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      Soil domestication by rice cultivation results in plant-soil feedback through shifts in soil microbiota

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          Abstract

          Background

          Soils are a key component of agricultural productivity, and soil microbiota determine the availability of many essential plant nutrients. Agricultural domestication of soils, that is, the conversion of previously uncultivated soils to a cultivated state, is frequently accompanied by intensive monoculture, especially in the developing world. However, there is limited understanding of how continuous cultivation alters the structure of prokaryotic soil microbiota after soil domestication, including to what extent crop plants impact soil microbiota composition, and how changes in microbiota composition arising from cultivation affect crop performance.

          Results

          We show here that continuous monoculture (> 8 growing seasons) of the major food crop rice under flooded conditions is associated with a pronounced shift in soil bacterial and archaeal microbiota structure towards a more consistent composition, thereby domesticating microbiota of previously uncultivated sites. Aside from the potential effects of agricultural cultivation practices, we provide evidence that rice plants themselves are important drivers of the domestication process, acting through selective enrichment of specific taxa, including methanogenic archaea, in their rhizosphere that differ from those of native plants growing in the same environment. Furthermore, we find that microbiota from soils domesticated by rice cultivation contribute to plant-soil feedback, by imparting a negative effect on rice seedling vigor.

          Conclusions

          Soil domestication through continuous monoculture cultivation of rice results in compositional changes in the soil microbiota, which are in part driven by the rice plants. The consequences include a negative impact on plant performance and increases in greenhouse gas emitting microbes.

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          Most cited references33

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          Controlling the False Discovery Rate: A Practical and Powerful Approach to Multiple Testing

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            Root exudate metabolites drive plant-soil feedbacks on growth and defense by shaping the rhizosphere microbiota

            By changing soil properties, plants can modify their growth environment. Although the soil microbiota is known to play a key role in the resulting plant-soil feedbacks, the proximal mechanisms underlying this phenomenon remain unknown. We found that benzoxazinoids, a class of defensive secondary metabolites that are released by roots of cereals such as wheat and maize, alter root-associated fungal and bacterial communities, decrease plant growth, increase jasmonate signaling and plant defenses, and suppress herbivore performance in the next plant generation. Complementation experiments demonstrate that the benzoxazinoid breakdown product 6-methoxy-benzoxazolin-2-one (MBOA), which accumulates in the soil during the conditioning phase, is both sufficient and necessary to trigger the observed phenotypic changes. Sterilization, fungal and bacterial profiling and complementation experiments reveal that MBOA acts indirectly by altering root-associated microbiota. Our results reveal a mechanism by which plants determine the composition of rhizosphere microbiota, plant performance and plant-herbivore interactions of the next generation.
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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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                Author and article information

                Contributors
                (530) 754 9677 , sundar@ucdavis.edu
                Journal
                Genome Biol
                Genome Biol
                Genome Biology
                BioMed Central (London )
                1474-7596
                1474-760X
                24 October 2019
                24 October 2019
                2019
                : 20
                : 221
                Affiliations
                [1 ]ISNI 0000 0004 1936 9684, GRID grid.27860.3b, Department of Plant Biology, , University of California, Davis, ; Life Sciences Addition, 1 Shields Ave., Davis, CA 95616 USA
                [2 ]ISNI 0000000121548364, GRID grid.55460.32, Present Address: Integrative Biology Department, , University of Texas, ; Austin 2415 Speedway, Austin, TX 78712 USA
                [3 ]ISNI 0000 0001 2169 5989, GRID grid.252381.f, Department of Agriculture, , Arkansas State University, ; 2105 Aggie Rd., Jonesboro, AR 72401 USA
                [4 ]ISNI 0000 0004 1936 9684, GRID grid.27860.3b, Department of Plant Sciences, , University of California, Davis, ; 1 Shields Ave., Davis, CA 95616 USA
                Author information
                http://orcid.org/0000-0002-4670-0630
                Article
                1825
                10.1186/s13059-019-1825-x
                6814045
                31651356
                b1376f04-329f-45ea-9187-0ba2317d7564
                © The Author(s). 2019

                Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License ( http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver ( http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

                History
                : 7 January 2019
                : 17 September 2019
                Funding
                Funded by: FundRef http://dx.doi.org/10.13039/100000001, National Science Foundation;
                Award ID: IOS 1444974
                Award Recipient :
                Funded by: FundRef http://dx.doi.org/10.13039/100000199, U.S. Department of Agriculture;
                Award ID: CA-D-XXX-6973-H
                Award Recipient :
                Funded by: University of California Institute for Mexico
                Funded by: FundRef http://dx.doi.org/10.13039/501100007350, Consejo Nacional de Ciencia y Tecnología;
                Funded by: Secretaría de Educación Pública (México)
                Funded by: National Science Foundation (US) Graduate Research Fellowship Program
                Categories
                Research
                Custom metadata
                © The Author(s) 2019

                Genetics
                Genetics

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