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Microbiome shifts with onset and progression of Sea Star Wasting Disease revealed through time course sampling

The recent outbreak of Sea Star Wasting Disease (SSWD) is one of the largest marine epizootics in history, but the host-associated microbial community changes specific to disease progression have not been characterized. Here, we sampled the microbiomes of ochre sea stars, Pisaster ochraceus, through...

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Autores principales: Lloyd, Melanie M., Pespeni, Melissa H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6220307/
https://www.ncbi.nlm.nih.gov/pubmed/30405146
http://dx.doi.org/10.1038/s41598-018-34697-w
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author Lloyd, Melanie M.
Pespeni, Melissa H.
author_facet Lloyd, Melanie M.
Pespeni, Melissa H.
author_sort Lloyd, Melanie M.
collection PubMed
description The recent outbreak of Sea Star Wasting Disease (SSWD) is one of the largest marine epizootics in history, but the host-associated microbial community changes specific to disease progression have not been characterized. Here, we sampled the microbiomes of ochre sea stars, Pisaster ochraceus, through time as animals stayed healthy or became sick and died with SSWD. We found community-wide differences in the microbiomes of sick and healthy sea stars, changes in microbial community composition through disease progression, and a decrease in species richness of the microbiome in late stages of SSWD. Known beneficial taxa (Pseudoalteromonas spp.) decreased in abundance at symptom onset and through disease progression, while known pathogenic (Tenacibaculum spp.) and putatively opportunistic bacteria (Polaribacter spp. and Phaeobacter spp.) increased in abundance in early and late disease stages. Functional profiling revealed microbes more abundant in healthy animals performed functions that inhibit growth of other microbes, including pathogen detection, biosynthesis of secondary metabolites, and degradation of xenobiotics. Changes in microbial composition with disease onset and progression suggest that a microbial imbalance of the host could lead to SSWD or be a consequence of infection by another pathogen. This work highlights the importance of the microbiome in SSWD and also suggests that a healthy microbiome may help confer resistance to SSWD.
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spelling pubmed-62203072018-11-08 Microbiome shifts with onset and progression of Sea Star Wasting Disease revealed through time course sampling Lloyd, Melanie M. Pespeni, Melissa H. Sci Rep Article The recent outbreak of Sea Star Wasting Disease (SSWD) is one of the largest marine epizootics in history, but the host-associated microbial community changes specific to disease progression have not been characterized. Here, we sampled the microbiomes of ochre sea stars, Pisaster ochraceus, through time as animals stayed healthy or became sick and died with SSWD. We found community-wide differences in the microbiomes of sick and healthy sea stars, changes in microbial community composition through disease progression, and a decrease in species richness of the microbiome in late stages of SSWD. Known beneficial taxa (Pseudoalteromonas spp.) decreased in abundance at symptom onset and through disease progression, while known pathogenic (Tenacibaculum spp.) and putatively opportunistic bacteria (Polaribacter spp. and Phaeobacter spp.) increased in abundance in early and late disease stages. Functional profiling revealed microbes more abundant in healthy animals performed functions that inhibit growth of other microbes, including pathogen detection, biosynthesis of secondary metabolites, and degradation of xenobiotics. Changes in microbial composition with disease onset and progression suggest that a microbial imbalance of the host could lead to SSWD or be a consequence of infection by another pathogen. This work highlights the importance of the microbiome in SSWD and also suggests that a healthy microbiome may help confer resistance to SSWD. Nature Publishing Group UK 2018-11-07 /pmc/articles/PMC6220307/ /pubmed/30405146 http://dx.doi.org/10.1038/s41598-018-34697-w Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Lloyd, Melanie M.
Pespeni, Melissa H.
Microbiome shifts with onset and progression of Sea Star Wasting Disease revealed through time course sampling
title Microbiome shifts with onset and progression of Sea Star Wasting Disease revealed through time course sampling
title_full Microbiome shifts with onset and progression of Sea Star Wasting Disease revealed through time course sampling
title_fullStr Microbiome shifts with onset and progression of Sea Star Wasting Disease revealed through time course sampling
title_full_unstemmed Microbiome shifts with onset and progression of Sea Star Wasting Disease revealed through time course sampling
title_short Microbiome shifts with onset and progression of Sea Star Wasting Disease revealed through time course sampling
title_sort microbiome shifts with onset and progression of sea star wasting disease revealed through time course sampling
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6220307/
https://www.ncbi.nlm.nih.gov/pubmed/30405146
http://dx.doi.org/10.1038/s41598-018-34697-w
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