10 results on '"Mary Madera"'
Search Results
2. Fungal community assembly in drought-stressed sorghum shows stochasticity, selection, and universal ecological dynamics
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Cheng Gao, Liliam Montoya, Ling Xu, Mary Madera, Joy Hollingsworth, Elizabeth Purdom, Vasanth Singan, John Vogel, Robert B. Hutmacher, Jeffery A. Dahlberg, Devin Coleman-Derr, Peggy G. Lemaux, and John W. Taylor
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Science - Abstract
Fungal community assembly on crop plants is thought to be driven by deterministic selection exerted by the host. Here Gao et al. use a sorghum system to show that stochastic forces act on fungal community assembly in leaves and roots early in host development and when sorghum is drought stressed.
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- 2020
- Full Text
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3. Cell Wall Compositions of Sorghum bicolor Leaves and Roots Remain Relatively Constant Under Drought Conditions
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Tess Scavuzzo-Duggan, Nelle Varoquaux, Mary Madera, John P. Vogel, Jeffery Dahlberg, Robert Hutmacher, Michael Belcher, Jasmine Ortega, Devin Coleman-Derr, Peggy Lemaux, Elizabeth Purdom, and Henrik V. Scheller
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Sorghum bicolor ,drought ,cell wall ,biomass conversion and expansion factor (BCEF) ,pre-flowering ,post-flowering ,Plant culture ,SB1-1110 - Abstract
Renewable fuels are needed to replace fossil fuels in the immediate future. Lignocellulosic bioenergy crops provide a renewable alternative that sequesters atmospheric carbon. To prevent displacement of food crops, it would be advantageous to grow biofuel crops on marginal lands. These lands will likely face more frequent and extreme drought conditions than conventional agricultural land, so it is crucial to see how proposed bioenergy crops fare under these conditions and how that may affect lignocellulosic biomass composition and saccharification properties. We found that while drought impacts the plant cell wall of Sorghum bicolor differently according to tissue and timing of drought induction, drought-induced cell wall compositional modifications are relatively minor and produce no negative effect on biomass conversion. This contrasts with the cell wall-related transcriptome, which had a varied range of highly variable genes (HVGs) within four cell wall-related GO categories, depending on the tissues surveyed and time of drought induction. Further, many HVGs had expression changes in which putative impacts were not seen in the physical cell wall or which were in opposition to their putative impacts. Interestingly, most pre-flowering drought-induced cell wall changes occurred in the leaf, with matrix and lignin compositional changes that did not persist after recovery from drought. Most measurable physical post-flowering cell wall changes occurred in the root, affecting mainly polysaccharide composition and cross-linking. This study couples transcriptomics to cell wall chemical analyses of a C4 grass experiencing progressive and differing drought stresses in the field. As such, we can analyze the cell wall-specific response to agriculturally relevant drought stresses on the transcriptomic level and see whether those changes translate to compositional or biomass conversion differences. Our results bolster the conclusion that drought stress does not substantially affect the cell wall composition of specific aerial and subterranean biomass nor impede enzymatic hydrolysis of leaf biomass, a positive result for biorefinery processes. Coupled with previously reported results on the root microbiome and rhizosphere and whole transcriptome analyses of this study, we can formulate and test hypotheses on individual gene candidates’ function in mediating drought stress in the grass cell wall, as demonstrated in sorghum.
