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Bacterial profiling of White Plague Disease across corals and oceans indicates a conserved and distinct disease microbiome

Coral diseases are characterized by microbial community shifts in coral mucus and tissue, but causes and consequences of these changes are vaguely understood due to the complexity and dynamics of coral-associated bacteria. We used 16S rRNA gene microarrays to assay differences in bacterial assemblag...

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Autores principales: Roder, Cornelia, Arif, Chatchanit, Daniels, Camille, Weil, Ernesto, Voolstra, Christian R
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BlackWell Publishing Ltd 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4285310/
https://www.ncbi.nlm.nih.gov/pubmed/24350609
http://dx.doi.org/10.1111/mec.12638
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author Roder, Cornelia
Arif, Chatchanit
Daniels, Camille
Weil, Ernesto
Voolstra, Christian R
author_facet Roder, Cornelia
Arif, Chatchanit
Daniels, Camille
Weil, Ernesto
Voolstra, Christian R
author_sort Roder, Cornelia
collection PubMed
description Coral diseases are characterized by microbial community shifts in coral mucus and tissue, but causes and consequences of these changes are vaguely understood due to the complexity and dynamics of coral-associated bacteria. We used 16S rRNA gene microarrays to assay differences in bacterial assemblages of healthy and diseased colonies displaying White Plague Disease (WPD) signs from two closely related Caribbean coral species, Orbicella faveolata and Orbicella franksi. Analysis of differentially abundant operational taxonomic units (OTUs) revealed strong differences between healthy and diseased specimens, but not between coral species. A subsequent comparison to data from two Indo-Pacific coral species (Pavona duerdeni and Porites lutea) revealed distinct microbial community patterns associated with ocean basin, coral species and health state. Coral species were clearly separated by site, but also, the relatedness of the underlying bacterial community structures resembled the phylogenetic relationship of the coral hosts. In diseased samples, bacterial richness increased and putatively opportunistic bacteria were consistently more abundant highlighting the role of opportunistic conditions in structuring microbial community patterns during disease. Our comparative analysis shows that it is possible to derive conserved bacterial footprints of diseased coral holobionts that might help in identifying key bacterial species related to the underlying etiopathology. Furthermore, our data demonstrate that similar-appearing disease phenotypes produce microbial community patterns that are consistent over coral species and oceans, irrespective of the putative underlying pathogen. Consequently, profiling coral diseases by microbial community structure over multiple coral species might allow the development of a comparative disease framework that can inform on cause and relatedness of coral diseases.
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spelling pubmed-42853102015-01-26 Bacterial profiling of White Plague Disease across corals and oceans indicates a conserved and distinct disease microbiome Roder, Cornelia Arif, Chatchanit Daniels, Camille Weil, Ernesto Voolstra, Christian R Mol Ecol Original Articles Coral diseases are characterized by microbial community shifts in coral mucus and tissue, but causes and consequences of these changes are vaguely understood due to the complexity and dynamics of coral-associated bacteria. We used 16S rRNA gene microarrays to assay differences in bacterial assemblages of healthy and diseased colonies displaying White Plague Disease (WPD) signs from two closely related Caribbean coral species, Orbicella faveolata and Orbicella franksi. Analysis of differentially abundant operational taxonomic units (OTUs) revealed strong differences between healthy and diseased specimens, but not between coral species. A subsequent comparison to data from two Indo-Pacific coral species (Pavona duerdeni and Porites lutea) revealed distinct microbial community patterns associated with ocean basin, coral species and health state. Coral species were clearly separated by site, but also, the relatedness of the underlying bacterial community structures resembled the phylogenetic relationship of the coral hosts. In diseased samples, bacterial richness increased and putatively opportunistic bacteria were consistently more abundant highlighting the role of opportunistic conditions in structuring microbial community patterns during disease. Our comparative analysis shows that it is possible to derive conserved bacterial footprints of diseased coral holobionts that might help in identifying key bacterial species related to the underlying etiopathology. Furthermore, our data demonstrate that similar-appearing disease phenotypes produce microbial community patterns that are consistent over coral species and oceans, irrespective of the putative underlying pathogen. Consequently, profiling coral diseases by microbial community structure over multiple coral species might allow the development of a comparative disease framework that can inform on cause and relatedness of coral diseases. BlackWell Publishing Ltd 2014-02 2014-01-29 /pmc/articles/PMC4285310/ /pubmed/24350609 http://dx.doi.org/10.1111/mec.12638 Text en © 2013 The Authors Molecular Ecology John Wiley & Sons Ltd. http://creativecommons.org/licenses/by/3.0/ This is an open access article under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Articles
Roder, Cornelia
Arif, Chatchanit
Daniels, Camille
Weil, Ernesto
Voolstra, Christian R
Bacterial profiling of White Plague Disease across corals and oceans indicates a conserved and distinct disease microbiome
title Bacterial profiling of White Plague Disease across corals and oceans indicates a conserved and distinct disease microbiome
title_full Bacterial profiling of White Plague Disease across corals and oceans indicates a conserved and distinct disease microbiome
title_fullStr Bacterial profiling of White Plague Disease across corals and oceans indicates a conserved and distinct disease microbiome
title_full_unstemmed Bacterial profiling of White Plague Disease across corals and oceans indicates a conserved and distinct disease microbiome
title_short Bacterial profiling of White Plague Disease across corals and oceans indicates a conserved and distinct disease microbiome
title_sort bacterial profiling of white plague disease across corals and oceans indicates a conserved and distinct disease microbiome
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4285310/
https://www.ncbi.nlm.nih.gov/pubmed/24350609
http://dx.doi.org/10.1111/mec.12638
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