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Unraveling the microbial processes of black band disease in corals through integrated genomics

Coral disease outbreaks contribute to the ongoing degradation of reef ecosystems, however, microbial mechanisms underlying the onset and progression of most coral diseases are poorly understood. Black band disease (BBD) manifests as a cyanobacterial-dominated microbial mat that destroys coral tissue...

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Autores principales: Sato, Yui, Ling, Edmund Y. S., Turaev, Dmitrij, Laffy, Patrick, Weynberg, Karen D., Rattei, Thomas, Willis, Bette L., Bourne, David G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5240343/
https://www.ncbi.nlm.nih.gov/pubmed/28094312
http://dx.doi.org/10.1038/srep40455
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author Sato, Yui
Ling, Edmund Y. S.
Turaev, Dmitrij
Laffy, Patrick
Weynberg, Karen D.
Rattei, Thomas
Willis, Bette L.
Bourne, David G.
author_facet Sato, Yui
Ling, Edmund Y. S.
Turaev, Dmitrij
Laffy, Patrick
Weynberg, Karen D.
Rattei, Thomas
Willis, Bette L.
Bourne, David G.
author_sort Sato, Yui
collection PubMed
description Coral disease outbreaks contribute to the ongoing degradation of reef ecosystems, however, microbial mechanisms underlying the onset and progression of most coral diseases are poorly understood. Black band disease (BBD) manifests as a cyanobacterial-dominated microbial mat that destroys coral tissues as it rapidly spreads over coral colonies. To elucidate BBD pathogenesis, we apply a comparative metagenomic and metatranscriptomic approach to identify taxonomic and functional changes within microbial lesions during in-situ development of BBD from a comparatively benign stage termed cyanobacterial patches. Results suggest that photosynthetic CO(2)-fixation in Cyanobacteria substantially enhances productivity of organic matter within the lesion during disease development. Photosynthates appear to subsequently promote sulfide-production by Deltaproteobacteria, facilitating the major virulence factor of BBD. Interestingly, our metagenome-enabled transcriptomic analysis reveals that BBD-associated cyanobacteria have a putative mechanism that enables them to adapt to higher levels of hydrogen sulfide within lesions, underpinning the pivotal roles of the dominant cyanobacterium within the polymicrobial lesions during the onset of BBD. The current study presents sequence-based evidence derived from whole microbial communities that unravel the mechanism of development and progression of BBD.
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spelling pubmed-52403432017-01-23 Unraveling the microbial processes of black band disease in corals through integrated genomics Sato, Yui Ling, Edmund Y. S. Turaev, Dmitrij Laffy, Patrick Weynberg, Karen D. Rattei, Thomas Willis, Bette L. Bourne, David G. Sci Rep Article Coral disease outbreaks contribute to the ongoing degradation of reef ecosystems, however, microbial mechanisms underlying the onset and progression of most coral diseases are poorly understood. Black band disease (BBD) manifests as a cyanobacterial-dominated microbial mat that destroys coral tissues as it rapidly spreads over coral colonies. To elucidate BBD pathogenesis, we apply a comparative metagenomic and metatranscriptomic approach to identify taxonomic and functional changes within microbial lesions during in-situ development of BBD from a comparatively benign stage termed cyanobacterial patches. Results suggest that photosynthetic CO(2)-fixation in Cyanobacteria substantially enhances productivity of organic matter within the lesion during disease development. Photosynthates appear to subsequently promote sulfide-production by Deltaproteobacteria, facilitating the major virulence factor of BBD. Interestingly, our metagenome-enabled transcriptomic analysis reveals that BBD-associated cyanobacteria have a putative mechanism that enables them to adapt to higher levels of hydrogen sulfide within lesions, underpinning the pivotal roles of the dominant cyanobacterium within the polymicrobial lesions during the onset of BBD. The current study presents sequence-based evidence derived from whole microbial communities that unravel the mechanism of development and progression of BBD. Nature Publishing Group 2017-01-17 /pmc/articles/PMC5240343/ /pubmed/28094312 http://dx.doi.org/10.1038/srep40455 Text en Copyright © 2017, The Author(s) 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
Sato, Yui
Ling, Edmund Y. S.
Turaev, Dmitrij
Laffy, Patrick
Weynberg, Karen D.
Rattei, Thomas
Willis, Bette L.
Bourne, David G.
Unraveling the microbial processes of black band disease in corals through integrated genomics
title Unraveling the microbial processes of black band disease in corals through integrated genomics
title_full Unraveling the microbial processes of black band disease in corals through integrated genomics
title_fullStr Unraveling the microbial processes of black band disease in corals through integrated genomics
title_full_unstemmed Unraveling the microbial processes of black band disease in corals through integrated genomics
title_short Unraveling the microbial processes of black band disease in corals through integrated genomics
title_sort unraveling the microbial processes of black band disease in corals through integrated genomics
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5240343/
https://www.ncbi.nlm.nih.gov/pubmed/28094312
http://dx.doi.org/10.1038/srep40455
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