Long Term Development of Gut Microbiota Composition in Atopic Children: Impact of Probiotics

PLoS One. 2015 Sep 17;10(9):e0137681. doi: 10.1371/journal.pone.0137681. eCollection 2015.

Abstract

Introduction: Imbalance of the human gut microbiota in early childhood is suggested as a risk factor for immune-mediated disorders such as allergies. With the objective to modulate the intestinal microbiota, probiotic supplementation during infancy has been used for prevention of allergic diseases in infants, with variable success. However, not much is known about the long-term consequences of neonatal use of probiotics on the microbiota composition. The aim of this study was to assess the composition and microbial diversity in stool samples of infants at high-risk for atopic disease, from birth onwards to six years of age, who were treated with probiotics or placebo during the first year of life.

Methods: In a double-blind, randomized, placebo-controlled trial, a probiotic mixture consisting of B. bifidum W23, B. lactis W52 and Lc. Lactis W58 (Ecologic® Panda) was administered to pregnant women during the last 6 weeks of pregnancy and to their offspring during the first year of life. During follow-up, faecal samples were collected from 99 children over a 6-year period with the following time points: first week, second week, first month, three months, first year, eighteen months, two years and six years. Bacterial profiling was performed by IS-pro. Differences in bacterial abundance and diversity were assessed by conventional statistics.

Results: The presence of the supplemented probiotic strains in faecal samples was confirmed, and the probiotic strains had a higher abundance and prevalence in the probiotic group during supplementation. Only minor and short term differences in composition of microbiota were found between the probiotic and placebo group and between children with or without atopy. The diversity of Bacteroidetes was significantly higher after two weeks in the placebo group, and at the age of two years atopic children had a significantly higher Proteobacteria diversity (p < 0.05). Gut microbiota development continued between two and six years, whereby microbiota composition at phylum level evolved more and more towards an adult-like configuration.

Conclusion: Perinatal supplementation with Ecologic® Panda, to children at high-risk for atopic disease, had minor effects on gut microbiota composition during the supplementation period. No long lasting differences were identified. Regardless of intervention or atopic disease status, children had a shared microbiota development over time determined by age that continued to develop between two and six years.

Publication types

  • Randomized Controlled Trial
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Bacterial Typing Techniques
  • Bifidobacterium
  • Biodiversity
  • Child
  • Child, Preschool
  • Dietary Supplements
  • Double-Blind Method
  • Female
  • Gastrointestinal Microbiome / drug effects*
  • Gastrointestinal Microbiome / genetics
  • Humans
  • Hypersensitivity / immunology
  • Infant
  • Infant, Newborn
  • Lactobacillus
  • Male
  • Metagenome / genetics*
  • Placebos / therapeutic use
  • Pregnancy
  • Probiotics / therapeutic use*
  • RNA, Ribosomal, 16S / genetics
  • RNA, Ribosomal, 23S / genetics

Substances

  • Placebos
  • RNA, Ribosomal, 16S
  • RNA, Ribosomal, 23S

Associated data

  • figshare/10.6084/M9.FIGSHARE.1520433
  • figshare/10.6084/M9.FIGSHARE.1520434
  • figshare/10.6084/M9.FIGSHARE.1520435
  • figshare/10.6084/M9.FIGSHARE.1520436,

Grants and funding

This research was supported financially by the Netherlands Enterprise Agency (Agentschap NL), grant number FND06015, http://english.rvo.nl/. Employees of this agency did not play any role in study design, data collection and analysis, nor in preparation of the manuscript and decision to publish. IB is an employee of Winclove Probiotics. Winclove Probiotics offers evidence based probiotic solutions for consumers, health professionals and business partners. This funder provided support in the form of salary for one author (IB) and did play a supportive role in the study design, as a public-private consortium of four parties (two hospitals and two companies) which together performed an innovative project entitled “Translational research to study the effect and mechanism of microbiota in paediatric immune-mediated diseases.” The parties had a cooperation agreement in the context of the grant scheme Food & Nutrition Delta Phase 2 from SenterNovem (Agentschap NL, nowadays RVO). The current study was designed as part of the above mentioned innovative project, in consultation with all the participating parties. Winclove Probiotics did not have any additional role in data collection and analysis, decision to publish, or preparation of the manuscript. The specific role of this author is articulated in the ‘authors contributions’ section.