Prevotella copri and microbiota members mediate the beneficial effects of a therapeutic food for malnutrition

Author:

Chang Hao-WeiORCID,Lee Evan M.,Wang Yi,Zhou CyrusORCID,Pruss Kali M.ORCID,Henrissat Suzanne,Chen Robert Y.,Kao ClaraORCID,Hibberd Matthew C.ORCID,Lynn Hannah M.ORCID,Webber Daniel M.ORCID,Crane MarieORCID,Cheng JiyeORCID,Rodionov Dmitry A.,Arzamasov Aleksandr A.ORCID,Castillo Juan J.ORCID,Couture Garret,Chen YeORCID,Balcazo Nikita P.ORCID,Lebrilla Carlito B.ORCID,Terrapon NicolasORCID,Henrissat BernardORCID,Ilkayeva OlgaORCID,Muehlbauer Michael J.,Newgard Christopher B.ORCID,Mostafa Ishita,Das Subhasish,Mahfuz Mustafa,Osterman Andrei L.ORCID,Barratt Michael J.,Ahmed Tahmeed,Gordon Jeffrey I.ORCID

Abstract

AbstractMicrobiota-directed complementary food (MDCF) formulations have been designed to repair the gut communities of malnourished children. A randomized controlled trial demonstrated that one formulation, MDCF-2, improved weight gain in malnourished Bangladeshi children compared to a more calorically dense standard nutritional intervention. Metagenome-assembled genomes from study participants revealed a correlation between ponderal growth and expression of MDCF-2 glycan utilization pathways by Prevotella copri strains. To test this correlation, here we use gnotobiotic mice colonized with defined consortia of age- and ponderal growth-associated gut bacterial strains, with or without P. copri isolates closely matching the metagenome-assembled genomes. Combining gut metagenomics and metatranscriptomics with host single-nucleus RNA sequencing and gut metabolomic analyses, we identify a key role of P. copri in metabolizing MDCF-2 glycans and uncover its interactions with other microbes including Bifidobacterium infantis. P. copri-containing consortia mediated weight gain and modulated energy metabolism within intestinal epithelial cells. Our results reveal structure–function relationships between MDCF-2 and members of the gut microbiota of malnourished children with potential implications for future therapies.

Funder

Bill and Melinda Gates Foundation

U.S. Department of Health & Human Services | National Institutes of Health

Helen Hay Whitney Foundation

Publisher

Springer Science and Business Media LLC

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3