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An Advanced Human Intestinal Coculture Model Reveals Compartmentalized Host and Pathogen Strategies during Salmonella Infection

A major obstacle in infection biology is the limited ability to recapitulate human disease trajectories in traditional cell culture and animal models, which impedes the translation of basic research into clinics. Here, we introduce a three-dimensional (3D) intestinal tissue model to study human ente...

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Autores principales: Schulte, Leon N., Schweinlin, Matthias, Westermann, Alexander J., Janga, Harshavardhan, Santos, Sara C., Appenzeller, Silke, Walles, Heike, Vogel, Jörg, Metzger, Marco
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Microbiology 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7029144/
https://www.ncbi.nlm.nih.gov/pubmed/32071273
http://dx.doi.org/10.1128/mBio.03348-19
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author Schulte, Leon N.
Schweinlin, Matthias
Westermann, Alexander J.
Janga, Harshavardhan
Santos, Sara C.
Appenzeller, Silke
Walles, Heike
Vogel, Jörg
Metzger, Marco
author_facet Schulte, Leon N.
Schweinlin, Matthias
Westermann, Alexander J.
Janga, Harshavardhan
Santos, Sara C.
Appenzeller, Silke
Walles, Heike
Vogel, Jörg
Metzger, Marco
author_sort Schulte, Leon N.
collection PubMed
description A major obstacle in infection biology is the limited ability to recapitulate human disease trajectories in traditional cell culture and animal models, which impedes the translation of basic research into clinics. Here, we introduce a three-dimensional (3D) intestinal tissue model to study human enteric infections at a level of detail that is not achieved by conventional two-dimensional monocultures. Our model comprises epithelial and endothelial layers, a primary intestinal collagen scaffold, and immune cells. Upon Salmonella infection, the model mimics human gastroenteritis, in that it restricts the pathogen to the epithelial compartment, an advantage over existing mouse models. Application of dual transcriptome sequencing to the Salmonella-infected model revealed the communication of epithelial, endothelial, monocytic, and natural killer cells among each other and with the pathogen. Our results suggest that Salmonella uses its type III secretion systems to manipulate STAT3-dependent inflammatory responses locally in the epithelium without accompanying alterations in the endothelial compartment. Our approach promises to reveal further human-specific infection strategies employed by Salmonella and other pathogens.
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spelling pubmed-70291442020-02-26 An Advanced Human Intestinal Coculture Model Reveals Compartmentalized Host and Pathogen Strategies during Salmonella Infection Schulte, Leon N. Schweinlin, Matthias Westermann, Alexander J. Janga, Harshavardhan Santos, Sara C. Appenzeller, Silke Walles, Heike Vogel, Jörg Metzger, Marco mBio Research Article A major obstacle in infection biology is the limited ability to recapitulate human disease trajectories in traditional cell culture and animal models, which impedes the translation of basic research into clinics. Here, we introduce a three-dimensional (3D) intestinal tissue model to study human enteric infections at a level of detail that is not achieved by conventional two-dimensional monocultures. Our model comprises epithelial and endothelial layers, a primary intestinal collagen scaffold, and immune cells. Upon Salmonella infection, the model mimics human gastroenteritis, in that it restricts the pathogen to the epithelial compartment, an advantage over existing mouse models. Application of dual transcriptome sequencing to the Salmonella-infected model revealed the communication of epithelial, endothelial, monocytic, and natural killer cells among each other and with the pathogen. Our results suggest that Salmonella uses its type III secretion systems to manipulate STAT3-dependent inflammatory responses locally in the epithelium without accompanying alterations in the endothelial compartment. Our approach promises to reveal further human-specific infection strategies employed by Salmonella and other pathogens. American Society for Microbiology 2020-02-18 /pmc/articles/PMC7029144/ /pubmed/32071273 http://dx.doi.org/10.1128/mBio.03348-19 Text en Copyright © 2020 Schulte et al. https://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Research Article
Schulte, Leon N.
Schweinlin, Matthias
Westermann, Alexander J.
Janga, Harshavardhan
Santos, Sara C.
Appenzeller, Silke
Walles, Heike
Vogel, Jörg
Metzger, Marco
An Advanced Human Intestinal Coculture Model Reveals Compartmentalized Host and Pathogen Strategies during Salmonella Infection
title An Advanced Human Intestinal Coculture Model Reveals Compartmentalized Host and Pathogen Strategies during Salmonella Infection
title_full An Advanced Human Intestinal Coculture Model Reveals Compartmentalized Host and Pathogen Strategies during Salmonella Infection
title_fullStr An Advanced Human Intestinal Coculture Model Reveals Compartmentalized Host and Pathogen Strategies during Salmonella Infection
title_full_unstemmed An Advanced Human Intestinal Coculture Model Reveals Compartmentalized Host and Pathogen Strategies during Salmonella Infection
title_short An Advanced Human Intestinal Coculture Model Reveals Compartmentalized Host and Pathogen Strategies during Salmonella Infection
title_sort advanced human intestinal coculture model reveals compartmentalized host and pathogen strategies during salmonella infection
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7029144/
https://www.ncbi.nlm.nih.gov/pubmed/32071273
http://dx.doi.org/10.1128/mBio.03348-19
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