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Isolation of an antimicrobial compound produced by bacteria associated with reef-building corals
Bacterial communities associated with healthy corals produce antimicrobial compounds that inhibit the colonization and growth of invasive microbes and potential pathogens. To date, however, bacteria-derived antimicrobial molecules have not been identified in reef-building corals. Here, we report the...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
PeerJ Inc.
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4994080/ https://www.ncbi.nlm.nih.gov/pubmed/27602265 http://dx.doi.org/10.7717/peerj.2275 |
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author | Raina, Jean-Baptiste Tapiolas, Dianne Motti, Cherie A. Foret, Sylvain Seemann, Torsten Tebben, Jan Willis, Bette L. Bourne, David G. |
author_facet | Raina, Jean-Baptiste Tapiolas, Dianne Motti, Cherie A. Foret, Sylvain Seemann, Torsten Tebben, Jan Willis, Bette L. Bourne, David G. |
author_sort | Raina, Jean-Baptiste |
collection | PubMed |
description | Bacterial communities associated with healthy corals produce antimicrobial compounds that inhibit the colonization and growth of invasive microbes and potential pathogens. To date, however, bacteria-derived antimicrobial molecules have not been identified in reef-building corals. Here, we report the isolation of an antimicrobial compound produced by Pseudovibrio sp. P12, a common and abundant coral-associated bacterium. This strain was capable of metabolizing dimethylsulfoniopropionate (DMSP), a sulfur molecule produced in high concentrations by reef-building corals and playing a role in structuring their bacterial communities. Bioassay-guided fractionation coupled with nuclear magnetic resonance (NMR) and mass spectrometry (MS), identified the antimicrobial as tropodithietic acid (TDA), a sulfur-containing compound likely derived from DMSP catabolism. TDA was produced in large quantities by Pseudovibrio sp., and prevented the growth of two previously identified coral pathogens, Vibrio coralliilyticus and V. owensii, at very low concentrations (0.5 μg/mL) in agar diffusion assays. Genome sequencing of Pseudovibrio sp. P12 identified gene homologs likely involved in the metabolism of DMSP and production of TDA. These results provide additional evidence for the integral role of DMSP in structuring coral-associated bacterial communities and underline the potential of these DMSP-metabolizing microbes to contribute to coral disease prevention. |
format | Online Article Text |
id | pubmed-4994080 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | PeerJ Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-49940802016-09-06 Isolation of an antimicrobial compound produced by bacteria associated with reef-building corals Raina, Jean-Baptiste Tapiolas, Dianne Motti, Cherie A. Foret, Sylvain Seemann, Torsten Tebben, Jan Willis, Bette L. Bourne, David G. PeerJ Marine Biology Bacterial communities associated with healthy corals produce antimicrobial compounds that inhibit the colonization and growth of invasive microbes and potential pathogens. To date, however, bacteria-derived antimicrobial molecules have not been identified in reef-building corals. Here, we report the isolation of an antimicrobial compound produced by Pseudovibrio sp. P12, a common and abundant coral-associated bacterium. This strain was capable of metabolizing dimethylsulfoniopropionate (DMSP), a sulfur molecule produced in high concentrations by reef-building corals and playing a role in structuring their bacterial communities. Bioassay-guided fractionation coupled with nuclear magnetic resonance (NMR) and mass spectrometry (MS), identified the antimicrobial as tropodithietic acid (TDA), a sulfur-containing compound likely derived from DMSP catabolism. TDA was produced in large quantities by Pseudovibrio sp., and prevented the growth of two previously identified coral pathogens, Vibrio coralliilyticus and V. owensii, at very low concentrations (0.5 μg/mL) in agar diffusion assays. Genome sequencing of Pseudovibrio sp. P12 identified gene homologs likely involved in the metabolism of DMSP and production of TDA. These results provide additional evidence for the integral role of DMSP in structuring coral-associated bacterial communities and underline the potential of these DMSP-metabolizing microbes to contribute to coral disease prevention. PeerJ Inc. 2016-08-18 /pmc/articles/PMC4994080/ /pubmed/27602265 http://dx.doi.org/10.7717/peerj.2275 Text en © 2016 Raina et al. http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, reproduction and adaptation in any medium and for any purpose provided that it is properly attributed. For attribution, the original author(s), title, publication source (PeerJ) and either DOI or URL of the article must be cited. |
spellingShingle | Marine Biology Raina, Jean-Baptiste Tapiolas, Dianne Motti, Cherie A. Foret, Sylvain Seemann, Torsten Tebben, Jan Willis, Bette L. Bourne, David G. Isolation of an antimicrobial compound produced by bacteria associated with reef-building corals |
title | Isolation of an antimicrobial compound produced by bacteria associated with reef-building corals |
title_full | Isolation of an antimicrobial compound produced by bacteria associated with reef-building corals |
title_fullStr | Isolation of an antimicrobial compound produced by bacteria associated with reef-building corals |
title_full_unstemmed | Isolation of an antimicrobial compound produced by bacteria associated with reef-building corals |
title_short | Isolation of an antimicrobial compound produced by bacteria associated with reef-building corals |
title_sort | isolation of an antimicrobial compound produced by bacteria associated with reef-building corals |
topic | Marine Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4994080/ https://www.ncbi.nlm.nih.gov/pubmed/27602265 http://dx.doi.org/10.7717/peerj.2275 |
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