E3-Ubiquitin Ligase SgATL31 Promotes Anthracnose Resistance in Stylosanthes by Modulating ROS Burst and Antioxidant Defence: A Proteomic and Functional Study.

IF 4.9 1区 农林科学 Q1 PLANT SCIENCES
Liyun Yang, Yunpiao Long, Mengze Gao, Shizi Zhang, Jing Gao, Lijuan Luo, Lingyan Jiang
{"title":"E3-Ubiquitin Ligase SgATL31 Promotes Anthracnose Resistance in Stylosanthes by Modulating ROS Burst and Antioxidant Defence: A Proteomic and Functional Study.","authors":"Liyun Yang, Yunpiao Long, Mengze Gao, Shizi Zhang, Jing Gao, Lijuan Luo, Lingyan Jiang","doi":"10.1111/mpp.70122","DOIUrl":null,"url":null,"abstract":"<p><p>Stylosanthes spp. (stylo) is an important leguminous forage cultivated in tropical areas. Anthracnose caused by Colletotrichum gloeosporioides is a destructive disease that limits the yield of stylo. Therefore, improving the resistance of stylo is crucial to control stylo anthracnose. In this study, the resistance evaluation of 40 Chinese stylo accessions was performed, including the main cultivar Stylosanthes guianensis 'Reyan No. 2' (RY2) as a susceptible control. Twelve stylo accessions were rated as highly resistant, with 2001-84 showing the strongest resistance. Compared to RY2, 2001-84 exhibited significantly milder disease symptoms, slower fungal colonisation, and higher pathogen-induced antioxidant enzyme activities. Integrated phosphoproteomics and plasma membrane (PM) enriched proteomics of both RY2 and 2001-84 revealed that pathogen-responsive proteins were predominantly associated with kinase signalling, transport processes, and oxidoreductase activity. A PM-localised E3 ubiquitin ligase, SgATL31, was identified as increasing in response to pathogen in both proteomic analyses. Functional characterisation demonstrated that SgATL31 overexpression in Arabidopsis enhanced resistance to C. gloeosporioides, promoted chitin-induced reactive oxygen species (ROS) production in both Arabidopsis and stylo protoplasts, and increased antioxidant enzyme activities following pathogen infection. Furthermore, the expression levels of SgATL31 were induced by pathogen infection in all 40 stylo accessions and accumulated to higher levels in resistant accessions. Overall, our findings not only identify 2001-84 as a valuable genetic resource for anthracnose resistance but also establish SgATL31 as a regulator of plant immunity against anthracnose, potentially through modulation of ROS and antioxidant pathways, providing important insights for improving disease resistance in stylo.</p>","PeriodicalId":18763,"journal":{"name":"Molecular plant pathology","volume":"26 7","pages":"e70122"},"PeriodicalIF":4.9000,"publicationDate":"2025-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12234378/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Molecular plant pathology","FirstCategoryId":"97","ListUrlMain":"https://doi.org/10.1111/mpp.70122","RegionNum":1,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"PLANT SCIENCES","Score":null,"Total":0}
引用次数: 0

Abstract

Stylosanthes spp. (stylo) is an important leguminous forage cultivated in tropical areas. Anthracnose caused by Colletotrichum gloeosporioides is a destructive disease that limits the yield of stylo. Therefore, improving the resistance of stylo is crucial to control stylo anthracnose. In this study, the resistance evaluation of 40 Chinese stylo accessions was performed, including the main cultivar Stylosanthes guianensis 'Reyan No. 2' (RY2) as a susceptible control. Twelve stylo accessions were rated as highly resistant, with 2001-84 showing the strongest resistance. Compared to RY2, 2001-84 exhibited significantly milder disease symptoms, slower fungal colonisation, and higher pathogen-induced antioxidant enzyme activities. Integrated phosphoproteomics and plasma membrane (PM) enriched proteomics of both RY2 and 2001-84 revealed that pathogen-responsive proteins were predominantly associated with kinase signalling, transport processes, and oxidoreductase activity. A PM-localised E3 ubiquitin ligase, SgATL31, was identified as increasing in response to pathogen in both proteomic analyses. Functional characterisation demonstrated that SgATL31 overexpression in Arabidopsis enhanced resistance to C. gloeosporioides, promoted chitin-induced reactive oxygen species (ROS) production in both Arabidopsis and stylo protoplasts, and increased antioxidant enzyme activities following pathogen infection. Furthermore, the expression levels of SgATL31 were induced by pathogen infection in all 40 stylo accessions and accumulated to higher levels in resistant accessions. Overall, our findings not only identify 2001-84 as a valuable genetic resource for anthracnose resistance but also establish SgATL31 as a regulator of plant immunity against anthracnose, potentially through modulation of ROS and antioxidant pathways, providing important insights for improving disease resistance in stylo.

e3 -泛素连接酶sgart31通过调节ROS爆发和抗氧化防御促进柱花草的炭疽病抗性:蛋白质组学和功能研究
柱花草属(Stylosanthes spp.)是热带地区重要的豆科牧草。炭疽菌引起的炭疽病是一种限制花柱产量的破坏性病害。因此,提高花柱的抗性是控制花柱炭疽病的关键。以主栽柱花草“热炎2号”(RY2)为敏感对照,对40份中国柱花草材料进行了抗性评价。12个品种被评为高抗性品种,其中2001 ~ 84抗性最强。与RY2相比,2001-84表现出明显较轻的疾病症状,较慢的真菌定植,较高的病原体诱导的抗氧化酶活性。综合磷酸化蛋白质组学和质膜(PM)富集的蛋白质组学显示,RY2和2001-84的病原体应答蛋白主要与激酶信号传导、运输过程和氧化还原酶活性相关。在两种蛋白质组学分析中,发现pm定位的E3泛素连接酶SgATL31在对病原体的反应中增加。功能表征表明,SgATL31在拟南芥中的过表达增强了对gloeosporioides的抗性,促进了几丁质诱导的活性氧(ROS)在拟南芥和柱头原生质体中的产生,并增加了病原体感染后的抗氧化酶活性。此外,在所有40个花柱材料中,SgATL31的表达水平均受病原菌感染的诱导,并在抗性材料中积累较高的表达水平。总的来说,我们的研究结果不仅确定了2001-84是有价值的炭疽病抗性遗传资源,而且还确定了SgATL31是植物对炭疽病免疫的调节剂,可能通过调节ROS和抗氧化途径,为提高花柱的抗病能力提供了重要的见解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
Molecular plant pathology
Molecular plant pathology 生物-植物科学
CiteScore
9.40
自引率
4.10%
发文量
120
审稿时长
6-12 weeks
期刊介绍: Molecular Plant Pathology is now an open access journal. Authors pay an article processing charge to publish in the journal and all articles will be freely available to anyone. BSPP members will be granted a 20% discount on article charges. The Editorial focus and policy of the journal has not be changed and the editorial team will continue to apply the same rigorous standards of peer review and acceptance criteria.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信