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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...

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Autores principales: 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.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2014
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.
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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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