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      MYB72-dependent coumarin exudation shapes root microbiome assembly to promote plant health

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          Significance

          Plant roots nurture a large diversity of soil microbes via exudation of chemical compounds into the rhizosphere. In turn, beneficial root microbiota promote plant growth and immunity. The root-specific transcription factor MYB72 has emerged as a central regulator in this process. Here, we show that MYB72 regulates the excretion of the coumarin scopoletin, an iron-mobilizing phenolic compound with selective antimicrobial activity that shapes the root-associated microbial community. Selected soil-borne fungal pathogens appeared to be highly sensitive to the antimicrobial activity of scopoletin, while two MYB72-inducing beneficial rhizobacteria were tolerant. Our results suggest that probiotic root-associated microbes that activate the iron-deficiency response during colonization stimulate MYB72-dependent excretion of scopoletin, thereby potentially improving their niche establishment and enhancing plant growth and protection.

          Abstract

          Plant roots nurture a tremendous diversity of microbes via exudation of photosynthetically fixed carbon sources. In turn, probiotic members of the root microbiome promote plant growth and protect the host plant against pathogens and pests. In the Arabidopsis thalianaPseudomonas simiae WCS417 model system the root-specific transcription factor MYB72 and the MYB72-controlled β-glucosidase BGLU42 emerged as important regulators of beneficial rhizobacteria-induced systemic resistance (ISR) and iron-uptake responses. MYB72 regulates the biosynthesis of iron-mobilizing fluorescent phenolic compounds, after which BGLU42 activity is required for their excretion into the rhizosphere. Metabolite fingerprinting revealed the antimicrobial coumarin scopoletin as a dominant metabolite that is produced in the roots and excreted into the rhizosphere in a MYB72- and BGLU42-dependent manner. Shotgun-metagenome sequencing of root-associated microbiota of Col-0, myb72, and the scopoletin biosynthesis mutant f6′h1 showed that scopoletin selectively impacts the assembly of the microbial community in the rhizosphere. We show that scopoletin selectively inhibits the soil-borne fungal pathogens Fusarium oxysporum and Verticillium dahliae, while the growth-promoting and ISR-inducing rhizobacteria P. simiae WCS417 and Pseudomonas capeferrum WCS358 are highly tolerant of the antimicrobial effect of scopoletin. Collectively, our results demonstrate a role for coumarins in microbiome assembly and point to a scenario in which plants and probiotic rhizobacteria join forces to trigger MYB72/BGLU42-dependent scopolin production and scopoletin excretion, resulting in improved niche establishment for the microbial partner and growth and immunity benefits for the host plant.

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          Most cited references55

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          Induced systemic resistance by beneficial microbes.

          Beneficial microbes in the microbiome of plant roots improve plant health. Induced systemic resistance (ISR) emerged as an important mechanism by which selected plant growth-promoting bacteria and fungi in the rhizosphere prime the whole plant body for enhanced defense against a broad range of pathogens and insect herbivores. A wide variety of root-associated mutualists, including Pseudomonas, Bacillus, Trichoderma, and mycorrhiza species sensitize the plant immune system for enhanced defense without directly activating costly defenses. This review focuses on molecular processes at the interface between plant roots and ISR-eliciting mutualists, and on the progress in our understanding of ISR signaling and systemic defense priming. The central role of the root-specific transcription factor MYB72 in the onset of ISR and the role of phytohormones and defense regulatory proteins in the expression of ISR in aboveground plant parts are highlighted. Finally, the ecological function of ISR-inducing microbes in the root microbiome is discussed.
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            Root microbiota drive direct integration of phosphate stress and immunity

            Plants live in biogeochemically diverse soils that harbor extraordinarily diverse microbiota. Plant organs associate intimately with a subset of these microbes; this community’s structure can be altered by soil nutrient content. Plant-associated microbes can compete with the plant and with each other for nutrients; they can also provide traits that increase plant productivity. It is unknown how the plant immune system coordinates microbial recognition with nutritional cues during microbiome assembly. We establish that a genetic network controlling phosphate stress response influences root microbiome community structure, even under non-stress phosphate conditions. We define a molecular mechanism regulating coordination between nutrition and defense in the presence of a synthetic bacterial community. We demonstrate that the master transcriptional regulators of phosphate stress response in Arabidopsis also directly repress defense, consistent with plant prioritization of nutritional stress over defense. Our work will impact efforts to define and deploy useful microbes to enhance plant performance.
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              A ferric-chelate reductase for iron uptake from soils.

