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Toward a porcine in vivo model to analyze the pathogenesis of TLR5-dependent enteropathies
Non-communicable diseases, such as the metabolic syndrome and inflammatory bowel disease, constitute serious public health threats in developed countries. Besides environmental factors, genetic predispositions contribute to the onset and progression of the disease. State-of-the-art mouse models rece...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Taylor & Francis
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7524303/ https://www.ncbi.nlm.nih.gov/pubmed/32715918 http://dx.doi.org/10.1080/19490976.2020.1782163 |
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author | Pieper, Robert van Best, Niels van Vorst, Kira Ebner, Friederike Reissmann, Monika Hornef, Mathias W. Fulde, Marcus |
author_facet | Pieper, Robert van Best, Niels van Vorst, Kira Ebner, Friederike Reissmann, Monika Hornef, Mathias W. Fulde, Marcus |
author_sort | Pieper, Robert |
collection | PubMed |
description | Non-communicable diseases, such as the metabolic syndrome and inflammatory bowel disease, constitute serious public health threats in developed countries. Besides environmental factors, genetic predispositions contribute to the onset and progression of the disease. State-of-the-art mouse models recently highlight the involvement of Toll-like receptor 5 (TLR5)–driven microbiota composition in the development of metabolic disorders. Here, we discuss the causes and consequences of an altered enteric microbiota and provide information on a similar mechanism in another species, the pig. We show for the first time that a single nucleotide polymorphism in the porcine TLR5 gene conferring impaired functionality is associated with changes in the intestinal microbiota in adult sows and neonatal piglets. Changes in the developing adaptive cellular immune response support the concept of TLR5-driven changes of the microbe-host interplay also in the pig. Together, these findings suggest that pigs with impaired TLR-functionality might represent a model for TLR5-driven diseases in humans. |
format | Online Article Text |
id | pubmed-7524303 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Taylor & Francis |
record_format | MEDLINE/PubMed |
spelling | pubmed-75243032020-10-06 Toward a porcine in vivo model to analyze the pathogenesis of TLR5-dependent enteropathies Pieper, Robert van Best, Niels van Vorst, Kira Ebner, Friederike Reissmann, Monika Hornef, Mathias W. Fulde, Marcus Gut Microbes Addendum Non-communicable diseases, such as the metabolic syndrome and inflammatory bowel disease, constitute serious public health threats in developed countries. Besides environmental factors, genetic predispositions contribute to the onset and progression of the disease. State-of-the-art mouse models recently highlight the involvement of Toll-like receptor 5 (TLR5)–driven microbiota composition in the development of metabolic disorders. Here, we discuss the causes and consequences of an altered enteric microbiota and provide information on a similar mechanism in another species, the pig. We show for the first time that a single nucleotide polymorphism in the porcine TLR5 gene conferring impaired functionality is associated with changes in the intestinal microbiota in adult sows and neonatal piglets. Changes in the developing adaptive cellular immune response support the concept of TLR5-driven changes of the microbe-host interplay also in the pig. Together, these findings suggest that pigs with impaired TLR-functionality might represent a model for TLR5-driven diseases in humans. Taylor & Francis 2020-07-25 /pmc/articles/PMC7524303/ /pubmed/32715918 http://dx.doi.org/10.1080/19490976.2020.1782163 Text en © 2020 The Author(s). Published with license by Taylor & Francis Group, LLC. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Addendum Pieper, Robert van Best, Niels van Vorst, Kira Ebner, Friederike Reissmann, Monika Hornef, Mathias W. Fulde, Marcus Toward a porcine in vivo model to analyze the pathogenesis of TLR5-dependent enteropathies |
title | Toward a porcine in vivo model to analyze the pathogenesis of TLR5-dependent enteropathies |
title_full | Toward a porcine in vivo model to analyze the pathogenesis of TLR5-dependent enteropathies |
title_fullStr | Toward a porcine in vivo model to analyze the pathogenesis of TLR5-dependent enteropathies |
title_full_unstemmed | Toward a porcine in vivo model to analyze the pathogenesis of TLR5-dependent enteropathies |
title_short | Toward a porcine in vivo model to analyze the pathogenesis of TLR5-dependent enteropathies |
title_sort | toward a porcine in vivo model to analyze the pathogenesis of tlr5-dependent enteropathies |
topic | Addendum |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7524303/ https://www.ncbi.nlm.nih.gov/pubmed/32715918 http://dx.doi.org/10.1080/19490976.2020.1782163 |
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