Engineered elicitin protein enhances Phytophthora resistance in plants by dual immune induction and pathogen inhibition.

IF 6.4
Zhengpeng Li, Yong Pei, Hao Zhou, Hui Wang, Yining Guo, Zhiyuan Yin, Daolong Dou
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Abstract

Phytophthora pathogens are devastating agricultural threats that cannot synthesize sterols and must scavenge them from host plants. This study exploits their sterol auxotrophy by engineering a dual-function elicitin protein, SOJ5V84F, for enhanced disease control. The V84F mutation in the sterol-binding pocket of the Phytophthora sojae elicitin SOJ5 abolishes sterol binding but retains interaction with the pathogen's sterol-sensing receptor kinase SSRK1. SOJ5V84F acts as a dominant-negative inhibitor: it competitively disrupts SSRK1-mediated sterol signaling (calcium influx, MAPK activation) and significantly inhibits P. sojae growth in an SSRK1-dependent manner. Crucially, SOJ5V84F retains its ability as a microbe-associated molecular pattern to robustly elicit reactive oxygen species burst in soybean, pepper, tomato, and potato plants. Consequently, pre-treatment with SOJ5V84F provided superior protection compared to wild-type SOJ5 against P. sojae in soybean, and against Phytophthora capsici and Phytophthora infestans in pepper, tomato, and potato under greenhouse conditions. This work demonstrates that engineered SOJ5V84F combines direct pathogen inhibition with host immune activation, establishing a novel dual-mechanism strategy for protein-based biocontrol against sterol-auxotrophic oomycetes.

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工程设计的卵磷脂蛋白通过双重免疫诱导和病原菌抑制增强植物对疫霉菌的抗性。
疫霉病原体是一种毁灭性的农业威胁,它不能合成甾醇,必须从寄主植物中清除它们。本研究通过设计一种双重功能的卵磷脂蛋白SOJ5V84F,利用它们的甾醇营养不良来增强疾病控制。SOJ5的甾醇结合口袋中的V84F突变消除了甾醇结合,但保留了与病原体的甾醇敏感受体激酶SSRK1的相互作用。SOJ5V84F作为显性阴性抑制剂:它竞争性地破坏ssrk1介导的甾醇信号(钙内流、MAPK激活),并以依赖ssrk1的方式显著抑制大豆卟卟菌的生长。最重要的是,SOJ5V84F保留了其作为微生物相关分子模式的能力,可以在大豆、辣椒、番茄和马铃薯植物中引发活性氧的爆发。结果表明,与野生型SOJ5相比,SOJ5V84F在温室条件下对大豆疫霉、辣椒疫霉、番茄疫霉和马铃薯疫霉具有更强的保护作用。本研究表明,工程SOJ5V84F结合了直接病原抑制和宿主免疫激活,建立了一种新的基于蛋白质的生物防治甾醇营养不良卵菌的双机制策略。
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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CiteScore
3.10
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