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You don’t have the guts: a diverse set of fungi survive passage through Macrotermes bellicosus termite guts

BACKGROUND: Monoculture farming poses significant disease challenges, but fungus-farming termites are able to successfully keep their monoculture crop free from contamination by other fungi. It has been hypothesised that obligate gut passage of all plant substrate used to manure the fungal symbiont...

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Autores principales: Bos, Nick, Guimaraes, Leandro, Palenzuela, Romen, Renelies-Hamilton, Justinn, Maccario, Lorrie, Silue, Simon Kolotchèlèma, Koné, N.’golo Abdoulaye, Poulsen, Michael
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7724875/
https://www.ncbi.nlm.nih.gov/pubmed/33297950
http://dx.doi.org/10.1186/s12862-020-01727-z
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author Bos, Nick
Guimaraes, Leandro
Palenzuela, Romen
Renelies-Hamilton, Justinn
Maccario, Lorrie
Silue, Simon Kolotchèlèma
Koné, N.’golo Abdoulaye
Poulsen, Michael
author_facet Bos, Nick
Guimaraes, Leandro
Palenzuela, Romen
Renelies-Hamilton, Justinn
Maccario, Lorrie
Silue, Simon Kolotchèlèma
Koné, N.’golo Abdoulaye
Poulsen, Michael
author_sort Bos, Nick
collection PubMed
description BACKGROUND: Monoculture farming poses significant disease challenges, but fungus-farming termites are able to successfully keep their monoculture crop free from contamination by other fungi. It has been hypothesised that obligate gut passage of all plant substrate used to manure the fungal symbiont is key to accomplish this. Here we refute this hypothesis in the fungus-farming termite species Macrotermes bellicosus. RESULTS: We first used ITS amplicon sequencing to show that plant substrate foraged on by termite workers harbour diverse fungal communities, which potentially could challenge the farming symbiosis. Subsequently, we cultivated fungi from dissected sections of termite guts to show that fungal diversity does not decrease during gut passage. Therefore, we investigated if healthy combs harboured these undesirable fungal genera, and whether the presence of workers affected fungal diversity within combs. Removal of workers led to a surge in fungal diversity in combs, implying that termite defences must be responsible for the near-complete absence of other fungi in functioning termite gardens. CONCLUSIONS: The rapid proliferation of some of these fungi when colonies are compromised indicates that some antagonists successfully employ a sit-and-wait strategy that allows them to remain dormant until conditions are favourable. Although this strategy requires potentially many years of waiting, it prevents these fungi from engaging in an evolutionary arms race with the termite host, which employs a series of complementary behavioural and chemical defences that may prove insurmountable.
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spelling pubmed-77248752020-12-09 You don’t have the guts: a diverse set of fungi survive passage through Macrotermes bellicosus termite guts Bos, Nick Guimaraes, Leandro Palenzuela, Romen Renelies-Hamilton, Justinn Maccario, Lorrie Silue, Simon Kolotchèlèma Koné, N.’golo Abdoulaye Poulsen, Michael BMC Evol Biol Research Article BACKGROUND: Monoculture farming poses significant disease challenges, but fungus-farming termites are able to successfully keep their monoculture crop free from contamination by other fungi. It has been hypothesised that obligate gut passage of all plant substrate used to manure the fungal symbiont is key to accomplish this. Here we refute this hypothesis in the fungus-farming termite species Macrotermes bellicosus. RESULTS: We first used ITS amplicon sequencing to show that plant substrate foraged on by termite workers harbour diverse fungal communities, which potentially could challenge the farming symbiosis. Subsequently, we cultivated fungi from dissected sections of termite guts to show that fungal diversity does not decrease during gut passage. Therefore, we investigated if healthy combs harboured these undesirable fungal genera, and whether the presence of workers affected fungal diversity within combs. Removal of workers led to a surge in fungal diversity in combs, implying that termite defences must be responsible for the near-complete absence of other fungi in functioning termite gardens. CONCLUSIONS: The rapid proliferation of some of these fungi when colonies are compromised indicates that some antagonists successfully employ a sit-and-wait strategy that allows them to remain dormant until conditions are favourable. Although this strategy requires potentially many years of waiting, it prevents these fungi from engaging in an evolutionary arms race with the termite host, which employs a series of complementary behavioural and chemical defences that may prove insurmountable. BioMed Central 2020-12-09 /pmc/articles/PMC7724875/ /pubmed/33297950 http://dx.doi.org/10.1186/s12862-020-01727-z Text en © The Author(s) 2020 Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research Article
Bos, Nick
Guimaraes, Leandro
Palenzuela, Romen
Renelies-Hamilton, Justinn
Maccario, Lorrie
Silue, Simon Kolotchèlèma
Koné, N.’golo Abdoulaye
Poulsen, Michael
You don’t have the guts: a diverse set of fungi survive passage through Macrotermes bellicosus termite guts
title You don’t have the guts: a diverse set of fungi survive passage through Macrotermes bellicosus termite guts
title_full You don’t have the guts: a diverse set of fungi survive passage through Macrotermes bellicosus termite guts
title_fullStr You don’t have the guts: a diverse set of fungi survive passage through Macrotermes bellicosus termite guts
title_full_unstemmed You don’t have the guts: a diverse set of fungi survive passage through Macrotermes bellicosus termite guts
title_short You don’t have the guts: a diverse set of fungi survive passage through Macrotermes bellicosus termite guts
title_sort you don’t have the guts: a diverse set of fungi survive passage through macrotermes bellicosus termite guts
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7724875/
https://www.ncbi.nlm.nih.gov/pubmed/33297950
http://dx.doi.org/10.1186/s12862-020-01727-z
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