Your browser doesn't support javascript.
loading
Enterococci enhance Clostridioides difficile pathogenesis.
Smith, Alexander B; Jenior, Matthew L; Keenan, Orlaith; Hart, Jessica L; Specker, Jonathan; Abbas, Arwa; Rangel, Paula C; Di, Chao; Green, Jamal; Bustin, Katelyn A; Gaddy, Jennifer A; Nicholson, Maribeth R; Laut, Clare; Kelly, Brendan J; Matthews, Megan L; Evans, Daniel R; Van Tyne, Daria; Furth, Emma E; Papin, Jason A; Bushman, Frederic D; Erlichman, Jessi; Baldassano, Robert N; Silverman, Michael A; Dunny, Gary M; Prentice, Boone M; Skaar, Eric P; Zackular, Joseph P.
Afiliación
  • Smith AB; Division of Protective Immunity, Children's Hospital of Philadelphia, Philadelphia, PA, USA.
  • Jenior ML; Department of Biomedical Engineering, University of Virginia, Charlottesville, VA, USA.
  • Keenan O; Division of Protective Immunity, Children's Hospital of Philadelphia, Philadelphia, PA, USA.
  • Hart JL; Division of Protective Immunity, Children's Hospital of Philadelphia, Philadelphia, PA, USA.
  • Specker J; Department of Chemistry, University of Florida, Gainesville, FL, USA.
  • Abbas A; Division of Protective Immunity, Children's Hospital of Philadelphia, Philadelphia, PA, USA.
  • Rangel PC; Division of Protective Immunity, Children's Hospital of Philadelphia, Philadelphia, PA, USA.
  • Di C; Department of Biomedical and Health Informatics, Children's Hospital of Philadelphia, Philadelphia, PA, USA.
  • Green J; Department of Pediatrics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA.
  • Bustin KA; Department of Chemistry, School of Arts and Sciences, University of Pennsylvania, Philadelphia, PA, USA.
  • Gaddy JA; Department of Pathology, Microbiology, and Immunology, Vanderbilt University School of Medicine, Nashville, TN, USA.
  • Nicholson MR; Department of Medicine, Vanderbilt University Medical Center, Nashville, TN, USA.
  • Laut C; Department of Pediatrics, Vanderbilt University School of Medicine, Nashville, TN, USA.
  • Kelly BJ; Department of Pathology, Microbiology, and Immunology, Vanderbilt University School of Medicine, Nashville, TN, USA.
  • Matthews ML; Department of Medicine, Division of Infectious Diseases & Department of Biostatistics, Epidemiology, and Informatics, University of Pennsylvania, Philadelphia, PA, USA.
  • Evans DR; Department of Chemistry, School of Arts and Sciences, University of Pennsylvania, Philadelphia, PA, USA.
  • Van Tyne D; Department of Medicine, Division of Infectious Diseases, University of Pittsburgh, Pittsburgh, PA, USA.
  • Furth EE; Department of Medicine, Division of Infectious Diseases, University of Pittsburgh, Pittsburgh, PA, USA.
  • Papin JA; Department of Microbiology, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA.
  • Bushman FD; Department of Biomedical Engineering, University of Virginia, Charlottesville, VA, USA.
  • Erlichman J; Department of Microbiology, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA.
  • Baldassano RN; Division of Gastroenterology, Hepatology, and Nutrition, Children's Hospital of Philadelphia, Philadelphia, PA, USA.
  • Silverman MA; Department of Pediatrics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA.
  • Dunny GM; Division of Gastroenterology, Hepatology, and Nutrition, Children's Hospital of Philadelphia, Philadelphia, PA, USA.
  • Prentice BM; Department of Pediatrics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA.
  • Skaar EP; Division of Pediatric Infectious Diseases, Children's Hospital of Philadelphia, Philadelphia, PA, USA.
  • Zackular JP; Department of Microbiology, University of Minnesota Medical School, Minneapolis, MN, USA.
Nature ; 611(7937): 780-786, 2022 11.
Article en En | MEDLINE | ID: mdl-36385534
ABSTRACT
Enteric pathogens are exposed to a dynamic polymicrobial environment in the gastrointestinal tract1. 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 pathogens2. Here we show that 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.
Asunto(s)

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Clostridioides difficile / Enterococcus / Interacciones Microbianas Tipo de estudio: Etiology_studies / Prognostic_studies Límite: Animals / Humans Idioma: En Revista: Nature Año: 2022 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Clostridioides difficile / Enterococcus / Interacciones Microbianas Tipo de estudio: Etiology_studies / Prognostic_studies Límite: Animals / Humans Idioma: En Revista: Nature Año: 2022 Tipo del documento: Article País de afiliación: Estados Unidos