Cargando…

Species- and Caste-Specific Gut Metabolomes in Fungus-Farming Termites

Fungus-farming termites host gut microbial communities that contribute to the pre-digestion of plant biomass for manuring the fungal mutualist, and potentially to the production of defensive compounds that suppress antagonists. Termite colonies are characterized by complex division of labor and diff...

Descripción completa

Detalles Bibliográficos
Autores principales: Vidkjær, Nanna Hjort, Schmidt, Suzanne, Hu, Haofu, Bodawatta, Kasun H., Beemelmanns, Christine, Poulsen, Michael
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8707012/
https://www.ncbi.nlm.nih.gov/pubmed/34940597
http://dx.doi.org/10.3390/metabo11120839
_version_ 1784622332496576512
author Vidkjær, Nanna Hjort
Schmidt, Suzanne
Hu, Haofu
Bodawatta, Kasun H.
Beemelmanns, Christine
Poulsen, Michael
author_facet Vidkjær, Nanna Hjort
Schmidt, Suzanne
Hu, Haofu
Bodawatta, Kasun H.
Beemelmanns, Christine
Poulsen, Michael
author_sort Vidkjær, Nanna Hjort
collection PubMed
description Fungus-farming termites host gut microbial communities that contribute to the pre-digestion of plant biomass for manuring the fungal mutualist, and potentially to the production of defensive compounds that suppress antagonists. Termite colonies are characterized by complex division of labor and differences in diet between termite size (minor and major) and morphological (worker and soldier) castes, and this extends to the composition of their gut microbial communities. We hypothesized that gut metabolomes should mirror these differences and tested this through untargeted LC-MS/MS analyses of three South African species of fungus-farming termites. We found distinct metabolomes between species and across castes, especially between soldiers and workers. Primary metabolites dominate the metabolomes and the high number of overlapping features with the mutualistic fungus and plant material show distinct impacts of diet and the environment. The identification of a few bioactive compounds of likely microbial origin underlines the potential for compound discovery among the many unannotated features. Our untargeted approach provides a first glimpse into the complex gut metabolomes and our dereplication suggests the presence of bioactive compounds with potential defensive roles to be targeted in future studies.
format Online
Article
Text
id pubmed-8707012
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher MDPI
record_format MEDLINE/PubMed
spelling pubmed-87070122021-12-25 Species- and Caste-Specific Gut Metabolomes in Fungus-Farming Termites Vidkjær, Nanna Hjort Schmidt, Suzanne Hu, Haofu Bodawatta, Kasun H. Beemelmanns, Christine Poulsen, Michael Metabolites Article Fungus-farming termites host gut microbial communities that contribute to the pre-digestion of plant biomass for manuring the fungal mutualist, and potentially to the production of defensive compounds that suppress antagonists. Termite colonies are characterized by complex division of labor and differences in diet between termite size (minor and major) and morphological (worker and soldier) castes, and this extends to the composition of their gut microbial communities. We hypothesized that gut metabolomes should mirror these differences and tested this through untargeted LC-MS/MS analyses of three South African species of fungus-farming termites. We found distinct metabolomes between species and across castes, especially between soldiers and workers. Primary metabolites dominate the metabolomes and the high number of overlapping features with the mutualistic fungus and plant material show distinct impacts of diet and the environment. The identification of a few bioactive compounds of likely microbial origin underlines the potential for compound discovery among the many unannotated features. Our untargeted approach provides a first glimpse into the complex gut metabolomes and our dereplication suggests the presence of bioactive compounds with potential defensive roles to be targeted in future studies. MDPI 2021-12-04 /pmc/articles/PMC8707012/ /pubmed/34940597 http://dx.doi.org/10.3390/metabo11120839 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Vidkjær, Nanna Hjort
Schmidt, Suzanne
Hu, Haofu
Bodawatta, Kasun H.
Beemelmanns, Christine
Poulsen, Michael
Species- and Caste-Specific Gut Metabolomes in Fungus-Farming Termites
title Species- and Caste-Specific Gut Metabolomes in Fungus-Farming Termites
title_full Species- and Caste-Specific Gut Metabolomes in Fungus-Farming Termites
title_fullStr Species- and Caste-Specific Gut Metabolomes in Fungus-Farming Termites
title_full_unstemmed Species- and Caste-Specific Gut Metabolomes in Fungus-Farming Termites
title_short Species- and Caste-Specific Gut Metabolomes in Fungus-Farming Termites
title_sort species- and caste-specific gut metabolomes in fungus-farming termites
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8707012/
https://www.ncbi.nlm.nih.gov/pubmed/34940597
http://dx.doi.org/10.3390/metabo11120839
work_keys_str_mv AT vidkjærnannahjort speciesandcastespecificgutmetabolomesinfungusfarmingtermites
AT schmidtsuzanne speciesandcastespecificgutmetabolomesinfungusfarmingtermites
AT huhaofu speciesandcastespecificgutmetabolomesinfungusfarmingtermites
AT bodawattakasunh speciesandcastespecificgutmetabolomesinfungusfarmingtermites
AT beemelmannschristine speciesandcastespecificgutmetabolomesinfungusfarmingtermites
AT poulsenmichael speciesandcastespecificgutmetabolomesinfungusfarmingtermites