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Captivity and Infection by the Fungal Pathogen Batrachochytrium salamandrivorans Perturb the Amphibian Skin Microbiome

The emerging fungal pathogen, Batrachochytrium salamandrivorans (Bsal) is responsible for the catastrophic decline of European salamanders and poses a threat to amphibians globally. The amphibian skin microbiome can influence disease outcome for several host-pathogen systems, yet little is known of...

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Autores principales: Bates, Kieran A., Shelton, Jennifer M. G., Mercier, Victoria L., Hopkins, Kevin P., Harrison, Xavier A., Petrovan, Silviu O., Fisher, Matthew C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6716147/
https://www.ncbi.nlm.nih.gov/pubmed/31507541
http://dx.doi.org/10.3389/fmicb.2019.01834
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author Bates, Kieran A.
Shelton, Jennifer M. G.
Mercier, Victoria L.
Hopkins, Kevin P.
Harrison, Xavier A.
Petrovan, Silviu O.
Fisher, Matthew C.
author_facet Bates, Kieran A.
Shelton, Jennifer M. G.
Mercier, Victoria L.
Hopkins, Kevin P.
Harrison, Xavier A.
Petrovan, Silviu O.
Fisher, Matthew C.
author_sort Bates, Kieran A.
collection PubMed
description The emerging fungal pathogen, Batrachochytrium salamandrivorans (Bsal) is responsible for the catastrophic decline of European salamanders and poses a threat to amphibians globally. The amphibian skin microbiome can influence disease outcome for several host-pathogen systems, yet little is known of its role in Bsal infection. In addition, many experimental in-vivo amphibian disease studies to date have relied on specimens that have been kept in captivity for long periods without considering the influence of environment on the microbiome and how this may impact the host response to pathogen exposure. We characterized the impact of captivity and exposure to Bsal on the skin bacterial and fungal communities of two co-occurring European newt species, the smooth newt, Lissotriton vulgaris and the great-crested newt, Triturus cristatus. We show that captivity led to significant losses in bacterial and fungal diversity of amphibian skin, which may be indicative of a decline in microbe-mediated protection. We further demonstrate that in both L. vulgaris and T. cristatus, Bsal infection was associated with changes in the composition of skin bacterial communities with possible negative consequences to host health. Our findings advance current understanding of the role of host-associated microbiota in Bsal infection and highlight important considerations for ex-situ amphibian conservation programmes.
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spelling pubmed-67161472019-09-10 Captivity and Infection by the Fungal Pathogen Batrachochytrium salamandrivorans Perturb the Amphibian Skin Microbiome Bates, Kieran A. Shelton, Jennifer M. G. Mercier, Victoria L. Hopkins, Kevin P. Harrison, Xavier A. Petrovan, Silviu O. Fisher, Matthew C. Front Microbiol Microbiology The emerging fungal pathogen, Batrachochytrium salamandrivorans (Bsal) is responsible for the catastrophic decline of European salamanders and poses a threat to amphibians globally. The amphibian skin microbiome can influence disease outcome for several host-pathogen systems, yet little is known of its role in Bsal infection. In addition, many experimental in-vivo amphibian disease studies to date have relied on specimens that have been kept in captivity for long periods without considering the influence of environment on the microbiome and how this may impact the host response to pathogen exposure. We characterized the impact of captivity and exposure to Bsal on the skin bacterial and fungal communities of two co-occurring European newt species, the smooth newt, Lissotriton vulgaris and the great-crested newt, Triturus cristatus. We show that captivity led to significant losses in bacterial and fungal diversity of amphibian skin, which may be indicative of a decline in microbe-mediated protection. We further demonstrate that in both L. vulgaris and T. cristatus, Bsal infection was associated with changes in the composition of skin bacterial communities with possible negative consequences to host health. Our findings advance current understanding of the role of host-associated microbiota in Bsal infection and highlight important considerations for ex-situ amphibian conservation programmes. Frontiers Media S.A. 2019-08-23 /pmc/articles/PMC6716147/ /pubmed/31507541 http://dx.doi.org/10.3389/fmicb.2019.01834 Text en Copyright © 2019 Bates, Shelton, Mercier, Hopkins, Harrison, Petrovan and Fisher. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Microbiology
Bates, Kieran A.
Shelton, Jennifer M. G.
Mercier, Victoria L.
Hopkins, Kevin P.
Harrison, Xavier A.
Petrovan, Silviu O.
Fisher, Matthew C.
Captivity and Infection by the Fungal Pathogen Batrachochytrium salamandrivorans Perturb the Amphibian Skin Microbiome
title Captivity and Infection by the Fungal Pathogen Batrachochytrium salamandrivorans Perturb the Amphibian Skin Microbiome
title_full Captivity and Infection by the Fungal Pathogen Batrachochytrium salamandrivorans Perturb the Amphibian Skin Microbiome
title_fullStr Captivity and Infection by the Fungal Pathogen Batrachochytrium salamandrivorans Perturb the Amphibian Skin Microbiome
title_full_unstemmed Captivity and Infection by the Fungal Pathogen Batrachochytrium salamandrivorans Perturb the Amphibian Skin Microbiome
title_short Captivity and Infection by the Fungal Pathogen Batrachochytrium salamandrivorans Perturb the Amphibian Skin Microbiome
title_sort captivity and infection by the fungal pathogen batrachochytrium salamandrivorans perturb the amphibian skin microbiome
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6716147/
https://www.ncbi.nlm.nih.gov/pubmed/31507541
http://dx.doi.org/10.3389/fmicb.2019.01834
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