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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...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Taylor & Francis
2018
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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. |
format | Online Article Text |
id | pubmed-6219641 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Taylor & Francis |
record_format | MEDLINE/PubMed |
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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