Stunted childhood growth is associated with decompartmentalization of the gastrointestinal tract and overgrowth of oropharyngeal taxa

Author:

Vonaesch Pascale,Morien Evan,Andrianonimiadana Lova,Sanke Hugues,Mbecko Jean-Robert,Huus Kelsey E.,Naharimanananirina Tanteliniaina,Gondje Bolmbaye Privat,Nigatoloum Synthia Nazita,Vondo Sonia Sandrine,Kaleb Kandou Jepthé Estimé,Randremanana Rindra,Rakotondrainipiana Maheninasy,Mazel Florent,Djorie Serge Ghislain,Gody Jean-Chrysostome,Finlay B. Brett,Rubbo Pierre-Alain,Wegener Parfrey Laura,Collard Jean-Marc,Sansonetti Philippe J.,

Abstract

Linear growth delay (stunting) affects roughly 155 million children under the age of 5 years worldwide. Treatment has been limited by a lack of understanding of the underlying pathophysiological mechanisms. Stunting is most likely associated with changes in the microbial community of the small intestine, a compartment vital for digestion and nutrient absorption. Efforts to better understand the pathophysiology have been hampered by difficulty of access to small intestinal fluids. Here, we describe the microbial community found in the upper gastrointestinal tract of stunted children aged 2–5 y living in sub-Saharan Africa. We studied 46 duodenal and 57 gastric samples from stunted children, as well as 404 fecal samples from stunted and nonstunted children living in Bangui, Central African Republic, and in Antananarivo, Madagascar, using 16S Illumina Amplicon sequencing and semiquantitative culture methods. The vast majority of the stunted children showed small intestinal bacterial overgrowth dominated by bacteria that normally reside in the oropharyngeal cavity. There was an overrepresentation of oral bacteria in fecal samples of stunted children, opening the way for developing noninvasive diagnostic markers. In addition, Escherichia coli/Shigella sp. and Campylobacter sp. were found to be more prevalent in stunted children, while Clostridia, well-known butyrate producers, were reduced. Our data suggest that stunting is associated with a microbiome “decompartmentalization” of the gastrointestinal tract characterized by an increased presence of oropharyngeal bacteria from the stomach to the colon, hence challenging the current view of stunting arising solely as a consequence of small intestine overstimulation through recurrent infections by enteric pathogens.

Funder

Total Corporate Foundation

Institut Pasteur

Fondation Pasteur Suisse

Nutricia Research Foundation

Early.Postdoc Mobility Fellowship Swiss National Science Foundation

Advanced.Postdoc Mobility Fellowship Swiss National Science Foundation

Roux-Cantarini Postdoctoral Fellowship

L'Oréal-UNESCO for Women in Science France Fellowship

Vanier Canada Graduate Scholarship

Banting Postdoctoral Fellowship

Human Frontier Science Program

Gouvernement du Canada | Canadian Institutes of Health Research

Canadian Institute for Advanced Research

Publisher

Proceedings of the National Academy of Sciences

Subject

Multidisciplinary

Reference102 articles.

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