Danone Nutricia Research, Utrecht, The Netherlands; Laboratory of Microbiology, Wageningen University, Wageningen, The Netherlands.
Department of Medicine, Section of Paediatrics, Imperial College London, London, United Kingdom.
J Allergy Clin Immunol. 2018 Apr;141(4):1334-1342.e5. doi: 10.1016/j.jaci.2017.05.054. Epub 2017 Sep 1.
Development of the gut microbiota in infancy is important in maturation of the immune system. Deviations in colonization patterns have been associated with allergic manifestations such as eczema, but exact microbiome dysfunctions underlying allergies remain unclear. We studied the gut microbiota of 138 infants at increased risk of allergy, participating in a clinical trial investigating the effectiveness of a partially hydrolyzed protein formula supplemented with nondigestible oligosaccharides on the prevention of eczema.
The effects of interventions and breast-feeding on fecal microbiota were investigated. Additionally, we aimed to identify microbial patterns associated with the onset of eczema.
Bacterial taxonomic compositions in the first 26 weeks of life were analyzed by using 16S rRNA gene sequencing. Additionally, fecal pH and microbial metabolite levels were measured.
Fecal microbial composition, metabolites, and pH of infants receiving partially hydrolyzed protein formula supplemented with nondigestible oligosaccharides was closer to that of breast-fed infants than that of infants receiving standard cow's milk formula. Infants with eczema by 18 months showed discordant development of bacterial genera of Enterobacteriaceae and Parabacteroides species in the first 26 weeks, as well as decreased acquisition of lactate-utilizing bacteria producing butyrate, namely Eubacterium and Anaerostipes species, supported by increased lactate and decreased butyrate levels.
We showed that a partially hydrolyzed protein infant formula with specific prebiotics modulated the gut microbiota closer to that of breast-fed infants. Additionally, we identified a potential link between microbial activity and onset of eczema, which might reflect a suboptimal implementation of gut microbiota at specific developmental stages in infants at high risk for allergy.
婴儿期肠道微生物群的发展对于免疫系统的成熟很重要。定植模式的偏差与特应性表现(如湿疹)有关,但过敏的确切微生物失调仍不清楚。我们研究了 138 名过敏风险增加的婴儿的肠道微生物群,他们参与了一项临床试验,该试验研究了部分水解蛋白配方与不可消化的低聚糖联合使用对预防湿疹的有效性。
研究干预措施和母乳喂养对粪便微生物群的影响。此外,我们旨在确定与特应性皮炎发病相关的微生物模式。
通过 16S rRNA 基因测序分析生命最初 26 周的细菌分类组成。此外,还测量了粪便 pH 值和微生物代谢产物水平。
接受部分水解蛋白配方与不可消化的低聚糖联合补充的婴儿的粪便微生物组成、代谢物和 pH 值更接近母乳喂养的婴儿,而不是接受标准牛奶配方的婴儿。18 个月时有湿疹的婴儿在最初 26 周内出现肠杆菌科和拟杆菌属细菌属的发育不一致,以及产生丁酸盐的乳杆菌和厌氧螺旋菌等利用乳酸的细菌的获得减少,这得到了乳酸水平升高和丁酸盐水平降低的支持。
我们表明,含有特定益生元的部分水解蛋白婴儿配方可使肠道微生物群更接近母乳喂养的婴儿。此外,我们发现微生物活性与特应性皮炎发病之间存在潜在联系,这可能反映出过敏高风险婴儿在特定发育阶段肠道微生物群的实施不理想。