Kumar Himanshu, Lund Riikka, Laiho Asta, Lundelin Krista, Ley Ruth E, Isolauri Erika, Salminen Seppo
Functional Food Forum, University of Turku, Turku, Finland
Finnish Microarray and Sequencing Centre, Turku Centre for Biotechnology, University of Turku and Åbo Akademi University, Turku, Finland.
mBio. 2014 Dec 16;5(6):e02113-14. doi: 10.1128/mBio.02113-14.
The core human gut microbiota contributes to the developmental origin of diseases by modifying metabolic pathways. To evaluate the predominant microbiota as an epigenetic modifier, we classified 8 pregnant women into two groups based on their dominant microbiota, i.e., Bacteroidetes, Firmicutes, and Proteobacteria. Deep sequencing of DNA methylomes revealed a clear association between bacterial predominance and epigenetic profiles. The genes with differentially methylated promoters in the group in which Firmicutes was dominant were linked to risk of disease, predominantly to cardiovascular disease and specifically to lipid metabolism, obesity, and the inflammatory response. This is one of the first studies that highlights the association of the predominant bacterial phyla in the gut with methylation patterns. Further longitudinal and in-depth studies targeting individual microbial species or metabolites are recommended to give us a deeper insight into the molecular mechanism of such epigenetic modifications.
Epigenetics encompasses genomic modifications that are due to environmental factors and do not affect the nucleotide sequence. The gut microbiota has an important role in human metabolism and could be a significant environmental factor affecting our epigenome. To investigate the association of gut microbiota with epigenetic changes, we assessed pregnant women and selected the participants based on their predominant gut microbiota for a study on their postpartum methylation profile. Intriguingly, we found that blood DNA methylation patterns were associated with gut microbiota profiles. The gut microbiota profiles, with either Firmicutes or Bacteroidetes as a dominant group, correlated with differential methylation status of gene promoters functionally associated with cardiovascular diseases. Furthermore, differential methylation of gene promoters linked to lipid metabolism and obesity was observed. For the first time, we report here a position of the predominant gut microbiota in epigenetic profiling, suggesting one potential mechanism in obesity with comorbidities, if proven in further in-depth studies.
核心人类肠道微生物群通过改变代谢途径促成疾病的发育起源。为了评估主要微生物群作为一种表观遗传修饰因子,我们根据8名孕妇的主要微生物群(即拟杆菌门、厚壁菌门和变形菌门)将她们分为两组。DNA甲基化组的深度测序揭示了细菌优势与表观遗传谱之间的明确关联。在厚壁菌门占主导的组中,启动子甲基化存在差异的基因与疾病风险相关,主要与心血管疾病相关,特别是与脂质代谢、肥胖和炎症反应相关。这是首批突出肠道中主要细菌门与甲基化模式之间关联的研究之一。建议针对个体微生物物种或代谢物进行进一步的纵向和深入研究,以便我们更深入地了解这种表观遗传修饰的分子机制。
表观遗传学包括由环境因素引起且不影响核苷酸序列的基因组修饰。肠道微生物群在人类代谢中具有重要作用,可能是影响我们表观基因组的一个重要环境因素。为了研究肠道微生物群与表观遗传变化的关联,我们评估了孕妇,并根据她们的主要肠道微生物群选择参与者,以研究她们产后的甲基化谱。有趣的是,我们发现血液DNA甲基化模式与肠道微生物群谱相关。以厚壁菌门或拟杆菌门为主导组的肠道微生物群谱与功能上与心血管疾病相关的基因启动子的甲基化差异状态相关。此外,还观察到与脂质代谢和肥胖相关的基因启动子的甲基化差异。我们首次在此报告主要肠道微生物群在表观遗传谱中的地位,这表明如果在进一步的深入研究中得到证实,这是肥胖合并症的一种潜在机制。