Broad Institute of MIT and Harvard, Cambridge, MA 02142, USA; Research Program for Clinical and Molecular Metabolism, Faculty of Medicine, University of Helsinki, Helsinki, Finland; Liggins Institute, University of Auckland, Auckland, New Zealand.
Broad Institute of MIT and Harvard, Cambridge, MA 02142, USA.
Cell. 2022 Dec 22;185(26):4921-4936.e15. doi: 10.1016/j.cell.2022.11.023.
The perinatal period represents a critical window for cognitive and immune system development, promoted by maternal and infant gut microbiomes and their metabolites. Here, we tracked the co-development of microbiomes and metabolomes from late pregnancy to 1 year of age using longitudinal multi-omics data from a cohort of 70 mother-infant dyads. We discovered large-scale mother-to-infant interspecies transfer of mobile genetic elements, frequently involving genes associated with diet-related adaptations. Infant gut metabolomes were less diverse than maternal but featured hundreds of unique metabolites and microbe-metabolite associations not detected in mothers. Metabolomes and serum cytokine signatures of infants who received regular-but not extensively hydrolyzed-formula were distinct from those of exclusively breastfed infants. Taken together, our integrative analysis expands the concept of vertical transmission of the gut microbiome and provides original insights into the development of maternal and infant microbiomes and metabolomes during late pregnancy and early life.
围产期是认知和免疫系统发育的关键时期,这一过程受到母婴肠道微生物组及其代谢产物的促进。在这里,我们使用来自 70 对母婴队列的纵向多组学数据,追踪了从妊娠晚期到 1 岁时微生物组和代谢组的共同发育。我们发现了大规模的母婴种间可移动遗传元件的转移,这些转移经常涉及与饮食相关适应有关的基因。婴儿肠道代谢组的多样性不如母体,但具有数百种母体中未检测到的独特代谢物和微生物-代谢物关联。接受常规但不是广泛水解配方的婴儿的代谢组和血清细胞因子特征与纯母乳喂养的婴儿不同。总的来说,我们的综合分析扩展了肠道微生物垂直传播的概念,并为妊娠晚期和生命早期母婴微生物组和代谢组的发育提供了新的见解。