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Porcine small intestinal organoids as a model to explore ETEC–host interactions in the gut

Small intestinal organoids, or enteroids, represent a valuable model to study host–pathogen interactions at the intestinal epithelial surface. Much research has been done on murine and human enteroids, however only a handful studies evaluated the development of enteroids in other species. Porcine en...

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Autores principales: Vermeire, Bjarne, Gonzalez, Liara M., Jansens, Robert J. J., Cox, Eric, Devriendt, Bert
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8235647/
https://www.ncbi.nlm.nih.gov/pubmed/34174960
http://dx.doi.org/10.1186/s13567-021-00961-7
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author Vermeire, Bjarne
Gonzalez, Liara M.
Jansens, Robert J. J.
Cox, Eric
Devriendt, Bert
author_facet Vermeire, Bjarne
Gonzalez, Liara M.
Jansens, Robert J. J.
Cox, Eric
Devriendt, Bert
author_sort Vermeire, Bjarne
collection PubMed
description Small intestinal organoids, or enteroids, represent a valuable model to study host–pathogen interactions at the intestinal epithelial surface. Much research has been done on murine and human enteroids, however only a handful studies evaluated the development of enteroids in other species. Porcine enteroid cultures have been described, but little is known about their functional responses to specific pathogens or their associated virulence factors. Here, we report that porcine enteroids respond in a similar manner as in vivo gut tissues to enterotoxins derived from enterotoxigenic Escherichia coli, an enteric pathogen causing postweaning diarrhoea in piglets. Upon enterotoxin stimulation, these enteroids not only display a dysregulated electrolyte and water balance as shown by their swelling, but also secrete inflammation markers. Porcine enteroids grown as a 2D-monolayer supported the adhesion of an F4(+) ETEC strain. Hence, these enteroids closely mimic in vivo intestinal epithelial responses to gut pathogens and are a promising model to study host–pathogen interactions in the pig gut. Insights obtained with this model might accelerate the design of veterinary therapeutics aimed at improving gut health. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13567-021-00961-7.
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spelling pubmed-82356472021-06-28 Porcine small intestinal organoids as a model to explore ETEC–host interactions in the gut Vermeire, Bjarne Gonzalez, Liara M. Jansens, Robert J. J. Cox, Eric Devriendt, Bert Vet Res Research Article Small intestinal organoids, or enteroids, represent a valuable model to study host–pathogen interactions at the intestinal epithelial surface. Much research has been done on murine and human enteroids, however only a handful studies evaluated the development of enteroids in other species. Porcine enteroid cultures have been described, but little is known about their functional responses to specific pathogens or their associated virulence factors. Here, we report that porcine enteroids respond in a similar manner as in vivo gut tissues to enterotoxins derived from enterotoxigenic Escherichia coli, an enteric pathogen causing postweaning diarrhoea in piglets. Upon enterotoxin stimulation, these enteroids not only display a dysregulated electrolyte and water balance as shown by their swelling, but also secrete inflammation markers. Porcine enteroids grown as a 2D-monolayer supported the adhesion of an F4(+) ETEC strain. Hence, these enteroids closely mimic in vivo intestinal epithelial responses to gut pathogens and are a promising model to study host–pathogen interactions in the pig gut. Insights obtained with this model might accelerate the design of veterinary therapeutics aimed at improving gut health. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13567-021-00961-7. BioMed Central 2021-06-26 2021 /pmc/articles/PMC8235647/ /pubmed/34174960 http://dx.doi.org/10.1186/s13567-021-00961-7 Text en © The Author(s) 2021, corrected publication 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research Article
Vermeire, Bjarne
Gonzalez, Liara M.
Jansens, Robert J. J.
Cox, Eric
Devriendt, Bert
Porcine small intestinal organoids as a model to explore ETEC–host interactions in the gut
title Porcine small intestinal organoids as a model to explore ETEC–host interactions in the gut
title_full Porcine small intestinal organoids as a model to explore ETEC–host interactions in the gut
title_fullStr Porcine small intestinal organoids as a model to explore ETEC–host interactions in the gut
title_full_unstemmed Porcine small intestinal organoids as a model to explore ETEC–host interactions in the gut
title_short Porcine small intestinal organoids as a model to explore ETEC–host interactions in the gut
title_sort porcine small intestinal organoids as a model to explore etec–host interactions in the gut
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8235647/
https://www.ncbi.nlm.nih.gov/pubmed/34174960
http://dx.doi.org/10.1186/s13567-021-00961-7
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