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- 2021
- Full Text
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4. Fungal community assembly in drought-stressed sorghum shows stochasticity, selection, and universal ecological dynamics
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Ling Xu, Elizabeth Purdom, Peggy G. Lemaux, Cheng Gao, John P. Vogel, Joy Hollingsworth, Jeffery A. Dahlberg, Devin Coleman-Derr, Mary Madera, John W. Taylor, Robert B. Hutmacher, Vasanth R. Singan, and Liliam Montoya
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0106 biological sciences ,0301 basic medicine ,Science ,Biodiversity ,General Physics and Astronomy ,010603 evolutionary biology ,01 natural sciences ,General Biochemistry, Genetics and Molecular Biology ,Article ,Microbial ecology ,03 medical and health sciences ,Ecosystem ,lcsh:Science ,Fungal ecology ,Selection (genetic algorithm) ,Soil Microbiology ,Sorghum ,Multidisciplinary ,biology ,Host (biology) ,Ecology ,fungi ,Fungi ,food and beverages ,General Chemistry ,biology.organism_classification ,Droughts ,030104 developmental biology ,Biological dispersal ,lcsh:Q ,Microbiome ,Soil microbiology ,Mycobiome - Abstract
Community assembly of crop-associated fungi is thought to be strongly influenced by deterministic selection exerted by the plant host, rather than stochastic processes. Here we use a simple, sorghum system with abundant sampling to show that stochastic forces (drift or stochastic dispersal) act on fungal community assembly in leaves and roots early in host development and when sorghum is drought stressed, conditions when mycobiomes are small. Unexpectedly, we find no signal for stochasticity when drought stress is relieved, likely due to renewed selection by the host. In our experimental system, the host compartment exerts the strongest effects on mycobiome assembly, followed by the timing of plant development and lastly by plant genotype. Using a dissimilarity-overlap approach, we find a universality in the forces of community assembly of the mycobiomes of the different sorghum compartments and in functional guilds of fungi., Fungal community assembly on crop plants is thought to be driven by deterministic selection exerted by the host. Here Gao et al. use a sorghum system to show that stochastic forces act on fungal community assembly in leaves and roots early in host development and when sorghum is drought stressed.
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- 2020
5. Transcriptomic analysis of field-droughted sorghum from seedling to maturity reveals biotic and metabolic responses
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Joy Hollingsworth, John P. Vogel, Robert B. Hutmacher, Vasanth R. Singan, Axel Visel, Grady Pierroz, Benjamin J. Cole, Mary Madera, John W. Taylor, Devin Coleman-Derr, Christer Jansson, Christopher R. Baker, Jeffery A. Dahlberg, Ronan C. O'Malley, Julie A. Sievert, Stephanie DeGraaf, Peggy G. Lemaux, Krishna K. Niyogi, Matthew J. Blow, Elizabeth Purdom, Tim L. Jeffers, Ling Xu, Yuko Yoshinaga, Maria J. Harrison, Cheng Gao, Judith A Owiti, Dhruv Patel, Nelle Varoquaux, Translational Innovation in Medicine and Complexity / Recherche Translationnelle et Innovation en Médecine et Complexité - UMR 5525 (TIMC ), VetAgro Sup - Institut national d'enseignement supérieur et de recherche en alimentation, santé animale, sciences agronomiques et de l'environnement (VAS)-Centre National de la Recherche Scientifique (CNRS)-Université Grenoble Alpes (UGA)-Institut polytechnique de Grenoble - Grenoble Institute of Technology (Grenoble INP ), Université Grenoble Alpes (UGA), Génomique et Évolution des Microorganismes (TIMC-IMAG-GEM ), Techniques de l'Ingénierie Médicale et de la Complexité - Informatique, Mathématiques et Applications Grenoble - UMR 5525 (TIMC-IMAG), and Université Grenoble Alpes (UGA)-VetAgro Sup - Institut national d'enseignement supérieur et de recherche en alimentation, santé animale, sciences agronomiques et de l'environnement (VAS)-Centre National de la Recherche Scientifique (CNRS)-Université Grenoble Alpes (UGA)-Institut polytechnique de Grenoble - Grenoble Institute of Technology (Grenoble INP )
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0106 biological sciences ,[SDV]Life Sciences [q-bio] ,Drought tolerance ,Plant Biology ,arbuscular mycorrhizal fungi ,drought ,Photosynthesis ,7. Clean energy ,01 natural sciences ,Crop ,03 medical and health sciences ,S. bicolor ,Symbiosis ,parasitic diseases ,RNA-Seq ,ComputingMilieux_MISCELLANEOUS ,030304 developmental biology ,2. Zero hunger ,0303 health sciences ,Multidisciplinary ,biology ,fungi ,food and beverages ,Plant physiology ,Biological Sciences ,15. Life on land ,biology.organism_classification ,Sorghum ,PNAS Plus ,Agronomy ,Seedling ,Sweet sorghum ,010606 plant biology & botany - Abstract
