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Chemical Interaction among Termite-Associated Microbes

Bacteria and fungi in shared environments compete with one another for common substrates, and this competition typically involves microbially-produced small molecules. An investigation of one shared environmental niche, the carton material of the Formosan subterranean termite Coptotermes formosanus,...

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Autores principales: Mevers, Emily, Chouvenc, Thomas, Su, Nan-Yao, Clardy, Jon
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5735195/
https://www.ncbi.nlm.nih.gov/pubmed/29134406
http://dx.doi.org/10.1007/s10886-017-0900-6
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author Mevers, Emily
Chouvenc, Thomas
Su, Nan-Yao
Clardy, Jon
author_facet Mevers, Emily
Chouvenc, Thomas
Su, Nan-Yao
Clardy, Jon
author_sort Mevers, Emily
collection PubMed
description Bacteria and fungi in shared environments compete with one another for common substrates, and this competition typically involves microbially-produced small molecules. An investigation of one shared environmental niche, the carton material of the Formosan subterranean termite Coptotermes formosanus, identified the participants on one of these molecular exchanges. Molecular characterization of several termite-associated actinobacteria strains identified eleven known antimicrobial metabolites that may aid in protecting the C. formosanus colony from pathogenic fungal infections. One particular actinobacterial-derived small molecule, bafilomycin C1, elicited a strong chemical response from Trichoderma harzianum, a common soil saprophyte. Upon purification and structure elucidation, three major fungal metabolites were identified, t22-azaphilone, cryptenol, and homodimericin A. Both t22-azaphilone and homodimericin A are strongly upregulated, 123- and 38-fold, respectively, when exposed to bafilomycin C1, suggesting each play a role in defending T. harzianum from the toxic effect of bafilomycin C1. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s10886-017-0900-6) contains supplementary material, which is available to authorized users.
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spelling pubmed-57351952017-12-26 Chemical Interaction among Termite-Associated Microbes Mevers, Emily Chouvenc, Thomas Su, Nan-Yao Clardy, Jon J Chem Ecol Article Bacteria and fungi in shared environments compete with one another for common substrates, and this competition typically involves microbially-produced small molecules. An investigation of one shared environmental niche, the carton material of the Formosan subterranean termite Coptotermes formosanus, identified the participants on one of these molecular exchanges. Molecular characterization of several termite-associated actinobacteria strains identified eleven known antimicrobial metabolites that may aid in protecting the C. formosanus colony from pathogenic fungal infections. One particular actinobacterial-derived small molecule, bafilomycin C1, elicited a strong chemical response from Trichoderma harzianum, a common soil saprophyte. Upon purification and structure elucidation, three major fungal metabolites were identified, t22-azaphilone, cryptenol, and homodimericin A. Both t22-azaphilone and homodimericin A are strongly upregulated, 123- and 38-fold, respectively, when exposed to bafilomycin C1, suggesting each play a role in defending T. harzianum from the toxic effect of bafilomycin C1. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s10886-017-0900-6) contains supplementary material, which is available to authorized users. Springer US 2017-11-13 2017 /pmc/articles/PMC5735195/ /pubmed/29134406 http://dx.doi.org/10.1007/s10886-017-0900-6 Text en © The Author(s) 2017 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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.
spellingShingle Article
Mevers, Emily
Chouvenc, Thomas
Su, Nan-Yao
Clardy, Jon
Chemical Interaction among Termite-Associated Microbes
title Chemical Interaction among Termite-Associated Microbes
title_full Chemical Interaction among Termite-Associated Microbes
title_fullStr Chemical Interaction among Termite-Associated Microbes
title_full_unstemmed Chemical Interaction among Termite-Associated Microbes
title_short Chemical Interaction among Termite-Associated Microbes
title_sort chemical interaction among termite-associated microbes
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5735195/
https://www.ncbi.nlm.nih.gov/pubmed/29134406
http://dx.doi.org/10.1007/s10886-017-0900-6
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