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Littoral lichens as a novel source of potentially bioactive Actinobacteria
Cultivable Actinobacteria are the largest source of microbially derived bioactive molecules. The high demand for novel antibiotics highlights the need for exploring novel sources of these bacteria. Microbial symbioses with sessile macro-organisms, known to contain bioactive compounds likely of bacte...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4626775/ https://www.ncbi.nlm.nih.gov/pubmed/26514347 http://dx.doi.org/10.1038/srep15839 |
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author | Parrot, Delphine Antony-Babu, Sanjay Intertaglia, Laurent Grube, Martin Tomasi, Sophie Suzuki, Marcelino T. |
author_facet | Parrot, Delphine Antony-Babu, Sanjay Intertaglia, Laurent Grube, Martin Tomasi, Sophie Suzuki, Marcelino T. |
author_sort | Parrot, Delphine |
collection | PubMed |
description | Cultivable Actinobacteria are the largest source of microbially derived bioactive molecules. The high demand for novel antibiotics highlights the need for exploring novel sources of these bacteria. Microbial symbioses with sessile macro-organisms, known to contain bioactive compounds likely of bacterial origin, represent an interesting and underexplored source of Actinobacteria. We studied the diversity and potential for bioactive-metabolite production of Actinobacteria associated with two marine lichens (Lichina confinis and L. pygmaea; from intertidal and subtidal zones) and one littoral lichen (Roccella fuciformis; from supratidal zone) from the Brittany coast (France), as well as the terrestrial lichen Collema auriforme (from a riparian zone, Austria). A total of 247 bacterial strains were isolated using two selective media. Isolates were identified and clustered into 101 OTUs (98% identity) including 51 actinobacterial OTUs. The actinobacterial families observed were: Brevibacteriaceae, Cellulomonadaceae, Gordoniaceae, Micrococcaceae, Mycobacteriaceae, Nocardioidaceae, Promicromonosporaceae, Pseudonocardiaceae, Sanguibacteraceae and Streptomycetaceae. Interestingly, the diversity was most influenced by the selective media rather than lichen species or the level of lichen thallus association. The potential for bioactive-metabolite biosynthesis of the isolates was confirmed by screening genes coding for polyketide synthases types I and II. These results show that littoral lichens are a source of diverse potentially bioactive Actinobacteria. |
format | Online Article Text |
id | pubmed-4626775 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-46267752015-11-03 Littoral lichens as a novel source of potentially bioactive Actinobacteria Parrot, Delphine Antony-Babu, Sanjay Intertaglia, Laurent Grube, Martin Tomasi, Sophie Suzuki, Marcelino T. Sci Rep Article Cultivable Actinobacteria are the largest source of microbially derived bioactive molecules. The high demand for novel antibiotics highlights the need for exploring novel sources of these bacteria. Microbial symbioses with sessile macro-organisms, known to contain bioactive compounds likely of bacterial origin, represent an interesting and underexplored source of Actinobacteria. We studied the diversity and potential for bioactive-metabolite production of Actinobacteria associated with two marine lichens (Lichina confinis and L. pygmaea; from intertidal and subtidal zones) and one littoral lichen (Roccella fuciformis; from supratidal zone) from the Brittany coast (France), as well as the terrestrial lichen Collema auriforme (from a riparian zone, Austria). A total of 247 bacterial strains were isolated using two selective media. Isolates were identified and clustered into 101 OTUs (98% identity) including 51 actinobacterial OTUs. The actinobacterial families observed were: Brevibacteriaceae, Cellulomonadaceae, Gordoniaceae, Micrococcaceae, Mycobacteriaceae, Nocardioidaceae, Promicromonosporaceae, Pseudonocardiaceae, Sanguibacteraceae and Streptomycetaceae. Interestingly, the diversity was most influenced by the selective media rather than lichen species or the level of lichen thallus association. The potential for bioactive-metabolite biosynthesis of the isolates was confirmed by screening genes coding for polyketide synthases types I and II. These results show that littoral lichens are a source of diverse potentially bioactive Actinobacteria. Nature Publishing Group 2015-10-30 /pmc/articles/PMC4626775/ /pubmed/26514347 http://dx.doi.org/10.1038/srep15839 Text en Copyright © 2015, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Parrot, Delphine Antony-Babu, Sanjay Intertaglia, Laurent Grube, Martin Tomasi, Sophie Suzuki, Marcelino T. Littoral lichens as a novel source of potentially bioactive Actinobacteria |
title | Littoral lichens as a novel source of potentially bioactive Actinobacteria |
title_full | Littoral lichens as a novel source of potentially bioactive Actinobacteria |
title_fullStr | Littoral lichens as a novel source of potentially bioactive Actinobacteria |
title_full_unstemmed | Littoral lichens as a novel source of potentially bioactive Actinobacteria |
title_short | Littoral lichens as a novel source of potentially bioactive Actinobacteria |
title_sort | littoral lichens as a novel source of potentially bioactive actinobacteria |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4626775/ https://www.ncbi.nlm.nih.gov/pubmed/26514347 http://dx.doi.org/10.1038/srep15839 |
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