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Gut bacterial dysbiosis in pediatric severe malaria associates with post-discharge mortality

Author

Listed:
  • Olivia J. Bednarski

    (Indiana University School of Medicine
    Indiana University School of Medicine)

  • Sawyer B. Lehman

    (Indiana University School of Medicine)

  • David Mzinza

    (Malawi University of Science and Technology
    Malawi University of Science and Technology
    Kamuzu University of Health Sciences)

  • Caroline Kazinga

    (Makerere University College of Health Sciences)

  • Ruth Namazzi

    (Makerere University College of Health Sciences
    Global Health Uganda)

  • Robert O. Opoka

    (Makerere University College of Health Sciences
    Global Health Uganda
    Aga Khan University East Africa Medical College)

  • Jie Ren

    (Indiana University School of Medicine)

  • Tuan M. Tran

    (Indiana University School of Medicine
    Indiana University School of Medicine
    Indiana University School of Medicine)

  • Terrie E. Taylor

    (Kamuzu University of Health Sciences
    Michigan State University)

  • Karl B. Seydel

    (Kamuzu University of Health Sciences
    Michigan State University)

  • Chandy C. John

    (Indiana University School of Medicine)

  • Andrea L. Conroy

    (Indiana University School of Medicine)

  • Nathan W. Schmidt

    (Indiana University School of Medicine
    Indiana University School of Medicine)

Abstract

Gut microbiota have been implicated in severe malaria in murine models, but their contribution to the pathogenesis of severe malaria in children is unknown. Here we show through analysis of gut bacteria in stool samples from two separate African studies enrolling children with severe malaria, and children from local communities, that children with severe malaria have gut bacteria dysbiosis. Among children with severe malaria, there is increased abundance of Enterobacteriaceae that associates with multiple clinical complications of severe malaria. Moreover, increased abundance of Escherichia coli was a predictor of post-discharge mortality. Metagenome analysis identify elevated metabolic pathways and genes supporting the utilization of host-derived molecules in children with severe malaria that have the potential to promote the survival and growth of Enterobacteriaceae. Treatments that target Enterobacteriaceae may have the potential to reduce post-discharge mortality in children with severe malaria.

Suggested Citation

  • Olivia J. Bednarski & Sawyer B. Lehman & David Mzinza & Caroline Kazinga & Ruth Namazzi & Robert O. Opoka & Jie Ren & Tuan M. Tran & Terrie E. Taylor & Karl B. Seydel & Chandy C. John & Andrea L. Conr, 2025. "Gut bacterial dysbiosis in pediatric severe malaria associates with post-discharge mortality," Nature Communications, Nature, vol. 16(1), pages 1-18, December.
  • Handle: RePEc:nat:natcom:v:16:y:2025:i:1:d:10.1038_s41467-025-64632-3
    DOI: 10.1038/s41467-025-64632-3
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