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Trehalose increases tomato drought tolerance, induces defenses, and increases resistance to bacterial wilt disease
Ralstonia solanacearum causes bacterial wilt disease, leading to severe crop losses. Xylem sap from R. solanacearum-infected tomato is enriched in the disaccharide trehalose. Water-stressed plants also accumulate trehalose, which increases drought tolerance via abscisic acid (ABA) signaling. Because...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9045674/ https://www.ncbi.nlm.nih.gov/pubmed/35476629 http://dx.doi.org/10.1371/journal.pone.0266254 |
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author | MacIntyre, April M. Meline, Valerian Gorman, Zachary Augustine, Steven P. Dye, Carolyn J. Hamilton, Corri D. Iyer-Pascuzzi, Anjali S. Kolomiets, Michael V. McCulloh, Katherine A. Allen, Caitilyn |
author_facet | MacIntyre, April M. Meline, Valerian Gorman, Zachary Augustine, Steven P. Dye, Carolyn J. Hamilton, Corri D. Iyer-Pascuzzi, Anjali S. Kolomiets, Michael V. McCulloh, Katherine A. Allen, Caitilyn |
author_sort | MacIntyre, April M. |
collection | PubMed |
description | Ralstonia solanacearum causes bacterial wilt disease, leading to severe crop losses. Xylem sap from R. solanacearum-infected tomato is enriched in the disaccharide trehalose. Water-stressed plants also accumulate trehalose, which increases drought tolerance via abscisic acid (ABA) signaling. Because R. solanacearum-infected plants suffer reduced water flow, we hypothesized that bacterial wilt physiologically mimics drought stress, which trehalose could mitigate. We found that R. solanacearum-infected plants differentially expressed drought-associated genes, including those involved in ABA and trehalose metabolism, and had more ABA in xylem sap. Consistent with this, treating tomato roots with ABA reduced both stomatal conductance and stem colonization by R. solanacearum. Treating roots with trehalose increased xylem sap ABA and reduced plant water use by lowering stomatal conductance and temporarily improving water use efficiency. Trehalose treatment also upregulated expression of salicylic acid (SA)-dependent tomato defense genes; increased xylem sap levels of SA and other antimicrobial compounds; and increased bacterial wilt resistance of SA-insensitive NahG tomato plants. Additionally, trehalose treatment increased xylem concentrations of jasmonic acid and related oxylipins. Finally, trehalose-treated plants were substantially more resistant to bacterial wilt disease. Together, these data show that exogenous trehalose reduced both water stress and bacterial wilt disease and triggered systemic disease resistance, possibly through a Damage Associated Molecular Pattern (DAMP) response pathway. This suite of responses revealed unexpected linkages between plant responses to biotic and abiotic stress and suggested that R. solanacearum-infected plants increase trehalose to improve water use efficiency and increase wilt disease resistance. The pathogen may degrade trehalose to counter these efforts. Together, these results suggest that treating tomatoes with exogenous trehalose could be a practical strategy for bacterial wilt management. |
format | Online Article Text |
id | pubmed-9045674 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-90456742022-04-28 Trehalose increases tomato drought tolerance, induces defenses, and increases resistance to bacterial wilt disease MacIntyre, April M. Meline, Valerian Gorman, Zachary Augustine, Steven P. Dye, Carolyn J. Hamilton, Corri D. Iyer-Pascuzzi, Anjali S. Kolomiets, Michael V. McCulloh, Katherine A. Allen, Caitilyn PLoS One Research Article Ralstonia solanacearum causes bacterial wilt disease, leading to severe crop losses. Xylem sap from R. solanacearum-infected tomato is enriched in the disaccharide trehalose. Water-stressed plants also accumulate trehalose, which increases drought tolerance via abscisic acid (ABA) signaling. Because R. solanacearum-infected plants suffer reduced water flow, we hypothesized that bacterial wilt physiologically mimics drought stress, which trehalose could mitigate. We found that R. solanacearum-infected plants differentially expressed drought-associated genes, including those involved in ABA and trehalose metabolism, and had more ABA in xylem sap. Consistent with this, treating tomato roots with ABA reduced both stomatal conductance and stem colonization by R. solanacearum. Treating roots with trehalose increased xylem sap ABA and reduced plant water use by lowering stomatal conductance and temporarily improving water use efficiency. Trehalose treatment also upregulated expression of salicylic acid (SA)-dependent tomato defense genes; increased xylem sap levels of SA and other antimicrobial compounds; and increased bacterial wilt resistance of SA-insensitive NahG tomato plants. Additionally, trehalose treatment increased xylem concentrations of jasmonic acid and related oxylipins. Finally, trehalose-treated plants were substantially more resistant to bacterial wilt disease. Together, these data show that exogenous trehalose reduced both water stress and bacterial wilt disease and triggered systemic disease resistance, possibly through a Damage Associated Molecular Pattern (DAMP) response pathway. This suite of responses revealed unexpected linkages between plant responses to biotic and abiotic stress and suggested that R. solanacearum-infected plants increase trehalose to improve water use efficiency and increase wilt disease resistance. The pathogen may degrade trehalose to counter these efforts. Together, these results suggest that treating tomatoes with exogenous trehalose could be a practical strategy for bacterial wilt management. Public Library of Science 2022-04-27 /pmc/articles/PMC9045674/ /pubmed/35476629 http://dx.doi.org/10.1371/journal.pone.0266254 Text en © 2022 MacIntyre et al https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article MacIntyre, April M. Meline, Valerian Gorman, Zachary Augustine, Steven P. Dye, Carolyn J. Hamilton, Corri D. Iyer-Pascuzzi, Anjali S. Kolomiets, Michael V. McCulloh, Katherine A. Allen, Caitilyn Trehalose increases tomato drought tolerance, induces defenses, and increases resistance to bacterial wilt disease |
title | Trehalose increases tomato drought tolerance, induces defenses, and increases resistance to bacterial wilt disease |
title_full | Trehalose increases tomato drought tolerance, induces defenses, and increases resistance to bacterial wilt disease |
title_fullStr | Trehalose increases tomato drought tolerance, induces defenses, and increases resistance to bacterial wilt disease |
title_full_unstemmed | Trehalose increases tomato drought tolerance, induces defenses, and increases resistance to bacterial wilt disease |
title_short | Trehalose increases tomato drought tolerance, induces defenses, and increases resistance to bacterial wilt disease |
title_sort | trehalose increases tomato drought tolerance, induces defenses, and increases resistance to bacterial wilt disease |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9045674/ https://www.ncbi.nlm.nih.gov/pubmed/35476629 http://dx.doi.org/10.1371/journal.pone.0266254 |
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