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Fecal microbiota transplantation reverses antibiotic and chemotherapy-induced gut dysbiosis in mice
Fecal microbiota transplantation (FMT) is now widely used to treat recurrent Clostridium difficile infection, but has been less studied as a means to restore microbiome diversity and composition following antibiotic or chemotherapy treatments. The purpose of our study was to assess the efficacy of F...
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/PMC5906603/ https://www.ncbi.nlm.nih.gov/pubmed/29670191 http://dx.doi.org/10.1038/s41598-018-24342-x |
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author | Le Bastard, Quentin Ward, Tonya Sidiropoulos, Dimitri Hillmann, Benjamin M. Chun, Chan Lan Sadowsky, Michael J. Knights, Dan Montassier, Emmanuel |
author_facet | Le Bastard, Quentin Ward, Tonya Sidiropoulos, Dimitri Hillmann, Benjamin M. Chun, Chan Lan Sadowsky, Michael J. Knights, Dan Montassier, Emmanuel |
author_sort | Le Bastard, Quentin |
collection | PubMed |
description | Fecal microbiota transplantation (FMT) is now widely used to treat recurrent Clostridium difficile infection, but has been less studied as a means to restore microbiome diversity and composition following antibiotic or chemotherapy treatments. The purpose of our study was to assess the efficacy of FMT to reverse antibiotic- and chemotherapy-induced gut dysbiosis in a mouse model. C57BL/6J mice were treated with ampicillin for 1 week and/or received a single intraperitoneal injection of 5-Fluorouracil. Fresh stool was collected and analyzed using shotgun metagenomics and the Illumina sequencing platform. Ampicillin caused a significant and immediate decrease in bacterial species richness and diversity that persisted for one week. In mice that received FMT, disruption of the intestinal microbiota was reversed immediately. Antibiotic and chemotherapy administration caused significant alteration in species distribution, including a decrease in the relative proportions of Clostridium scindens and Faecalibacterium prausnitzii, and an increase in known pathogenic species. In mice receiving FMT, we observed a significant increase in species known to exhibit anti-inflammatory properties. Moreover, chemotherapy led to a critical decrease in key ‘health-promoting’ species and to an altered functional profile, especially when chemotherapy was administered in tandem with antibiotics, and that FMT can ameliorate these effects. |
format | Online Article Text |
id | pubmed-5906603 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-59066032018-04-30 Fecal microbiota transplantation reverses antibiotic and chemotherapy-induced gut dysbiosis in mice Le Bastard, Quentin Ward, Tonya Sidiropoulos, Dimitri Hillmann, Benjamin M. Chun, Chan Lan Sadowsky, Michael J. Knights, Dan Montassier, Emmanuel Sci Rep Article Fecal microbiota transplantation (FMT) is now widely used to treat recurrent Clostridium difficile infection, but has been less studied as a means to restore microbiome diversity and composition following antibiotic or chemotherapy treatments. The purpose of our study was to assess the efficacy of FMT to reverse antibiotic- and chemotherapy-induced gut dysbiosis in a mouse model. C57BL/6J mice were treated with ampicillin for 1 week and/or received a single intraperitoneal injection of 5-Fluorouracil. Fresh stool was collected and analyzed using shotgun metagenomics and the Illumina sequencing platform. Ampicillin caused a significant and immediate decrease in bacterial species richness and diversity that persisted for one week. In mice that received FMT, disruption of the intestinal microbiota was reversed immediately. Antibiotic and chemotherapy administration caused significant alteration in species distribution, including a decrease in the relative proportions of Clostridium scindens and Faecalibacterium prausnitzii, and an increase in known pathogenic species. In mice receiving FMT, we observed a significant increase in species known to exhibit anti-inflammatory properties. Moreover, chemotherapy led to a critical decrease in key ‘health-promoting’ species and to an altered functional profile, especially when chemotherapy was administered in tandem with antibiotics, and that FMT can ameliorate these effects. Nature Publishing Group UK 2018-04-18 /pmc/articles/PMC5906603/ /pubmed/29670191 http://dx.doi.org/10.1038/s41598-018-24342-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 Le Bastard, Quentin Ward, Tonya Sidiropoulos, Dimitri Hillmann, Benjamin M. Chun, Chan Lan Sadowsky, Michael J. Knights, Dan Montassier, Emmanuel Fecal microbiota transplantation reverses antibiotic and chemotherapy-induced gut dysbiosis in mice |
title | Fecal microbiota transplantation reverses antibiotic and chemotherapy-induced gut dysbiosis in mice |
title_full | Fecal microbiota transplantation reverses antibiotic and chemotherapy-induced gut dysbiosis in mice |
title_fullStr | Fecal microbiota transplantation reverses antibiotic and chemotherapy-induced gut dysbiosis in mice |
title_full_unstemmed | Fecal microbiota transplantation reverses antibiotic and chemotherapy-induced gut dysbiosis in mice |
title_short | Fecal microbiota transplantation reverses antibiotic and chemotherapy-induced gut dysbiosis in mice |
title_sort | fecal microbiota transplantation reverses antibiotic and chemotherapy-induced gut dysbiosis in mice |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5906603/ https://www.ncbi.nlm.nih.gov/pubmed/29670191 http://dx.doi.org/10.1038/s41598-018-24342-x |
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