Anna Koprivova, Miroslav Berka, Veronika Berková, Daniela Ristova, Gözde Merve Türksoy, Melina Schwier, Philipp Westhoff, Martin Cerny, Stanislav Kopriva
{"title":"Multilevel Analysis of Response to Plant Growth Promoting and Pathogenic Bacteria in Arabidopsis Roots.","authors":"Anna Koprivova, Miroslav Berka, Veronika Berková, Daniela Ristova, Gözde Merve Türksoy, Melina Schwier, Philipp Westhoff, Martin Cerny, Stanislav Kopriva","doi":"10.1094/MPMI-09-25-0125-R","DOIUrl":null,"url":null,"abstract":"<p><p>A major challenge in plant-microbe interaction research is understanding how plants distinguish between commensal and pathogenic microorganisms. We compared Arabidopsis responses to two contrasting bacterial strains, the plant growth promoting (PGP) <i>Pseudomonas</i> sp. CH267 and the pathogen <i>Burkholderia glumeae</i> PG1, using integrated multi-omics analyses. The pathogen triggered stronger transcriptional reprogramming and proteomic changes in roots than the PGP strain, while both strains also affected numerous leaf proteins indicating systemic responses. Interaction with both strains increased the abundance of sulfur containing metabolites: camalexin, glutathione, and cysteine, in particular under pathogen treatment, which corresponded with elevated total sulfur in the leaves. Root and root exudate metabolomes significantly changed, with amino acids and tricarboxylic acid cycle intermediates accumulating in roots but being diminished in the exudates. Integrative analysis across the omics datasets revealed strong correlations between metabolite levels, protein abundance, and transcript levels, highlighting new links between sulfur metabolism, defense pathways, and mineral nutrition, including iron. Together, these findings uncover the complex multi-layered nature of Arabidopsis responses to commensal and pathogenic bacteria and identify new connections across different regulatory levels.</p>","PeriodicalId":19009,"journal":{"name":"Molecular Plant-microbe Interactions","volume":" ","pages":""},"PeriodicalIF":3.4000,"publicationDate":"2025-09-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Molecular Plant-microbe Interactions","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1094/MPMI-09-25-0125-R","RegionNum":3,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"BIOCHEMISTRY & MOLECULAR BIOLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
A major challenge in plant-microbe interaction research is understanding how plants distinguish between commensal and pathogenic microorganisms. We compared Arabidopsis responses to two contrasting bacterial strains, the plant growth promoting (PGP) Pseudomonas sp. CH267 and the pathogen Burkholderia glumeae PG1, using integrated multi-omics analyses. The pathogen triggered stronger transcriptional reprogramming and proteomic changes in roots than the PGP strain, while both strains also affected numerous leaf proteins indicating systemic responses. Interaction with both strains increased the abundance of sulfur containing metabolites: camalexin, glutathione, and cysteine, in particular under pathogen treatment, which corresponded with elevated total sulfur in the leaves. Root and root exudate metabolomes significantly changed, with amino acids and tricarboxylic acid cycle intermediates accumulating in roots but being diminished in the exudates. Integrative analysis across the omics datasets revealed strong correlations between metabolite levels, protein abundance, and transcript levels, highlighting new links between sulfur metabolism, defense pathways, and mineral nutrition, including iron. Together, these findings uncover the complex multi-layered nature of Arabidopsis responses to commensal and pathogenic bacteria and identify new connections across different regulatory levels.
期刊介绍:
Molecular Plant-Microbe Interactions® (MPMI) publishes fundamental and advanced applied research on the genetics, genomics, molecular biology, biochemistry, and biophysics of pathological, symbiotic, and associative interactions of microbes, insects, nematodes, or parasitic plants with plants.