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Transplantation of human microbiota into conventional mice durably reshapes the gut microbiota
Human microbiota-associated (HMA) mice are an important model to study the relationship between liver diseases and intestinal microbiota. We describe a new method to humanize conventional mice based on bowel cleansing with polyethylene glycol followed by fecal microbiota transplantation (FMT) from a...
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/PMC5931539/ https://www.ncbi.nlm.nih.gov/pubmed/29717179 http://dx.doi.org/10.1038/s41598-018-25300-3 |
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author | Wrzosek, Laura Ciocan, Dragos Borentain, Patrick Spatz, Madeleine Puchois, Virginie Hugot, Cindy Ferrere, Gladys Mayeur, Camille Perlemuter, Gabriel Cassard, Anne-Marie |
author_facet | Wrzosek, Laura Ciocan, Dragos Borentain, Patrick Spatz, Madeleine Puchois, Virginie Hugot, Cindy Ferrere, Gladys Mayeur, Camille Perlemuter, Gabriel Cassard, Anne-Marie |
author_sort | Wrzosek, Laura |
collection | PubMed |
description | Human microbiota-associated (HMA) mice are an important model to study the relationship between liver diseases and intestinal microbiota. We describe a new method to humanize conventional mice based on bowel cleansing with polyethylene glycol followed by fecal microbiota transplantation (FMT) from a human donor. Four successive bowel cleansings were sufficient to empty the intestine and decrease the microbiota by 90%. We then compared four different strategies based on the frequency of FMT over four weeks: (1) twice a week; (2) once a week; (3) two FMTs; (4) one FMT. We were able to transfer human bacteria to mice, irrespective of the strategy used. We detected human bacteria after four weeks, even if only one FMT was performed, but there was a shift of the microbiota over time. FMT twice a week for four weeks was too frequent and perturbed the stability of the newly formed ecosystem. FMT once a week appears to be the best compromise as it allowed engraftment of Faecalibacterium, and a higher diversity of bacteria belonging to the Bacteroidales order. Our easy to establish HMA mouse model could be used as an alternative to classical HMA mice to study the relationship between the liver and the microbiota. |
format | Online Article Text |
id | pubmed-5931539 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-59315392018-08-29 Transplantation of human microbiota into conventional mice durably reshapes the gut microbiota Wrzosek, Laura Ciocan, Dragos Borentain, Patrick Spatz, Madeleine Puchois, Virginie Hugot, Cindy Ferrere, Gladys Mayeur, Camille Perlemuter, Gabriel Cassard, Anne-Marie Sci Rep Article Human microbiota-associated (HMA) mice are an important model to study the relationship between liver diseases and intestinal microbiota. We describe a new method to humanize conventional mice based on bowel cleansing with polyethylene glycol followed by fecal microbiota transplantation (FMT) from a human donor. Four successive bowel cleansings were sufficient to empty the intestine and decrease the microbiota by 90%. We then compared four different strategies based on the frequency of FMT over four weeks: (1) twice a week; (2) once a week; (3) two FMTs; (4) one FMT. We were able to transfer human bacteria to mice, irrespective of the strategy used. We detected human bacteria after four weeks, even if only one FMT was performed, but there was a shift of the microbiota over time. FMT twice a week for four weeks was too frequent and perturbed the stability of the newly formed ecosystem. FMT once a week appears to be the best compromise as it allowed engraftment of Faecalibacterium, and a higher diversity of bacteria belonging to the Bacteroidales order. Our easy to establish HMA mouse model could be used as an alternative to classical HMA mice to study the relationship between the liver and the microbiota. Nature Publishing Group UK 2018-05-01 /pmc/articles/PMC5931539/ /pubmed/29717179 http://dx.doi.org/10.1038/s41598-018-25300-3 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 Wrzosek, Laura Ciocan, Dragos Borentain, Patrick Spatz, Madeleine Puchois, Virginie Hugot, Cindy Ferrere, Gladys Mayeur, Camille Perlemuter, Gabriel Cassard, Anne-Marie Transplantation of human microbiota into conventional mice durably reshapes the gut microbiota |
title | Transplantation of human microbiota into conventional mice durably reshapes the gut microbiota |
title_full | Transplantation of human microbiota into conventional mice durably reshapes the gut microbiota |
title_fullStr | Transplantation of human microbiota into conventional mice durably reshapes the gut microbiota |
title_full_unstemmed | Transplantation of human microbiota into conventional mice durably reshapes the gut microbiota |
title_short | Transplantation of human microbiota into conventional mice durably reshapes the gut microbiota |
title_sort | transplantation of human microbiota into conventional mice durably reshapes the gut microbiota |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5931539/ https://www.ncbi.nlm.nih.gov/pubmed/29717179 http://dx.doi.org/10.1038/s41598-018-25300-3 |
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