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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,...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer US
2017
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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. |
format | Online Article Text |
id | pubmed-5735195 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Springer US |
record_format | MEDLINE/PubMed |
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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