School of Pharmacy, Shanghai Jiao Tong University, Shanghai 200240, China; Center for Instrumental Analysis, Shanghai Jiao Tong University, Shanghai 200240, China.
School of Chemistry and Chemical Engineering, Shanghai Jiao Tong University, Shanghai 200240, China.
Anal Chim Acta. 2017 Dec 1;995:21-33. doi: 10.1016/j.aca.2017.09.042. Epub 2017 Oct 19.
In this paper, an optimized method based on gas chromatography/time-of-flight mass spectrometry (GC-TOFMS) platform has been developed for the analysis of gut microbial-host related co-metabolites in fecal samples. The optimization was performed with proportion of chloroform (C), methanol (M) and water (W) for the extraction of specific metabolic pathways of interest. Loading Bi-plots from the PLS regression model revealed that high concentration of chloroform emphasized the extraction of short chain fatty acids and TCA intermediates, while the higher concentration of methanol emphasized indole and phenyl derivatives. Low level of organic solution emphasized some TCA intermediates but not for indole and phenyl species. The highest sum of the peak area and the distribution of metabolites corresponded to the extraction of methanol/chloroform/water of 225:75:300 (v/v/v), which was then selected for method validation and utilized in our application. Excellent linearity was obtained with 62 reference standards representing different classes of gut microbial-host related co-metabolites, with correlation coefficients (r) higher than 0.99. Limit of detections (LODs) and limit of qualifications (LOQs) for these standards were below 0.9 nmol and 1.6 nmol, respectively. The reproducibility and repeatability of the majority of tested metabolites in fecal samples were observed with RSDs lower than 15%. Chinese rhubarb-treated rats had elevated indole and phenyl species, and decreased levels of polyamine such as putrescine, and several amino acids. Our optimized method has revealed host-microbe relationships of potential importance for intestinal microbial metabolite receptors such as pregnane X receptor (PXR) and aryl hydrocarbon receptor (AHR) activity, and for enzymes such as ornithine decarboxylase (ODC).
本文建立了一种基于气相色谱/飞行时间质谱(GC-TOFMS)平台的优化方法,用于分析粪便样本中肠道微生物-宿主相关共代谢物。通过优化提取特定代谢途径感兴趣的比例的氯仿(C)、甲醇(M)和水(W)来进行优化。PLS 回归模型的加载双平面图显示,高浓度的氯仿强调了短链脂肪酸和 TCA 中间体的提取,而高浓度的甲醇则强调了吲哚和苯衍生物。低水平的有机溶剂强调了一些 TCA 中间体,但不包括吲哚和苯类物质。峰面积总和最高且代谢物分布对应的是甲醇/氯仿/水为 225:75:300(v/v/v)的提取,然后选择该方法进行验证并应用于我们的研究中。以 62 种不同类别的肠道微生物-宿主相关共代谢物的参考标准品进行测定,得到了极好的线性关系,相关系数(r)均高于 0.99。这些标准品的检测限(LOD)和定量限(LOQ)均低于 0.9 nmol 和 1.6 nmol。在粪便样本中,大多数测试代谢物的重现性和重复性的 RSD 均低于 15%。大黄素处理的大鼠粪便中吲哚和苯类物质水平升高,腐胺和几种氨基酸等多胺水平降低。我们的优化方法揭示了肠道微生物代谢物受体(如孕烷 X 受体(PXR)和芳香烃受体(AHR)活性)和酶(如鸟氨酸脱羧酶(ODC))的宿主-微生物关系的重要性。