生物
毒力
烟草
基因
突变体
微生物学
细胞壁
细胞生物学
过敏反应
遗传学
植物对草食的防御
真菌
程序性细胞死亡
真菌蛋白
细枝
寄主(生物学)
液泡
细胞
基因组
基因敲除
基因表达调控
分泌蛋白
菌丝
基因表达
蛋白质结构域
富含亮氨酸重复
防御机制
植物
作者
Pei-Shan Wu,Zhe-Zheng Zeng,Yuan-Ling Xiao,Wen-Kai Wei,Min-Zheng Cai,Weixiao Yin,Guido Schnabel,Chaoxi Luo
出处
期刊:Plant Disease
[American Phytopathological Society]
日期:2026-01-03
标识
DOI:10.1094/pdis-10-25-2125-re
摘要
Monilinia fructicola, the most widely distributed species among the Monilinia genus globally, causes blossom blight, twig canker, and fruit rot on Rosaceae fruits. Despite previous studies, limitations still exist regarding virulence of M. fructicola. In this study, we identified a gene significantly upregulated during the early stages of infection. Bioinformatic analysis revealed that this gene encoded a protein containing the HAD_SAK_1 domain (abbreviated as HS1), and we named it MfHS1. Knockout and complemented transformants were generated and evaluated for environmental fitness. Results revealed that MfHS1 was involved in the regulation of osmotic stress and cell wall integrity. Additionally, microscopic observations showed that MfHS1 participated in the differentiation process of hyphal tips. Virulence assays indicated that the knockout transformant ΔMfHS1 exhibited significantly reduced virulence. Considering that MfHS1 is predicted as a non-classical secreted protein, it was transiently expressed in Nicotiana benthamiana leaves, and the induced plant cell death was observed, indicating that MfHS1 might trigger plant defense responses, e.g., programmed cell death, and supply nutrients to necrotic pathogens, thus aiding host infection. This study offers a new perspective for further understanding the pathogenic mechanisms of M. fructicola and developing control strategies.
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