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Gut microbial diversity impacts carbohydrate fermentation by children with severe acute malnutrition

  • Akshay Bisht
  • , Jennifer Ahn-Jarvis
  • , Kendall Corbin
  • , Suzanne Harris
  • , Perla Troncoso-Rey
  • , Peter Olupot-Olupot
  • , Nuala Calder
  • , Kevin Walsh
  • , Kathryn Maitland
  • , Gary Frost
  • , Frederick J. Warren

Research output: Contribution to journalArticlepeer-review

Abstract

African children suffering from severe acute malnutrition (SAM) have a disrupted gut microbiome and low short-chain fatty acids (SCFAs). These are linked to persistently high mortality and morbidity rates. Supplementing recovery feeding regimes with suitable fermentable carbohydrate may improve outcomes in SAM. We adapted in vitro colon models to investigate the ability of children with SAM to utilize four carbohydrate substrates: milk powders (with and without human milk-like oligosaccharides), chickpea-enriched feed, and inulin. All substrates, except inulin, were fermented to produce SCFAs. The inability to utilize inulin ex vivo, a widely used prebiotic, is attributed to low microbial diversity, enriched with Proteobacteria. Stool samples obtained after partial anthropometric recovery showed increased microbial diversity and higher levels of GH32 enzyme family, responsible for inulin metabolism. These findings can inform the design of future therapeutic feeds for the treatment of SAM, where inulin has been found ineffective during initial hospitalization. Alternative carbohydrates appear to be more effective in supporting gut recovery during both the initial and later treatment phases.

Original languageEnglish
Article number114640
Number of pages17
JournaliScience
Volume29
Issue number2
DOIs
StatePublished - Feb 20 2026

Bibliographical note

Publisher Copyright:
© 2026 The Author(s)

Funding

We gratefully acknowledge the technical assistance of David Baker with library preparation and Alise Ponsero with the dbCAN pipeline setup. We thank all the participants and trial staff who participated in the MIMBLE trials. The authors gratefully acknowledge the support of the Biotechnology and Biological Sciences Research Council (BBSRC); this research was funded by the BBSRC Institute Strategic Programme Food Microbiome and Health BB/X011054/1 and its constituent projects BBS/E/QU/230001A and BBS/E/QU/230001B.

FundersFunder number
Biotechnology and Biological Sciences Research CouncilBBS/E/QU/230001A, BB/X011054/1, BBS/E/QU/230001B

    UN SDGs

    This output contributes to the following UN Sustainable Development Goals (SDGs)

    1. SDG 2 - Zero Hunger
      SDG 2 Zero Hunger
    2. SDG 3 - Good Health and Well-being
      SDG 3 Good Health and Well-being

    Keywords

    • Microbiology
    • Microbiome
    • Pediatrics

    ASJC Scopus subject areas

    • General

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