4.7 Article

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

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CELL HOST & MICROBE
卷 29, 期 11, 页码 1680-+

出版社

CELL PRESS
DOI: 10.1016/j.chom.2021.09.004

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资金

  1. D-A-CH Programme [DFG STE 1971/7-1]
  2. DFG Priority Programme SPP1656 [DFG STE 1971/4-2]
  3. European Research Council (EVOGUTHEALTH) [865615]
  4. German Center for Infection Research (DZIF)
  5. Center for Gastrointestinal Microbiome Research (CEGIMIR)
  6. DFG [CRC1371]
  7. European Research Council (ERC) [865615] Funding Source: European Research Council (ERC)

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The composition of the intrinsic microbial communities plays a crucial role in determining whether invading pathogens can establish colonization or be blocked by commensal bacteria. This study found that E. coli can provide colonization resistance against Salmonella Typhimurium by depleting specific carbon sources in a microbial context that supports the removal of simple sugars from the intestine. In certain cases, the presence of other bacterial groups is essential for the colonization resistance mediated by commensal E. coli.
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.

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