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Hordeum vulgare differentiates its response to beneficial bacteria
BACKGROUND: In nature, beneficial bacteria triggering induced systemic resistance (ISR) may protect plants from potential diseases, reducing yield losses caused by diverse pathogens. However, little is known about how the host plant initially responds to different beneficial bacteria. To reveal the...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10548682/ https://www.ncbi.nlm.nih.gov/pubmed/37789272 http://dx.doi.org/10.1186/s12870-023-04484-5 |
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author | Duan, Yongming Han, Min Grimm, Maja Schierstaedt, Jasper Imani, Jafargholi Cardinale, Massimiliano Le Jean, Marie Nesme, Joseph Sørensen, Søren J. Schikora, Adam |
author_facet | Duan, Yongming Han, Min Grimm, Maja Schierstaedt, Jasper Imani, Jafargholi Cardinale, Massimiliano Le Jean, Marie Nesme, Joseph Sørensen, Søren J. Schikora, Adam |
author_sort | Duan, Yongming |
collection | PubMed |
description | BACKGROUND: In nature, beneficial bacteria triggering induced systemic resistance (ISR) may protect plants from potential diseases, reducing yield losses caused by diverse pathogens. However, little is known about how the host plant initially responds to different beneficial bacteria. To reveal the impact of different bacteria on barley (Hordeum vulgare), bacterial colonization patterns, gene expression, and composition of seed endophytes were explored. RESULTS: This study used the soil-borne Ensifer meliloti, as well as Pantoea sp. and Pseudomonas sp. isolated from barley seeds, individually. The results demonstrated that those bacteria persisted in the rhizosphere but with different colonization patterns. Although root-leaf translocation was not observed, all three bacteria induced systemic resistance (ISR) against foliar fungal pathogens. Transcriptome analysis revealed that ion- and stress-related genes were regulated in plants that first encountered bacteria. Iron homeostasis and heat stress responses were involved in the response to E. meliloti and Pantoea sp., even if the iron content was not altered. Heat shock protein-encoding genes responded to inoculation with Pantoea sp. and Pseudomonas sp. Furthermore, bacterial inoculation affected the composition of seed endophytes. Investigation of the following generation indicated that the enhanced resistance was not heritable. CONCLUSIONS: Here, using barley as a model, we highlighted different responses to three different beneficial bacteria as well as the influence of soil-borne Ensifer meliloti on the seed microbiome. In total, these results can help to understand the interaction between ISR-triggering bacteria and a crop plant, which is essential for the application of biological agents in sustainable agriculture. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12870-023-04484-5. |
format | Online Article Text |
id | pubmed-10548682 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-105486822023-10-05 Hordeum vulgare differentiates its response to beneficial bacteria Duan, Yongming Han, Min Grimm, Maja Schierstaedt, Jasper Imani, Jafargholi Cardinale, Massimiliano Le Jean, Marie Nesme, Joseph Sørensen, Søren J. Schikora, Adam BMC Plant Biol Research BACKGROUND: In nature, beneficial bacteria triggering induced systemic resistance (ISR) may protect plants from potential diseases, reducing yield losses caused by diverse pathogens. However, little is known about how the host plant initially responds to different beneficial bacteria. To reveal the impact of different bacteria on barley (Hordeum vulgare), bacterial colonization patterns, gene expression, and composition of seed endophytes were explored. RESULTS: This study used the soil-borne Ensifer meliloti, as well as Pantoea sp. and Pseudomonas sp. isolated from barley seeds, individually. The results demonstrated that those bacteria persisted in the rhizosphere but with different colonization patterns. Although root-leaf translocation was not observed, all three bacteria induced systemic resistance (ISR) against foliar fungal pathogens. Transcriptome analysis revealed that ion- and stress-related genes were regulated in plants that first encountered bacteria. Iron homeostasis and heat stress responses were involved in the response to E. meliloti and Pantoea sp., even if the iron content was not altered. Heat shock protein-encoding genes responded to inoculation with Pantoea sp. and Pseudomonas sp. Furthermore, bacterial inoculation affected the composition of seed endophytes. Investigation of the following generation indicated that the enhanced resistance was not heritable. CONCLUSIONS: Here, using barley as a model, we highlighted different responses to three different beneficial bacteria as well as the influence of soil-borne Ensifer meliloti on the seed microbiome. In total, these results can help to understand the interaction between ISR-triggering bacteria and a crop plant, which is essential for the application of biological agents in sustainable agriculture. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12870-023-04484-5. BioMed Central 2023-10-04 /pmc/articles/PMC10548682/ /pubmed/37789272 http://dx.doi.org/10.1186/s12870-023-04484-5 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Duan, Yongming Han, Min Grimm, Maja Schierstaedt, Jasper Imani, Jafargholi Cardinale, Massimiliano Le Jean, Marie Nesme, Joseph Sørensen, Søren J. Schikora, Adam Hordeum vulgare differentiates its response to beneficial bacteria |
title | Hordeum vulgare differentiates its response to beneficial bacteria |
title_full | Hordeum vulgare differentiates its response to beneficial bacteria |
title_fullStr | Hordeum vulgare differentiates its response to beneficial bacteria |
title_full_unstemmed | Hordeum vulgare differentiates its response to beneficial bacteria |
title_short | Hordeum vulgare differentiates its response to beneficial bacteria |
title_sort | hordeum vulgare differentiates its response to beneficial bacteria |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10548682/ https://www.ncbi.nlm.nih.gov/pubmed/37789272 http://dx.doi.org/10.1186/s12870-023-04484-5 |
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