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Enterococci enhance Clostridioides difficile pathogenesis

Author

Listed:
  • Alexander B. Smith

    (Division of Protective Immunity, Children’s Hospital of Philadelphia)

  • Matthew L. Jenior

    (University of Virginia)

  • Orlaith Keenan

    (Division of Protective Immunity, Children’s Hospital of Philadelphia)

  • Jessica L. Hart

    (Division of Protective Immunity, Children’s Hospital of Philadelphia)

  • Jonathan Specker

    (University of Florida)

  • Arwa Abbas

    (Division of Protective Immunity, Children’s Hospital of Philadelphia)

  • Paula C. Rangel

    (Division of Protective Immunity, Children’s Hospital of Philadelphia)

  • Chao Di

    (Children’s Hospital of Philadelphia)

  • Jamal Green

    (University of Pennsylvania)

  • Katelyn A. Bustin

    (University of Pennsylvania)

  • Jennifer A. Gaddy

    (Vanderbilt University School of Medicine
    Vanderbilt University Medical Center)

  • Maribeth R. Nicholson

    (Vanderbilt University School of Medicine)

  • Clare Laut

    (Vanderbilt University School of Medicine)

  • Brendan J. Kelly

    (University of Pennsylvania)

  • Megan L. Matthews

    (University of Pennsylvania)

  • Daniel R. Evans

    (University of Pittsburgh)

  • Daria Van Tyne

    (University of Pittsburgh)

  • Emma E. Furth

    (University of Pennsylvania)

  • Jason A. Papin

    (University of Virginia)

  • Frederic D. Bushman

    (University of Pennsylvania)

  • Jessi Erlichman

    (Children’s Hospital of Philadelphia)

  • Robert N. Baldassano

    (University of Pennsylvania
    Children’s Hospital of Philadelphia)

  • Michael A. Silverman

    (University of Pennsylvania
    Children’s Hospital of Philadelphia)

  • Gary M. Dunny

    (University of Minnesota Medical School)

  • Boone M. Prentice

    (University of Florida)

  • Eric P. Skaar

    (Vanderbilt University School of Medicine)

  • Joseph P. Zackular

    (Division of Protective Immunity, Children’s Hospital of Philadelphia
    University of Pennsylvania
    Perelman School of Medicine, University of Pennsylvania)

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.

Suggested Citation

  • Alexander B. Smith & Matthew L. Jenior & Orlaith Keenan & Jessica L. Hart & Jonathan Specker & Arwa Abbas & Paula C. Rangel & Chao Di & Jamal Green & Katelyn A. Bustin & Jennifer A. Gaddy & Maribeth R, 2022. "Enterococci enhance Clostridioides difficile pathogenesis," Nature, Nature, vol. 611(7937), pages 780-786, November.
  • Handle: RePEc:nat:nature:v:611:y:2022:i:7937:d:10.1038_s41586-022-05438-x
    DOI: 10.1038/s41586-022-05438-x
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    Cited by:

    1. Huan Yang & Xiaoxiao Wu & Xiao Li & Wanqing Zang & Zhou Zhou & Yuan Zhou & Wenwen Cui & Yanbo Kou & Liang Wang & Ankang Hu & Lianlian Wu & Zhinan Yin & Quangang Chen & Ying Chen & Zhutao Huang & Yugan, 2024. "A commensal protozoan attenuates Clostridioides difficile pathogenesis in mice via arginine-ornithine metabolism and host intestinal immune response," Nature Communications, Nature, vol. 15(1), pages 1-18, December.
    2. Marijana Bosnjak & Avinash V. Karpe & Thi Thu Hao Van & Despina Kotsanas & Grant A. Jenkin & Samuel P. Costello & Priscilla Johanesen & Robert J. Moore & David J. Beale & Yogitha N. Srikhanta & Enzo A, 2023. "Multi-omics analysis of hospital-acquired diarrhoeal patients reveals biomarkers of enterococcal proliferation and Clostridioides difficile infection," Nature Communications, Nature, vol. 14(1), pages 1-16, December.

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