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Snake fungal disease alters skin bacterial and fungal diversity in an endangered rattlesnake

Snake Fungal Disease (SFD), caused by Ophidiomyces ophiodiicola, is the most recently described fungal disease afflicting wildlife populations across North America and Europe. It has been proposed as a significant conservation threat yielding high mortality and yet much its ecology is unknown. We co...

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Autores principales: Allender, Matthew C., Baker, Sarah, Britton, Megan, Kent, Angela D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6092386/
https://www.ncbi.nlm.nih.gov/pubmed/30108369
http://dx.doi.org/10.1038/s41598-018-30709-x
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author Allender, Matthew C.
Baker, Sarah
Britton, Megan
Kent, Angela D.
author_facet Allender, Matthew C.
Baker, Sarah
Britton, Megan
Kent, Angela D.
author_sort Allender, Matthew C.
collection PubMed
description Snake Fungal Disease (SFD), caused by Ophidiomyces ophiodiicola, is the most recently described fungal disease afflicting wildlife populations across North America and Europe. It has been proposed as a significant conservation threat yielding high mortality and yet much its ecology is unknown. We collected 144 skin swabs from Eastern Massasaugas (Sistrurus catenatus) in 2015 and 2016 to determine document ongoing prevalence and assess differences in microbial assemblages between positive and negative individuals. Alpha diversity of fungi was reduced in SFD positive animals, while beta diversity identified distinct assemblages of microbes between SFD–positive and –negative samples. Ophidiomyces was present on the skin of affected animals, even on body sites distant to lesions indicating that the microbiome on entire surface of the skin is altered. Ophidiomyces was not detected in any non-SFD snake. There were smaller, but significant, influences of year sampled. Bacterial genera Janthinobacterium and Serratia were significantly increased in SFD snakes, while Xylanimicrobium, Cellulosimicrobium, and Rhodococcus were the only bacterial taxa significantly reduced. The relative abundance of fungi within the orders Pleosporales and Canopdiales was reduced in SFD-positive samples, though Pyrenochaetopsis pratorum was the only species found to differ significantly. This is the first study to determine the impact that this fungal pathogen has on the skin microbiome.
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spelling pubmed-60923862018-08-20 Snake fungal disease alters skin bacterial and fungal diversity in an endangered rattlesnake Allender, Matthew C. Baker, Sarah Britton, Megan Kent, Angela D. Sci Rep Article Snake Fungal Disease (SFD), caused by Ophidiomyces ophiodiicola, is the most recently described fungal disease afflicting wildlife populations across North America and Europe. It has been proposed as a significant conservation threat yielding high mortality and yet much its ecology is unknown. We collected 144 skin swabs from Eastern Massasaugas (Sistrurus catenatus) in 2015 and 2016 to determine document ongoing prevalence and assess differences in microbial assemblages between positive and negative individuals. Alpha diversity of fungi was reduced in SFD positive animals, while beta diversity identified distinct assemblages of microbes between SFD–positive and –negative samples. Ophidiomyces was present on the skin of affected animals, even on body sites distant to lesions indicating that the microbiome on entire surface of the skin is altered. Ophidiomyces was not detected in any non-SFD snake. There were smaller, but significant, influences of year sampled. Bacterial genera Janthinobacterium and Serratia were significantly increased in SFD snakes, while Xylanimicrobium, Cellulosimicrobium, and Rhodococcus were the only bacterial taxa significantly reduced. The relative abundance of fungi within the orders Pleosporales and Canopdiales was reduced in SFD-positive samples, though Pyrenochaetopsis pratorum was the only species found to differ significantly. This is the first study to determine the impact that this fungal pathogen has on the skin microbiome. Nature Publishing Group UK 2018-08-14 /pmc/articles/PMC6092386/ /pubmed/30108369 http://dx.doi.org/10.1038/s41598-018-30709-x 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
Allender, Matthew C.
Baker, Sarah
Britton, Megan
Kent, Angela D.
Snake fungal disease alters skin bacterial and fungal diversity in an endangered rattlesnake
title Snake fungal disease alters skin bacterial and fungal diversity in an endangered rattlesnake
title_full Snake fungal disease alters skin bacterial and fungal diversity in an endangered rattlesnake
title_fullStr Snake fungal disease alters skin bacterial and fungal diversity in an endangered rattlesnake
title_full_unstemmed Snake fungal disease alters skin bacterial and fungal diversity in an endangered rattlesnake
title_short Snake fungal disease alters skin bacterial and fungal diversity in an endangered rattlesnake
title_sort snake fungal disease alters skin bacterial and fungal diversity in an endangered rattlesnake
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6092386/
https://www.ncbi.nlm.nih.gov/pubmed/30108369
http://dx.doi.org/10.1038/s41598-018-30709-x
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