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Chemical warfare between leafcutter ant symbionts and a co-evolved pathogen

Acromyrmex leafcutter ants form a mutually beneficial symbiosis with the fungus Leucoagaricus gongylophorus and with Pseudonocardia bacteria. Both are vertically transmitted and actively maintained by the ants. The fungus garden is manured with freshly cut leaves and provides the sole food for the a...

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Autores principales: Heine, Daniel, Holmes, Neil A., Worsley, Sarah F., Santos, Ana Carolina A., Innocent, Tabitha M., Scherlach, Kirstin, Patrick, Elaine H., Yu, Douglas W., Murrell, J. Colin, Vieria, Paulo C., Boomsma, Jacobus J., Hertweck, Christian, Hutchings, Matthew I., Wilkinson, Barrie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5992151/
https://www.ncbi.nlm.nih.gov/pubmed/29880868
http://dx.doi.org/10.1038/s41467-018-04520-1
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author Heine, Daniel
Holmes, Neil A.
Worsley, Sarah F.
Santos, Ana Carolina A.
Innocent, Tabitha M.
Scherlach, Kirstin
Patrick, Elaine H.
Yu, Douglas W.
Murrell, J. Colin
Vieria, Paulo C.
Boomsma, Jacobus J.
Hertweck, Christian
Hutchings, Matthew I.
Wilkinson, Barrie
author_facet Heine, Daniel
Holmes, Neil A.
Worsley, Sarah F.
Santos, Ana Carolina A.
Innocent, Tabitha M.
Scherlach, Kirstin
Patrick, Elaine H.
Yu, Douglas W.
Murrell, J. Colin
Vieria, Paulo C.
Boomsma, Jacobus J.
Hertweck, Christian
Hutchings, Matthew I.
Wilkinson, Barrie
author_sort Heine, Daniel
collection PubMed
description Acromyrmex leafcutter ants form a mutually beneficial symbiosis with the fungus Leucoagaricus gongylophorus and with Pseudonocardia bacteria. Both are vertically transmitted and actively maintained by the ants. The fungus garden is manured with freshly cut leaves and provides the sole food for the ant larvae, while Pseudonocardia cultures are reared on the ant-cuticle and make antifungal metabolites to help protect the cultivar against disease. If left unchecked, specialized parasitic Escovopsis fungi can overrun the fungus garden and lead to colony collapse. We report that Escovopsis upregulates the production of two specialized metabolites when it infects the cultivar. These compounds inhibit Pseudonocardia and one, shearinine D, also reduces worker behavioral defenses and is ultimately lethal when it accumulates in ant tissues. Our results are consistent with an active evolutionary arms race between Pseudonocardia and Escovopsis, which modifies both bacterial and behavioral defenses such that colony collapse is unavoidable once Escovopsis infections escalate.
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spelling pubmed-59921512018-06-11 Chemical warfare between leafcutter ant symbionts and a co-evolved pathogen Heine, Daniel Holmes, Neil A. Worsley, Sarah F. Santos, Ana Carolina A. Innocent, Tabitha M. Scherlach, Kirstin Patrick, Elaine H. Yu, Douglas W. Murrell, J. Colin Vieria, Paulo C. Boomsma, Jacobus J. Hertweck, Christian Hutchings, Matthew I. Wilkinson, Barrie Nat Commun Article Acromyrmex leafcutter ants form a mutually beneficial symbiosis with the fungus Leucoagaricus gongylophorus and with Pseudonocardia bacteria. Both are vertically transmitted and actively maintained by the ants. The fungus garden is manured with freshly cut leaves and provides the sole food for the ant larvae, while Pseudonocardia cultures are reared on the ant-cuticle and make antifungal metabolites to help protect the cultivar against disease. If left unchecked, specialized parasitic Escovopsis fungi can overrun the fungus garden and lead to colony collapse. We report that Escovopsis upregulates the production of two specialized metabolites when it infects the cultivar. These compounds inhibit Pseudonocardia and one, shearinine D, also reduces worker behavioral defenses and is ultimately lethal when it accumulates in ant tissues. Our results are consistent with an active evolutionary arms race between Pseudonocardia and Escovopsis, which modifies both bacterial and behavioral defenses such that colony collapse is unavoidable once Escovopsis infections escalate. Nature Publishing Group UK 2018-06-07 /pmc/articles/PMC5992151/ /pubmed/29880868 http://dx.doi.org/10.1038/s41467-018-04520-1 Text en © The Author(s) 2018 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
Heine, Daniel
Holmes, Neil A.
Worsley, Sarah F.
Santos, Ana Carolina A.
Innocent, Tabitha M.
Scherlach, Kirstin
Patrick, Elaine H.
Yu, Douglas W.
Murrell, J. Colin
Vieria, Paulo C.
Boomsma, Jacobus J.
Hertweck, Christian
Hutchings, Matthew I.
Wilkinson, Barrie
Chemical warfare between leafcutter ant symbionts and a co-evolved pathogen
title Chemical warfare between leafcutter ant symbionts and a co-evolved pathogen
title_full Chemical warfare between leafcutter ant symbionts and a co-evolved pathogen
title_fullStr Chemical warfare between leafcutter ant symbionts and a co-evolved pathogen
title_full_unstemmed Chemical warfare between leafcutter ant symbionts and a co-evolved pathogen
title_short Chemical warfare between leafcutter ant symbionts and a co-evolved pathogen
title_sort chemical warfare between leafcutter ant symbionts and a co-evolved pathogen
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5992151/
https://www.ncbi.nlm.nih.gov/pubmed/29880868
http://dx.doi.org/10.1038/s41467-018-04520-1
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