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Routes to roots: direct evidence of water transport by arbuscular mycorrhizal fungi to host plants
Arbuscular mycorrhizal fungi (AMF) can help mitigate plant responses to water stress, but it is unclear whether AMF do so by indirect mechanisms, direct water transport to roots, or a combination of the two. Here, we investigated if and how the AMF Rhizophagus intraradices transported water to the h...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9543596/ https://www.ncbi.nlm.nih.gov/pubmed/35633108 http://dx.doi.org/10.1111/nph.18281 |
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author | Kakouridis, Anne Hagen, John A. Kan, Megan P. Mambelli, Stefania Feldman, Lewis J. Herman, Donald J. Weber, Peter K. Pett‐Ridge, Jennifer Firestone, Mary K. |
author_facet | Kakouridis, Anne Hagen, John A. Kan, Megan P. Mambelli, Stefania Feldman, Lewis J. Herman, Donald J. Weber, Peter K. Pett‐Ridge, Jennifer Firestone, Mary K. |
author_sort | Kakouridis, Anne |
collection | PubMed |
description | Arbuscular mycorrhizal fungi (AMF) can help mitigate plant responses to water stress, but it is unclear whether AMF do so by indirect mechanisms, direct water transport to roots, or a combination of the two. Here, we investigated if and how the AMF Rhizophagus intraradices transported water to the host plant Avena barbata, wild oat. We used two‐compartment microcosms, isotopically labeled water, and a fluorescent dye to directly track and quantify water transport by AMF across an air gap to host plants. Plants grown with AMF that had access to a physically separated compartment containing (18)O‐labeled water transpired almost twice as much as plants with AMF excluded from that compartment. Using an isotopic mixing model, we estimated that water transported by AMF across the air gap accounted for 34.6% of the water transpired by host plants. In addition, a fluorescent dye indicated that hyphae were able to transport some water via an extracytoplasmic pathway. Our study provides direct evidence that AMF can act as extensions of the root system along the soil–plant–air continuum of water movement, with plant transpiration driving water flow along hyphae outside of the hyphal cell membrane. |
format | Online Article Text |
id | pubmed-9543596 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-95435962022-10-14 Routes to roots: direct evidence of water transport by arbuscular mycorrhizal fungi to host plants Kakouridis, Anne Hagen, John A. Kan, Megan P. Mambelli, Stefania Feldman, Lewis J. Herman, Donald J. Weber, Peter K. Pett‐Ridge, Jennifer Firestone, Mary K. New Phytol Research Arbuscular mycorrhizal fungi (AMF) can help mitigate plant responses to water stress, but it is unclear whether AMF do so by indirect mechanisms, direct water transport to roots, or a combination of the two. Here, we investigated if and how the AMF Rhizophagus intraradices transported water to the host plant Avena barbata, wild oat. We used two‐compartment microcosms, isotopically labeled water, and a fluorescent dye to directly track and quantify water transport by AMF across an air gap to host plants. Plants grown with AMF that had access to a physically separated compartment containing (18)O‐labeled water transpired almost twice as much as plants with AMF excluded from that compartment. Using an isotopic mixing model, we estimated that water transported by AMF across the air gap accounted for 34.6% of the water transpired by host plants. In addition, a fluorescent dye indicated that hyphae were able to transport some water via an extracytoplasmic pathway. Our study provides direct evidence that AMF can act as extensions of the root system along the soil–plant–air continuum of water movement, with plant transpiration driving water flow along hyphae outside of the hyphal cell membrane. John Wiley and Sons Inc. 2022-07-01 2022-10 /pmc/articles/PMC9543596/ /pubmed/35633108 http://dx.doi.org/10.1111/nph.18281 Text en © 2022 The Authors. New Phytologist © 2022 New Phytologist Foundation. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Research Kakouridis, Anne Hagen, John A. Kan, Megan P. Mambelli, Stefania Feldman, Lewis J. Herman, Donald J. Weber, Peter K. Pett‐Ridge, Jennifer Firestone, Mary K. Routes to roots: direct evidence of water transport by arbuscular mycorrhizal fungi to host plants |
title | Routes to roots: direct evidence of water transport by arbuscular mycorrhizal fungi to host plants |
title_full | Routes to roots: direct evidence of water transport by arbuscular mycorrhizal fungi to host plants |
title_fullStr | Routes to roots: direct evidence of water transport by arbuscular mycorrhizal fungi to host plants |
title_full_unstemmed | Routes to roots: direct evidence of water transport by arbuscular mycorrhizal fungi to host plants |
title_short | Routes to roots: direct evidence of water transport by arbuscular mycorrhizal fungi to host plants |
title_sort | routes to roots: direct evidence of water transport by arbuscular mycorrhizal fungi to host plants |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9543596/ https://www.ncbi.nlm.nih.gov/pubmed/35633108 http://dx.doi.org/10.1111/nph.18281 |
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