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Root-associated fungal microbiota of nonmycorrhizal Arabis alpina and its contribution to plant phosphorus nutrition

Most land plants live in association with arbuscular mycorrhizal (AM) fungi and rely on this symbiosis to scavenge phosphorus (P) from soil. The ability to establish this partnership has been lost in some plant lineages like the Brassicaceae, which raises the question of what alternative nutrition s...

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Autores principales: Almario, Juliana, Jeena, Ganga, Wunder, Jörg, Langen, Gregor, Zuccaro, Alga, Coupland, George, Bucher, Marcel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: National Academy of Sciences 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5676915/
https://www.ncbi.nlm.nih.gov/pubmed/28973917
http://dx.doi.org/10.1073/pnas.1710455114
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author Almario, Juliana
Jeena, Ganga
Wunder, Jörg
Langen, Gregor
Zuccaro, Alga
Coupland, George
Bucher, Marcel
author_facet Almario, Juliana
Jeena, Ganga
Wunder, Jörg
Langen, Gregor
Zuccaro, Alga
Coupland, George
Bucher, Marcel
author_sort Almario, Juliana
collection PubMed
description Most land plants live in association with arbuscular mycorrhizal (AM) fungi and rely on this symbiosis to scavenge phosphorus (P) from soil. The ability to establish this partnership has been lost in some plant lineages like the Brassicaceae, which raises the question of what alternative nutrition strategies such plants have to grow in P-impoverished soils. To understand the contribution of plant–microbiota interactions, we studied the root-associated fungal microbiome of Arabis alpina (Brassicaceae) with the hypothesis that some of its components can promote plant P acquisition. Using amplicon sequencing of the fungal internal transcribed spacer 2, we studied the root and rhizosphere fungal communities of A. alpina growing under natural and controlled conditions including low-P soils and identified a set of 15 fungal taxa consistently detected in its roots. This cohort included a Helotiales taxon exhibiting high abundance in roots of wild A. alpina growing in an extremely P-limited soil. Consequently, we isolated and subsequently reintroduced a specimen from this taxon into its native P-poor soil in which it improved plant growth and P uptake. The fungus exhibited mycorrhiza-like traits including colonization of the root endosphere and P transfer to the plant. Genome analysis revealed a link between its endophytic lifestyle and the expansion of its repertoire of carbohydrate-active enzymes. We report the discovery of a plant–fungus interaction facilitating the growth of a nonmycorrhizal plant under native P-limited conditions, thus uncovering a previously underestimated role of root fungal microbiota in P cycling.
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spelling pubmed-56769152017-11-15 Root-associated fungal microbiota of nonmycorrhizal Arabis alpina and its contribution to plant phosphorus nutrition Almario, Juliana Jeena, Ganga Wunder, Jörg Langen, Gregor Zuccaro, Alga Coupland, George Bucher, Marcel Proc Natl Acad Sci U S A PNAS Plus Most land plants live in association with arbuscular mycorrhizal (AM) fungi and rely on this symbiosis to scavenge phosphorus (P) from soil. The ability to establish this partnership has been lost in some plant lineages like the Brassicaceae, which raises the question of what alternative nutrition strategies such plants have to grow in P-impoverished soils. To understand the contribution of plant–microbiota interactions, we studied the root-associated fungal microbiome of Arabis alpina (Brassicaceae) with the hypothesis that some of its components can promote plant P acquisition. Using amplicon sequencing of the fungal internal transcribed spacer 2, we studied the root and rhizosphere fungal communities of A. alpina growing under natural and controlled conditions including low-P soils and identified a set of 15 fungal taxa consistently detected in its roots. This cohort included a Helotiales taxon exhibiting high abundance in roots of wild A. alpina growing in an extremely P-limited soil. Consequently, we isolated and subsequently reintroduced a specimen from this taxon into its native P-poor soil in which it improved plant growth and P uptake. The fungus exhibited mycorrhiza-like traits including colonization of the root endosphere and P transfer to the plant. Genome analysis revealed a link between its endophytic lifestyle and the expansion of its repertoire of carbohydrate-active enzymes. We report the discovery of a plant–fungus interaction facilitating the growth of a nonmycorrhizal plant under native P-limited conditions, thus uncovering a previously underestimated role of root fungal microbiota in P cycling. National Academy of Sciences 2017-10-31 2017-10-02 /pmc/articles/PMC5676915/ /pubmed/28973917 http://dx.doi.org/10.1073/pnas.1710455114 Text en Freely available online through the PNAS open access option.
spellingShingle PNAS Plus
Almario, Juliana
Jeena, Ganga
Wunder, Jörg
Langen, Gregor
Zuccaro, Alga
Coupland, George
Bucher, Marcel
Root-associated fungal microbiota of nonmycorrhizal Arabis alpina and its contribution to plant phosphorus nutrition
title Root-associated fungal microbiota of nonmycorrhizal Arabis alpina and its contribution to plant phosphorus nutrition
title_full Root-associated fungal microbiota of nonmycorrhizal Arabis alpina and its contribution to plant phosphorus nutrition
title_fullStr Root-associated fungal microbiota of nonmycorrhizal Arabis alpina and its contribution to plant phosphorus nutrition
title_full_unstemmed Root-associated fungal microbiota of nonmycorrhizal Arabis alpina and its contribution to plant phosphorus nutrition
title_short Root-associated fungal microbiota of nonmycorrhizal Arabis alpina and its contribution to plant phosphorus nutrition
title_sort root-associated fungal microbiota of nonmycorrhizal arabis alpina and its contribution to plant phosphorus nutrition
topic PNAS Plus
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5676915/
https://www.ncbi.nlm.nih.gov/pubmed/28973917
http://dx.doi.org/10.1073/pnas.1710455114
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