灰葡萄孢菌
生物
RNA干扰
RNA沉默
植物抗病性
基因
细胞生物学
基因沉默
病菌
核糖核酸
病原真菌
免疫系统
细胞
转基因作物
茉莉酸
微生物学
接种
小RNA
基因表达
水杨酸
杀菌剂
细胞壁
基因敲除
三型分泌系统
植物病害
真菌
效应器
内吞作用
核糖核酸酶P
植物
反义RNA
菌丝体
花瓣
作者
Yaping Yin,Rui Wang,JuMei Hou,Yuhang Fu,Yingtong Chen,Lin Wang,Aatika Sikandar,Yuejiao Li,Tong Liu
标识
DOI:10.1016/j.xplc.2025.101615
摘要
Gray mold, caused by the fungal pathogen Botrytis cinerea, is a major threat to global agriculture. Conventional pesticide control exacerbates environmental pollution and the risk of resistance development. Although RNA interference (RNAi) holds potential for disease control, its application is limited by instability of RNA and ambiguous targeting. This study demonstrates that tomato microRNA393 (miR393) can cross-kingdom into B. cinerea and reduce its pathogenicity. Using RT-qPCR, GUS staining, and 5' RLM-RACE, we confirmed that miR393 specifically targets nucleotides 1777-1778 of the BcFKS1 gene in B. cinerea, thereby inhibiting its expression and disrupting the fungal cell wall. To protect against miRNA degradation, we constructed a nanocarrier delivery system based on Star Polycation (SPc) was constructed. This nanomaterial extended the degradation half-life of miR393's by 6-fold under RNase A and RNase III conditions (up to 2 h) and increased delivery efficiency by 35%-65%. SPc-loaded miR393 enhanced tomato immunity by activating the jasmonic acid/salicylic acid (JA/SA) pathways, suppressing auxin receptor genes, and inducing PR1 protein accumulation (6.8-fold). Furthermore, inoculation assays showed that dsmiR393 reduced gray mold lesion areas by 67% in tomato, 88% in strawberry, and 41% in grape. This study elucidates the dual mechanism of miR393 to control gray mold, including cross-kingdom regulation for pathogenic fungi and modulation of plant immunity. This work provides a new strategy for disease prevention and control in sustainable agriculture.
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