Plant salicylic acid signaling is inhibited by a cooperative strategy of two powdery mildew effectors.

IF 5.1 1区 生物学 Q1 MICROBIOLOGY
mBio Pub Date : 2025-04-09 Epub Date: 2025-03-17 DOI:10.1128/mbio.03959-24
Yuhan Liu, Xiao Li, Qiguang He, Minghao Zuo, Yinjie Guo, Lijuan Liu, Jinyao Yin, Lijuan He, Xiaoli Li, Jiaxin Shan, Wenbo Liu, Chunhua Lin, Weiguo Miao
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引用次数: 0

Abstract

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 Erysiphe quercicola 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.

Importance: 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 Erysiphe quercicola 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 E. quercicola 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.

两种白粉病效应因子的合作策略抑制了植物水杨酸信号传递。
白粉病对农作物和有经济价值的植物构成全球性威胁。水杨酸(SA)信号在植物对生物营养性寄生虫的抗性中起重要作用然而,白粉病真菌如何绕过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传递效应物以维持感染。在这项研究中,我们发现橡胶树白粉病真菌Erysiphe quercicola通过两个效应蛋白EqCmu和EqPdt抑制宿主SA的生物合成。这些效应蛋白可以通过其酶活性进入植物细胞,水解SA的主要前体choris酸。值得注意的是,EqCmu和EqPdt可以相互作用,对植物泛素-蛋白酶体系统介导的蛋白质降解提供相互保护。这种相互作用增强了它们水解氯酸盐的活性。我们的研究揭示了一种新的致病策略,通过两种白粉病效应蛋白合作,通过抑制宿主免疫系统来逃避识别。重要性:白粉病真菌可能通过多种途径干扰植物体内水杨酸(SA)信号,而水杨酸在激活免疫中起着重要作用,目前对这些途径知之甚少。结果表明,槲寄生效应蛋白EqCmu可以在感染阶段转运到宿主细胞中,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,从而诱导EqCmu降解。为了避开UPS, EqCmu与另一种槲寄生效应蛋白EqPdt相互作用,以防止泛素化。EqPdt还通过其预苯酸脱水酶活性抑制宿主SA的生物合成。综上所述,这两种白粉病效应蛋白在干扰宿主SA信号方面产生协同效应。我们的研究还表明,增强SA信号是增强对白粉病真菌免疫的必要条件。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
mBio
mBio MICROBIOLOGY-
CiteScore
10.50
自引率
3.10%
发文量
762
审稿时长
1 months
期刊介绍: mBio® is ASM''s first broad-scope, online-only, open access journal. mBio offers streamlined review and publication of the best research in microbiology and allied fields.
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