Volatile 2-Phenylethanol and β-Cyclocitral Trigger Defense-Related Transcriptional and Metabolic Changes in Grapevine Leaves Against Downy Mildew.

IF 5.4 2区 生物学 Q1 PLANT SCIENCES
Sara Avesani, Valentina Lazazzara, Matteo Buti, Michael Oberhuber, Peter Robatscher, Michele Perazzolli
{"title":"Volatile 2-Phenylethanol and β-Cyclocitral Trigger Defense-Related Transcriptional and Metabolic Changes in Grapevine Leaves Against Downy Mildew.","authors":"Sara Avesani, Valentina Lazazzara, Matteo Buti, Michael Oberhuber, Peter Robatscher, Michele Perazzolli","doi":"10.1111/ppl.70412","DOIUrl":null,"url":null,"abstract":"<p><p>Volatile organic compounds (VOCs) are produced by grapevine leaves in response to phytopathogen infection. In particular, 2-phenylethanol and β-cyclocitral were triggered by Plasmopara viticola inoculation in downy mildew-resistant genotypes, but no information is available on their involvement in plant resistance induction. This study aimed to clarify transcriptional and metabolic changes associated with VOC-induced resistance activated by 2-phenylethanol and β-cyclocitral treatments against P. viticola. Both VOCs decreased downy mildew severity on grapevine leaf disks by complex reprogramming of the grapevine transcriptome at 1 and 6 days post inoculation. RNA-Seq analysis showed the modulation of transcripts related to defense (chitinases, defense-related proteins, and pathogenesis-related proteins), oxidative stress (glutathione S-transferases and peroxidases), secondary metabolism (nitrilases, stilbene synthases, and terpene synthases), signal transduction (e.g., kinases, receptor kinases, and calmodulins), and transcription (bHLH, ERF, MYB, NAC, and WRKY transcription factors) in leaf disks treated with 2-phenylethanol and β-cyclocitral. VOC treatments also caused changes in the leaf metabolome, and pathway analysis of metabolic features with significant changes in abundance in 2-phenylethanol- and β-cyclocitral-treated leaf disks revealed the reprogramming of amino acid, carbohydrate, flavonoid, phenylpropanoid, and terpenoid metabolism. In particular, compounds with increases in abundance belonged to putative carbohydrates, carboxylic acids, and phenylpropanoids in 2-phenylethanol-treated samples, or carboxylic acids and terpenoids in β-cyclocitral-treated samples, including molecules possibly associated with plant defense against pathogens, such as 3-dehydroquinic acid, 4-thujanol, aromadendrin, camphor, p-coumaryl alcohol, and perillaldehyde. Correlation analysis between transcriptomic and metabolomic data indicated that 2-phenylethanol and β-cyclocitral act as resistance inducers against downy mildew in grapevine.</p>","PeriodicalId":20164,"journal":{"name":"Physiologia plantarum","volume":"177 4","pages":"e70412"},"PeriodicalIF":5.4000,"publicationDate":"2025-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Physiologia plantarum","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1111/ppl.70412","RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"PLANT SCIENCES","Score":null,"Total":0}
引用次数: 0

