Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Liu, Fanghua, Wickham, Jacob D., Cao, Qingjie, Lu, Min, Sun, Jianghua
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
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
_version_ 1783632364834914304
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
work_keys_str_mv AT liufanghua aninvasivebeetlefunguscomplexismaintainedbyfungalnutritionalcompensationmediatedbybacterialvolatiles
AT wickhamjacobd aninvasivebeetlefunguscomplexismaintainedbyfungalnutritionalcompensationmediatedbybacterialvolatiles
AT caoqingjie aninvasivebeetlefunguscomplexismaintainedbyfungalnutritionalcompensationmediatedbybacterialvolatiles
AT lumin aninvasivebeetlefunguscomplexismaintainedbyfungalnutritionalcompensationmediatedbybacterialvolatiles
AT sunjianghua aninvasivebeetlefunguscomplexismaintainedbyfungalnutritionalcompensationmediatedbybacterialvolatiles
AT liufanghua invasivebeetlefunguscomplexismaintainedbyfungalnutritionalcompensationmediatedbybacterialvolatiles
AT wickhamjacobd invasivebeetlefunguscomplexismaintainedbyfungalnutritionalcompensationmediatedbybacterialvolatiles
AT caoqingjie invasivebeetlefunguscomplexismaintainedbyfungalnutritionalcompensationmediatedbybacterialvolatiles
AT lumin invasivebeetlefunguscomplexismaintainedbyfungalnutritionalcompensationmediatedbybacterialvolatiles
AT sunjianghua invasivebeetlefunguscomplexismaintainedbyfungalnutritionalcompensationmediatedbybacterialvolatiles