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The gut microbiome is required for full protection against acute arsenic toxicity in mouse models
Arsenic poisons an estimated 200 million people worldwide through contaminated food and drinking water. Confusingly, the gut microbiome has been suggested to both mitigate and exacerbate arsenic toxicity. Here, we show that the microbiome protects mice from arsenic-induced mortality. Both antibiotic...
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/PMC6303300/ https://www.ncbi.nlm.nih.gov/pubmed/30575732 http://dx.doi.org/10.1038/s41467-018-07803-9 |
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author | Coryell, Michael McAlpine, Mark Pinkham, Nicholas V. McDermott, Timothy R. Walk, Seth T. |
author_facet | Coryell, Michael McAlpine, Mark Pinkham, Nicholas V. McDermott, Timothy R. Walk, Seth T. |
author_sort | Coryell, Michael |
collection | PubMed |
description | Arsenic poisons an estimated 200 million people worldwide through contaminated food and drinking water. Confusingly, the gut microbiome has been suggested to both mitigate and exacerbate arsenic toxicity. Here, we show that the microbiome protects mice from arsenic-induced mortality. Both antibiotic-treated and germ-free mice excrete less arsenic in stool and accumulate more arsenic in organs compared to control mice. Mice lacking the primary arsenic detoxification enzyme (As3mt) are hypersensitive to arsenic after antibiotic treatment or when derived germ-free, compared to wild-type and/or conventional counterparts. Human microbiome (stool) transplants protect germ-free As3mt-KO mice from arsenic-induced mortality, but protection depends on microbiome stability and the presence of specific bacteria, including Faecalibacterium. Our results demonstrate that both a functional As3mt and specific microbiome members are required for protection against acute arsenic toxicity in mouse models. We anticipate that the gut microbiome will become an important explanatory factor of disease (arsenicosis) penetrance in humans, and a novel target for prevention and treatment strategies. |
format | Online Article Text |
id | pubmed-6303300 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-63033002018-12-23 The gut microbiome is required for full protection against acute arsenic toxicity in mouse models Coryell, Michael McAlpine, Mark Pinkham, Nicholas V. McDermott, Timothy R. Walk, Seth T. Nat Commun Article Arsenic poisons an estimated 200 million people worldwide through contaminated food and drinking water. Confusingly, the gut microbiome has been suggested to both mitigate and exacerbate arsenic toxicity. Here, we show that the microbiome protects mice from arsenic-induced mortality. Both antibiotic-treated and germ-free mice excrete less arsenic in stool and accumulate more arsenic in organs compared to control mice. Mice lacking the primary arsenic detoxification enzyme (As3mt) are hypersensitive to arsenic after antibiotic treatment or when derived germ-free, compared to wild-type and/or conventional counterparts. Human microbiome (stool) transplants protect germ-free As3mt-KO mice from arsenic-induced mortality, but protection depends on microbiome stability and the presence of specific bacteria, including Faecalibacterium. Our results demonstrate that both a functional As3mt and specific microbiome members are required for protection against acute arsenic toxicity in mouse models. We anticipate that the gut microbiome will become an important explanatory factor of disease (arsenicosis) penetrance in humans, and a novel target for prevention and treatment strategies. Nature Publishing Group UK 2018-12-21 /pmc/articles/PMC6303300/ /pubmed/30575732 http://dx.doi.org/10.1038/s41467-018-07803-9 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 Coryell, Michael McAlpine, Mark Pinkham, Nicholas V. McDermott, Timothy R. Walk, Seth T. The gut microbiome is required for full protection against acute arsenic toxicity in mouse models |
title | The gut microbiome is required for full protection against acute arsenic toxicity in mouse models |
title_full | The gut microbiome is required for full protection against acute arsenic toxicity in mouse models |
title_fullStr | The gut microbiome is required for full protection against acute arsenic toxicity in mouse models |
title_full_unstemmed | The gut microbiome is required for full protection against acute arsenic toxicity in mouse models |
title_short | The gut microbiome is required for full protection against acute arsenic toxicity in mouse models |
title_sort | gut microbiome is required for full protection against acute arsenic toxicity in mouse models |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6303300/ https://www.ncbi.nlm.nih.gov/pubmed/30575732 http://dx.doi.org/10.1038/s41467-018-07803-9 |
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