A short chain fatty acid-centric view of Clostridioides difficile pathogenesis

被引:31
作者
Gregory, Anna L. [1 ,2 ,3 ]
Pensinger, Daniel A. [1 ,2 ]
Hryckowian, Andrew J. [1 ,2 ]
机构
[1] Univ Wisconsin, Dept Med, Sch Med & Publ Hlth, Madison, WI 53706 USA
[2] Univ Wisconsin, Dept Med Microbiol & Immunol, Sch Med & Publ Hlth, Madison, WI 53706 USA
[3] Univ Wisconsin, Microbiol Doctoral Training Program, Madison, WI USA
关键词
KAPPA-B ACTIVATION; ESCHERICHIA-COLI; GUT MICROBIOTA; COLONIZATION RESISTANCE; ANTIBIOTIC-TREATMENT; ENERGY-METABOLISM; BUTYRATE; ACETATE; GROWTH; INHIBITION;
D O I
10.1371/journal.ppat.1009959
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Clostridioides difficile is an opportunistic diarrheal pathogen responsible for significant morbidity and mortality worldwide. A disrupted (dysbiotic) gut microbiome, commonly engendered by antibiotic treatment, is the primary risk factor for C. difficile infection, highlighting that C. difficile-microbiome interactions are critical for determining the fitness of this pathogen. Here, we review short chain fatty acids (SCFAs): a major class of metabolites present in the gut, their production by the gut microbiome, and their impacts on the biology of the host and of C. difficile. We use these observations to illustrate a conceptual model whereby C. difficile senses and responds to SCFAs as a marker of a healthy gut and tunes its virulence accordingly in order to maintain dysbiosis. Future work to learn the molecular mechanisms and genetic circuitry underlying the relationships between C. difficile and SCFAs will help to identify precision approaches, distinct from antibiotics and fecal transplant, for mitigating disease caused by C. difficile and will inform similar investigations into other gastrointestinal pathogens.</p>
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页数:15
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