Untangling human milk oligosaccharides and infant gut microbiome

被引:60
|
作者
Masi, Andrea C. [1 ]
Stewart, Christopher J. [1 ]
机构
[1] Newcastle Univ, Fac Med Sci, Translat & Clin Res Inst, 3rd Floor Leech Bldg, Newcastle Upon Tyne NE2 4HH, Tyne & Wear, England
基金
英国惠康基金;
关键词
LONGUM SUBSP INFANTIS; N-BIOSE PHOSPHORYLASE; ALPHA-L-FUCOSIDASES; CHAIN FATTY-ACIDS; BIFIDOBACTERIUM-BIFIDUM; BETA-GALACTOSIDASES; MOLECULAR-CLONING; DEGRADATION; CONSUMPTION; FORMULA;
D O I
10.1016/j.isci.2021.103542
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The developing gut microbiome in infancy plays a key role in shaping the host immune system and metabolic state, and human milk is the main factor influencing its composition. Human milk does not only serve to feed the baby, but also to help the new-born adapt to its new environment and microbial exposures. Human milk protects the infant by providing multiple bioactive molecules, including human milk oligosaccharides (HMOs), which are the third most abundant solid component after lipids and lactose. The infant is unable to digest HMOs, so they reach the small and large intestines intact where they have many roles, including acting as prebiotics. Bifidobacterium spp. are the main, but not the only, commensals equipped with genes for HMO degradation. In this review we will outline the HMOs structures and functions, list the genes needed for their digestion, and describe the main strategies adopted by bacteria for their utilization.
引用
收藏
页数:15
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