{"title":"代谢组学和双重蛋白质组学发现了芦笋嫩枝受镰刀菌感染后主要通路受影响的对比模式","authors":"Katja Witzel, Roxana Djalali Farahani-Kofoet, Stefanie Döll, Viktoria Lindemann, Benedikt Cramer, Hans-Ulrich Humpf, Rita Zrenner","doi":"10.1007/s11104-024-07069-9","DOIUrl":null,"url":null,"abstract":"<h3 data-test=\"abstract-sub-heading\">Aims</h3><p>Infections with soil-borne pathogens have considerable detrimental effects on asparagus (<i>Asparagus officinalis</i>) growth and production, notably caused by the Fusarium species <i>F. oxysporum</i> f.sp. <i>asparagi</i>, <i>F. proliferatum,</i> and <i>F. redolens</i>. To get insight into the systemic effects of fungal infection on plant physiology to identify candidate resistance traits, we investigated this interaction using a multi omics approach.</p><h3 data-test=\"abstract-sub-heading\">Methods</h3><p>Asparagus plants were inoculated with one of the three Fusarium species. After 8 weeks, basal stem parts were harvested and subjected to metabolome and proteome analysis as well as detection of fungal DNA.</p><h3 data-test=\"abstract-sub-heading\">Results</h3><p>Upon infection, the pathogen spreads systemically from the root to the shoot and, consequently, fungal DNA and mycotoxins were detected in the basal part of the plant stem. Metabolite data revealed that the main pathway affected by Fusarium infections was “Fatty acids”, specifically the superclasses “Glycerophospholipids”, “Glycerolipids” and “Sphingolipids” being lower abundant upon infection. Another main pathway identified in the analysis was “Shikimates and Phenylpropanoids” with compounds assigned to these classes being mainly enriched upon infection. Proteome data revealed an induction of pathogen-defense proteins upon infection in asparagus, while proteins involved in vesicle trafficking and lipid metabolism were lower abundant.</p><h3 data-test=\"abstract-sub-heading\">Conclusions</h3><p>This indicates that not only lipid-based signaling processes are distorted by Fusarium, but also fundamental processes such as vesicle formation, membrane integrity and cell wall organization. <i>In planta</i> proteome analysis of <i>F. oxysporum</i> led to the identification of 1,488 fungal proteins, including proteins involved in metabolic and cellular processes as well as putative virulence factors.</p>","PeriodicalId":20223,"journal":{"name":"Plant and Soil","volume":"145 1","pages":""},"PeriodicalIF":3.9000,"publicationDate":"2024-11-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Metabolomics and dual proteomics identify contrasting patterns of major pathways affected in asparagus shoot upon Fusarium infection\",\"authors\":\"Katja Witzel, Roxana Djalali Farahani-Kofoet, Stefanie Döll, Viktoria Lindemann, Benedikt Cramer, Hans-Ulrich Humpf, Rita Zrenner\",\"doi\":\"10.1007/s11104-024-07069-9\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<h3 data-test=\\\"abstract-sub-heading\\\">Aims</h3><p>Infections with soil-borne pathogens have considerable detrimental effects on asparagus (<i>Asparagus officinalis</i>) growth and production, notably caused by the Fusarium species <i>F. oxysporum</i> f.sp. <i>asparagi</i>, <i>F. proliferatum,</i> and <i>F. redolens</i>. To get insight into the systemic effects of fungal infection on plant physiology to identify candidate resistance traits, we investigated this interaction using a multi omics approach.</p><h3 data-test=\\\"abstract-sub-heading\\\">Methods</h3><p>Asparagus plants were inoculated with one of the three Fusarium species. After 8 weeks, basal stem parts were harvested and subjected to metabolome and proteome analysis as well as detection of fungal DNA.</p><h3 data-test=\\\"abstract-sub-heading\\\">Results</h3><p>Upon infection, the pathogen spreads systemically from the root to the shoot and, consequently, fungal DNA and mycotoxins were detected in the basal part of the plant stem. Metabolite data revealed that the main pathway affected by Fusarium infections was “Fatty acids”, specifically the superclasses “Glycerophospholipids”, “Glycerolipids” and “Sphingolipids” being lower abundant upon infection. Another main pathway identified in the analysis was “Shikimates and Phenylpropanoids” with compounds assigned to these classes being mainly enriched upon infection. Proteome data revealed an induction of pathogen-defense proteins upon infection in asparagus, while proteins involved in vesicle trafficking and lipid metabolism were lower abundant.