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Bioactive glycans in a microbiome-directed food for children with malnutrition.
Hibberd, Matthew C; Webber, Daniel M; Rodionov, Dmitry A; Henrissat, Suzanne; Chen, Robert Y; Zhou, Cyrus; Lynn, Hannah M; Wang, Yi; Chang, Hao-Wei; Lee, Evan M; Lelwala-Guruge, Janaki; Kazanov, Marat D; Arzamasov, Aleksandr A; Leyn, Semen A; Lombard, Vincent; Terrapon, Nicolas; Henrissat, Bernard; Castillo, Juan J; Couture, Garret; Bacalzo, Nikita P; Chen, Ye; Lebrilla, Carlito B; Mostafa, Ishita; Das, Subhasish; Mahfuz, Mustafa; Barratt, Michael J; Osterman, Andrei L; Ahmed, Tahmeed; Gordon, Jeffrey I.
Affiliation
  • Hibberd MC; Edison Family Center for Genome Sciences and Systems Biology, Washington University School of Medicine, St Louis, MO, USA.
  • Webber DM; Center for Gut Microbiome and Nutrition Research, Washington University School of Medicine, St Louis, MO, USA.
  • Rodionov DA; Department of Pathology and Immunology, Washington University School of Medicine, St Louis, MO, USA.
  • Henrissat S; Edison Family Center for Genome Sciences and Systems Biology, Washington University School of Medicine, St Louis, MO, USA.
  • Chen RY; Center for Gut Microbiome and Nutrition Research, Washington University School of Medicine, St Louis, MO, USA.
  • Zhou C; Department of Pathology and Immunology, Washington University School of Medicine, St Louis, MO, USA.
  • Lynn HM; Infectious and Inflammatory Disease Center, Sanford Burnham Prebys Medical Discovery Institute, La Jolla, CA, USA.
  • Wang Y; Edison Family Center for Genome Sciences and Systems Biology, Washington University School of Medicine, St Louis, MO, USA.
  • Chang HW; Center for Gut Microbiome and Nutrition Research, Washington University School of Medicine, St Louis, MO, USA.
  • Lee EM; Architecture et Fonction des Macromolécules Biologiques, CNRS, Aix-Marseille University, Marseille, France.
  • Lelwala-Guruge J; Edison Family Center for Genome Sciences and Systems Biology, Washington University School of Medicine, St Louis, MO, USA.
  • Kazanov MD; Center for Gut Microbiome and Nutrition Research, Washington University School of Medicine, St Louis, MO, USA.
  • Arzamasov AA; Edison Family Center for Genome Sciences and Systems Biology, Washington University School of Medicine, St Louis, MO, USA.
  • Leyn SA; Center for Gut Microbiome and Nutrition Research, Washington University School of Medicine, St Louis, MO, USA.
  • Lombard V; Edison Family Center for Genome Sciences and Systems Biology, Washington University School of Medicine, St Louis, MO, USA.
  • Terrapon N; Center for Gut Microbiome and Nutrition Research, Washington University School of Medicine, St Louis, MO, USA.
  • Henrissat B; Edison Family Center for Genome Sciences and Systems Biology, Washington University School of Medicine, St Louis, MO, USA.
  • Castillo JJ; Center for Gut Microbiome and Nutrition Research, Washington University School of Medicine, St Louis, MO, USA.
  • Couture G; Edison Family Center for Genome Sciences and Systems Biology, Washington University School of Medicine, St Louis, MO, USA.
  • Bacalzo NP; Center for Gut Microbiome and Nutrition Research, Washington University School of Medicine, St Louis, MO, USA.
  • Chen Y; Edison Family Center for Genome Sciences and Systems Biology, Washington University School of Medicine, St Louis, MO, USA.
  • Lebrilla CB; Center for Gut Microbiome and Nutrition Research, Washington University School of Medicine, St Louis, MO, USA.
  • Mostafa I; Edison Family Center for Genome Sciences and Systems Biology, Washington University School of Medicine, St Louis, MO, USA.
  • Das S; Center for Gut Microbiome and Nutrition Research, Washington University School of Medicine, St Louis, MO, USA.
  • Mahfuz M; Faculty of Engineering and Natural Sciences, Sabanci University, Istanbul, Turkey.
  • Barratt MJ; Infectious and Inflammatory Disease Center, Sanford Burnham Prebys Medical Discovery Institute, La Jolla, CA, USA.
  • Osterman AL; Infectious and Inflammatory Disease Center, Sanford Burnham Prebys Medical Discovery Institute, La Jolla, CA, USA.
  • Ahmed T; Architecture et Fonction des Macromolécules Biologiques, CNRS, Aix-Marseille University, Marseille, France.
  • Gordon JI; Architecture et Fonction des Macromolécules Biologiques, CNRS, Aix-Marseille University, Marseille, France.
Nature ; 625(7993): 157-165, 2024 Jan.
Article in En | MEDLINE | ID: mdl-38093016
ABSTRACT
Evidence is accumulating that perturbed postnatal development of the gut microbiome contributes to childhood malnutrition1-4. Here we analyse biospecimens from a randomized, controlled trial of a microbiome-directed complementary food (MDCF-2) that produced superior rates of weight gain compared with a calorically more dense conventional ready-to-use supplementary food in 12-18-month-old Bangladeshi children with moderate acute malnutrition4. We reconstructed 1,000 bacterial genomes (metagenome-assembled genomes (MAGs)) from the faecal microbiomes of trial participants, identified 75 MAGs of which the abundances were positively associated with ponderal growth (change in weight-for-length Z score (WLZ)), characterized changes in MAG gene expression as a function of treatment type and WLZ response, and quantified carbohydrate structures in MDCF-2 and faeces. The results reveal that two Prevotella copri MAGs that are positively associated with WLZ are the principal contributors to MDCF-2-induced expression of metabolic pathways involved in utilizing the component glycans of MDCF-2. The predicted specificities of carbohydrate-active enzymes expressed by their polysaccharide-utilization loci are correlated with (1) the in vitro growth of Bangladeshi P. copri strains, possessing varying degrees of polysaccharide-utilization loci and genomic conservation with these MAGs, in defined medium containing different purified glycans representative of those in MDCF-2, and (2) the levels of faecal carbohydrate structures in the trial participants. These associations suggest that identifying bioactive glycan structures in MDCFs metabolized by growth-associated bacterial taxa will help to guide recommendations about their use in children with acute malnutrition and enable the development of additional formulations.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Polysaccharides / Malnutrition / Gastrointestinal Microbiome / Food Limits: Humans / Infant Country/Region as subject: Asia Language: En Journal: Nature Year: 2024 Document type: Article Affiliation country: United States

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Polysaccharides / Malnutrition / Gastrointestinal Microbiome / Food Limits: Humans / Infant Country/Region as subject: Asia Language: En Journal: Nature Year: 2024 Document type: Article Affiliation country: United States