              Iron deficiency afflicts more than three billion people worldwide, and plants are the principal source of iron in most diets. Low availability of iron often limits plant growth because iron forms insoluble ferric oxides, leaving only a small, organically complexed fraction in soil solutions. The enzyme ferric-chelate reductase is required for most plants to acquire soluble iron. Here we report the isolation of the FRO2 gene, which is expressed in iron-deficient roots of Arabidopsis. FRO2 belongs to a superfamily of flavocytochromes that transport electrons across membranes. It possesses intramembranous binding sites for haem and cytoplasmic binding sites for nucleotide cofactors that donate and transfer electrons. We show that FRO2 is allelic to the frd1 mutations that impair the activity of ferric-chelate reductase. There is a nonsense mutation within the first exon of FRO2 in frd1-1 and a missense mutation within FRO2 in frd1-3. Introduction of functional FRO2 complements the frd1-1 phenotype in transgenic plants. The isolation of FRO2 has implications for the generation of crops with improved nutritional quality and increased growth in iron-deficient soils.
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                Author and article information

                Journal
                Proc Natl Acad Sci U S A
                Proc. Natl. Acad. Sci. U.S.A
                pnas
                pnas
                PNAS
                Proceedings of the National Academy of Sciences of the United States of America
                National Academy of Sciences
                0027-8424
                1091-6490
                29 May 2018
                23 April 2018
                23 April 2018
                : 115
                : 22
                : E5213-E5222
                Affiliations
                [1] aPlant–Microbe Interactions, Department of Biology, Science4Life, Utrecht University , 3508 TB Utrecht, The Netherlands;
                [2] bDepartment of Plant Biochemistry, Albrecht-von-Haller-Institute for Plant Sciences, University of Göttingen , 37077 Göttingen, Germany;
                [3] cDepartment of Plant Systems Biology, Vlaams Instituut voor Biotechnologie , 9052 Ghent, Belgium;
                [4] dDepartment of Plant Biotechnology and Bioinformatics, Ghent University , 9052 Ghent, Belgium;
                [5] eDepartment of Plant Biochemistry, Göttingen Center for Molecular Biosciences, University of Göttingen , 37077 Göttingen, Germany
                Author notes
                2To whom correspondence should be addressed. Email: c.m.j.pieterse@ 123456uu.nl .

                Edited by Jeffery L. Dangl, University of North Carolina at Chapel Hill, Chapel Hill, NC, and approved April 3, 2018 (received for review December 22, 2017)

                Author contributions: I.A.S., K.Y., K.F., M.C.V.V., R.L.B., P.A.H.M.B., I.F., and C.M.J.P. designed research; I.A.S., K.Y., K.F., and S.V.B. performed research; I.A.S., K.Y., K.F., and R.d.J. analyzed data; and I.A.S. and C.M.J.P. wrote the paper.

                1I.A.S., K.Y., and K.F. contributed equally to this work.

                Author information
                http://orcid.org/0000-0001-7128-597X
                http://orcid.org/0000-0001-5065-8538
                http://orcid.org/0000-0003-2707-8919
                http://orcid.org/0000-0002-5473-4646
                Article
                201722335
                10.1073/pnas.1722335115
                5984513
                29686086
                f3bd780b-12c2-4f8a-b777-8aefa1238eb7
                Copyright © 2018 the Author(s). Published by PNAS.

                This open access article is distributed under Creative Commons Attribution-NonCommercial-NoDerivatives License 4.0 (CC BY-NC-ND).

                History
                Page count
                Pages: 10
                Funding
                Funded by: EC | FP7 | FP7 Ideas: European Research Council (FP7 Ideas) 100011199
                Award ID: 269072
                Funded by: China Scholarship Council (CSC) 501100004543
                Award ID: 201306300051
                Funded by: Fonds Wetenschappelijk Onderzoek (FWO) 501100003130
                Award ID: 12B8116N
                Funded by: Deutsche Forschungsgemeinschaft (DFG) 501100001659
                Award ID: ZUK 45/2010
                Categories
                PNAS Plus
                Biological Sciences
                Plant Biology
                From the Cover
                PNAS Plus

                root metabolome,coumarin,induced systemic resistance,iron-deficiency response,microbiome assembly

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