
Human milk oligosaccharides (HMO) constitute the third most abundant class of molecules in breast milk. Since infants lack the enzymes required for milk glycan digestion, this group of carbohydrates passes undigested to the lower part of the intestinal tract, where they can be consumed by specific members of the infant gut microbiota. We review proposed mechanisms for the depletion and metabolism of HMO by two major bacterial genera within the infant intestinal microbiota, Bifidobacterium and Bacteroides.
Microbiology (medical), Milk, Human, Infant, Newborn, Oligosaccharides, infant gut, Bifidobacterium, human milk oligosaccharides, Gastrointestinal Tract, Infectious Diseases, Bacteroides, Carbohydrate Metabolism, Humans, Metagenome, Bifidobacterium
Microbiology (medical), Milk, Human, Infant, Newborn, Oligosaccharides, infant gut, Bifidobacterium, human milk oligosaccharides, Gastrointestinal Tract, Infectious Diseases, Bacteroides, Carbohydrate Metabolism, Humans, Metagenome, Bifidobacterium
| citations This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically). | 261 | |
| popularity This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network. | Top 1% | |
| influence This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically). | Top 10% | |
| impulse This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network. | Top 1% |
