Intestinal inflammation responds to microbial tissue load independent of pathogen/non-pathogen discrimination.

The intestinal immune system mounts inflammatory responses to pathogens but tolerates harmless commensal microbiota. Various mechanisms for pathogen/non-pathogen discrimination have been proposed but their general relevance for inflammation control is unclear. Here, we compared intestinal responses...

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Main Authors: Yvonne Willer, Beatrice Müller, Dirk Bumann
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2012-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC3346762?pdf=render
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spelling doaj-d5ce5b473e9648fbbbf1624cc6f78a032020-11-25T01:58:14ZengPublic Library of Science (PLoS)PLoS ONE1932-62032012-01-0175e3599210.1371/journal.pone.0035992Intestinal inflammation responds to microbial tissue load independent of pathogen/non-pathogen discrimination.Yvonne WillerBeatrice MüllerDirk BumannThe intestinal immune system mounts inflammatory responses to pathogens but tolerates harmless commensal microbiota. Various mechanisms for pathogen/non-pathogen discrimination have been proposed but their general relevance for inflammation control is unclear. Here, we compared intestinal responses to pathogenic Salmonella and non-pathogenic E. coli. Both microbes entered intestinal Peyer's patches and, surprisingly, induced qualitatively and quantitatively similar initial inflammatory responses revealing a striking discrimination failure. Diverging inflammatory responses only occurred when Salmonella subsequently proliferated and induced escalating neutrophil infiltration, while harmless E. coli was rapidly cleared from the tissue and inflammation resolved. Transient intestinal inflammation induced by harmless E. coli tolerized against subsequent exposure thereby preventing chronic inflammation during repeated exposure. These data revealed a striking failure of the intestinal immune system to discriminate pathogens from harmless microbes based on distinct molecular signatures. Instead, appropriate intestinal responses to gut microbiota might be ensured by immediate inflammatory responses to any rise in microbial tissue loads, and desensitization after bacterial clearance.http://europepmc.org/articles/PMC3346762?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Yvonne Willer
Beatrice Müller
Dirk Bumann
spellingShingle Yvonne Willer
Beatrice Müller
Dirk Bumann
Intestinal inflammation responds to microbial tissue load independent of pathogen/non-pathogen discrimination.
PLoS ONE
author_facet Yvonne Willer
Beatrice Müller
Dirk Bumann
author_sort Yvonne Willer
title Intestinal inflammation responds to microbial tissue load independent of pathogen/non-pathogen discrimination.
title_short Intestinal inflammation responds to microbial tissue load independent of pathogen/non-pathogen discrimination.
title_full Intestinal inflammation responds to microbial tissue load independent of pathogen/non-pathogen discrimination.
title_fullStr Intestinal inflammation responds to microbial tissue load independent of pathogen/non-pathogen discrimination.
title_full_unstemmed Intestinal inflammation responds to microbial tissue load independent of pathogen/non-pathogen discrimination.
title_sort intestinal inflammation responds to microbial tissue load independent of pathogen/non-pathogen discrimination.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2012-01-01
description The intestinal immune system mounts inflammatory responses to pathogens but tolerates harmless commensal microbiota. Various mechanisms for pathogen/non-pathogen discrimination have been proposed but their general relevance for inflammation control is unclear. Here, we compared intestinal responses to pathogenic Salmonella and non-pathogenic E. coli. Both microbes entered intestinal Peyer's patches and, surprisingly, induced qualitatively and quantitatively similar initial inflammatory responses revealing a striking discrimination failure. Diverging inflammatory responses only occurred when Salmonella subsequently proliferated and induced escalating neutrophil infiltration, while harmless E. coli was rapidly cleared from the tissue and inflammation resolved. Transient intestinal inflammation induced by harmless E. coli tolerized against subsequent exposure thereby preventing chronic inflammation during repeated exposure. These data revealed a striking failure of the intestinal immune system to discriminate pathogens from harmless microbes based on distinct molecular signatures. Instead, appropriate intestinal responses to gut microbiota might be ensured by immediate inflammatory responses to any rise in microbial tissue loads, and desensitization after bacterial clearance.
url http://europepmc.org/articles/PMC3346762?pdf=render
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AT beatricemuller intestinalinflammationrespondstomicrobialtissueloadindependentofpathogennonpathogendiscrimination
AT dirkbumann intestinalinflammationrespondstomicrobialtissueloadindependentofpathogennonpathogendiscrimination
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