</p><h3 data-test=\\\"abstract-sub-heading\\\">Conclusions</h3><p>This indicates that not only lipid-based signaling processes are distorted by Fusarium, but also fundamental processes such as vesicle formation, membrane integrity and cell wall organization. <i>In planta</i> proteome analysis of <i>F. oxysporum</i> led to the identification of 1,488 fungal proteins, including proteins involved in metabolic and cellular processes as well as putative virulence factors.</p>\",\"PeriodicalId\":20223,\"journal\":{\"name\":\"Plant and Soil\",\"volume\":\"145 1\",\"pages\":\"\"},\"PeriodicalIF\":3.9000,\"publicationDate\":\"2024-11-19\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Plant and Soil\",\"FirstCategoryId\":\"97\",\"ListUrlMain\":\"https://doi.org/10.1007/s11104-024-07069-9\",\"RegionNum\":2,\"RegionCategory\":\"农林科学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"AGRONOMY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Plant and Soil","FirstCategoryId":"97","ListUrlMain":"https://doi.org/10.1007/s11104-024-07069-9","RegionNum":2,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"AGRONOMY","Score":null,"Total":0}
引用次数: 0
摘要
目的土传病原体感染对芦笋(Asparagus officinalis)的生长和产量有相当大的不利影响,主要是由镰刀菌 F. oxysporum f.sp. asparagi、F. proliferatum 和 F. redolens 引起的。为了深入了解真菌感染对植物生理的系统性影响,以确定候选抗性性状,我们采用多omics方法研究了这种相互作用。8周后,收获茎基部,进行代谢组和蛋白质组分析,并检测真菌DNA。结果感染后,病原体从根部向嫩枝系统性扩散,因此在植物茎基部检测到真菌DNA和霉菌毒素。代谢物数据显示,镰刀菌感染影响的主要途径是 "脂肪酸",特别是 "甘油磷脂"、"甘油脂类 "和 "鞘氨醇脂类 "等超类在感染后含量较低。分析中发现的另一个主要途径是 "莽草酸盐和苯丙酸盐",这些类别的化合物在感染后主要富集。蛋白质组数据显示,芦笋感染后病原体防御蛋白被诱导,而参与囊泡运输和脂质代谢的蛋白质含量较低。通过对 F. oxysporum 的植物蛋白质组分析,鉴定了 1,488 种真菌蛋白质,其中包括参与代谢和细胞过程的蛋白质以及假定的毒力因子。
Metabolomics and dual proteomics identify contrasting patterns of major pathways affected in asparagus shoot upon Fusarium infection
Aims
Infections with soil-borne pathogens have considerable detrimental effects on asparagus (Asparagus officinalis) growth and production, notably caused by the Fusarium species F. oxysporum f.sp. asparagi, F. proliferatum, and F. redolens. To get insight into the systemic effects of fungal infection on plant physiology to identify candidate resistance traits, we investigated this interaction using a multi omics approach.
Methods
Asparagus plants were inoculated with one of the three Fusarium species. After 8 weeks, basal stem parts were harvested and subjected to metabolome and proteome analysis as well as detection of fungal DNA.
Results
Upon infection, the pathogen spreads systemically from the root to the shoot and, consequently, fungal DNA and mycotoxins were detected in the basal part of the plant stem. Metabolite data revealed that the main pathway affected by Fusarium infections was “Fatty acids”, specifically the superclasses “Glycerophospholipids”, “Glycerolipids” and “Sphingolipids” being lower abundant upon infection. Another main pathway identified in the analysis was “Shikimates and Phenylpropanoids” with compounds assigned to these classes being mainly enriched upon infection. Proteome data revealed an induction of pathogen-defense proteins upon infection in asparagus, while proteins involved in vesicle trafficking and lipid metabolism were lower abundant.
Conclusions
This indicates that not only lipid-based signaling processes are distorted by Fusarium, but also fundamental processes such as vesicle formation, membrane integrity and cell wall organization. In planta proteome analysis of F. oxysporum led to the identification of 1,488 fungal proteins, including proteins involved in metabolic and cellular processes as well as putative virulence factors.
期刊介绍:
Plant and Soil publishes original papers and review articles exploring the interface of plant biology and soil sciences, and that enhance our mechanistic understanding of plant-soil interactions. We focus on the interface of plant biology and soil sciences, and seek those manuscripts with a strong mechanistic component which develop and test hypotheses aimed at understanding underlying mechanisms of plant-soil interactions. Manuscripts can include both fundamental and applied aspects of mineral nutrition, plant water relations, symbiotic and pathogenic plant-microbe interactions, root anatomy and morphology, soil biology, ecology, agrochemistry and agrophysics, as long as they are hypothesis-driven and enhance our mechanistic understanding. Articles including a major molecular or modelling component also fall within the scope of the journal. All contributions appear in the English language, with consistent spelling, using either American or British English.