCmu can be translocated into host cells and inhibit host SA levels during the infection stage; however, it is targeted by the plant ubiquitin-proteasome system (UPS) and ubiquitinated, which induces EqCmu degradation. To evade the UPS, EqCmu interacts with EqPdt, another effector protein, to prevent that ubiquitination. EqPdt also inhibits host SA biosynthesis through its prephenate dehydratase activity. Taken together, these two powdery mildew effector proteins cause a synergistic effect in disturbing host SA signaling. Our study also suggests that enhancing SA signaling is required for boosting immunity against powdery mildew fungus.
白粉病对农作物和具有经济价值的植物构成全球威胁。水杨酸(SA)信号传导在植物对活体营养型寄生菌的抗性中起重要作用;然而,白粉病真菌规避SA介导的抗性背后的机制仍不清楚。许多植物病原微生物向宿主输送效应蛋白以维持感染。在本研究中,我们表明橡胶树白粉病真菌通过利用两种效应蛋白EqCmu和EqPdt抑制宿主SA生物合成。这些效应蛋白可通过其酶活性被输送到植物细胞中以水解SA的主要前体分支酸。值得注意的是,EqCmu和EqPdt可以相互作用,提供针对植物泛素 - 蛋白酶体系统介导的蛋白质降解的相互保护。这种相互作用增强了它们在分支酸水解中的活性。我们的研究揭示了一种新的致病策略,即两种白粉病效应蛋白通过抑制宿主免疫系统来协同逃避识别。
白粉病真菌可能会制定多种策略来干扰植物中的水杨酸(SA)信号传导,SA信号传导在激活免疫中起重要作用,而对这些策略知之甚少。我们的结果表明,效应蛋白EqCmu在感染阶段可转移到宿主细胞中并抑制宿主SA水平;然而,它被植物泛素 - 蛋白酶体系统(UPS)靶向并泛素化,这会诱导EqCmu降解。为了逃避UPS,EqCmu与另一种效应蛋白EqPdt相互作用以防止泛素化。EqPdt还通过其苯丙酮酸脱水酶活性抑制宿主SA生物合成。综上所述,这两种白粉病效应蛋白在干扰宿主SA信号传导方面产生协同作用。我们的研究还表明,增强SA信号传导对于增强对白粉病真菌的免疫力是必要的。