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Lifespan and functionality of mycorrhizal fungal mycelium are uncoupled from host plant lifespan
Arbuscular mycorrhizal fungi (AMF) are obligate symbionts, living in associations with the roots of most land plants. AMF produce wide networks of extraradical mycelium (ERM) of indeterminate length, spreading from host roots into the surrounding soil and establishing belowground interconnections am...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6035242/ https://www.ncbi.nlm.nih.gov/pubmed/29980700 http://dx.doi.org/10.1038/s41598-018-28354-5 |
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author | Pepe, Alessandra Giovannetti, Manuela Sbrana, Cristiana |
author_facet | Pepe, Alessandra Giovannetti, Manuela Sbrana, Cristiana |
author_sort | Pepe, Alessandra |
collection | PubMed |
description | Arbuscular mycorrhizal fungi (AMF) are obligate symbionts, living in associations with the roots of most land plants. AMF produce wide networks of extraradical mycelium (ERM) of indeterminate length, spreading from host roots into the surrounding soil and establishing belowground interconnections among plants belonging to the same or to different taxa. Whether their lifespan and functionality are limited by host plant viability or can be extended beyond this limit is unknown. To address this issue, we performed time-course studies to investigate viability and functionality of ERM produced in an in vivo whole-plant system by Funneliformis mosseae and Rhizoglomus irregulare, after shoot detachment. Our data revealed that viability and functionality of F. mosseae and R. irregulare extraradical hyphae were uncoupled from host plant lifespan. Indeed, ERM spreading from roots of intact or shootless plants showed comparable levels of viability, similar structural traits and ability to establish mycorrhizal symbioses with new plants, as long as five months after shoot removal. Our findings expand the current knowledge on AMF biology and life cycle, providing data on ERM long-term survival in the soil of two Glomeracean species, functional to the prompt establishment of mycorrhizal symbioses and to the maintenance of soil biological fertility. |
format | Online Article Text |
id | pubmed-6035242 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-60352422018-07-12 Lifespan and functionality of mycorrhizal fungal mycelium are uncoupled from host plant lifespan Pepe, Alessandra Giovannetti, Manuela Sbrana, Cristiana Sci Rep Article Arbuscular mycorrhizal fungi (AMF) are obligate symbionts, living in associations with the roots of most land plants. AMF produce wide networks of extraradical mycelium (ERM) of indeterminate length, spreading from host roots into the surrounding soil and establishing belowground interconnections among plants belonging to the same or to different taxa. Whether their lifespan and functionality are limited by host plant viability or can be extended beyond this limit is unknown. To address this issue, we performed time-course studies to investigate viability and functionality of ERM produced in an in vivo whole-plant system by Funneliformis mosseae and Rhizoglomus irregulare, after shoot detachment. Our data revealed that viability and functionality of F. mosseae and R. irregulare extraradical hyphae were uncoupled from host plant lifespan. Indeed, ERM spreading from roots of intact or shootless plants showed comparable levels of viability, similar structural traits and ability to establish mycorrhizal symbioses with new plants, as long as five months after shoot removal. Our findings expand the current knowledge on AMF biology and life cycle, providing data on ERM long-term survival in the soil of two Glomeracean species, functional to the prompt establishment of mycorrhizal symbioses and to the maintenance of soil biological fertility. Nature Publishing Group UK 2018-07-06 /pmc/articles/PMC6035242/ /pubmed/29980700 http://dx.doi.org/10.1038/s41598-018-28354-5 Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Pepe, Alessandra Giovannetti, Manuela Sbrana, Cristiana Lifespan and functionality of mycorrhizal fungal mycelium are uncoupled from host plant lifespan |
title | Lifespan and functionality of mycorrhizal fungal mycelium are uncoupled from host plant lifespan |
title_full | Lifespan and functionality of mycorrhizal fungal mycelium are uncoupled from host plant lifespan |
title_fullStr | Lifespan and functionality of mycorrhizal fungal mycelium are uncoupled from host plant lifespan |
title_full_unstemmed | Lifespan and functionality of mycorrhizal fungal mycelium are uncoupled from host plant lifespan |
title_short | Lifespan and functionality of mycorrhizal fungal mycelium are uncoupled from host plant lifespan |
title_sort | lifespan and functionality of mycorrhizal fungal mycelium are uncoupled from host plant lifespan |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6035242/ https://www.ncbi.nlm.nih.gov/pubmed/29980700 http://dx.doi.org/10.1038/s41598-018-28354-5 |
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