Natural Products Targeting the Fungal Unfolded Protein Response as an Alternative Crop Protection Strategy

灰葡萄孢菌 杀菌剂 生物 植物对草食的防御 葡萄球菌炎 效应器 生物化学 植物 基因
作者
Thomas H. Charpentier,Guillaume Viault,Anne‐Marie Le Ray,Nelly Bataillé‐Simoneau,Jean-Jacques Hélesbeux,N Blon,Franck Bastide,Muriel Marchi,Sophie Aligon,Antoine Bruguière,Chau-Phi Dinh,Z. Benbelkacem,Jean‐Félix Dallery,Philippe Simoneau,Pascal Richomme,Thomas Guillemette
出处
期刊:Journal of Agricultural and Food Chemistry [American Chemical Society]
卷期号:71 (37): 13706-13716
标识
DOI:10.1021/acs.jafc.3c03602
摘要

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 in vitro cell-based screening assay allowed for the identification of seven potential IRE1 inhibitors with a focus on polyhydroxylated prenylated xanthones. Inhibition of hac1 mRNA splicing, which is mediated by IRE1, was then validated for the most active compound, namely, γ-mangostin 3. 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 Brassica oleracea inoculated with Alternaria brassicicola and Botrytis cinerea.
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