Department of Pediatrics, School of Public Health, University of Alberta, Edmonton, AB, Canada; Department of Pediatrics & Child Health, Children's Hospital Research Institute of Manitoba, University of Manitoba, Winnipeg, MB, Canada.
Clin Exp Allergy. 2015 Mar;45(3):632-43. doi: 10.1111/cea.12487.
The gut microbiota is established during infancy and plays a fundamental role in shaping host immunity. Colonization patterns may influence the development of atopic disease, but existing evidence is limited and conflicting.
To explore associations of infant gut microbiota and food sensitization.
Food sensitization at 1 year was determined by skin prick testing in 166 infants from the population-based Canadian Healthy Infant Longitudinal Development (CHILD) study. Faecal samples were collected at 3 and 12 months, and microbiota was characterized by Illumina 16S rRNA sequencing.
Twelve infants (7.2%) were sensitized to ≥ 1 common food allergen at 1 year. Enterobacteriaceae were overrepresented and Bacteroidaceae were underrepresented in the gut microbiota of food-sensitized infants at 3 months and 1 year, whereas lower microbiota richness was evident only at 3 months. Each quartile increase in richness at 3 months was associated with a 55% reduction in risk for food sensitization by 1 year (adjusted odds ratio 0.45, 95% confidence interval 0.23-0.87). Independently, each quartile increase in Enterobacteriaceae/Bacteroidaceae ratio was associated with a twofold increase in risk (2.02, 1.07-3.80). These associations were upheld in a sensitivity analysis among infants who were vaginally delivered, exclusively breastfed and unexposed to antibiotics. At 1 year, the Enterobacteriaceae/Bacteroidaceae ratio remained elevated among sensitized infants, who also tended to have decreased abundance of Ruminococcaceae.
Low gut microbiota richness and an elevated Enterobacteriaceae/Bacteroidaceae ratio in early infancy are associated with subsequent food sensitization, suggesting that early gut colonization may contribute to the development of atopic disease, including food allergy.
肠道微生物群在婴儿期建立,对宿主免疫起着至关重要的作用。定植模式可能会影响特应性疾病的发展,但现有证据有限且相互矛盾。
探索婴儿肠道微生物群与食物致敏的关系。
通过加拿大基于人群的健康婴儿纵向发展(CHILD)研究中 166 名婴儿的皮肤点刺试验,确定 1 岁时的食物致敏情况。在 3 个月和 12 个月时采集粪便样本,并通过 Illumina 16S rRNA 测序对微生物群进行特征分析。
12 名婴儿(7.2%)在 1 岁时对≥1 种常见食物过敏原过敏。致敏婴儿的肠道微生物群中,肠杆菌科在 3 个月和 1 岁时过度表达,拟杆菌科表达不足,而微生物丰富度仅在 3 个月时降低。3 个月时丰富度每增加一个四分位间距,1 岁时食物致敏的风险降低 55%(调整后的优势比 0.45,95%置信区间 0.23-0.87)。独立地,肠杆菌科/拟杆菌科比值每增加一个四分位间距,风险增加两倍(2.02,1.07-3.80)。这些关联在阴道分娩、纯母乳喂养和未暴露于抗生素的婴儿中进行敏感性分析时仍然成立。在 1 岁时,致敏婴儿的肠杆菌科/拟杆菌科比值仍然升高,其瘤胃球菌科的丰度也趋于降低。
婴儿早期肠道微生物群丰富度低,肠杆菌科/拟杆菌科比值升高与随后的食物致敏相关,这表明早期肠道定植可能有助于特应性疾病(包括食物过敏)的发展。