| Autor: |
Hryckowian AJ; Department of Microbiology and Immunology, Stanford University School of Medicine, Stanford, CA, USA., Van Treuren W; Department of Microbiology and Immunology, Stanford University School of Medicine, Stanford, CA, USA., Smits SA; Department of Microbiology and Immunology, Stanford University School of Medicine, Stanford, CA, USA., Davis NM; Department of Microbiology and Immunology, Stanford University School of Medicine, Stanford, CA, USA., Gardner JO; Department of Microbiology and Immunology, Stanford University School of Medicine, Stanford, CA, USA., Bouley DM; Department of Comparative Medicine, Stanford University School of Medicine, Stanford, CA, USA., Sonnenburg JL; Department of Microbiology and Immunology, Stanford University School of Medicine, Stanford, CA, USA. jsonnenburg@stanford.edu. |
| Abstrakt: |
Clostridium difficile is an opportunistic diarrhoeal pathogen, and C. difficile infection (CDI) represents a major health care concern, causing an estimated 15,000 deaths per year in the United States alone 1 . Several enteric pathogens, including C. difficile, leverage inflammation and the accompanying microbial dysbiosis to thrive in the distal gut 2 . Although diet is among the most powerful available tools for affecting the health of humans and their relationship with their microbiota, investigation into the effects of diet on CDI has been limited. Here, we show in mice that the consumption of microbiota-accessible carbohydrates (MACs) found in dietary plant polysaccharides has a significant effect on CDI. Specifically, using a model of antibiotic-induced CDI that typically resolves within 12 days of infection, we demonstrate that MAC-deficient diets perpetuate CDI. We show that C. difficile burdens are suppressed through the addition of either a diet containing a complex mixture of MACs or a simplified diet containing inulin as the sole MAC source. We show that switches between these dietary conditions are coincident with changes to microbiota membership, its metabolic output and C. difficile-mediated inflammation. Together, our data demonstrate the outgrowth of MAC-utilizing taxa and the associated end products of MAC metabolism, namely, the short-chain fatty acids acetate, propionate and butyrate, are associated with decreased C. difficile fitness despite increased C. difficile toxin expression in the gut. Our findings, when placed into the context of the known fibre deficiencies of a human Western diet, provide rationale for pursuing MAC-centric dietary strategies as an alternate line of investigation for mitigating CDI. |
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