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Transfer of gut microbiota from lean and obese mice to antibiotic-treated mice
Transferring gut microbiota from one individual to another may enable researchers to “humanize” the gut of animal models and transfer phenotypes between species. To date, most studies of gut microbiota transfer are performed in germ-free mice. In the studies presented, it was tested whether an antib...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4118149/ https://www.ncbi.nlm.nih.gov/pubmed/25082483 http://dx.doi.org/10.1038/srep05922 |
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author | Ellekilde, Merete Selfjord, Ellika Larsen, Christian S. Jakesevic, Maja Rune, Ida Tranberg, Britt Vogensen, Finn K. Nielsen, Dennis S. Bahl, Martin I. Licht, Tine R. Hansen, Axel K. Hansen, Camilla H. F. |
author_facet | Ellekilde, Merete Selfjord, Ellika Larsen, Christian S. Jakesevic, Maja Rune, Ida Tranberg, Britt Vogensen, Finn K. Nielsen, Dennis S. Bahl, Martin I. Licht, Tine R. Hansen, Axel K. Hansen, Camilla H. F. |
author_sort | Ellekilde, Merete |
collection | PubMed |
description | Transferring gut microbiota from one individual to another may enable researchers to “humanize” the gut of animal models and transfer phenotypes between species. To date, most studies of gut microbiota transfer are performed in germ-free mice. In the studies presented, it was tested whether an antibiotic treatment approach could be used instead. C57BL/6 mice were treated with ampicillin prior to inoculation at weaning or eight weeks of age with gut microbiota from lean or obese donors. The gut microbiota and clinical parameters of the recipients was characterized one and six weeks after inoculation. The results demonstrate, that the donor gut microbiota was introduced, established, and changed the gut microbiota of the recipients. Six weeks after inoculation, the differences persisted, however alteration of the gut microbiota occurred with time within the groups. The clinical parameters of the donor phenotype were partly transmissible from obese to lean mice, in particularly β cell hyperactivity in the obese recipients. Thus, a successful inoculation of gut microbiota was not age dependent in order for the microbes to colonize, and transferring different microbial compositions to conventional antibiotic-treated mice was possible at least for a time period during which the microbiota may permanently modulate important host functions. |
format | Online Article Text |
id | pubmed-4118149 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-41181492014-08-15 Transfer of gut microbiota from lean and obese mice to antibiotic-treated mice Ellekilde, Merete Selfjord, Ellika Larsen, Christian S. Jakesevic, Maja Rune, Ida Tranberg, Britt Vogensen, Finn K. Nielsen, Dennis S. Bahl, Martin I. Licht, Tine R. Hansen, Axel K. Hansen, Camilla H. F. Sci Rep Article Transferring gut microbiota from one individual to another may enable researchers to “humanize” the gut of animal models and transfer phenotypes between species. To date, most studies of gut microbiota transfer are performed in germ-free mice. In the studies presented, it was tested whether an antibiotic treatment approach could be used instead. C57BL/6 mice were treated with ampicillin prior to inoculation at weaning or eight weeks of age with gut microbiota from lean or obese donors. The gut microbiota and clinical parameters of the recipients was characterized one and six weeks after inoculation. The results demonstrate, that the donor gut microbiota was introduced, established, and changed the gut microbiota of the recipients. Six weeks after inoculation, the differences persisted, however alteration of the gut microbiota occurred with time within the groups. The clinical parameters of the donor phenotype were partly transmissible from obese to lean mice, in particularly β cell hyperactivity in the obese recipients. Thus, a successful inoculation of gut microbiota was not age dependent in order for the microbes to colonize, and transferring different microbial compositions to conventional antibiotic-treated mice was possible at least for a time period during which the microbiota may permanently modulate important host functions. Nature Publishing Group 2014-08-01 /pmc/articles/PMC4118149/ /pubmed/25082483 http://dx.doi.org/10.1038/srep05922 Text en Copyright © 2014, Macmillan Publishers Limited. All rights reserved http://creativecommons.org/licenses/by-nc-nd/4.0/ This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International License. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder in order to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-nd/4.0/ |
spellingShingle | Article Ellekilde, Merete Selfjord, Ellika Larsen, Christian S. Jakesevic, Maja Rune, Ida Tranberg, Britt Vogensen, Finn K. Nielsen, Dennis S. Bahl, Martin I. Licht, Tine R. Hansen, Axel K. Hansen, Camilla H. F. Transfer of gut microbiota from lean and obese mice to antibiotic-treated mice |
title | Transfer of gut microbiota from lean and obese mice to antibiotic-treated mice |
title_full | Transfer of gut microbiota from lean and obese mice to antibiotic-treated mice |
title_fullStr | Transfer of gut microbiota from lean and obese mice to antibiotic-treated mice |
title_full_unstemmed | Transfer of gut microbiota from lean and obese mice to antibiotic-treated mice |
title_short | Transfer of gut microbiota from lean and obese mice to antibiotic-treated mice |
title_sort | transfer of gut microbiota from lean and obese mice to antibiotic-treated mice |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4118149/ https://www.ncbi.nlm.nih.gov/pubmed/25082483 http://dx.doi.org/10.1038/srep05922 |
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