E. coli enhance colonization resistance against Salmonella Typhimurium by competing for galactitol, a context-dependent limiting carbon source

The composition of intrinsic microbial communities determines if invading pathogens will find a suitable niche for colonization and cause infection or be eliminated. Here, we investigate how commensal E. coli mediate colonization resistance (CR) against Salmonella Typhimurium (S. Tm). Using syntheti...

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Veröffentlicht in:Cell host & microbe 2021-11, Vol.29 (11), p.1680-1692.e7
Hauptverfasser: Eberl, Claudia, Weiss, Anna S., Jochum, Lara M., Durai Raj, Abilash Chakravarthy, Ring, Diana, Hussain, Saib, Herp, Simone, Meng, Chen, Kleigrewe, Karin, Gigl, Michael, Basic, Marijana, Stecher, Bärbel
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container_end_page 1692.e7
container_issue 11
container_start_page 1680
container_title Cell host & microbe
container_volume 29
creator Eberl, Claudia
Weiss, Anna S.
Jochum, Lara M.
Durai Raj, Abilash Chakravarthy
Ring, Diana
Hussain, Saib
Herp, Simone
Meng, Chen
Kleigrewe, Karin
Gigl, Michael
Basic, Marijana
Stecher, Bärbel
description The composition of intrinsic microbial communities determines if invading pathogens will find a suitable niche for colonization and cause infection or be eliminated. Here, we investigate how commensal E. coli mediate colonization resistance (CR) against Salmonella Typhimurium (S. Tm). Using synthetic bacterial communities, we show that the capacity of E. coli Mt1B1 to block S. Tm colonization depends on the microbial context. In an infection-permissive context, E. coli utilized a high diversity of carbon sources and was unable to block S. Tm invasion. In mice that were stably colonized by twelve phylogenetically diverse murine gut bacteria (OMM12), establishing a protective context, E. coli depleted galactitol, a substrate otherwise fueling S. Tm colonization. Here, Lachnospiraceae, capable of consuming C5 and C6 sugars, critically contributed to CR. We propose that E. coli provides CR by depleting a limited carbon source when in a microbial community adept at removing simple sugars from the intestine. [Display omitted] •E. coli mediates colonization resistance against Salmonella in a specific microbiota•E. coli can prevent Salmonella invasion by depleting galactitol•Lachnospiraceae consume free sugars and contribute to colonization resistance Eberl et al. show that E. coli provides colonization resistance (CR) against Salmonella by competing for the limiting carbon source galactitol in a specific microbial context. In this protective context, Lachnospiraceae that consume C5 and C6 sugars play an essential role.
doi_str_mv 10.1016/j.chom.2021.09.004
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Here, we investigate how commensal E. coli mediate colonization resistance (CR) against Salmonella Typhimurium (S. Tm). Using synthetic bacterial communities, we show that the capacity of E. coli Mt1B1 to block S. Tm colonization depends on the microbial context. In an infection-permissive context, E. coli utilized a high diversity of carbon sources and was unable to block S. Tm invasion. In mice that were stably colonized by twelve phylogenetically diverse murine gut bacteria (OMM12), establishing a protective context, E. coli depleted galactitol, a substrate otherwise fueling S. Tm colonization. Here, Lachnospiraceae, capable of consuming C5 and C6 sugars, critically contributed to CR. We propose that E. coli provides CR by depleting a limited carbon source when in a microbial community adept at removing simple sugars from the intestine. [Display omitted] •E. coli mediates colonization resistance against Salmonella in a specific microbiota•E. coli can prevent Salmonella invasion by depleting galactitol•Lachnospiraceae consume free sugars and contribute to colonization resistance Eberl et al. show that E. coli provides colonization resistance (CR) against Salmonella by competing for the limiting carbon source galactitol in a specific microbial context. 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Here, we investigate how commensal E. coli mediate colonization resistance (CR) against Salmonella Typhimurium (S. Tm). Using synthetic bacterial communities, we show that the capacity of E. coli Mt1B1 to block S. Tm colonization depends on the microbial context. In an infection-permissive context, E. coli utilized a high diversity of carbon sources and was unable to block S. Tm invasion. In mice that were stably colonized by twelve phylogenetically diverse murine gut bacteria (OMM12), establishing a protective context, E. coli depleted galactitol, a substrate otherwise fueling S. Tm colonization. Here, Lachnospiraceae, capable of consuming C5 and C6 sugars, critically contributed to CR. We propose that E. coli provides CR by depleting a limited carbon source when in a microbial community adept at removing simple sugars from the intestine. 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subjects Animals
Blautia coccoides
Carbon
ecosystem invasion
Enterocloster clostridioformis
Enterococcus faecalis
Escherichia coli
Freter
Galactitol
Mice
Microbiota
niche pre-emption
nutrient-niche hypothesis
Oligo-MM
Salmonella typhimurium - genetics
sDMDMm2
title E. coli enhance colonization resistance against Salmonella Typhimurium by competing for galactitol, a context-dependent limiting carbon source
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