{"title":"Antagonistic manipulation of ER-protein quality control between biotrophic pathogenic fungi and host induced defense","authors":"Theoni Margaritopoulou , Konstantinos Kotsaridis , Martina Samiotaki , Spyridon Nastos , Marinos Maratos , Ieronymos Zoidakis , Despoina Tsiriva , Stergios Pispas , Emilia Markellou","doi":"10.1016/j.stress.2024.100693","DOIUrl":null,"url":null,"abstract":"<div><div>The interaction of plants with pathogens during infection is a multifaceted process involving various molecules deriving from both partners. A current goal in combating pathogen virulence is to induce plant resistance using environmentally friendly compounds. Here, we show that chitosan-based nanoparticles loaded with the defense hormone salicylic acid, can efficiently activate defense responses and reactive oxygen species (ROS) production and <em>PATHOGENESIS RELATED-1</em> (<em>PR1</em>) expression in <em>Arabidopsis thaliana</em> leaves, and reduce conidial germination of the biotrophic pathogenic fungus <em>Podosphaera xanthii</em>. Transcriptomic and proteomic analyses identified immune response-related upregulated transcripts and proteins after nanoparticle application, highlighting the Leucine Rich Repeat (LRR)-, Systemic Acquired Resistance (SAR)-, and glutathione-related protein groups. Examination of <em>P. xanthii</em> during infection at control conditions, identified ribosomal, hydrolase-related, putative secreted and effector proteins, while nanoparticle application significantly downregulated their expression. An in-depth investigation of the highly expressed proteins in <em>P. xanthii</em> and Arabidopsis revealed the involvement of components of endoplasmic reticulum protein quality control (ERQC) in the pathogen-host interaction. The RPS27A effector protein was identified in fungal virulence, while endoplasmic reticulum (ER) protein processing- and glycosyltransferase-related proteins were implicated in plant's induced defense response following nanoparticle application. Overall, these findings demonstrate that the ERQC is dynamically manipulated by both the pathogen for efficient virulence and by elicitors for plant induced defense.</div></div>","PeriodicalId":34736,"journal":{"name":"Plant Stress","volume":"14 ","pages":"Article 100693"},"PeriodicalIF":6.8000,"publicationDate":"2024-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Plant Stress","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2667064X24003464","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"PLANT SCIENCES","Score":null,"Total":0}
引用次数: 0
Abstract
The interaction of plants with pathogens during infection is a multifaceted process involving various molecules deriving from both partners. A current goal in combating pathogen virulence is to induce plant resistance using environmentally friendly compounds. Here, we show that chitosan-based nanoparticles loaded with the defense hormone salicylic acid, can efficiently activate defense responses and reactive oxygen species (ROS) production and PATHOGENESIS RELATED-1 (PR1) expression in Arabidopsis thaliana leaves, and reduce conidial germination of the biotrophic pathogenic fungus Podosphaera xanthii. Transcriptomic and proteomic analyses identified immune response-related upregulated transcripts and proteins after nanoparticle application, highlighting the Leucine Rich Repeat (LRR)-, Systemic Acquired Resistance (SAR)-, and glutathione-related protein groups. Examination of P. xanthii during infection at control conditions, identified ribosomal, hydrolase-related, putative secreted and effector proteins, while nanoparticle application significantly downregulated their expression. An in-depth investigation of the highly expressed proteins in P. xanthii and Arabidopsis revealed the involvement of components of endoplasmic reticulum protein quality control (ERQC) in the pathogen-host interaction. The RPS27A effector protein was identified in fungal virulence, while endoplasmic reticulum (ER) protein processing- and glycosyltransferase-related proteins were implicated in plant's induced defense response following nanoparticle application. Overall, these findings demonstrate that the ERQC is dynamically manipulated by both the pathogen for efficient virulence and by elicitors for plant induced defense.
期刊介绍:
The journal Plant Stress deals with plant (or other photoautotrophs, such as algae, cyanobacteria and lichens) responses to abiotic and biotic stress factors that can result in limited growth and productivity. Such responses can be analyzed and described at a physiological, biochemical and molecular level. Experimental approaches/technologies aiming to improve growth and productivity with a potential for downstream validation under stress conditions will also be considered. Both fundamental and applied research manuscripts are welcome, provided that clear mechanistic hypotheses are made and descriptive approaches are avoided. In addition, high-quality review articles will also be considered, provided they follow a critical approach and stimulate thought for future research avenues.
Plant Stress welcomes high-quality manuscripts related (but not limited) to interactions between plants and:
Lack of water (drought) and excess (flooding),
Salinity stress,
Elevated temperature and/or low temperature (chilling and freezing),
Hypoxia and/or anoxia,
Mineral nutrient excess and/or deficiency,
Heavy metals and/or metalloids,
Plant priming (chemical, biological, physiological, nanomaterial, biostimulant) approaches for improved stress protection,
Viral, phytoplasma, bacterial and fungal plant-pathogen interactions.
The journal welcomes basic and applied research articles, as well as review articles and short communications. All submitted manuscripts will be subject to a thorough peer-reviewing process.