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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...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Society for Microbiology
2015
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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. |
format | Online Article Text |
id | pubmed-4468523 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | American Society for Microbiology |
record_format | MEDLINE/PubMed |
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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