Abstract

The interest for naturally-occurring oligosaccharides from plant origin having prebiotic properties is growing, with special focus being paid to supplemented products for infants. Currently, non-fructosylated α-galactooligosaccharides (α-GOS) from peas have peaked interest as a result of their prebiotic activity in adults and their mitigated side-effects on gas production from colonic bacterial fermentation. In this study, commercially available non-fructosylated α-GOS from peas and β-galactooligosaccharides (β-GOS) derived from lactose were fermented using fecal slurries from children aged 11 to 24 months old during 6 and 24 h. The modulatory effect of both GOS on different bacterial groups and bifidobacteria species was assessed; non-fructosylated α-GOS consumption was monitored throughout the fermentation process and the amounts of lactic acid and short-chain fatty acids (SCFA) generated were analyzed. Non-fructosylated α-GOS, composed mainly of manninotriose and verbascotetraose and small amounts of melibiose, were fully metabolized and presented remarkable bifidogenic activity, similar to that obtained with β-GOS. Furthermore, non-fructosylated α-GOS selectively caused an increase on the population of Bifidobacterium longum subsp. longum and Bifidobacterium catenulatum/pseudo-catenulatum. In conclusion, non-fructosylated α-GOS could be used as potential ingredient in infant formula supplemented with prebiotic oligosaccharides.

Highlights

  • The colonisation of the gastrointestinal tract (GIT) by microorganisms is an essential process in our life cycle and starts during the gestation period [1,2]

  • The continued succession of microorganisms during the first years of life has an important effect on the long-term maturity of the GIT microbiota, which is affected by diet, mode of delivery, antibiotic treatments, genetics, intestinal mucin glycosylation and other factors [4]

  • The bifidogenic effect in non-fructosylated α-GOS and β-GOS groups was significantly greater than that found in control samples

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Summary

Introduction

The colonisation of the gastrointestinal tract (GIT) by microorganisms is an essential process in our life cycle and starts during the gestation period [1,2]. Evidence shows that the GIT colonisation rapidly increases after birth by aerobic microorganisms that decrease the concentration of oxygen. This lowering of redox potentially allows the colonisation of anaerobic bacteria [3]. Non-digestible dietary ingredients are capable of modulating composition and metabolic function of gut microbiota. In this context, the prebiotic concept was recently defined by the International

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