Impact of short-chain galactooligosaccharides on the gut microbiome of lactose-intolerant individuals

Directed modulation of the colonic bacteria to metabolize lactose effectively is a potentially useful approach to improve lactose digestion and tolerance. A randomized, double-blind, multisite placebo-controlled trial conducted in human subjects demonstrated that administration of a highly purified...

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Published inProceedings of the National Academy of Sciences - PNAS Vol. 114; no. 3; pp. E367 - E375
Main Authors Azcarate-Peril, M. Andrea, Ritter, Andrew J., Savaiano, Dennis, Monteagudo-Mera, Andrea, Anderson, Carlton, Magness, Scott T., Klaenhammer, Todd R.
Format Journal Article
LanguageEnglish
Published United States National Academy of Sciences 17.01.2017
SeriesPNAS Plus
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Summary:Directed modulation of the colonic bacteria to metabolize lactose effectively is a potentially useful approach to improve lactose digestion and tolerance. A randomized, double-blind, multisite placebo-controlled trial conducted in human subjects demonstrated that administration of a highly purified (>95%) short-chain galactooligosaccharide (GOS), designated “RP-G28,” significantly improved clinical outcomes for lactose digestion and tolerance. In these individuals, stool samples were collected pretreatment (day 0), after GOS treatment (day 36), and 30 d after GOS feeding stopped and consumption of dairy products was encouraged (day 66). In this study, changes in the fecal microbiome were investigated using 16S rRNA amplicon pyrosequencing and high-throughput quantitative PCR. At day 36, bifidobacterial populations were increased in 27 of 30 of GOS subjects (90%), demonstrating a bifidogenic response in vivo. Relative abundance of lactose-fermenting Bifidobacterium, Faecalibacterium, and Lactobacillus were significantly increased in response to GOS. When dairy was introduced into the diet, lactose-fermenting Roseburia species increased from day 36 to day 66. The results indicated a definitive change in the fecal microbiome of lactose-intolerant individuals, increasing the abundance of lactose-metabolizing bacteria that were responsive to dietary adaptation to GOS. This change correlated with clinical outcomes of improved lactose tolerance.
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1Present address: Division of Gastroenterology and Hepatology, Department of Medicine, School of Medicine, University of North Carolina at Chapel Hill, Chapel Hill, NC 27514.
Author contributions: M.A.A.-P., A.J.R., D.S., and T.R.K. designed research; M.A.A.-P., A.J.R., D.S., A.M.-M., C.A., and T.R.K. performed research; M.A.A.-P., S.T.M., and T.R.K. contributed new reagents/analytic tools; M.A.A.-P., A.J.R., and T.R.K. analyzed data; and M.A.A.-P., A.J.R., D.S., and T.R.K. wrote the paper.
Edited by Ralph R. Isberg, Howard Hughes Medical Institute/Tufts University School of Medicine, Boston, MA, and approved November 30, 2016 (received for review May 6, 2016)
ISSN:0027-8424
1091-6490
1091-6490
DOI:10.1073/pnas.1606722113