Significance Understanding the molecular response of plants to drought is critical to efforts to improve agricultural yields under increasingly frequent droughts. We grew 2 cultivars of the naturally drought-tolerant food crop sorghum in the field under drought stress. We sequenced the mRNA from weekly samples of these plants, resulting in a molecular profile of drought response over the growing season. We find molecular differences in the 2 cultivars that help explain their differing tolerances to drought and evidence of a disruption in the plant’s symbiosis with arbuscular mycorrhizal fungi. Our findings are of practical importance for agricultural breeding programs, while the resulting data are a resource for the plant and microbial communities for studying the dynamics of drought response., Drought is the most important environmental stress limiting crop yields. The C4 cereal sorghum [Sorghum bicolor (L.) Moench] is a critical food, forage, and emerging bioenergy crop that is notably drought-tolerant. We conducted a large-scale field experiment, imposing preflowering and postflowering drought stress on 2 genotypes of sorghum across a tightly resolved time series, from plant emergence to postanthesis, resulting in a dataset of nearly 400 transcriptomes. We observed a fast and global transcriptomic response in leaf and root tissues with clear temporal patterns, including modulation of well-known drought pathways. We also identified genotypic differences in core photosynthesis and reactive oxygen species scavenging pathways, highlighting possible mechanisms of drought tolerance and of the delayed senescence, characteristic of the stay-green phenotype. Finally, we discovered a large-scale depletion in the expression of genes critical to arbuscular mycorrhizal (AM) symbiosis, with a corresponding drop in AM fungal mass in the plants’ roots.
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- 2019
6. Genome-resolved metagenomics reveals role of iron metabolism in drought-induced rhizosphere microbiome dynamics
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Peggy G. Lemaux, Siwen Deng, Daniel F. Caddell, Nelle Varoquaux, Mary Lou Guerinot, Dawn Chiniquy, Ling Xu, Heidi M.-L. Wipf, Jeffery A. Dahlberg, Mary Madera, John W. Taylor, Elizabeth Purdom, Spencer Diamond, Cheng Gao, Zhaobin Dong, Robert B. Hutmacher, Devin Coleman-Derr, Tuesday Simmons, Jillian F. Banfield, Grady Pierroz, Adam M. Deutschbauer, University of California [Berkeley], University of California, China State Key Laboratory of Plant Physiology and Biochemistry, China Agricultural University (CAU), Lawrence Berkeley National Laboratory [Berkeley] (LBNL), USDA-ARS : Agricultural Research Service, Translational microbial Evolution and Engineering (TIMC-TrEE), Translational Innovation in Medicine and Complexity / Recherche Translationnelle et Innovation en Médecine et Complexité - UMR 5525 (TIMC ), VetAgro Sup - Institut national d'enseignement supérieur et de recherche en alimentation, santé animale, sciences agronomiques et de l'environnement (VAS)-Centre National de la Recherche Scientifique (CNRS)-Université Grenoble Alpes (UGA)-Institut polytechnique de Grenoble - Grenoble Institute of Technology (Grenoble INP ), Université Grenoble Alpes (UGA)-VetAgro Sup - Institut national d'enseignement supérieur et de recherche en alimentation, santé animale, sciences agronomiques et de l'environnement (VAS)-Centre National de la Recherche Scientifique (CNRS)-Université Grenoble Alpes (UGA)-Institut polytechnique de Grenoble - Grenoble Institute of Technology (Grenoble INP ), Université Grenoble Alpes (UGA), University of California [Davis] (UC Davis), and Dartmouth College [Hanover]
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0106 biological sciences ,0301 basic medicine ,Acclimatization ,[SDV]Life Sciences [q-bio] ,General Physics and Astronomy ,01 natural sciences ,Plant Roots ,2.1 Biological and endogenous factors ,RNA-Seq ,Aetiology ,Soil Microbiology ,2. Zero hunger ,Genetics ,Rhizosphere ,Multidisciplinary ,Microbiota ,food and beverages ,Crop Production ,Droughts ,Actinobacteria ,Soil microbiology ,Plant molecular biology ,Science ,Iron ,Physiological ,Drought tolerance ,Biology ,Stress ,General Biochemistry, Genetics and Molecular Biology ,Article ,03 medical and health sciences ,Stress, Physiological ,parasitic diseases ,Microbe ,Microbiome ,Sorghum ,Comparative genomics ,Drought ,Human Genome ,fungi ,Root microbiome ,General Chemistry ,15. Life on land ,biology.organism_classification ,030104 developmental biology ,13. Climate action ,Metagenomics ,Food Security ,010606 plant biology & botany - Abstract
