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An invasive beetle–fungus complex is maintained by fungal nutritional-compensation mediated by bacterial volatiles
Mutualisms between symbiotic microbes and animals have been well documented, and nutritional relationships provide the foundation for maintaining beneficial associations. The well-studied mutualism between bark beetles and their fungi has become a classic model system in the study of symbioses. Desp...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7784882/ https://www.ncbi.nlm.nih.gov/pubmed/32814865 http://dx.doi.org/10.1038/s41396-020-00740-w |
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author | Liu, Fanghua Wickham, Jacob D. Cao, Qingjie Lu, Min Sun, Jianghua |
author_facet | Liu, Fanghua Wickham, Jacob D. Cao, Qingjie Lu, Min Sun, Jianghua |
author_sort | Liu, Fanghua |
collection | PubMed |
description | Mutualisms between symbiotic microbes and animals have been well documented, and nutritional relationships provide the foundation for maintaining beneficial associations. The well-studied mutualism between bark beetles and their fungi has become a classic model system in the study of symbioses. Despite the nutritional competition between bark beetles and beneficial fungi in the same niche due to poor nutritional feeding substrates, bark beetles still maintain mutualistic associations with beneficial fungi over time. The mechanism behind this phenomenon, however, remains largely unknown. Here, we demonstrated the bark beetle Dendroctonus valens LeConte relies on the symbiotic bacterial volatile ammonia, as a nitrogen source, to regulate carbohydrate metabolism of its mutualistic fungus Leptographium procerum to alleviate nutritional competition, thereby maintaining the stability of the bark beetle–fungus mutualism. Ammonia significantly reduces competition of L. procerum for carbon resources for D. valens larval growth and increases fungal growth. Using stable isotope analysis, we show the fungus breakdown of phloem starch into d-glucose by switching on amylase genes only in the presence of ammonia. Deletion of amylase genes interferes with the conversion of starch to glucose. The acceleration of carbohydrate consumption and the conversion of starch into glucose benefit this invasive beetle–fungus complex. The nutrient consumption–compensation strategy mediated by tripartite beetle–fungus–bacterium aids the maintenance of this invasive mutualism under limited nutritional conditions, exacerbating its invasiveness with this competitive nutritional edge. |
format | Online Article Text |
id | pubmed-7784882 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-77848822021-01-14 An invasive beetle–fungus complex is maintained by fungal nutritional-compensation mediated by bacterial volatiles Liu, Fanghua Wickham, Jacob D. Cao, Qingjie Lu, Min Sun, Jianghua ISME J Article Mutualisms between symbiotic microbes and animals have been well documented, and nutritional relationships provide the foundation for maintaining beneficial associations. The well-studied mutualism between bark beetles and their fungi has become a classic model system in the study of symbioses. Despite the nutritional competition between bark beetles and beneficial fungi in the same niche due to poor nutritional feeding substrates, bark beetles still maintain mutualistic associations with beneficial fungi over time. The mechanism behind this phenomenon, however, remains largely unknown. Here, we demonstrated the bark beetle Dendroctonus valens LeConte relies on the symbiotic bacterial volatile ammonia, as a nitrogen source, to regulate carbohydrate metabolism of its mutualistic fungus Leptographium procerum to alleviate nutritional competition, thereby maintaining the stability of the bark beetle–fungus mutualism. Ammonia significantly reduces competition of L. procerum for carbon resources for D. valens larval growth and increases fungal growth. Using stable isotope analysis, we show the fungus breakdown of phloem starch into d-glucose by switching on amylase genes only in the presence of ammonia. Deletion of amylase genes interferes with the conversion of starch to glucose. The acceleration of carbohydrate consumption and the conversion of starch into glucose benefit this invasive beetle–fungus complex. The nutrient consumption–compensation strategy mediated by tripartite beetle–fungus–bacterium aids the maintenance of this invasive mutualism under limited nutritional conditions, exacerbating its invasiveness with this competitive nutritional edge. Nature Publishing Group UK 2020-08-19 2020-11 /pmc/articles/PMC7784882/ /pubmed/32814865 http://dx.doi.org/10.1038/s41396-020-00740-w Text en © The Author(s) 2020 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 Liu, Fanghua Wickham, Jacob D. Cao, Qingjie Lu, Min Sun, Jianghua An invasive beetle–fungus complex is maintained by fungal nutritional-compensation mediated by bacterial volatiles |
title | An invasive beetle–fungus complex is maintained by fungal nutritional-compensation mediated by bacterial volatiles |
title_full | An invasive beetle–fungus complex is maintained by fungal nutritional-compensation mediated by bacterial volatiles |
title_fullStr | An invasive beetle–fungus complex is maintained by fungal nutritional-compensation mediated by bacterial volatiles |
title_full_unstemmed | An invasive beetle–fungus complex is maintained by fungal nutritional-compensation mediated by bacterial volatiles |
title_short | An invasive beetle–fungus complex is maintained by fungal nutritional-compensation mediated by bacterial volatiles |
title_sort | invasive beetle–fungus complex is maintained by fungal nutritional-compensation mediated by bacterial volatiles |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7784882/ https://www.ncbi.nlm.nih.gov/pubmed/32814865 http://dx.doi.org/10.1038/s41396-020-00740-w |
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