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Interaction of Salmonella enterica Serovar Typhimurium with Intestinal Organoids Derived from Human Induced Pluripotent Stem Cells

The intestinal mucosa forms the first line of defense against infections mediated by enteric pathogens such as salmonellae. Here we exploited intestinal “organoids” (iHOs) generated from human induced pluripotent stem cells (hIPSCs) to explore the interaction of Salmonella enterica serovar Typhimuri...

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Autores principales: Forbester, Jessica L., Goulding, David, Vallier, Ludovic, Hannan, Nicholas, Hale, Christine, Pickard, Derek, Mukhopadhyay, Subhankar, Dougan, Gordon
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Microbiology 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4468523/
https://www.ncbi.nlm.nih.gov/pubmed/25964470
http://dx.doi.org/10.1128/IAI.00161-15
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author Forbester, Jessica L.
Goulding, David
Vallier, Ludovic
Hannan, Nicholas
Hale, Christine
Pickard, Derek
Mukhopadhyay, Subhankar
Dougan, Gordon
author_facet Forbester, Jessica L.
Goulding, David
Vallier, Ludovic
Hannan, Nicholas
Hale, Christine
Pickard, Derek
Mukhopadhyay, Subhankar
Dougan, Gordon
author_sort Forbester, Jessica L.
collection PubMed
description The intestinal mucosa forms the first line of defense against infections mediated by enteric pathogens such as salmonellae. Here we exploited intestinal “organoids” (iHOs) generated from human induced pluripotent stem cells (hIPSCs) to explore the interaction of Salmonella enterica serovar Typhimurium with iHOs. Imaging and RNA sequencing were used to analyze these interactions, and clear changes in transcriptional signatures were detected, including altered patterns of cytokine expression after the exposure of iHOs to bacteria. S. Typhimurium microinjected into the lumen of iHOs was able to invade the epithelial barrier, with many bacteria residing within Salmonella-containing vacuoles. An S. Typhimurium invA mutant defective in the Salmonella pathogenicity island 1 invasion apparatus was less capable of invading the iHO epithelium. Hence, we provide evidence that hIPSC-derived organoids are a promising model of the intestinal epithelium for assessing interactions with enteric pathogens.
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spelling pubmed-44685232015-06-19 Interaction of Salmonella enterica Serovar Typhimurium with Intestinal Organoids Derived from Human Induced Pluripotent Stem Cells Forbester, Jessica L. Goulding, David Vallier, Ludovic Hannan, Nicholas Hale, Christine Pickard, Derek Mukhopadhyay, Subhankar Dougan, Gordon Infect Immun Host Response and Inflammation The intestinal mucosa forms the first line of defense against infections mediated by enteric pathogens such as salmonellae. Here we exploited intestinal “organoids” (iHOs) generated from human induced pluripotent stem cells (hIPSCs) to explore the interaction of Salmonella enterica serovar Typhimurium with iHOs. Imaging and RNA sequencing were used to analyze these interactions, and clear changes in transcriptional signatures were detected, including altered patterns of cytokine expression after the exposure of iHOs to bacteria. S. Typhimurium microinjected into the lumen of iHOs was able to invade the epithelial barrier, with many bacteria residing within Salmonella-containing vacuoles. An S. Typhimurium invA mutant defective in the Salmonella pathogenicity island 1 invasion apparatus was less capable of invading the iHO epithelium. Hence, we provide evidence that hIPSC-derived organoids are a promising model of the intestinal epithelium for assessing interactions with enteric pathogens. American Society for Microbiology 2015-06-15 2015-07 /pmc/articles/PMC4468523/ /pubmed/25964470 http://dx.doi.org/10.1128/IAI.00161-15 Text en Copyright © 2015 Forbester et al. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution 3.0 Unported license (http://creativecommons.org/licenses/by/3.0/) .
spellingShingle Host Response and Inflammation
Forbester, Jessica L.
Goulding, David
Vallier, Ludovic
Hannan, Nicholas
Hale, Christine
Pickard, Derek
Mukhopadhyay, Subhankar
Dougan, Gordon
Interaction of Salmonella enterica Serovar Typhimurium with Intestinal Organoids Derived from Human Induced Pluripotent Stem Cells
title Interaction of Salmonella enterica Serovar Typhimurium with Intestinal Organoids Derived from Human Induced Pluripotent Stem Cells
title_full Interaction of Salmonella enterica Serovar Typhimurium with Intestinal Organoids Derived from Human Induced Pluripotent Stem Cells
title_fullStr Interaction of Salmonella enterica Serovar Typhimurium with Intestinal Organoids Derived from Human Induced Pluripotent Stem Cells
title_full_unstemmed Interaction of Salmonella enterica Serovar Typhimurium with Intestinal Organoids Derived from Human Induced Pluripotent Stem Cells
title_short Interaction of Salmonella enterica Serovar Typhimurium with Intestinal Organoids Derived from Human Induced Pluripotent Stem Cells
title_sort interaction of salmonella enterica serovar typhimurium with intestinal organoids derived from human induced pluripotent stem cells
topic Host Response and Inflammation
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4468523/
https://www.ncbi.nlm.nih.gov/pubmed/25964470
http://dx.doi.org/10.1128/IAI.00161-15
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