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Plant Transcriptome Reprograming and Bacterial Extracellular Metabolites Underlying Tomato Drought Resistance Triggered by a Beneficial Soil Bacteria

Water deficit is one of the major constraints to crop production and food security worldwide. Some plant growth-promoting rhizobacteria (PGPR) strains are capable of increasing plant drought resistance. Knowledge about the mechanisms underlying bacteria-induced plant drought resistance is important...

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Autores principales: Morcillo, Rafael J. L., Vílchez, Juan I., Zhang, Song, Kaushal, Richa, He, Danxia, Zi, Hailing, Liu, Renyi, Niehaus, Karsten, Handa, Avtar K., Zhang, Huiming
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8230097/
https://www.ncbi.nlm.nih.gov/pubmed/34207663
http://dx.doi.org/10.3390/metabo11060369
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author Morcillo, Rafael J. L.
Vílchez, Juan I.
Zhang, Song
Kaushal, Richa
He, Danxia
Zi, Hailing
Liu, Renyi
Niehaus, Karsten
Handa, Avtar K.
Zhang, Huiming
author_facet Morcillo, Rafael J. L.
Vílchez, Juan I.
Zhang, Song
Kaushal, Richa
He, Danxia
Zi, Hailing
Liu, Renyi
Niehaus, Karsten
Handa, Avtar K.
Zhang, Huiming
author_sort Morcillo, Rafael J. L.
collection PubMed
description Water deficit is one of the major constraints to crop production and food security worldwide. Some plant growth-promoting rhizobacteria (PGPR) strains are capable of increasing plant drought resistance. Knowledge about the mechanisms underlying bacteria-induced plant drought resistance is important for PGPR applications in agriculture. In this study, we show the drought stress-mitigating effects on tomato plants by the Bacillus megaterium strain TG1-E1, followed by the profiling of plant transcriptomic responses to TG1-E1 and the profiling of bacterial extracellular metabolites. Comparison between the transcriptomes of drought-stressed plants with and without TG1-E1 inoculation revealed bacteria-induced transcriptome reprograming, with highlights on differentially expressed genes belonging to the functional categories including transcription factors, signal transduction, and cell wall biogenesis and organization. Mass spectrometry-based analysis identified over 40 bacterial extracellular metabolites, including several important regulators or osmoprotectant precursors for increasing plant drought resistance. These results demonstrate the importance of plant transcriptional regulation and bacterial metabolites in PGPR-induced plant drought resistance.
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spelling pubmed-82300972021-06-26 Plant Transcriptome Reprograming and Bacterial Extracellular Metabolites Underlying Tomato Drought Resistance Triggered by a Beneficial Soil Bacteria Morcillo, Rafael J. L. Vílchez, Juan I. Zhang, Song Kaushal, Richa He, Danxia Zi, Hailing Liu, Renyi Niehaus, Karsten Handa, Avtar K. Zhang, Huiming Metabolites Article Water deficit is one of the major constraints to crop production and food security worldwide. Some plant growth-promoting rhizobacteria (PGPR) strains are capable of increasing plant drought resistance. Knowledge about the mechanisms underlying bacteria-induced plant drought resistance is important for PGPR applications in agriculture. In this study, we show the drought stress-mitigating effects on tomato plants by the Bacillus megaterium strain TG1-E1, followed by the profiling of plant transcriptomic responses to TG1-E1 and the profiling of bacterial extracellular metabolites. Comparison between the transcriptomes of drought-stressed plants with and without TG1-E1 inoculation revealed bacteria-induced transcriptome reprograming, with highlights on differentially expressed genes belonging to the functional categories including transcription factors, signal transduction, and cell wall biogenesis and organization. Mass spectrometry-based analysis identified over 40 bacterial extracellular metabolites, including several important regulators or osmoprotectant precursors for increasing plant drought resistance. These results demonstrate the importance of plant transcriptional regulation and bacterial metabolites in PGPR-induced plant drought resistance. MDPI 2021-06-09 /pmc/articles/PMC8230097/ /pubmed/34207663 http://dx.doi.org/10.3390/metabo11060369 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Morcillo, Rafael J. L.
Vílchez, Juan I.
Zhang, Song
Kaushal, Richa
He, Danxia
Zi, Hailing
Liu, Renyi
Niehaus, Karsten
Handa, Avtar K.
Zhang, Huiming
Plant Transcriptome Reprograming and Bacterial Extracellular Metabolites Underlying Tomato Drought Resistance Triggered by a Beneficial Soil Bacteria
title Plant Transcriptome Reprograming and Bacterial Extracellular Metabolites Underlying Tomato Drought Resistance Triggered by a Beneficial Soil Bacteria
title_full Plant Transcriptome Reprograming and Bacterial Extracellular Metabolites Underlying Tomato Drought Resistance Triggered by a Beneficial Soil Bacteria
title_fullStr Plant Transcriptome Reprograming and Bacterial Extracellular Metabolites Underlying Tomato Drought Resistance Triggered by a Beneficial Soil Bacteria
title_full_unstemmed Plant Transcriptome Reprograming and Bacterial Extracellular Metabolites Underlying Tomato Drought Resistance Triggered by a Beneficial Soil Bacteria
title_short Plant Transcriptome Reprograming and Bacterial Extracellular Metabolites Underlying Tomato Drought Resistance Triggered by a Beneficial Soil Bacteria
title_sort plant transcriptome reprograming and bacterial extracellular metabolites underlying tomato drought resistance triggered by a beneficial soil bacteria
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8230097/
https://www.ncbi.nlm.nih.gov/pubmed/34207663
http://dx.doi.org/10.3390/metabo11060369
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