4.8 Article

Enterococci enhance Clostridioides difficile pathogenesis

期刊

NATURE
卷 611, 期 7937, 页码 780-+

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NATURE PORTFOLIO
DOI: 10.1038/s41586-022-05438-x

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资金

  1. National Institutes of Health [K22AI7220, R35GM138369, R01AI138581, R01AI145992, R01AI164587, R01AT010253, K23AI156132-01, K23 AI121485]
  2. Children's Hospital of Philadelphia Junior Faculty Pilot Grant
  3. Cell and Molecular Biology Training Grant [T32GM07229]
  4. UVA TransUniversity Microbiome Initiative Pilot Grant
  5. Chemical and Biology Interface Training Grant [5T32GM071339-15]
  6. National Institutes of Health/National Center for Advancing Translational Sciences Grant Support [UL1TR000445]
  7. Centers for Disease Control and Prevention [BAA 200-2016-91937]
  8. Perelman School of Medicine/Children's Hospital of Philadelphia PennCHOP Microbiome Program
  9. Crohn's and Colitis Foundation
  10. Penn Center for AIDS Research [P30-AI045008]
  11. Commonwealth Universal Research Enhancement programme grant SAP [4100068710]

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Enterococci can shape the metabolic environment in the gut and enhance the fitness and pathogenesis of Clostridioides difficile through nutrient restriction and cross-feeding. This microbial interaction plays a role in the susceptibility to and the severity of C. difficile infection.
Enteric pathogens are exposed to a dynamic polymicrobial environment in the gastrointestinal tract(1). This microbial community has been shown to be important during infection, but there are few examples illustrating how microbial interactions can influence the virulence of invading pathogens(2). Here we showthat expansion of a group of antibiotic-resistant, opportunistic pathogens in the gut-the enterococci-enhances the fitness and pathogenesis of Clostridioides difficile. Through a parallel process of nutrient restriction and cross-feeding, enterococci shape the metabolic environment in the gut and reprogramme C. difficile metabolism. Enterococci provide fermentable amino acids, including leucine and ornithine, which increase C. difficile fitness in the antibiotic-perturbed gut. Parallel depletion of arginine by enterococci through arginine catabolism provides a metabolic cue for C. difficile that facilitates increased virulence. We find evidence of microbial interaction between these two pathogenic organisms in multiple mouse models of infection and patients infected with C. difficile. These findings provide mechanistic insights into the role of pathogenic microbiota in the susceptibility to and the severity of C. difficile infection.

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