Abstract

BackgroundProbiotics are increasingly applied to prevent and treat a range of infectious, immune related and gastrointestinal diseases. Despite this, the mechanisms behind the putative effects of probiotics are poorly understood. One of the suggested modes of probiotic action is modulation of the endogenous gut microbiota, however probiotic intervention studies in adults have failed to show significant effects on gut microbiota composition. The gut microbiota of young children is known to be unstable and more responsive to external factors than that of adults. Therefore, potential effects of probiotic intervention on gut microbiota may be easier detectable in early life. We thus investigated the effects of a 6 month placebo-controlled probiotic intervention with Bifidobacterium animalis subsp. lactis (BB-12®) and Lactobacillus rhamnosus (LGG®) on gut microbiota composition and diversity in more than 200 Danish infants (N = 290 enrolled; N = 201 all samples analyzed), as assessed by 16S rRNA amplicon sequencing. Further, we evaluated probiotic presence and proliferation by use of specific quantitative polymerase chain reaction (qPCR).ResultsProbiotic administration did not significantly alter gut microbiota community structure or diversity as compared to placebo. The probiotic strains were detected in 91.3% of the fecal samples from children receiving probiotics and in 1% of the placebo treated children. Baseline gut microbiota was not found to predict the ability of probiotics to establish in the gut after the 6 month intervention. Within the probiotics group, proliferation of the strains LGG® and BB-12® in the gut was detected in 44.7% and 83.5% of the participants, respectively. A sub-analysis of the gut microbiota including only individuals with detected growth of the probiotics LGG® or BB-12® and comparing these to placebo revealed no differences in community structure or diversity.ConclusionSix months of probiotic administration during early life did not change gut microbiota community structure or diversity, despite active proliferation of the administered probiotic strains. Therefore, alteration of the healthy infant gut microbiota is not likely to be a prominent mechanism by which these specific probiotics works to exert beneficial effects on host health.Trial registrationNCT02180581. Registered 30 June 2014.

Highlights

  • Introduction of selected foodsCow’s milk 8.0 (7.0–12.0) 9.0 (6.0–11.0)Meat 6.0 (6.0–7.0)FishBreastfeeding prevalence 1st visit (%) 2nd visit (%) Age1st visit

  • Principle Coordinate Analysis (PCoA) of both weighted and unweighted UniFrac distances did not result in visible separation of samples according to treatment group (Fig. 1a), Adonis testing revealed a significant difference between the unweighted distances caused by the specific presence of the probiotics as described

  • A BLAST search against the 16S rRNA gene database revealed that they had 100% homology to the V3 regions of the two probiotic strains included in the intervention, namely B. animalis subsp. lactis and L. rhamnosus strains, respectively (Table 2)

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Summary

Introduction

We investigated the effects of a 6 month placebo-controlled probiotic intervention with Bifidobacterium animalis subsp. If alteration of the gut microbiota composition is a mechanism by which probiotics exert their beneficial effect, this would be expected to be evident in early life interventions. We have analyzed the fecal microbiota of healthy infants at the age of starting daycare (age 8–13 months), sampled before and after a 6 months intervention with a single daily dose of Lactobacillus rhamnosus (LGG®) and Bifidobacterium animalis subsp. In contrast to previous studies, we assessed the presence and proliferation of the probiotic strains in the gut, and evaluated the effect on the endogenous microbial composition and diversity based on probiotic propagation

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