Department of Genetics and Genomic Sciences, Icahn School of Medicine at Mount Sinai, New York, NY.
Department of Pediatrics, Icahn School of Medicine at Mount Sinai, New York, NY.
J Allergy Clin Immunol. 2023 Dec;152(6):1569-1580. doi: 10.1016/j.jaci.2023.08.012. Epub 2023 Aug 22.
Rising rates of peanut allergy (PA) motivate investigations of its development to inform prevention and therapy. Microbiota and the metabolites they produce shape food allergy risk.
We sought to gain insight into gut microbiome and metabolome dynamics in the development of PA.
We performed a longitudinal, integrative study of the gut microbiome and metabolome of infants with allergy risk factors but no PA from a multicenter cohort followed through mid-childhood. We performed 16S rRNA sequencing, short chain fatty acid measurements, and global metabolome profiling of fecal samples at infancy and at mid-childhood.
In this longitudinal, multicenter sample (n = 122), 28.7% of infants developed PA by mid-childhood (mean age 9 years). Lower infant gut microbiome diversity was associated with PA development (P = .014). Temporal changes in the relative abundance of specific microbiota and gut metabolite levels significantly differed in children who developed PA. PA-bound children had different abundance trajectories of Clostridium sensu stricto 1 sp (false discovery rate (FDR) = 0.015) and Bifidobacterium sp (FDR = 0.033), with butyrate (FDR = 0.045) and isovalerate (FDR = 0.036) decreasing over time. Metabolites associated with PA development clustered within the histidine metabolism pathway. Positive correlations between microbiota, butyrate, and isovalerate and negative correlations with histamine marked the PA-free network.
The temporal dynamics of the gut microbiome and metabolome in early childhood are distinct for children who develop PA. These findings inform our thinking on the mechanisms underlying and strategies for potentially preventing PA.
花生过敏(PA)发病率的上升促使人们对其发病机制进行研究,以便为预防和治疗提供信息。微生物群及其产生的代谢产物影响食物过敏的风险。
我们旨在深入了解过敏风险婴儿 PA 发病过程中的肠道微生物组和代谢组动态。
我们对来自多中心队列的过敏风险因素但无 PA 的婴儿进行了纵向、综合的肠道微生物组和代谢组研究,随访至儿童中期。我们对婴儿期和儿童中期的粪便样本进行了 16S rRNA 测序、短链脂肪酸测量和全代谢组谱分析。
在这项纵向、多中心样本(n=122)中,28.7%的婴儿在儿童中期发展为 PA(平均年龄 9 岁)。婴儿肠道微生物组多样性较低与 PA 发病相关(P=0.014)。PA 发病儿童肠道微生物群和肠道代谢物水平的时间变化明显不同。PA 相关儿童的 Clostridium sensu stricto 1 sp(错误发现率(FDR)=0.015)和双歧杆菌属(FDR=0.033)相对丰度轨迹不同,丁酸(FDR=0.045)和异戊酸(FDR=0.036)随时间推移而降低。与 PA 发病相关的代谢物聚类在组氨酸代谢途径内。微生物群、丁酸和异戊酸与组胺呈正相关,标志着 PA 无网络。
儿童早期肠道微生物组和代谢组的时间动态在发展为 PA 的儿童中是不同的。这些发现为我们思考潜在预防 PA 的发病机制和策略提供了信息。