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      Root microbiota drive direct integration of phosphate stress and immunity

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          Abstract

          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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          Most cited references41

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          Soil microorganisms mediating phosphorus availability update on microbial phosphorus.

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            PHOSPHATE ACQUISITION.

            Phosphorus is one of the major plant nutrients that is least available in the soil. Consequently, plants have developed numerous morphological, physiological, biochemical, and molecular adaptations to acquire phosphate (Pi). Enhanced ability to acquire Pi and altered gene expression are the hallmarks of plant adaptation to Pi deficiency. The intricate mechanisms involved in maintaining Pi homeostasis reflect the complexity of Pi acquisition and translocation in plants. Recent discoveries of multiple Pi transporters have opened up opportunities to study the molecular basis of Pi acquisition by plants. An increasing number of genes are now known to be activated under Pi starvation. Some of these genes may be involved in Pi acquisition, transfer, and signal transduction during Pi stress. This review provides an overview of plant adaptations leading to enhanced Pi acquisition, with special emphasis on recent developments in the molecular biology of Pi acquisition.
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              Microbiota and Host Nutrition across Plant and Animal Kingdoms.

              Plants and animals each have evolved specialized organs dedicated to nutrient acquisition, and these harbor specific bacterial communities that extend the host's metabolic repertoire. Similar forces driving microbial community establishment in the gut and plant roots include diet/soil-type, host genotype, and immune system as well as microbe-microbe interactions. Here we show that there is no overlap of abundant bacterial taxa between the microbiotas of the mammalian gut and plant roots, whereas taxa overlap does exist between fish gut and plant root communities. A comparison of root and gut microbiota composition in multiple host species belonging to the same evolutionary lineage reveals host phylogenetic signals in both eukaryotic kingdoms. The reasons underlying striking differences in microbiota composition in independently evolved, yet functionally related, organs in plants and animals remain unclear but might include differences in start inoculum and niche-specific factors such as oxygen levels, temperature, pH, and organic carbon availability.
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                Author and article information

                Journal
                0410462
                6011
                Nature
                Nature
                Nature
                0028-0836
                1476-4687
                7 February 2017
                15 March 2017
                23 March 2017
                15 September 2017
                : 543
                : 7646
                : 513-518
                Affiliations
                [1 ]Department of Biology, University of North Carolina, Chapel Hill, NC 27599-3280, USA
                [2 ]Howard Hughes Medical Institute, University of North Carolina, Chapel Hill, NC 27599-3280, USA
                [3 ]Curriculum in Bioinformatics and Computational Biology, University of North Carolina, Chapel Hill, NC 27599-3280, USA
                [4 ]Department of Plant Molecular Genetics, Centro Nacional de Biotecnología, CNB-CSIC, Darwin 3, 28049 Madrid, Spain
                [5 ]Department of Genetics, University of North Carolina, Chapel Hill, NC, USA
                [6 ]Lineberger Comprehensive Cancer Center, University of North Carolina, Chapel Hill, NC 27599-3280, USA
                [7 ]Carolina Center for Genome Sciences, University of North Carolina, Chapel Hill, NC 27599-3280, USA
                [8 ]Curriculum in Genetics and Molecular Biology, University of North Carolina, Chapel Hill, NC 27599-3280, USA
                [9 ]Department of Microbiology and Immunology, University of North Carolina, Chapel Hill, NC 27599-3280, USA
                Author notes
                Correspondence and requests for materials should be addressed to J.L.D. ( dangl@ 123456email.unc.edu )
                [*]

                Indicates co-first author

                Current addresses:

                NB – NewLeaf Symbiotics, St. Louis, MO 63132 USA

                LdL -- Department of Plant and Soil Sciences, University of Kentucky, Lexington, KY 40546 USA.

                Article
                HHMIMS846966
                10.1038/nature21417
                5364063
                28297714
                b9849677-171b-4001-a775-ae49335ff8f8

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