Karagas Margaret R, McRitchie Susan, Hoen Anne G, Takigawa Cindy, Jackson Brian, Baker Emily R, Madan Juliette, Sumner Susan J, Pathmasiri Wimal
Department of Epidemiology, Geisel School of Medicine at Dartmouth College, Hanover, NH, USA.
Nutrition Research Institute, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA.
Expo Health. 2022 Dec;14(4):941-949. doi: 10.1007/s12403-022-00468-2. Epub 2022 Feb 3.
In utero and early life exposure to inorganic arsenic (iAs) alters immune response in experimental animals and is associated with an increased risk of infant infections. iAs exposure is related to differences in the gut microbiota diversity, community structure, and the relative abundance of individual microbial taxa both in laboratory and human studies. Metabolomics permits a direct measure of molecular products of microbial and host metabolic processes. We conducted NMR metabolomics analysis on infant stool samples and quantified the relative concentrations of 34 known microbial-related metabolites. We examined these metabolites in relation to both in utero and infant log urinary total arsenic concentrations (utAs, the sum of iAs and iAs metabolites) collected at approximately 6 weeks of age using linear regression models, adjusted for infant sex, age at sample collection, type of delivery (vaginal vs. cesarean section), feeding mode (breast milk vs. any formula), and specific gravity. Increased fecal butyrate ( = 214.24), propionate ( = 518.33), cholate ( = 8.79), tryptophan (= 14.23), asparagine ( = 28.80), isoleucine ( = 65.58), leucine ( = 95.91), malonate ( = 50.43), and uracil ( = 36.13), concentrations were associated with a doubling of infant utAs concentrations ( 0.05). These associations were largely among infants who were formula fed. No clear associations were observed with maternal utAs and infant fecal metabolites. Metabolomic analyses of infant stool samples lend further evidence that the infant gut microbiota is sensitive to As exposure, and these effects may have functional consequences.
子宫内及生命早期暴露于无机砷(iAs)会改变实验动物的免疫反应,并与婴儿感染风险增加有关。在实验室研究和人体研究中,iAs暴露均与肠道微生物群多样性、群落结构以及单个微生物分类群的相对丰度差异有关。代谢组学能够直接测量微生物和宿主代谢过程的分子产物。我们对婴儿粪便样本进行了核磁共振代谢组学分析,并对34种已知的微生物相关代谢物的相对浓度进行了定量。我们使用线性回归模型,在调整了婴儿性别、样本采集时的年龄、分娩方式(阴道分娩与剖宫产)、喂养方式(母乳喂养与任何配方奶喂养)以及比重后,研究了这些代谢物与大约6周龄时采集的婴儿尿总砷浓度(utAs,iAs及其代谢物的总和)对数之间的关系。粪便中丁酸盐(= 214.24)、丙酸盐(= 518.33)、胆酸盐(= 8.79)、色氨酸(= 14.23)、天冬酰胺(= 28.80)、异亮氨酸(= 65.58)、亮氨酸(= 95.91)、丙二酸(= 50.43)和尿嘧啶(= 36.13)浓度的增加与婴儿utAs浓度翻倍相关(P < 0.05)。这些关联主要存在于配方奶喂养的婴儿中。未观察到母体utAs与婴儿粪便代谢物之间有明显关联。对婴儿粪便样本的代谢组学分析进一步证明,婴儿肠道微生物群对砷暴露敏感,且这些影响可能具有功能后果。