Université Angers, SONAS, SFR QUASAV, F-49000 Angers, France.
Université Angers, Institut Agro, INRAE, IRHS, SFR QUASAV, 49070 Beaucouzé, France.
J Agric Food Chem. 2023 Sep 20;71(37):13706-13716. doi: 10.1021/acs.jafc.3c03602. Epub 2023 Sep 11.
Discovering new solutions for crop protection is a major challenge for the next decades as a result of the ecotoxicological impact of classical fungicides, the emergence of fungicide resistances, and the consequence of climate change on pathogen distribution. Previous work on fungal mutants deficient in the unfolded protein response (UPR) supported that targeting this pathway is a promising plant disease control strategy. In particular, we showed that the UPR is involved in fungal virulence by altering cell protection against host defense compounds, such as phytoalexins and phytoanticipins. In this study, we evaluated natural products targeting fungal IRE1 protein (UPR effector) and consequently increasing fungal susceptibility to plant defenses. Developing an cell-based screening assay allowed for the identification of seven potential IRE1 inhibitors with a focus on polyhydroxylated prenylated xanthones. Inhibition of 1 mRNA splicing, which is mediated by IRE1, was then validated for the most active compound, namely, γ-mangostin . To study the mode of interaction between the binding site of IRE1 and active xanthones, molecular docking was also undertaken, revealing similar and novel interactions between the known inhibitor and the binding site. Eventually, active xanthones applied at subtoxic doses induced a significant reduction in necrosis size for leaves of inoculated with and .
由于经典杀菌剂的生态毒性影响、杀菌剂抗性的出现以及气候变化对病原体分布的影响,在未来几十年里,寻找新的作物保护解决方案是一个主要挑战。先前关于真菌突变体中 unfolded protein response(UPR)缺陷的研究支持靶向该途径是一种有前途的植物病害控制策略。特别是,我们表明 UPR 通过改变细胞对植物防御化合物(如植物抗毒素和植物防御素)的保护作用来参与真菌的毒力。在这项研究中,我们评估了靶向真菌 IRE1 蛋白(UPR 效应物)的天然产物,从而提高真菌对植物防御的敏感性。开发基于细胞的筛选测定法可鉴定出七种潜在的 IRE1 抑制剂,重点是多羟基化的prenylated xanthones。然后针对最有效的化合物γ-mangostin验证了对 1 mRNA 剪接的抑制作用,该剪接是由 IRE1 介导的。为了研究 IRE1 结合位点与活性黄烷酮之间的相互作用模式,还进行了分子对接,揭示了已知抑制剂和结合位点之间的相似和新的相互作用。最终,在亚毒性剂量下应用活性黄烷酮可显著减少接种 和 的叶片坏死面积。