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Fecal microbiota variation across the lifespan of the healthy laboratory rat

Laboratory rats are commonly used in life science research as a model for human biology and disease, but the composition and development of their gut microbiota during life is poorly understood. We determined the fecal microbiota composition of healthy Sprague Dawley laboratory rats from 3 weeks to...

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Autores principales: Flemer, Burkhardt, Gaci, Nadia, Borrel, Guillaume, Sanderson, Ian R., Chaudhary, Prem P., Tottey, William, O'Toole, Paul W., Brugère, Jean-François
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5628645/
https://www.ncbi.nlm.nih.gov/pubmed/28586297
http://dx.doi.org/10.1080/19490976.2017.1334033
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author Flemer, Burkhardt
Gaci, Nadia
Borrel, Guillaume
Sanderson, Ian R.
Chaudhary, Prem P.
Tottey, William
O'Toole, Paul W.
Brugère, Jean-François
author_facet Flemer, Burkhardt
Gaci, Nadia
Borrel, Guillaume
Sanderson, Ian R.
Chaudhary, Prem P.
Tottey, William
O'Toole, Paul W.
Brugère, Jean-François
author_sort Flemer, Burkhardt
collection PubMed
description Laboratory rats are commonly used in life science research as a model for human biology and disease, but the composition and development of their gut microbiota during life is poorly understood. We determined the fecal microbiota composition of healthy Sprague Dawley laboratory rats from 3 weeks to 2 y of age, kept under controlled environmental and dietary conditions. Additionally, we determined fecal short-chain fatty acid profiles, and we compared the rat fecal microbiota with that of mice and humans. Gut microbiota and to a lesser extent SCFAs profiles separated rats into 3 different clusters according to age: before weaning, first year of life (12- to 26-week-old animals) and second year of life (52- to 104-week-old). A core of 46 bacterial species was present in all rats but its members' relative abundance progressively decreased with age. This was accompanied by an increase of microbiota α-diversity, likely due to the acquisition of environmental microorganisms during the lifespan. Contrastingly, the functional profile of the microbiota across animal species became more similar upon aging. Lastly, the microbiota of rats and mice were most similar to each other but at the same time the microbiota profile of rats was more similar to that of humans than was the microbiota profile of mice. These data offer an explanation as to why germ-free rats are more efficient recipients and retainers of human microbiota than mice. Furthermore, experimental design should take into account dynamic changes in the microbiota of model animals considering that their changing gut microbiota interacts with their physiology.
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spelling pubmed-56286452017-10-12 Fecal microbiota variation across the lifespan of the healthy laboratory rat Flemer, Burkhardt Gaci, Nadia Borrel, Guillaume Sanderson, Ian R. Chaudhary, Prem P. Tottey, William O'Toole, Paul W. Brugère, Jean-François Gut Microbes Research Paper/Report Laboratory rats are commonly used in life science research as a model for human biology and disease, but the composition and development of their gut microbiota during life is poorly understood. We determined the fecal microbiota composition of healthy Sprague Dawley laboratory rats from 3 weeks to 2 y of age, kept under controlled environmental and dietary conditions. Additionally, we determined fecal short-chain fatty acid profiles, and we compared the rat fecal microbiota with that of mice and humans. Gut microbiota and to a lesser extent SCFAs profiles separated rats into 3 different clusters according to age: before weaning, first year of life (12- to 26-week-old animals) and second year of life (52- to 104-week-old). A core of 46 bacterial species was present in all rats but its members' relative abundance progressively decreased with age. This was accompanied by an increase of microbiota α-diversity, likely due to the acquisition of environmental microorganisms during the lifespan. Contrastingly, the functional profile of the microbiota across animal species became more similar upon aging. Lastly, the microbiota of rats and mice were most similar to each other but at the same time the microbiota profile of rats was more similar to that of humans than was the microbiota profile of mice. These data offer an explanation as to why germ-free rats are more efficient recipients and retainers of human microbiota than mice. Furthermore, experimental design should take into account dynamic changes in the microbiota of model animals considering that their changing gut microbiota interacts with their physiology. Taylor & Francis 2017-06-06 /pmc/articles/PMC5628645/ /pubmed/28586297 http://dx.doi.org/10.1080/19490976.2017.1334033 Text en © 2017 The Author(s). Published with license by Taylor & Francis http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivatives License (http://creativecommons.org/licenses/by-nc-nd/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited, and is not altered, transformed, or built upon in any way.
spellingShingle Research Paper/Report
Flemer, Burkhardt
Gaci, Nadia
Borrel, Guillaume
Sanderson, Ian R.
Chaudhary, Prem P.
Tottey, William
O'Toole, Paul W.
Brugère, Jean-François
Fecal microbiota variation across the lifespan of the healthy laboratory rat
title Fecal microbiota variation across the lifespan of the healthy laboratory rat
title_full Fecal microbiota variation across the lifespan of the healthy laboratory rat
title_fullStr Fecal microbiota variation across the lifespan of the healthy laboratory rat
title_full_unstemmed Fecal microbiota variation across the lifespan of the healthy laboratory rat
title_short Fecal microbiota variation across the lifespan of the healthy laboratory rat
title_sort fecal microbiota variation across the lifespan of the healthy laboratory rat
topic Research Paper/Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5628645/
https://www.ncbi.nlm.nih.gov/pubmed/28586297
http://dx.doi.org/10.1080/19490976.2017.1334033
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