Make the environment protect you from disease: elevated CO2 inhibits antagonists of the fungus-farming termite symbiosis

Research output: Contribution to journalJournal articleResearchpeer-review

Standard

Make the environment protect you from disease : elevated CO2 inhibits antagonists of the fungus-farming termite symbiosis. / Schmidt, Suzanne; Bos, Nick; Murphy, Robert; Koné, N’Golo A.; Silué, Kolotchelema S.; Meyling, Nicolai V.; Poulsen, Michael.

In: Frontiers in Ecology and Evolution, Vol. 11, 1134492, 2023.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Schmidt, S, Bos, N, Murphy, R, Koné, NGA, Silué, KS, Meyling, NV & Poulsen, M 2023, 'Make the environment protect you from disease: elevated CO2 inhibits antagonists of the fungus-farming termite symbiosis', Frontiers in Ecology and Evolution, vol. 11, 1134492. https://doi.org/10.3389/fevo.2023.1134492

APA

Schmidt, S., Bos, N., Murphy, R., Koné, NG. A., Silué, K. S., Meyling, N. V., & Poulsen, M. (2023). Make the environment protect you from disease: elevated CO2 inhibits antagonists of the fungus-farming termite symbiosis. Frontiers in Ecology and Evolution, 11, [1134492]. https://doi.org/10.3389/fevo.2023.1134492

Vancouver

Schmidt S, Bos N, Murphy R, Koné NGA, Silué KS, Meyling NV et al. Make the environment protect you from disease: elevated CO2 inhibits antagonists of the fungus-farming termite symbiosis. Frontiers in Ecology and Evolution. 2023;11. 1134492. https://doi.org/10.3389/fevo.2023.1134492

Author

Schmidt, Suzanne ; Bos, Nick ; Murphy, Robert ; Koné, N’Golo A. ; Silué, Kolotchelema S. ; Meyling, Nicolai V. ; Poulsen, Michael. / Make the environment protect you from disease : elevated CO2 inhibits antagonists of the fungus-farming termite symbiosis. In: Frontiers in Ecology and Evolution. 2023 ; Vol. 11.

Bibtex

@article{9a19375fbd944ce29ebca7c805db809d,
title = "Make the environment protect you from disease: elevated CO2 inhibits antagonists of the fungus-farming termite symbiosis",
abstract = "Fungus-farming termite colonies maintain monoculture fungus combs in underground chambers without apparent problems with diseases. Multiple lines of defense contribute to the suppression or removal of antagonists of the symbiosis, but the role of the termite-manipulated environment within mounds has yet to be tested. Specifically, termite mounds have extremely high levels of CO2 compared to atmospheric levels. We tested the effect of 5% CO2 on the growth of fungal crops from Macrotermes bellicosus colonies, generalist fungi that could challenge the symbiosis, as well as a specialist stowaway fungus, Pseudoxylaria. For sporulating fungi, we also quantified the effects on conidia production. We found that elevated CO2 significantly reduces mycelial growth and conidia production of the generalist fungi Aspergillus sp., Beauveria bassiana, and Metarhizium brunneum, whereas it overall had a net positive effect on the growth of the fungal crop Termitomyces and Pseudoxylaria; albeit, with variation between fungal strains within genera. Our findings point to elevated CO2 being of adaptive significance to the fungus-farming termite symbiosis as an additional layer of defense that helps keep termite fungus gardens free from fungal infections. The mound-building activities that make termites ecosystem engineers may thus also generate environmental conditions that impact the fate of fungi inhabiting the extended phenotypes that massive termite mounds represent.",
keywords = "defense, extended phenotype, Macrotermes bellicosus, Macrotermitinae, Pseudoxylaria, Termitomyces",
author = "Suzanne Schmidt and Nick Bos and Robert Murphy and Kon{\'e}, {N{\textquoteright}Golo A.} and Silu{\'e}, {Kolotchelema S.} and Meyling, {Nicolai V.} and Michael Poulsen",
note = "Publisher Copyright: Copyright {\textcopyright} 2023 Schmidt, Bos, Murphy, Kon{\'e}, Silu{\'e}, Meyling and Poulsen.",
year = "2023",
doi = "10.3389/fevo.2023.1134492",
language = "English",
volume = "11",
journal = "Frontiers in Ecology and Evolution",
issn = "2296-701X",
publisher = "Frontiers Media",

