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Modeling Longitudinal Metabonomics and Microbiota Interactions in C57BL/6 Mice Fed a High Fat Diet

机译:喂养高脂饮食的C57BL / 6小鼠的纵向代谢组学和微生物群相互作用的建模

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Longitudinal studies aim typically at following populations of subjects over time and are important to understand the global evolution of biological processes. When it comes to longitudinal omics data, it will often depend on the overall objective of the study, and constraints imposed by the data, to define the appropriate modeling tools. Here, we report the use of multilevel simultaneous component analysis (MSCA), orthogonal projection on latent structures (OPLS), and regularized canonical correlation analysis (rCCA) to study associations between specific longitudinal urine metabonomics data and microbiome data in a diet-induced obesity model using C57BL/6 mice. H-1 NMR urine metabolic profiling was performed on samples collected weekly over a period of 13 weeks, and stool microbial composition was assessed using 16S rRNA gene sequencing at three specific time periods (baseline, first week response, end of study). MSCA and OPLS allowed us to explore longitudinal urine metabonomics data in relation to the dietary groups, as well as dietary effects on body weight. In addition, we report a data integration strategy based on regularized CCA and correlation analyses of urine metabonomics data and 16S rRNA gene sequencing data to investigate the functional relationships between metabolites and gut microbial composition. Thanks to this workflow enabling the breakdown of this data set complexity, the most relevant patterns could be extracted to further explore physiological processes at an anthropometric, cellular, and molecular level.
机译:纵向研究通常针对随时间推移的受试者群体,对于理解生物过程的全球演变非常重要。对于纵向组学数据,通常将取决于研究的总体目标以及数据所施加的约束条件,以定义适当的建模工具。在这里,我们报告使用多级同时成分分析(MSCA),在潜在结构上的正交投影(OPLS)和正则规范相关分析(rCCA)来研究饮食引起的肥胖症中特定纵向尿液代谢组学数据与微生物组数据之间的关联使用C57BL / 6小鼠的模型。对在13周内每周收集的样品进行H-1 NMR尿液代谢谱分析,并在三个特定时间段(基线,第一周反应,研究结束)使用16S rRNA基因测序评估粪便微生物组成。 MSCA和OPLS使我们能够探索与饮食组有关的纵向尿液代谢组学数据,以及饮食对体重的影响。此外,我们报告了基于规范化CCA的数据整合策略以及尿液代谢组学数据和16S rRNA基因测序数据的相关分析,以研究代谢物与肠道微生物组成之间的功能关系。由于此工作流程能够分解此数据集的复杂性,因此可以提取最相关的模式,以进一步在人体测量,细胞和分子水平上探索生理过程。

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