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Phosphate Suppression of Arbuscular Mycorrhizal Symbiosis Involves Gibberellic Acid Signaling

Most land plants entertain a mutualistic symbiosis known as arbuscular mycorrhiza with fungi (Glomeromycota) that provide them with essential mineral nutrients, in particular phosphate (P(i)), and protect them from biotic and abiotic stress. Arbuscular mycorrhizal (AM) symbiosis increases plant prod...

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Autores principales: Nouri, Eva, Surve, Rohini, Bapaume, Laure, Stumpe, Michael, Chen, Min, Zhang, Yunmeng, Ruyter-Spira, Carolien, Bouwmeester, Harro, Glauser, Gaëtan, Bruisson, Sébastien, Reinhardt, Didier
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8504448/
https://www.ncbi.nlm.nih.gov/pubmed/34037236
http://dx.doi.org/10.1093/pcp/pcab063
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author Nouri, Eva
Surve, Rohini
Bapaume, Laure
Stumpe, Michael
Chen, Min
Zhang, Yunmeng
Ruyter-Spira, Carolien
Bouwmeester, Harro
Glauser, Gaëtan
Bruisson, Sébastien
Reinhardt, Didier
author_facet Nouri, Eva
Surve, Rohini
Bapaume, Laure
Stumpe, Michael
Chen, Min
Zhang, Yunmeng
Ruyter-Spira, Carolien
Bouwmeester, Harro
Glauser, Gaëtan
Bruisson, Sébastien
Reinhardt, Didier
author_sort Nouri, Eva
collection PubMed
description Most land plants entertain a mutualistic symbiosis known as arbuscular mycorrhiza with fungi (Glomeromycota) that provide them with essential mineral nutrients, in particular phosphate (P(i)), and protect them from biotic and abiotic stress. Arbuscular mycorrhizal (AM) symbiosis increases plant productivity and biodiversity and is therefore relevant for both natural plant communities and crop production. However, AM fungal populations suffer from intense farming practices in agricultural soils, in particular P(i) fertilization. The dilemma between natural fertilization from AM symbiosis and chemical fertilization has raised major concern and emphasizes the need to better understand the mechanisms by which P(i) suppresses AM symbiosis. Here, we test the hypothesis that P(i) may interfere with AM symbiosis via the phytohormone gibberellic acid (GA) in the Solanaceous model systems Petunia hybrida and Nicotiana tabacum. Indeed, we find that GA is inhibitory to AM symbiosis and that P(i) may cause GA levels to increase in mycorrhizal roots. Consistent with a role of endogenous GA as an inhibitor of AM development, GA-defective N. tabacum lines expressing a GA-metabolizing enzyme (GA methyltransferase—GAMT) are colonized more quickly by the AM fungus Rhizoglomus irregulare, and exogenous P(i) is less effective in inhibiting AM colonization in these lines. Systematic gene expression analysis of GA-related genes reveals a complex picture, in which GA degradation by GA2 oxidase plays a prominent role. These findings reveal potential targets for crop breeding that could reduce P(i) suppression of AM symbiosis, thereby reconciling the advantages of P(i) fertilization with the diverse benefits of AM symbiosis.
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spelling pubmed-85044482021-10-13 Phosphate Suppression of Arbuscular Mycorrhizal Symbiosis Involves Gibberellic Acid Signaling Nouri, Eva Surve, Rohini Bapaume, Laure Stumpe, Michael Chen, Min Zhang, Yunmeng Ruyter-Spira, Carolien Bouwmeester, Harro Glauser, Gaëtan Bruisson, Sébastien Reinhardt, Didier Plant Cell Physiol Regular Paper Most land plants entertain a mutualistic symbiosis known as arbuscular mycorrhiza with fungi (Glomeromycota) that provide them with essential mineral nutrients, in particular phosphate (P(i)), and protect them from biotic and abiotic stress. Arbuscular mycorrhizal (AM) symbiosis increases plant productivity and biodiversity and is therefore relevant for both natural plant communities and crop production. However, AM fungal populations suffer from intense farming practices in agricultural soils, in particular P(i) fertilization. The dilemma between natural fertilization from AM symbiosis and chemical fertilization has raised major concern and emphasizes the need to better understand the mechanisms by which P(i) suppresses AM symbiosis. Here, we test the hypothesis that P(i) may interfere with AM symbiosis via the phytohormone gibberellic acid (GA) in the Solanaceous model systems Petunia hybrida and Nicotiana tabacum. Indeed, we find that GA is inhibitory to AM symbiosis and that P(i) may cause GA levels to increase in mycorrhizal roots. Consistent with a role of endogenous GA as an inhibitor of AM development, GA-defective N. tabacum lines expressing a GA-metabolizing enzyme (GA methyltransferase—GAMT) are colonized more quickly by the AM fungus Rhizoglomus irregulare, and exogenous P(i) is less effective in inhibiting AM colonization in these lines. Systematic gene expression analysis of GA-related genes reveals a complex picture, in which GA degradation by GA2 oxidase plays a prominent role. These findings reveal potential targets for crop breeding that could reduce P(i) suppression of AM symbiosis, thereby reconciling the advantages of P(i) fertilization with the diverse benefits of AM symbiosis. Oxford University Press 2021-06-28 /pmc/articles/PMC8504448/ /pubmed/34037236 http://dx.doi.org/10.1093/pcp/pcab063 Text en © The Author(s) 2021. Published by Oxford University Press on behalf of Japanese Society of Plant Physiologists. https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial License (https://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Regular Paper
Nouri, Eva
Surve, Rohini
Bapaume, Laure
Stumpe, Michael
Chen, Min
Zhang, Yunmeng
Ruyter-Spira, Carolien
Bouwmeester, Harro
Glauser, Gaëtan
Bruisson, Sébastien
Reinhardt, Didier
Phosphate Suppression of Arbuscular Mycorrhizal Symbiosis Involves Gibberellic Acid Signaling
title Phosphate Suppression of Arbuscular Mycorrhizal Symbiosis Involves Gibberellic Acid Signaling
title_full Phosphate Suppression of Arbuscular Mycorrhizal Symbiosis Involves Gibberellic Acid Signaling
title_fullStr Phosphate Suppression of Arbuscular Mycorrhizal Symbiosis Involves Gibberellic Acid Signaling
title_full_unstemmed Phosphate Suppression of Arbuscular Mycorrhizal Symbiosis Involves Gibberellic Acid Signaling
title_short Phosphate Suppression of Arbuscular Mycorrhizal Symbiosis Involves Gibberellic Acid Signaling
title_sort phosphate suppression of arbuscular mycorrhizal symbiosis involves gibberellic acid signaling
topic Regular Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8504448/
https://www.ncbi.nlm.nih.gov/pubmed/34037236
http://dx.doi.org/10.1093/pcp/pcab063
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