Exclusively Breastfed Infant Microbiota Develops over Time and Is Associated with Human Milk Oligosaccharide Intakes

被引:20
作者
Cheema, Ali Sadiq [1 ]
Trevenen, Michelle Louise [2 ]
Turlach, Berwin Ashoka [2 ]
Furst, Annalee June [3 ,4 ]
Roman, Ana Sophia [3 ,4 ]
Bode, Lars [3 ,4 ]
Gridneva, Zoya [1 ]
Lai, Ching Tat [1 ]
Stinson, Lisa Faye [1 ]
Payne, Matthew Scott [5 ,6 ]
Geddes, Donna Tracy [1 ]
机构
[1] Univ Western Australia, Sch Mol Sci, Crawley, WA 6009, Australia
[2] Univ Western Australia, Ctr Appl Stat, Crawley, WA 6009, Australia
[3] Univ Calif San Diego, Larsson Rosenquist Fdn Mother Milk Infant Ctr Res, La Jolla, CA 92093 USA
[4] Univ Calif San Diego, Dept Pediat, La Jolla, CA 92093 USA
[5] Univ Western Australia, Sch Med, Div Obstet & Gynaecol, Subiaco, WA 6008, Australia
[6] Women & Infants Res Fdn, Subiaco, WA 6008, Australia
基金
英国医学研究理事会;
关键词
maternal faecal; human milk; human milk oligosaccharides; human milk bacteria; infant oral; infant faecal; microbiome; 16S rRNA gene; breastfeeding; body composition; intake; concentration; lactation; HUMAN GUT MICROBIOME; STAPHYLOCOCCUS-EPIDERMIDIS; LONGITUDINAL CHANGES; COMMUNITY STRUCTURE; 1ST YEAR; LACTATION; HEALTHY; COLONIZATION; TRANSMISSION; BIFIDOBACTERIA;
D O I
10.3390/ijms23052804
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Temporal development of maternal and infant microbiomes during early life impacts short- and long-term infant health. This study aimed to characterize bacterial dynamics within maternal faecal, human milk (HM), infant oral, and infant faecal samples during the exclusive breastfeeding period and to document associations between human milk oligosaccharide (HMO) intakes and infant oral and faecal bacterial profiles. Maternal and infant samples (n = 10) were collected at 2-5, 30, 60, 90 and 120 days postpartum and the full-length 16S ribosomal RNA (rRNA) gene was sequenced. Nineteen HMOs were quantitated using high-performance liquid chromatography. Bacterial profiles were unique to each sample type and changed significantly over time, with a large degree of intra- and inter-individual variation in all sample types. Beta diversity was stable over time within infant faecal, maternal faecal and HM samples, however, the infant oral microbiota at day 2-5 significantly differed from all other time points (all p < 0.02). HMO concentrations and intakes significantly differed over time, and HMO intakes showed differential associations with taxa observed in infant oral and faecal samples. The direct clinical relevance of this, however, is unknown. Regardless, future studies should account for intakes of HMOs when modelling the impact of HM on infant growth, as it may have implications for infant microbiota development.
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