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The Microbiota Mediates Pathogen Clearance from the Gut Lumen after Non-Typhoidal Salmonella Diarrhea

Many enteropathogenic bacteria target the mammalian gut. The mechanisms protecting the host from infection are poorly understood. We have studied the protective functions of secretory antibodies (sIgA) and the microbiota, using a mouse model for S. typhimurium diarrhea. This pathogen is a common cau...

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Autores principales: Endt, Kathrin, Stecher, Bärbel, Chaffron, Samuel, Slack, Emma, Tchitchek, Nicolas, Benecke, Arndt, Van Maele, Laurye, Sirard, Jean-Claude, Mueller, Andreas J., Heikenwalder, Mathias, Macpherson, Andrew J., Strugnell, Richard, von Mering, Christian, Hardt, Wolf-Dietrich
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2936549/
https://www.ncbi.nlm.nih.gov/pubmed/20844578
http://dx.doi.org/10.1371/journal.ppat.1001097
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author Endt, Kathrin
Stecher, Bärbel
Chaffron, Samuel
Slack, Emma
Tchitchek, Nicolas
Benecke, Arndt
Van Maele, Laurye
Sirard, Jean-Claude
Mueller, Andreas J.
Heikenwalder, Mathias
Macpherson, Andrew J.
Strugnell, Richard
von Mering, Christian
Hardt, Wolf-Dietrich
author_facet Endt, Kathrin
Stecher, Bärbel
Chaffron, Samuel
Slack, Emma
Tchitchek, Nicolas
Benecke, Arndt
Van Maele, Laurye
Sirard, Jean-Claude
Mueller, Andreas J.
Heikenwalder, Mathias
Macpherson, Andrew J.
Strugnell, Richard
von Mering, Christian
Hardt, Wolf-Dietrich
author_sort Endt, Kathrin
collection PubMed
description Many enteropathogenic bacteria target the mammalian gut. The mechanisms protecting the host from infection are poorly understood. We have studied the protective functions of secretory antibodies (sIgA) and the microbiota, using a mouse model for S. typhimurium diarrhea. This pathogen is a common cause of diarrhea in humans world-wide. S. typhimurium (S. tm (att), sseD) causes a self-limiting gut infection in streptomycin-treated mice. After 40 days, all animals had overcome the disease, developed a sIgA response, and most had cleared the pathogen from the gut lumen. sIgA limited pathogen access to the mucosal surface and protected from gut inflammation in challenge infections. This protection was O-antigen specific, as demonstrated with pathogens lacking the S. typhimurium O-antigen (wbaP, S. enteritidis) and sIgA-deficient mice (TCRβ(−/−)δ(−/−), J(H) (−/−), IgA(−/−), pIgR(−/−)). Surprisingly, sIgA-deficiency did not affect the kinetics of pathogen clearance from the gut lumen. Instead, this was mediated by the microbiota. This was confirmed using ‘L-mice’ which harbor a low complexity gut flora, lack colonization resistance and develop a normal sIgA response, but fail to clear S. tm (att) from the gut lumen. In these mice, pathogen clearance was achieved by transferring a normal complex microbiota. Thus, besides colonization resistance ( = pathogen blockage by an intact microbiota), the microbiota mediates a second, novel protective function, i.e. pathogen clearance. Here, the normal microbiota re-grows from a state of depletion and disturbed composition and gradually clears even very high pathogen loads from the gut lumen, a site inaccessible to most “classical” immune effector mechanisms. In conclusion, sIgA and microbiota serve complementary protective functions. The microbiota confers colonization resistance and mediates pathogen clearance in primary infections, while sIgA protects from disease if the host re-encounters the same pathogen. This has implications for curing S. typhimurium diarrhea and for preventing transmission.
