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健康成年人的粪便微生物组成不能预测饮食诱导的 TMAO 生成。

Fecal Microbiome Composition Does Not Predict Diet-Induced TMAO Production in Healthy Adults.

机构信息

Department of Cardiovascular and Metabolic Sciences Lerner Research Institute Cleveland Clinic Cleveland OH.

Department of Systems Biology and Bioinformatics Case Western Reserve University Cleveland OH.

出版信息

J Am Heart Assoc. 2021 Nov 2;10(21):e021934. doi: 10.1161/JAHA.121.021934. Epub 2021 Oct 29.

Abstract

Background Trimethylamine--oxide (TMAO) is a small molecule derived from the metabolism of dietary nutrients by gut microbes and contributes to cardiovascular disease. Plasma TMAO increases following consumption of red meat. This metabolic change is thought to be partly because of the expansion of gut microbes able to use nutrients abundant in red meat. Methods and Results We used data from a randomized crossover study to estimate the degree to which TMAO can be estimated from fecal microbial composition. Healthy participants received a series of 3 diets that differed in protein source (red meat, white meat, and non-meat), and fecal, plasma, and urine samples were collected following 4 weeks of exposure to each diet. TMAO was quantitated in plasma and urine, while shotgun metagenomic sequencing was performed on fecal DNA. While the cai gene cluster was weakly correlated with plasma TMAO (rho=0.17, =0.0007), elastic net models of TMAO were not improved by abundances of bacterial genes known to contribute to TMAO synthesis. A global analysis of all taxonomic groups, genes, and gene families found no meaningful predictors of TMAO. We postulated that abundances of known genes related to TMAO production do not predict bacterial metabolism, and we measured choline- and carnitine-trimethylamine lyase activity during fecal culture. Trimethylamine lyase genes were only weakly correlated with the activity of the enzymes they encode. Conclusions Fecal microbiome composition does not predict systemic TMAO because, in this case, gene copy number does not predict bacterial metabolic activity. Registration URL: https://www.clinicaltrials.gov; Unique identifier: NCT01427855.

摘要

背景

三甲胺氧化物(TMAO)是一种小分子,来源于肠道微生物对饮食营养素的代谢,与心血管疾病有关。食用红肉后,血浆 TMAO 增加。这种代谢变化部分是由于能够利用红肉中丰富营养物质的肠道微生物的扩张。

方法和结果

我们使用一项随机交叉研究的数据来估计从粪便微生物组成中估算 TMAO 的程度。健康参与者接受了 3 种不同蛋白质来源(红肉、白肉和非肉类)的饮食,在每种饮食暴露 4 周后收集粪便、血浆和尿液样本。测定血浆和尿液中的 TMAO,同时对粪便 DNA 进行 shotgun 宏基因组测序。虽然 cai 基因簇与血浆 TMAO 呈弱相关(rho=0.17,=0.0007),但已知有助于 TMAO 合成的细菌基因丰度并不能改善 TMAO 的弹性网络模型。对所有分类群、基因和基因家族的全局分析未发现 TMAO 的有意义预测因子。我们推测,已知与 TMAO 产生相关的基因丰度不能预测细菌代谢,并且我们在粪便培养期间测量了胆碱和肉碱三甲胺裂解酶的活性。三甲胺裂解酶基因与它们编码的酶的活性仅呈弱相关。

结论

粪便微生物组组成不能预测系统性 TMAO,因为在这种情况下,基因拷贝数不能预测细菌的代谢活性。注册网址:https://www.clinicaltrials.gov;唯一标识符:NCT01427855。

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