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4D live imaging and computational modeling of a functional gut-on-a-chip evaluate how peristalsis facilitates enteric pathogen invasion

Physical forces are essential to biological function, but their impact at the tissue level is not fully understood. The gut is under continuous mechanical stress because of peristalsis. To assess the influence of mechanical cues on enteropathogen invasion, we combine computational imaging with a mec...

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Autores principales: Boquet-Pujadas, Aleix, Feaugas, Thomas, Petracchini, Alba, Grassart, Alexandre, Mary, Héloïse, Manich, Maria, Gobaa, Samy, Olivo-Marin, Jean-Christophe, Sauvonnet, Nathalie, Labruyère, Elisabeth
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Association for the Advancement of Science 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9586479/
https://www.ncbi.nlm.nih.gov/pubmed/36269830
http://dx.doi.org/10.1126/sciadv.abo5767
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author Boquet-Pujadas, Aleix
Feaugas, Thomas
Petracchini, Alba
Grassart, Alexandre
Mary, Héloïse
Manich, Maria
Gobaa, Samy
Olivo-Marin, Jean-Christophe
Sauvonnet, Nathalie
Labruyère, Elisabeth
author_facet Boquet-Pujadas, Aleix
Feaugas, Thomas
Petracchini, Alba
Grassart, Alexandre
Mary, Héloïse
Manich, Maria
Gobaa, Samy
Olivo-Marin, Jean-Christophe
Sauvonnet, Nathalie
Labruyère, Elisabeth
author_sort Boquet-Pujadas, Aleix
collection PubMed
description Physical forces are essential to biological function, but their impact at the tissue level is not fully understood. The gut is under continuous mechanical stress because of peristalsis. To assess the influence of mechanical cues on enteropathogen invasion, we combine computational imaging with a mechanically active gut-on-a-chip. After infecting the device with either of two microbes, we image their behavior in real time while mapping the mechanical stress within the tissue. This is achieved by reconstructing three-dimensional videos of the ongoing invasion and leveraging on-manifold inverse problems together with viscoelastic rheology. Our results show that peristalsis accelerates the destruction and invasion of intestinal tissue by Entamoeba histolytica and colonization by Shigella flexneri. Local tension facilitates parasite penetration and activates virulence genes in the bacteria. Overall, our work highlights the fundamental role of physical cues during host-pathogen interactions and introduces a framework that opens the door to study mechanobiology on deformable tissues.
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spelling pubmed-95864792022-10-26 4D live imaging and computational modeling of a functional gut-on-a-chip evaluate how peristalsis facilitates enteric pathogen invasion Boquet-Pujadas, Aleix Feaugas, Thomas Petracchini, Alba Grassart, Alexandre Mary, Héloïse Manich, Maria Gobaa, Samy Olivo-Marin, Jean-Christophe Sauvonnet, Nathalie Labruyère, Elisabeth Sci Adv Biomedicine and Life Sciences Physical forces are essential to biological function, but their impact at the tissue level is not fully understood. The gut is under continuous mechanical stress because of peristalsis. To assess the influence of mechanical cues on enteropathogen invasion, we combine computational imaging with a mechanically active gut-on-a-chip. After infecting the device with either of two microbes, we image their behavior in real time while mapping the mechanical stress within the tissue. This is achieved by reconstructing three-dimensional videos of the ongoing invasion and leveraging on-manifold inverse problems together with viscoelastic rheology. Our results show that peristalsis accelerates the destruction and invasion of intestinal tissue by Entamoeba histolytica and colonization by Shigella flexneri. Local tension facilitates parasite penetration and activates virulence genes in the bacteria. Overall, our work highlights the fundamental role of physical cues during host-pathogen interactions and introduces a framework that opens the door to study mechanobiology on deformable tissues. American Association for the Advancement of Science 2022-10-21 /pmc/articles/PMC9586479/ /pubmed/36269830 http://dx.doi.org/10.1126/sciadv.abo5767 Text en Copyright © 2022 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works. Distributed under a Creative Commons Attribution License 4.0 (CC BY). https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution license (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 Biomedicine and Life Sciences
Boquet-Pujadas, Aleix
Feaugas, Thomas
Petracchini, Alba
Grassart, Alexandre
Mary, Héloïse
Manich, Maria
Gobaa, Samy
Olivo-Marin, Jean-Christophe
Sauvonnet, Nathalie
Labruyère, Elisabeth
4D live imaging and computational modeling of a functional gut-on-a-chip evaluate how peristalsis facilitates enteric pathogen invasion
title 4D live imaging and computational modeling of a functional gut-on-a-chip evaluate how peristalsis facilitates enteric pathogen invasion
title_full 4D live imaging and computational modeling of a functional gut-on-a-chip evaluate how peristalsis facilitates enteric pathogen invasion
title_fullStr 4D live imaging and computational modeling of a functional gut-on-a-chip evaluate how peristalsis facilitates enteric pathogen invasion
title_full_unstemmed 4D live imaging and computational modeling of a functional gut-on-a-chip evaluate how peristalsis facilitates enteric pathogen invasion
title_short 4D live imaging and computational modeling of a functional gut-on-a-chip evaluate how peristalsis facilitates enteric pathogen invasion
title_sort 4d live imaging and computational modeling of a functional gut-on-a-chip evaluate how peristalsis facilitates enteric pathogen invasion
topic Biomedicine and Life Sciences
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9586479/
https://www.ncbi.nlm.nih.gov/pubmed/36269830
http://dx.doi.org/10.1126/sciadv.abo5767
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