Cargando…
Unravelling the Microbiome of Eggs of the Endangered Sea Turtle Eretmochelys imbricata Identifies Bacteria with Activity against the Emerging Pathogen Fusarium falciforme
Habitat bioaugmentation and introduction of protective microbiota have been proposed as potential conservation strategies to rescue endangered mammals and amphibians from emerging diseases. For both strategies, insight into the microbiomes of the endangered species and their habitats is essential. H...
Autores principales: | , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2014
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3990731/ https://www.ncbi.nlm.nih.gov/pubmed/24743166 http://dx.doi.org/10.1371/journal.pone.0095206 |
_version_ | 1782312333601669120 |
---|---|
author | Sarmiento-Ramírez, Jullie M. van der Voort, Menno Raaijmakers, Jos M. Diéguez-Uribeondo, Javier |
author_facet | Sarmiento-Ramírez, Jullie M. van der Voort, Menno Raaijmakers, Jos M. Diéguez-Uribeondo, Javier |
author_sort | Sarmiento-Ramírez, Jullie M. |
collection | PubMed |
description | Habitat bioaugmentation and introduction of protective microbiota have been proposed as potential conservation strategies to rescue endangered mammals and amphibians from emerging diseases. For both strategies, insight into the microbiomes of the endangered species and their habitats is essential. Here, we sampled nests of the endangered sea turtle species Eretmochelys imbricata that were infected with the fungal pathogen Fusarium falciforme. Metagenomic analysis of the bacterial communities associated with the shells of the sea turtle eggs revealed approximately 16,664 operational taxonomic units, with Proteobacteria, Actinobacteria, Firmicutes and Bacteroidetes as the most dominant phyla. Subsequent isolation of Actinobacteria from the eggshells led to the identification of several genera (Streptomyces, Amycolaptosis, Micromomospora Plantactinospora and Solwaraspora) that inhibit hyphal growth of the pathogen F. falciforme. These bacterial genera constitute a first set of microbial indicators to evaluate the potential role of microbiota in conservation of endangered sea turtle species. |
format | Online Article Text |
id | pubmed-3990731 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-39907312014-04-21 Unravelling the Microbiome of Eggs of the Endangered Sea Turtle Eretmochelys imbricata Identifies Bacteria with Activity against the Emerging Pathogen Fusarium falciforme Sarmiento-Ramírez, Jullie M. van der Voort, Menno Raaijmakers, Jos M. Diéguez-Uribeondo, Javier PLoS One Research Article Habitat bioaugmentation and introduction of protective microbiota have been proposed as potential conservation strategies to rescue endangered mammals and amphibians from emerging diseases. For both strategies, insight into the microbiomes of the endangered species and their habitats is essential. Here, we sampled nests of the endangered sea turtle species Eretmochelys imbricata that were infected with the fungal pathogen Fusarium falciforme. Metagenomic analysis of the bacterial communities associated with the shells of the sea turtle eggs revealed approximately 16,664 operational taxonomic units, with Proteobacteria, Actinobacteria, Firmicutes and Bacteroidetes as the most dominant phyla. Subsequent isolation of Actinobacteria from the eggshells led to the identification of several genera (Streptomyces, Amycolaptosis, Micromomospora Plantactinospora and Solwaraspora) that inhibit hyphal growth of the pathogen F. falciforme. These bacterial genera constitute a first set of microbial indicators to evaluate the potential role of microbiota in conservation of endangered sea turtle species. Public Library of Science 2014-04-17 /pmc/articles/PMC3990731/ /pubmed/24743166 http://dx.doi.org/10.1371/journal.pone.0095206 Text en © 2014 Sarmiento-Ramírez 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, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Sarmiento-Ramírez, Jullie M. van der Voort, Menno Raaijmakers, Jos M. Diéguez-Uribeondo, Javier Unravelling the Microbiome of Eggs of the Endangered Sea Turtle Eretmochelys imbricata Identifies Bacteria with Activity against the Emerging Pathogen Fusarium falciforme |
title | Unravelling the Microbiome of Eggs of the Endangered Sea Turtle Eretmochelys imbricata Identifies Bacteria with Activity against the Emerging Pathogen Fusarium falciforme
|
title_full | Unravelling the Microbiome of Eggs of the Endangered Sea Turtle Eretmochelys imbricata Identifies Bacteria with Activity against the Emerging Pathogen Fusarium falciforme
|
title_fullStr | Unravelling the Microbiome of Eggs of the Endangered Sea Turtle Eretmochelys imbricata Identifies Bacteria with Activity against the Emerging Pathogen Fusarium falciforme
|
title_full_unstemmed | Unravelling the Microbiome of Eggs of the Endangered Sea Turtle Eretmochelys imbricata Identifies Bacteria with Activity against the Emerging Pathogen Fusarium falciforme
|
title_short | Unravelling the Microbiome of Eggs of the Endangered Sea Turtle Eretmochelys imbricata Identifies Bacteria with Activity against the Emerging Pathogen Fusarium falciforme
|
title_sort | unravelling the microbiome of eggs of the endangered sea turtle eretmochelys imbricata identifies bacteria with activity against the emerging pathogen fusarium falciforme |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3990731/ https://www.ncbi.nlm.nih.gov/pubmed/24743166 http://dx.doi.org/10.1371/journal.pone.0095206 |
work_keys_str_mv | AT sarmientoramirezjulliem unravellingthemicrobiomeofeggsoftheendangeredseaturtleeretmochelysimbricataidentifiesbacteriawithactivityagainsttheemergingpathogenfusariumfalciforme AT vandervoortmenno unravellingthemicrobiomeofeggsoftheendangeredseaturtleeretmochelysimbricataidentifiesbacteriawithactivityagainsttheemergingpathogenfusariumfalciforme AT raaijmakersjosm unravellingthemicrobiomeofeggsoftheendangeredseaturtleeretmochelysimbricataidentifiesbacteriawithactivityagainsttheemergingpathogenfusariumfalciforme AT dieguezuribeondojavier unravellingthemicrobiomeofeggsoftheendangeredseaturtleeretmochelysimbricataidentifiesbacteriawithactivityagainsttheemergingpathogenfusariumfalciforme |