Respiration of Microbiota-Derived 1,2-propanediol Drives Salmonella Expansion during Colitis.

Intestinal inflammation caused by Salmonella enterica serovar Typhimurium increases the availability of electron acceptors that fuel a respiratory growth of the pathogen in the intestinal lumen. Here we show that one of the carbon sources driving this respiratory expansion in the mouse model is 1,2-...

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Main Authors: Franziska Faber, Parameth Thiennimitr, Luisella Spiga, Mariana X Byndloss, Yael Litvak, Sara Lawhon, Helene L Andrews-Polymenis, Sebastian E Winter, Andreas J Bäumler
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2017-01-01
Series:PLoS Pathogens
Online Access:http://europepmc.org/articles/PMC5215881?pdf=render
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spelling doaj-7c73770af8b24168a0c4417adb8902812020-11-25T00:29:42ZengPublic Library of Science (PLoS)PLoS Pathogens1553-73661553-73742017-01-01131e100612910.1371/journal.ppat.1006129Respiration of Microbiota-Derived 1,2-propanediol Drives Salmonella Expansion during Colitis.Franziska FaberParameth ThiennimitrLuisella SpigaMariana X ByndlossYael LitvakSara LawhonHelene L Andrews-PolymenisSebastian E WinterAndreas J BäumlerIntestinal inflammation caused by Salmonella enterica serovar Typhimurium increases the availability of electron acceptors that fuel a respiratory growth of the pathogen in the intestinal lumen. Here we show that one of the carbon sources driving this respiratory expansion in the mouse model is 1,2-propanediol, a microbial fermentation product. 1,2-propanediol utilization required intestinal inflammation induced by virulence factors of the pathogen. S. Typhimurium used both aerobic and anaerobic respiration to consume 1,2-propanediol and expand in the murine large intestine. 1,2-propanediol-utilization did not confer a benefit in germ-free mice, but the pdu genes conferred a fitness advantage upon S. Typhimurium in mice mono-associated with Bacteroides fragilis or Bacteroides thetaiotaomicron. Collectively, our data suggest that intestinal inflammation enables S. Typhimurium to sidestep nutritional competition by respiring a microbiota-derived fermentation product.http://europepmc.org/articles/PMC5215881?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Franziska Faber
Parameth Thiennimitr
Luisella Spiga
Mariana X Byndloss
Yael Litvak
Sara Lawhon
Helene L Andrews-Polymenis
Sebastian E Winter
Andreas J Bäumler
spellingShingle Franziska Faber
Parameth Thiennimitr
Luisella Spiga
Mariana X Byndloss
Yael Litvak
Sara Lawhon
Helene L Andrews-Polymenis
Sebastian E Winter
Andreas J Bäumler
Respiration of Microbiota-Derived 1,2-propanediol Drives Salmonella Expansion during Colitis.
PLoS Pathogens
author_facet Franziska Faber
Parameth Thiennimitr
Luisella Spiga
Mariana X Byndloss
Yael Litvak
Sara Lawhon
Helene L Andrews-Polymenis
Sebastian E Winter
Andreas J Bäumler
author_sort Franziska Faber
title Respiration of Microbiota-Derived 1,2-propanediol Drives Salmonella Expansion during Colitis.
title_short Respiration of Microbiota-Derived 1,2-propanediol Drives Salmonella Expansion during Colitis.
title_full Respiration of Microbiota-Derived 1,2-propanediol Drives Salmonella Expansion during Colitis.
title_fullStr Respiration of Microbiota-Derived 1,2-propanediol Drives Salmonella Expansion during Colitis.
title_full_unstemmed Respiration of Microbiota-Derived 1,2-propanediol Drives Salmonella Expansion during Colitis.
title_sort respiration of microbiota-derived 1,2-propanediol drives salmonella expansion during colitis.
publisher Public Library of Science (PLoS)
series PLoS Pathogens
issn 1553-7366
1553-7374
publishDate 2017-01-01
description Intestinal inflammation caused by Salmonella enterica serovar Typhimurium increases the availability of electron acceptors that fuel a respiratory growth of the pathogen in the intestinal lumen. Here we show that one of the carbon sources driving this respiratory expansion in the mouse model is 1,2-propanediol, a microbial fermentation product. 1,2-propanediol utilization required intestinal inflammation induced by virulence factors of the pathogen. S. Typhimurium used both aerobic and anaerobic respiration to consume 1,2-propanediol and expand in the murine large intestine. 1,2-propanediol-utilization did not confer a benefit in germ-free mice, but the pdu genes conferred a fitness advantage upon S. Typhimurium in mice mono-associated with Bacteroides fragilis or Bacteroides thetaiotaomicron. Collectively, our data suggest that intestinal inflammation enables S. Typhimurium to sidestep nutritional competition by respiring a microbiota-derived fermentation product.
url http://europepmc.org/articles/PMC5215881?pdf=render
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