Recent studies have demonstrated that drought leads to dramatic, highly conserved shifts in the root microbiome. At present, the molecular mechanisms underlying these responses remain largely uncharacterized. Here we employ genome-resolved metagenomics and comparative genomics to demonstrate that carbohydrate and secondary metabolite transport functionalities are overrepresented within drought-enriched taxa. These data also reveal that bacterial iron transport and metabolism functionality is highly correlated with drought enrichment. Using time-series root RNA-Seq data, we demonstrate that iron homeostasis within the root is impacted by drought stress, and that loss of a plant phytosiderophore iron transporter impacts microbial community composition, leading to significant increases in the drought-enriched lineage, Actinobacteria. Finally, we show that exogenous application of iron disrupts the drought-induced enrichment of Actinobacteria, as well as their improvement in host phenotype during drought stress. Collectively, our findings implicate iron metabolism in the root microbiome’s response to drought and may inform efforts to improve plant drought tolerance to increase food security., Advances in omics provide a tool to understand mechanisms for plant–microbial interactions under stress. Here the authors apply genome-resolved metagenomics to investigate sorghum and its microbiome responses to drought, identifying an unexpected role of iron metabolism.
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- 2021
7. Isolation of Histone from Sorghum Leaf Tissue for Top Down Mass Spectrometry Profiling of Potential Epigenetic Markers
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Shadan H Abdali, Lifeng Liu, Robert B. Hutmacher, Kim K. Hixson, Tanya E. Winkler, Benjamin J. Cole, Christer Jansson, Julie A. Sievert, Ljiljana Paša-Tolić, Amir H. Ahkami, Mary Madera, Neha Malhan, Mowei Zhou, Joy Hollingsworth, Peggy G. Lemaux, Jeff Dahlberg, Judith A Owiti, and David Dilworth
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General Chemical Engineering ,1.1 Normal biological development and functioning ,Buffers ,Proteomics ,General Biochemistry, Genetics and Molecular Biology ,Mass Spectrometry ,Epigenesis, Genetic ,Histones ,chemistry.chemical_compound ,Genetic ,Gene expression ,Genetics ,Nucleosome ,Psychology ,Epigenetics ,Amino Acid Sequence ,Peptide sequence ,Sorghum ,Protein Processing ,Plant Proteins ,Cell Nucleus ,Chromatography ,Liquid ,General Immunology and Microbiology ,biology ,General Neuroscience ,fungi ,Post-Translational ,food and beverages ,Chromatin ,Cell biology ,Plant Leaves ,Histone ,chemistry ,biology.protein ,Cognitive Sciences ,Biochemistry and Cell Biology ,Protein Processing, Post-Translational ,DNA ,Biomarkers ,Chromatography, Liquid ,Epigenesis - Abstract
Histones belong to a family of highly conserved proteins in eukaryotes. They pack DNA into nucleosomes as functional units of chromatin. Post-translational modifications (PTMs) of histones, which are highly dynamic and can be added or removed by enzymes, play critical roles in regulating gene expression. In plants, epigenetic factors, including histone PTMs, are related to their adaptive responses to the environment. Understanding the molecular mechanisms of epigenetic control can bring unprecedented opportunities for innovative bioengineering solutions. Herein, we describe a protocol to isolate the nuclei and purify histones from sorghum leaf tissue. The extracted histones can be analyzed in their intact forms by top-down mass spectrometry (MS) coupled with online reversed-phase (RP) liquid chromatography (LC). Combinations and stoichiometry of multiple PTMs on the same histone proteoform can be readily identified. In addition, histone tail clipping can be detected using the top-down LC-MS workflow, thus, yielding the global PTM profile of core histones (H4, H2A, H2B, H3). We have applied this protocol previously to profile histone PTMs from sorghum leaf tissue collected from a large-scale field study, aimed at identifying epigenetic markers of drought resistance. The protocol could potentially be adapted and optimized for chromatin immunoprecipitation-sequencing (ChIP-seq), or for studying histone PTMs in similar plants.