}

RIS

TY - JOUR

T1 - Make the environment protect you from disease

T2 - elevated CO2 inhibits antagonists of the fungus-farming termite symbiosis

AU - Schmidt, Suzanne

AU - Bos, Nick

AU - Murphy, Robert

AU - Koné, N’Golo A.

AU - Silué, Kolotchelema S.

AU - Meyling, Nicolai V.

AU - Poulsen, Michael

N1 - Publisher Copyright: Copyright © 2023 Schmidt, Bos, Murphy, Koné, Silué, Meyling and Poulsen.

PY - 2023

Y1 - 2023

N2 - Fungus-farming termite colonies maintain monoculture fungus combs in underground chambers without apparent problems with diseases. Multiple lines of defense contribute to the suppression or removal of antagonists of the symbiosis, but the role of the termite-manipulated environment within mounds has yet to be tested. Specifically, termite mounds have extremely high levels of CO2 compared to atmospheric levels. We tested the effect of 5% CO2 on the growth of fungal crops from Macrotermes bellicosus colonies, generalist fungi that could challenge the symbiosis, as well as a specialist stowaway fungus, Pseudoxylaria. For sporulating fungi, we also quantified the effects on conidia production. We found that elevated CO2 significantly reduces mycelial growth and conidia production of the generalist fungi Aspergillus sp., Beauveria bassiana, and Metarhizium brunneum, whereas it overall had a net positive effect on the growth of the fungal crop Termitomyces and Pseudoxylaria; albeit, with variation between fungal strains within genera. Our findings point to elevated CO2 being of adaptive significance to the fungus-farming termite symbiosis as an additional layer of defense that helps keep termite fungus gardens free from fungal infections. The mound-building activities that make termites ecosystem engineers may thus also generate environmental conditions that impact the fate of fungi inhabiting the extended phenotypes that massive termite mounds represent.

AB - Fungus-farming termite colonies maintain monoculture fungus combs in underground chambers without apparent problems with diseases. Multiple lines of defense contribute to the suppression or removal of antagonists of the symbiosis, but the role of the termite-manipulated environment within mounds has yet to be tested. Specifically, termite mounds have extremely high levels of CO2 compared to atmospheric levels. We tested the effect of 5% CO2 on the growth of fungal crops from Macrotermes bellicosus colonies, generalist fungi that could challenge the symbiosis, as well as a specialist stowaway fungus, Pseudoxylaria. For sporulating fungi, we also quantified the effects on conidia production. We found that elevated CO2 significantly reduces mycelial growth and conidia production of the generalist fungi Aspergillus sp., Beauveria bassiana, and Metarhizium brunneum, whereas it overall had a net positive effect on the growth of the fungal crop Termitomyces and Pseudoxylaria; albeit, with variation between fungal strains within genera. Our findings point to elevated CO2 being of adaptive significance to the fungus-farming termite symbiosis as an additional layer of defense that helps keep termite fungus gardens free from fungal infections. The mound-building activities that make termites ecosystem engineers may thus also generate environmental conditions that impact the fate of fungi inhabiting the extended phenotypes that massive termite mounds represent.

KW - defense

KW - extended phenotype

KW - Macrotermes bellicosus

KW - Macrotermitinae

KW - Pseudoxylaria

KW - Termitomyces

U2 - 10.3389/fevo.2023.1134492

DO - 10.3389/fevo.2023.1134492

M3 - Journal article

AN - SCOPUS:85161008481

VL - 11

JO - Frontiers in Ecology and Evolution

JF - Frontiers in Ecology and Evolution

SN - 2296-701X

M1 - 1134492

ER -

ID: 357271180