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Environmental radiation alters the gut microbiome of the bank vole Myodes glareolus
Gut microbiota composition depends on many factors, although the impact of environmental pollution is largely unknown. We used amplicon sequencing of bacterial 16S rRNA genes to quantify whether anthropogenic radionuclides at Chernobyl (Ukraine) impact the gut microbiome of the bank vole Myodes glar...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6193954/ https://www.ncbi.nlm.nih.gov/pubmed/29988064 http://dx.doi.org/10.1038/s41396-018-0214-x |
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author | Lavrinienko, Anton Mappes, Tapio Tukalenko, Eugene Mousseau, Timothy A. Møller, Anders P. Knight, Rob Morton, James T. Thompson, Luke R. Watts, Phillip C. |
author_facet | Lavrinienko, Anton Mappes, Tapio Tukalenko, Eugene Mousseau, Timothy A. Møller, Anders P. Knight, Rob Morton, James T. Thompson, Luke R. Watts, Phillip C. |
author_sort | Lavrinienko, Anton |
collection | PubMed |
description | Gut microbiota composition depends on many factors, although the impact of environmental pollution is largely unknown. We used amplicon sequencing of bacterial 16S rRNA genes to quantify whether anthropogenic radionuclides at Chernobyl (Ukraine) impact the gut microbiome of the bank vole Myodes glareolus. Exposure to elevated levels of environmental radionuclides had no detectable effect on the gut community richness but was associated with an almost two-fold increase in the Firmicutes:Bacteroidetes ratio. Animals inhabiting uncontaminated areas had remarkably similar gut communities irrespective of their proximity to the nuclear power plant. Hence, samples could be classified to high-radiation or low-radiation sites based solely on microbial community with >90% accuracy. Radiation-associated bacteria had distinct inferred functional profiles, including pathways involved in degradation, assimilation and transport of carbohydrates, xenobiotics biodegradation, and DNA repair. Our results suggest that exposure to environmental radionuclides significantly alters vertebrate gut microbiota. |
format | Online Article Text |
id | pubmed-6193954 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-61939542018-10-22 Environmental radiation alters the gut microbiome of the bank vole Myodes glareolus Lavrinienko, Anton Mappes, Tapio Tukalenko, Eugene Mousseau, Timothy A. Møller, Anders P. Knight, Rob Morton, James T. Thompson, Luke R. Watts, Phillip C. ISME J Brief Communication Gut microbiota composition depends on many factors, although the impact of environmental pollution is largely unknown. We used amplicon sequencing of bacterial 16S rRNA genes to quantify whether anthropogenic radionuclides at Chernobyl (Ukraine) impact the gut microbiome of the bank vole Myodes glareolus. Exposure to elevated levels of environmental radionuclides had no detectable effect on the gut community richness but was associated with an almost two-fold increase in the Firmicutes:Bacteroidetes ratio. Animals inhabiting uncontaminated areas had remarkably similar gut communities irrespective of their proximity to the nuclear power plant. Hence, samples could be classified to high-radiation or low-radiation sites based solely on microbial community with >90% accuracy. Radiation-associated bacteria had distinct inferred functional profiles, including pathways involved in degradation, assimilation and transport of carbohydrates, xenobiotics biodegradation, and DNA repair. Our results suggest that exposure to environmental radionuclides significantly alters vertebrate gut microbiota. Nature Publishing Group UK 2018-07-09 2018-11 /pmc/articles/PMC6193954/ /pubmed/29988064 http://dx.doi.org/10.1038/s41396-018-0214-x Text en © International Society for Microbial Ecology 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 | Brief Communication Lavrinienko, Anton Mappes, Tapio Tukalenko, Eugene Mousseau, Timothy A. Møller, Anders P. Knight, Rob Morton, James T. Thompson, Luke R. Watts, Phillip C. Environmental radiation alters the gut microbiome of the bank vole Myodes glareolus |
title | Environmental radiation alters the gut microbiome of the bank vole Myodes glareolus |
title_full | Environmental radiation alters the gut microbiome of the bank vole Myodes glareolus |
title_fullStr | Environmental radiation alters the gut microbiome of the bank vole Myodes glareolus |
title_full_unstemmed | Environmental radiation alters the gut microbiome of the bank vole Myodes glareolus |
title_short | Environmental radiation alters the gut microbiome of the bank vole Myodes glareolus |
title_sort | environmental radiation alters the gut microbiome of the bank vole myodes glareolus |
topic | Brief Communication |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6193954/ https://www.ncbi.nlm.nih.gov/pubmed/29988064 http://dx.doi.org/10.1038/s41396-018-0214-x |
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