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- 2021
8. Top-down mass spectrometry of histone modifications in sorghum reveals potential epigenetic markers for drought acclimation
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Ljiljana Paša-Tolić, Mary Madera, Joy Hollingsworth, Amir H. Ahkami, Jeffery A. Dahlberg, Mowei Zhou, Peggy G. Lemaux, Kristin Engbrecht, Gabriel L. Myers, Neha Malhan, Julie A. Sievert, Robert B. Hutmacher, Kim K. Hixson, and Christer Jansson
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Acclimatization ,General Biochemistry, Genetics and Molecular Biology ,Mass Spectrometry ,Epigenesis, Genetic ,Histones ,03 medical and health sciences ,Gene Expression Regulation, Plant ,Genotype ,Pyruvic Acid ,Epigenetics ,Molecular Biology ,Sorghum ,030304 developmental biology ,Plant Proteins ,0303 health sciences ,Chromatography, Reverse-Phase ,biology ,030302 biochemistry & molecular biology ,food and beverages ,biology.organism_classification ,Cell biology ,Chromatin ,Droughts ,Histone Code ,Histone ,Acetylation ,biology.protein ,Reprogramming ,Protein Processing, Post-Translational - Abstract
Sorghum [Sorghum bicolor (L.) Moench] is an important cereal crop noted for its ability to survive water-limiting conditions. Herein, we present an analytical workflow to explore the changes in histone modifications through plant developmental stages and two drought stresses in two sorghum genotypes that differ in their response to drought. Top-down mass spectrometry (MS) is an ideal method to profile histone modifications and distinguish closely related histone proteoforms. We analyzed leaves of 48 plants and identified 26 unique histone proteins and 677 unique histone proteoforms (124 full-length and 553 truncated proteoforms). We detected trimethylation on nearly all H2B N-termini where acetylation is commonly expected. In addition, an unexpected modification on H2A histones was assigned to N-pyruvic acid 2-iminylation based on its unique neutral loss of CO2. Interestingly, some of the truncated histones, in particular H4 and H3.2, showed significant changes that correlated with the growth and water conditions. The histone proteoforms could serve as targets in search of chromatin modifiers and ultimately have important ramifications in future attempts of studying plant epigenetic reprogramming under stress.