Abstract

Volatile organic compounds (VOCs) are produced by grapevine leaves in response to phytopathogen infection. In particular, 2-phenylethanol and β-cyclocitral were triggered by Plasmopara viticola inoculation in downy mildew-resistant genotypes, but no information is available on their involvement in plant resistance induction. This study aimed to clarify transcriptional and metabolic changes associated with VOC-induced resistance activated by 2-phenylethanol and β-cyclocitral treatments against P. viticola. Both VOCs decreased downy mildew severity on grapevine leaf disks by complex reprogramming of the grapevine transcriptome at 1 and 6 days post inoculation. RNA-Seq analysis showed the modulation of transcripts related to defense (chitinases, defense-related proteins, and pathogenesis-related proteins), oxidative stress (glutathione S-transferases and peroxidases), secondary metabolism (nitrilases, stilbene synthases, and terpene synthases), signal transduction (e.g., kinases, receptor kinases, and calmodulins), and transcription (bHLH, ERF, MYB, NAC, and WRKY transcription factors) in leaf disks treated with 2-phenylethanol and β-cyclocitral. VOC treatments also caused changes in the leaf metabolome, and pathway analysis of metabolic features with significant changes in abundance in 2-phenylethanol- and β-cyclocitral-treated leaf disks revealed the reprogramming of amino acid, carbohydrate, flavonoid, phenylpropanoid, and terpenoid metabolism. In particular, compounds with increases in abundance belonged to putative carbohydrates, carboxylic acids, and phenylpropanoids in 2-phenylethanol-treated samples, or carboxylic acids and terpenoids in β-cyclocitral-treated samples, including molecules possibly associated with plant defense against pathogens, such as 3-dehydroquinic acid, 4-thujanol, aromadendrin, camphor, p-coumaryl alcohol, and perillaldehyde. Correlation analysis between transcriptomic and metabolomic data indicated that 2-phenylethanol and β-cyclocitral act as resistance inducers against downy mildew in grapevine.

挥发性2-苯乙醇和β-环柠檬醛引发葡萄叶片抗霜霉病相关的转录和代谢变化。
葡萄叶片对植物病原菌感染产生挥发性有机化合物(VOCs)。特别是,2-苯乙醇和β-环柠檬醛在抗霜霉病基因型中被葡萄浆原菌接种引发,但没有关于它们参与植物抗性诱导的信息。本研究旨在阐明2-苯基乙醇和β-环柠檬醛处理激活的挥发性有机化合物(voc)诱导的抗葡萄假单胞菌抗性的转录和代谢变化。两种挥发性有机化合物通过在接种后1天和6天对葡萄转录组进行复杂的重编程,降低了葡萄叶片霜霉病的严重程度。RNA-Seq分析显示,在2-苯乙醇和β-环戊二醛处理的叶片中,与防御相关的转录物(几丁质酶、防御相关蛋白和致病相关蛋白)、氧化应激(谷胱甘肽s-转移酶和过氧化物酶)、次级代谢(腈酶、二苯乙烯合成酶和萜烯合成酶)、信号转导(如激酶、受体激酶和钙调素)和转录(bHLH、ERF、MYB、NAC和WRKY转录因子)相关的转录物被调节。VOC处理也引起了叶片代谢组的变化,代谢特征的途径分析显示,2-苯乙醇和β-环柠檬醇处理的叶片代谢特征丰度发生了显著变化,表明氨基酸、碳水化合物、类黄酮、苯丙素和萜类代谢发生了重编程。特别是,丰度增加的化合物在2-苯乙醇处理的样品中属于假定的碳水化合物、羧酸和苯丙素,或在β-环柠檬酸处理的样品中属于羧酸和萜类,包括可能与植物防御病原体有关的分子,如3-脱氢醌酸、4-土豆醇、芳香腺嘌呤、樟脑、对香豆醇和紫苏醛。转录组学和代谢组学的相关分析表明,2-苯乙醇和β-环柠檬醛是葡萄霜霉病的抗性诱导剂。
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
Physiologia plantarum
Physiologia plantarum 生物-植物科学
CiteScore
11.00
自引率
3.10%
发文量
224
审稿时长
3.9 months
期刊介绍: Physiologia Plantarum is an international journal committed to publishing the best full-length original research papers that advance our understanding of primary mechanisms of plant development, growth and productivity as well as plant interactions with the biotic and abiotic environment. All organisational levels of experimental plant biology – from molecular and cell biology, biochemistry and biophysics to ecophysiology and global change biology – fall within the scope of the journal. The content is distributed between 5 main subject areas supervised by Subject Editors specialised in the respective domain: (1) biochemistry and metabolism, (2) ecophysiology, stress and adaptation, (3) uptake, transport and assimilation, (4) development, growth and differentiation, (5) photobiology and photosynthesis.
×
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