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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Series: | PLoS Pathogens |
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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 |
work_keys_str_mv |
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