Zhang Jun, Liu Siwen, Yang Wenlong, Xie Yanling, Shao Chuange, Zhang Zhi-Ren, Li Chunyu, Yao Xiaoqiang
Department of Cardiology, The First Affiliated Hospital of Harbin Medical University, NHC Key Laboratory of Cell Transplantation, Key Laboratories of Education Ministry for Myocardial Ischemia Mechanism and Treatment, Harbin, China.
Institute of Fruit Tree Research, Guangdong Academy of Agricultural Sciences, Key Laboratory of South Subtropical Fruit Biology and Genetic Research Utilization, Ministry of Agriculture and Rural Affairs, Guangdong Provincial Key Laboratory of Tropical and Subtropical Fruit Tree Research, Guangzhou, China.
PLoS Pathog. 2025 Apr 9;21(4):e1013066. doi: 10.1371/journal.ppat.1013066. eCollection 2025 Apr.
Our previous studies have demonstrated that the phytotoxin fusaric acid (FSA), secreted by several Fusarium species, acts as a key factor in the development of plant diseases; however, the underlying mechanism remains unknown. In this study, we showed that the symptoms of Fusarium wilt in banana seedlings closely resembled those observed in plants grown under potassium (K+) deficiency conditions. Mechanistically, we found that FSA induces the accumulation of intracellular reactive oxygen species (ROS), which in turn inhibits banana K+ in banana roots. This inhibition occurs via S-glutathionylation of the banana AKT1 (MaAKT1) channel, leading to reduced K+ influx and reduced K+ content in banana roots. Through mutagenesis, electrophysiological studies, immunofluorescence staining, and co-immunoprecipitation experiment, we demonstrated that mutation of Cys202, a highly conserved site in the transmembrane segment 5 of MaAKT1, diminished the biochemical interaction of glutathione (GSH) and the channel induced by FSA, and alleviated Fusarium oxysporum f. sp. cubense tropical race 4 (Foc TR4) and FSA-induced yellowing symptom. The evolutionarily conserved function of this site for S-glutathionylation was also observed in Arabidopsis AKT1 (AtAKT1) channel, as mutation of its homologue site in AtAKT1 similarly reduced the GSH-AtAKT1 interaction under FSA stress. Collectively, our results suggest that FSA contributes to disease progression by decreasing K+ absorption through S-glutathionylation of MaAKT1 channel at the conserved Cys202 residue. These findings uncover a previously unrecognized role of FSA in regulating K+ homeostasis in bananas, and provide a foundation for future strategies to treat Fusarium wilt and increase banana production by targeting the conserved S-glutathionylation site in MaAKT1 channel.
我们之前的研究表明,几种镰刀菌属物种分泌的植物毒素镰刀菌酸(FSA)是植物病害发展的关键因素;然而,其潜在机制仍不清楚。在本研究中,我们发现香蕉幼苗枯萎病的症状与在钾(K+)缺乏条件下生长的植物所观察到的症状非常相似。从机制上讲,我们发现FSA诱导细胞内活性氧(ROS)的积累,进而抑制香蕉根中的K+。这种抑制是通过香蕉AKT1(MaAKT1)通道的S-谷胱甘肽化发生的,导致K+流入减少和香蕉根中K+含量降低。通过诱变、电生理研究、免疫荧光染色和免疫共沉淀实验,我们证明了MaAKT1跨膜段5中高度保守的位点Cys202的突变减少了谷胱甘肽(GSH)与FSA诱导的通道之间的生化相互作用,并减轻了尖孢镰刀菌古巴专化型热带4号小种(Foc TR4)和FSA诱导的黄化症状。在拟南芥AKT1(AtAKT1)通道中也观察到该位点S-谷胱甘肽化的进化保守功能,因为AtAKT1中其同源位点的突变同样降低了FSA胁迫下GSH与AtAKT1的相互作用。总的来说,我们的结果表明,FSA通过在保守的Cys202残基处对MaAKT1通道进行S-谷胱甘肽化来减少K+吸收,从而促进疾病进展。这些发现揭示了FSA在调节香蕉K+稳态方面以前未被认识的作用,并为未来通过靶向MaAKT1通道中保守的S-谷胱甘肽化位点来治疗枯萎病和提高香蕉产量的策略提供了基础。