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Nutrients ; 12(11)2020 Oct 24.
Article in English | MEDLINE | ID: mdl-33114404

ABSTRACT

Certain non-digestible oligosaccharides (NDO) are specifically fermented by bifidobacteria along the human gastrointestinal tract, selectively favoring their growth and the production of health-promoting metabolites. In the present study, the ability of the probiotic strain Bifidobacterium longum subsp. infantis CECT7210 (herein referred to as B. infantis IM-1®) to utilize a large range of oligosaccharides, or a mixture of oligosaccharides, was investigated. The strain was able to utilize all prebiotics screened. However, galactooligosaccharides (GOS), and GOS-containing mixtures, effectively increased its growth to a higher extent than the other prebiotics. The best synbiotic combination was used to examine the antimicrobial activity against Escherichia coli, Cronobacter sakazakii, Listeria monocytogenes and Clostridium difficile in co-culture experiments. C. difficile was inhibited by the synbiotic, but it failed to inhibit E. coli. Moreover, Cr. sakazakii growth decreased during co-culture with B. infantis IM-1®. Furthermore, adhesion experiments using the intestinal cell line HT29 showed that the strain IM-1® was able to displace some pathogens from the enterocyte layer, especially Cr. sakazakii and Salmonella enterica, and prevented the adhesion of Cr. sakazakii and Shigella sonnei. In conclusion, a new synbiotic (probiotic strain B. infantis IM-1® and GOS) appears to be a potential effective supplement for maintaining infant health. However, further studies are needed to go more deeply into the mechanisms that allow B.infantis IM-1® to compete with enteropathogens.


Subject(s)
Anti-Bacterial Agents/pharmacology , Bifidobacterium longum subspecies infantis , Intestines/microbiology , Oligosaccharides/pharmacology , Probiotics/pharmacology , Clostridioides difficile/drug effects , Coculture Techniques , Complex Mixtures , Cronobacter sakazakii/drug effects , Escherichia coli/drug effects , Female , Gastrointestinal Tract/microbiology , HT29 Cells , Humans , Infant , Infant, Newborn , Listeria monocytogenes/drug effects , Male , Prebiotics/microbiology , Salmonella enterica/drug effects , Synbiotics
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