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spelling pubmed-29365492010-09-15 The Microbiota Mediates Pathogen Clearance from the Gut Lumen after Non-Typhoidal Salmonella Diarrhea Endt, Kathrin Stecher, Bärbel Chaffron, Samuel Slack, Emma Tchitchek, Nicolas Benecke, Arndt Van Maele, Laurye Sirard, Jean-Claude Mueller, Andreas J. Heikenwalder, Mathias Macpherson, Andrew J. Strugnell, Richard von Mering, Christian Hardt, Wolf-Dietrich PLoS Pathog Research Article Many enteropathogenic bacteria target the mammalian gut. The mechanisms protecting the host from infection are poorly understood. We have studied the protective functions of secretory antibodies (sIgA) and the microbiota, using a mouse model for S. typhimurium diarrhea. This pathogen is a common cause of diarrhea in humans world-wide. S. typhimurium (S. tm (att), sseD) causes a self-limiting gut infection in streptomycin-treated mice. After 40 days, all animals had overcome the disease, developed a sIgA response, and most had cleared the pathogen from the gut lumen. sIgA limited pathogen access to the mucosal surface and protected from gut inflammation in challenge infections. This protection was O-antigen specific, as demonstrated with pathogens lacking the S. typhimurium O-antigen (wbaP, S. enteritidis) and sIgA-deficient mice (TCRβ(−/−)δ(−/−), J(H) (−/−), IgA(−/−), pIgR(−/−)). Surprisingly, sIgA-deficiency did not affect the kinetics of pathogen clearance from the gut lumen. Instead, this was mediated by the microbiota. This was confirmed using ‘L-mice’ which harbor a low complexity gut flora, lack colonization resistance and develop a normal sIgA response, but fail to clear S. tm (att) from the gut lumen. In these mice, pathogen clearance was achieved by transferring a normal complex microbiota. Thus, besides colonization resistance ( = pathogen blockage by an intact microbiota), the microbiota mediates a second, novel protective function, i.e. pathogen clearance. Here, the normal microbiota re-grows from a state of depletion and disturbed composition and gradually clears even very high pathogen loads from the gut lumen, a site inaccessible to most “classical” immune effector mechanisms. In conclusion, sIgA and microbiota serve complementary protective functions. The microbiota confers colonization resistance and mediates pathogen clearance in primary infections, while sIgA protects from disease if the host re-encounters the same pathogen. This has implications for curing S. typhimurium diarrhea and for preventing transmission. Public Library of Science 2010-09-09 /pmc/articles/PMC2936549/ /pubmed/20844578 http://dx.doi.org/10.1371/journal.ppat.1001097 Text en Endt et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Endt, Kathrin
Stecher, Bärbel
Chaffron, Samuel
Slack, Emma
Tchitchek, Nicolas
Benecke, Arndt
Van Maele, Laurye
Sirard, Jean-Claude
Mueller, Andreas J.
Heikenwalder, Mathias
Macpherson, Andrew J.
Strugnell, Richard
von Mering, Christian
Hardt, Wolf-Dietrich
The Microbiota Mediates Pathogen Clearance from the Gut Lumen after Non-Typhoidal Salmonella Diarrhea
title The Microbiota Mediates Pathogen Clearance from the Gut Lumen after Non-Typhoidal Salmonella Diarrhea
title_full The Microbiota Mediates Pathogen Clearance from the Gut Lumen after Non-Typhoidal Salmonella Diarrhea
title_fullStr The Microbiota Mediates Pathogen Clearance from the Gut Lumen after Non-Typhoidal Salmonella Diarrhea
title_full_unstemmed The Microbiota Mediates Pathogen Clearance from the Gut Lumen after Non-Typhoidal Salmonella Diarrhea
title_short The Microbiota Mediates Pathogen Clearance from the Gut Lumen after Non-Typhoidal Salmonella Diarrhea
title_sort microbiota mediates pathogen clearance from the gut lumen after non-typhoidal salmonella diarrhea
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2936549/
https://www.ncbi.nlm.nih.gov/pubmed/20844578
http://dx.doi.org/10.1371/journal.ppat.1001097
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