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Inflammasomes make the case for littermate-controlled experimental design in studying host-microbiota interactions

Several human diseases are thought to evolve due to a combination of host genetic mutations and environmental factors that include alterations in intestinal microbiota composition termed dysbiosis. Although in some cases, host genetics may shape the gut microbiota and enable it to provoke disease, e...

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Autores principales: Mamantopoulos, Michail, Ronchi, Francesca, McCoy, Kathy D., Wullaert, Andy
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6219641/
https://www.ncbi.nlm.nih.gov/pubmed/29672197
http://dx.doi.org/10.1080/19490976.2017.1421888
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author Mamantopoulos, Michail
Ronchi, Francesca
McCoy, Kathy D.
Wullaert, Andy
author_facet Mamantopoulos, Michail
Ronchi, Francesca
McCoy, Kathy D.
Wullaert, Andy
author_sort Mamantopoulos, Michail
collection PubMed
description Several human diseases are thought to evolve due to a combination of host genetic mutations and environmental factors that include alterations in intestinal microbiota composition termed dysbiosis. Although in some cases, host genetics may shape the gut microbiota and enable it to provoke disease, experimentally disentangling cause and consequence in such host-microbe interactions requires strict control over non-genetic confounding factors. Mouse genetic studies previously proposed Nlrp6/ASC inflammasomes as innate immunity regulators of the intestinal ecosystem. In contrast, using littermate-controlled experimental setups, we recently showed that Nlrp6/ASC inflammasomes do not alter the gut microbiota composition. Our analyses indicated that maternal inheritance and long-term separate housing are non-genetic confounders that preclude the use of non-littermate mice when analyzing host genetic effects on intestinal ecology. Here, we summarize and discuss our gut microbiota analyses in inflammasome-deficient mice for illustrating the importance of littermate experimental design in studying host-microbiota interactions.
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spelling pubmed-62196412018-11-07 Inflammasomes make the case for littermate-controlled experimental design in studying host-microbiota interactions Mamantopoulos, Michail Ronchi, Francesca McCoy, Kathy D. Wullaert, Andy Gut Microbes Addendum Several human diseases are thought to evolve due to a combination of host genetic mutations and environmental factors that include alterations in intestinal microbiota composition termed dysbiosis. Although in some cases, host genetics may shape the gut microbiota and enable it to provoke disease, experimentally disentangling cause and consequence in such host-microbe interactions requires strict control over non-genetic confounding factors. Mouse genetic studies previously proposed Nlrp6/ASC inflammasomes as innate immunity regulators of the intestinal ecosystem. In contrast, using littermate-controlled experimental setups, we recently showed that Nlrp6/ASC inflammasomes do not alter the gut microbiota composition. Our analyses indicated that maternal inheritance and long-term separate housing are non-genetic confounders that preclude the use of non-littermate mice when analyzing host genetic effects on intestinal ecology. Here, we summarize and discuss our gut microbiota analyses in inflammasome-deficient mice for illustrating the importance of littermate experimental design in studying host-microbiota interactions. Taylor & Francis 2018-04-19 /pmc/articles/PMC6219641/ /pubmed/29672197 http://dx.doi.org/10.1080/19490976.2017.1421888 Text en © 2018 The Author(s). Published with license by Taylor & Francis Group, LLC 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 Addendum
Mamantopoulos, Michail
Ronchi, Francesca
McCoy, Kathy D.
Wullaert, Andy
Inflammasomes make the case for littermate-controlled experimental design in studying host-microbiota interactions
title Inflammasomes make the case for littermate-controlled experimental design in studying host-microbiota interactions
title_full Inflammasomes make the case for littermate-controlled experimental design in studying host-microbiota interactions
title_fullStr Inflammasomes make the case for littermate-controlled experimental design in studying host-microbiota interactions
title_full_unstemmed Inflammasomes make the case for littermate-controlled experimental design in studying host-microbiota interactions
title_short Inflammasomes make the case for littermate-controlled experimental design in studying host-microbiota interactions
title_sort inflammasomes make the case for littermate-controlled experimental design in studying host-microbiota interactions
topic Addendum
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6219641/
https://www.ncbi.nlm.nih.gov/pubmed/29672197
http://dx.doi.org/10.1080/19490976.2017.1421888
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