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Soil chemistry determines whether defensive plant secondary metabolites promote or suppress herbivore growth

Plant secondary (or specialized) metabolites mediate important interactions in both the rhizosphere and the phyllosphere. If and how such compartmentalized functions interact to determine plant–environment interactions is not well understood. Here, we investigated how the dual role of maize benzoxaz...

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Autores principales: Hu, Lingfei, Wu, Zhenwei, Robert, Christelle A. M., Ouyang, Xiao, Züst, Tobias, Mestrot, Adrien, Xu, Jianming, Erb, Matthias
Formato: Online Artículo Texto
Lenguaje:English
Publicado: National Academy of Sciences 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8639379/
https://www.ncbi.nlm.nih.gov/pubmed/34675080
http://dx.doi.org/10.1073/pnas.2109602118
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author Hu, Lingfei
Wu, Zhenwei
Robert, Christelle A. M.
Ouyang, Xiao
Züst, Tobias
Mestrot, Adrien
Xu, Jianming
Erb, Matthias
author_facet Hu, Lingfei
Wu, Zhenwei
Robert, Christelle A. M.
Ouyang, Xiao
Züst, Tobias
Mestrot, Adrien
Xu, Jianming
Erb, Matthias
author_sort Hu, Lingfei
collection PubMed
description Plant secondary (or specialized) metabolites mediate important interactions in both the rhizosphere and the phyllosphere. If and how such compartmentalized functions interact to determine plant–environment interactions is not well understood. Here, we investigated how the dual role of maize benzoxazinoids as leaf defenses and root siderophores shapes the interaction between maize and a major global insect pest, the fall armyworm. We find that benzoxazinoids suppress fall armyworm growth when plants are grown in soils with very low available iron but enhance growth in soils with higher available iron. Manipulation experiments confirm that benzoxazinoids suppress herbivore growth under iron-deficient conditions and in the presence of chelated iron but enhance herbivore growth in the presence of free iron in the growth medium. This reversal of the protective effect of benzoxazinoids is not associated with major changes in plant primary metabolism. Plant defense activation is modulated by the interplay between soil iron and benzoxazinoids but does not explain fall armyworm performance. Instead, increased iron supply to the fall armyworm by benzoxazinoids in the presence of free iron enhances larval performance. This work identifies soil chemistry as a decisive factor for the impact of plant secondary metabolites on herbivore growth. It also demonstrates how the multifunctionality of plant secondary metabolites drives interactions between abiotic and biotic factors, with potential consequences for plant resistance in variable environments.
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spelling pubmed-86393792021-12-12 Soil chemistry determines whether defensive plant secondary metabolites promote or suppress herbivore growth Hu, Lingfei Wu, Zhenwei Robert, Christelle A. M. Ouyang, Xiao Züst, Tobias Mestrot, Adrien Xu, Jianming Erb, Matthias Proc Natl Acad Sci U S A Biological Sciences Plant secondary (or specialized) metabolites mediate important interactions in both the rhizosphere and the phyllosphere. If and how such compartmentalized functions interact to determine plant–environment interactions is not well understood. Here, we investigated how the dual role of maize benzoxazinoids as leaf defenses and root siderophores shapes the interaction between maize and a major global insect pest, the fall armyworm. We find that benzoxazinoids suppress fall armyworm growth when plants are grown in soils with very low available iron but enhance growth in soils with higher available iron. Manipulation experiments confirm that benzoxazinoids suppress herbivore growth under iron-deficient conditions and in the presence of chelated iron but enhance herbivore growth in the presence of free iron in the growth medium. This reversal of the protective effect of benzoxazinoids is not associated with major changes in plant primary metabolism. Plant defense activation is modulated by the interplay between soil iron and benzoxazinoids but does not explain fall armyworm performance. Instead, increased iron supply to the fall armyworm by benzoxazinoids in the presence of free iron enhances larval performance. This work identifies soil chemistry as a decisive factor for the impact of plant secondary metabolites on herbivore growth. It also demonstrates how the multifunctionality of plant secondary metabolites drives interactions between abiotic and biotic factors, with potential consequences for plant resistance in variable environments. National Academy of Sciences 2021-10-21 2021-10-26 /pmc/articles/PMC8639379/ /pubmed/34675080 http://dx.doi.org/10.1073/pnas.2109602118 Text en Copyright © 2021 the Author(s). Published by PNAS. https://creativecommons.org/licenses/by-nc-nd/4.0/This open access article is distributed under Creative Commons Attribution-NonCommercial-NoDerivatives License 4.0 (CC BY-NC-ND) (https://creativecommons.org/licenses/by-nc-nd/4.0/) .
spellingShingle Biological Sciences
Hu, Lingfei
Wu, Zhenwei
Robert, Christelle A. M.
Ouyang, Xiao
Züst, Tobias
Mestrot, Adrien
Xu, Jianming
Erb, Matthias
Soil chemistry determines whether defensive plant secondary metabolites promote or suppress herbivore growth
title Soil chemistry determines whether defensive plant secondary metabolites promote or suppress herbivore growth
title_full Soil chemistry determines whether defensive plant secondary metabolites promote or suppress herbivore growth
title_fullStr Soil chemistry determines whether defensive plant secondary metabolites promote or suppress herbivore growth
title_full_unstemmed Soil chemistry determines whether defensive plant secondary metabolites promote or suppress herbivore growth
title_short Soil chemistry determines whether defensive plant secondary metabolites promote or suppress herbivore growth
title_sort soil chemistry determines whether defensive plant secondary metabolites promote or suppress herbivore growth
topic Biological Sciences
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8639379/
https://www.ncbi.nlm.nih.gov/pubmed/34675080
http://dx.doi.org/10.1073/pnas.2109602118
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