Sterrett John D, Quinn Kevin D, Doenges Katrina A, Nusbacher Nichole M, Levens Cassandra L, Armstrong Mike L, Reisdorph Richard M, Smith Harry, Saba Laura M, Kuhn Kristine A, Lozupone Catherine A, Reisdorph Nichole A
Department of Integrative Physiology, University of Colorado, Boulder, Colorado, USA.
Interdisciplinary Quantitative Biology, University of Colorado, Boulder, Colorado, USA.
Microbiol Spectr. 2025 Feb 4;13(2):e0179924. doi: 10.1128/spectrum.01799-24. Epub 2025 Jan 10.
Studies have suggested that phytochemicals in green tea have systemic anti-inflammatory and neuroprotective effects. However, the mechanisms behind these effects are poorly understood, possibly due to the differential metabolism of phytochemicals resulting from variations in gut microbiome composition. To unravel this complex relationship, our team utilized a novel combined microbiome analysis and metabolomics approach applied to low complexity microbiome (LCM) and human colonized (HU) gnotobiotic mice treated with an acute dose of powdered matcha green tea. A total of 20 LCM mice received 10 distinct human fecal slurries for an = 2 mice per human gut microbiome; 9 LCM mice remained un-colonized with human slurries throughout the experiment. We performed untargeted metabolomics on green tea and plasma to identify green tea compounds that were found in the plasma of LCM and HU mice that had consumed green tea. 16S ribosomal RNA gene sequencing was performed on feces of all mice at study end to assess microbiome composition. We found multiple green tea compounds in plasma associated with microbiome presence and diversity (including acetylagmatine, lactiflorin, and aspartic acid negatively associated with diversity). Additionally, we detected strong associations between bioactive green tea compounds in plasma and specific gut bacteria, including associations between spiramycin and and between wildforlide and . Notably, some of the physiologically relevant green tea compounds are likely derived from plant-associated microbes, highlighting the importance of considering foods and food products as meta-organisms. Overall, we describe a novel workflow for discovering relationships between individual food compounds and the composition of the gut microbiome.
Foods contain thousands of unique and biologically important compounds beyond the macro- and micro-nutrients listed on nutrition facts labels. In mammals, many of these compounds are metabolized or co-metabolized by the community of microbes in the colon. These microbes may impact the thousands of biologically important compounds we consume; therefore, understanding microbial metabolism of food compounds will be important for understanding how foods impact health. We used metabolomics to track green tea compounds in plasma of mice with and without complex microbiomes. From this, we can start to recognize certain groups of green tea-derived compounds that are impacted by mammalian microbiomes. This research presents a novel technique for understanding microbial metabolism of food-derived compounds in the gut, which can be applied to other foods.
研究表明,绿茶中的植物化学物质具有全身抗炎和神经保护作用。然而,这些作用背后的机制尚不清楚,这可能是由于肠道微生物群组成的变化导致植物化学物质的代谢差异所致。为了阐明这种复杂的关系,我们的团队采用了一种新颖的微生物组分析与代谢组学相结合的方法,应用于用急性剂量的抹茶绿茶粉末处理的低复杂性微生物组(LCM)和人定殖(HU)无菌小鼠。总共20只LCM小鼠接受了10种不同的人类粪便悬液,每种人类肠道微生物组有2只小鼠;9只LCM小鼠在整个实验过程中未用人悬液定殖。我们对绿茶和血浆进行了非靶向代谢组学分析,以鉴定在饮用绿茶的LCM和HU小鼠血浆中发现的绿茶化合物。在研究结束时,对所有小鼠的粪便进行16S核糖体RNA基因测序,以评估微生物组组成。我们在血浆中发现了多种与微生物组的存在和多样性相关的绿茶化合物(包括与多样性呈负相关的胍基丁胺、蒙花苷和天冬氨酸)。此外,我们检测到血浆中生物活性绿茶化合物与特定肠道细菌之间有很强的关联,包括螺旋霉素与[具体细菌名称1]之间以及野黄芩苷与[具体细菌名称2]之间的关联。值得注意的是,一些生理相关的绿茶化合物可能来源于与植物相关的微生物,这突出了将食物和食品视为元生物体的重要性。总体而言,我们描述了一种发现单个食物化合物与肠道微生物组组成之间关系的新颖工作流程。
食物中含有数千种独特且具有生物学重要性的化合物,超出了营养成分标签上列出的宏量和微量营养素。在哺乳动物中,许多这些化合物由结肠中的微生物群落进行代谢或共代谢。这些微生物可能会影响我们摄入的数千种具有生物学重要性的化合物;因此,了解食物化合物的微生物代谢对于理解食物如何影响健康至关重要。我们使用代谢组学来追踪有无复杂微生物组的小鼠血浆中的绿茶化合物。由此,我们可以开始识别某些受哺乳动物微生物组影响的绿茶衍生化合物组。这项研究提出了一种理解肠道中食物衍生化合物微生物代谢的新技术,该技术可应用于其他食物。