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- 2019
9. Strong succession in arbuscular mycorrhizal fungal communities
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Devin Coleman-Derr, Peggy G. Lemaux, Joy Hollingsworth, Mary Madera, Cheng Gao, John W. Taylor, Robert B. Hutmacher, Ling Xu, Elizabeth Purdom, Liliam Montoya, and Jeffery A. Dahlberg
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Technology ,Ecological succession ,Plant Roots ,Microbiology ,Article ,03 medical and health sciences ,Soil ,Symbiosis ,Mycorrhizae ,DNA, Fungal ,Ecology, Evolution, Behavior and Systematics ,Sorghum ,Soil Microbiology ,030304 developmental biology ,0303 health sciences ,Rhizosphere ,Extinction ,biology ,Ecology ,030306 microbiology ,fungi ,Fungal genetics ,Agriculture ,DNA ,Biological Sciences ,biology.organism_classification ,Fungal ,Seedling ,Nestedness ,Soil microbiology ,Environmental Sciences ,Mycobiome - Abstract
The ecology of fungi lags behind that of plants and animals because most fungi are microscopic and hidden in their substrates. Here, we address the basic ecological process of fungal succession in nature using the microscopic, arbuscular mycorrhizal fungi (AMF) that form essential mutualisms with 70-90% of plants. We find a signal for temporal change in AMF community similarity that is 40-fold stronger than seen in the most recent studies, likely due to weekly samplings of roots, rhizosphere and soil throughout the 17 weeks from seedling to fruit maturity and the use of the fungal DNA barcode to recognize species in a simple, agricultural environment. We demonstrate the patterns of nestedness and turnover and the microbial equivalents of the processes of immigration and extinction, that is, appearance and disappearance. We also provide the first evidence that AMF species co-exist rather than simply co-occur by demonstrating negative, density-dependent population growth for multiple species. Our study shows the advantages of using fungi to test basic ecological hypotheses (e.g., nestedness v. turnover, immigration v. extinction, and coexistence theory) over periods as short as one season.
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- 2019
10. Drought delays development of the sorghum root microbiome and enriches for monoderm bacteria
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Erika M. Zink, Ling Xu, Young-Mo Kim, Cheng Gao, Yi Wang, Devon Birdseye, Julie A. Sievert, Stephanie DeGraaf, Devin Coleman-Derr, Grady Pierroz, Kristin Engbrecht, Henrik Vibe Scheller, Joy Hollingsworth, Kim K. Hixson, Christer Jansson, Jeffery A. Dahlberg, Zhaobin Dong, Peggy G. Lemaux, Tuesday Simmons, Robert B. Hutmacher, Dan Naylor, Mary Madera, and John W. Taylor
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0301 basic medicine ,16S ,microbiome ,drought ,Corrections ,Plant Roots ,Crop ,03 medical and health sciences ,Metabolomics ,Bacterial Proteins ,Cell Wall ,RNA, Ribosomal, 16S ,metatranscriptome ,Colonization ,Microbiome ,Sorghum ,Ribosomal ,Multidisciplinary ,biology ,Bacteria ,Dehydration ,business.industry ,Microbiota ,fungi ,Root microbiome ,Bacterial ,food and beverages ,biology.organism_classification ,root ,RNA, Bacterial ,030104 developmental biology ,Agronomy ,Agriculture ,RNA ,ATP-Binding Cassette Transporters ,sorghum ,business - Abstract
© 2018 National Academy of Sciences. All Rights Reserved. Drought stress is a major obstacle to crop productivity, and the severity and frequency of drought are expected to increase in the coming century. Certain root-associated bacteria have been shown to mitigate the negative effects of drought stress on plant growth, and manipulation of the crop microbiome is an emerging strategy for overcoming drought stress in agricultural systems, yet the effect of drought on the development of the root microbiome is poorly understood. Through 16S rRNA amplicon and metatranscriptome sequencing, as well as root metabolomics, we demonstrate that drought delays the development of the early sorghum root microbiome and causes increased abundance and activity of monoderm bacteria, which lack an outer cell membrane and contain thick cell walls. Our data suggest that altered plant metabolism and increased activity of bacterial ATP-binding cassette (ABC) transporter genes are correlated with these shifts in community composition. Finally, inoculation experiments with monoderm isolates indicate that increased colonization of the root during drought can positively impact plant growth. Collectively, these results demonstrate the role that drought plays in restructuring the root microbiome and highlight the importance of temporal sampling when studying plant-associated microbiomes.
- Published
- 2018
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