Skaggs School of Pharmacy and Pharmaceutical Sciences, University of California at San Diego, San Diego, California 92093, United States.
Anal Chem. 2012 Nov 6;84(21):9259-67. doi: 10.1021/ac302039u. Epub 2012 Oct 10.
The communities constituting our microbiotas are emerging as mediators of the health-disease continuum. However, deciphering the functional impact of microbial communities on host pathophysiology represents a formidable challenge, due to the heterogeneous distribution of chemical and microbial species within the gastrointestinal (GI) tract. Herein, we apply imaging mass spectrometry (IMS) to localize metabolites from the interaction between the host and colonizing microbiota. This approach complements other molecular imaging methodologies in that analytes need not be known a priori, offering the possibility of untargeted analysis. Localized molecules within the GI tract were then identified in situ by surface sampling with nanodesorption electrospray ionization Fourier transform ion cyclotron resonance-mass spectrometry (nanoDESI FTICR-MS). Products from diverse structural classes were identified including cholesterol-derived lipids, glycans, and polar metabolites. Specific chemical transformations performed by the microbiota were validated with bacteria in culture. This study illustrates how untargeted spatial characterization of metabolites can be applied to the molecular dissection of complex biology in situ.
构成我们微生物组的群落正在成为健康-疾病连续体的介导者。然而,由于胃肠道 (GI) 道内化学物质和微生物种类的不均匀分布,破译微生物群落对宿主病理生理学的功能影响是一项艰巨的挑战。在这里,我们应用成像质谱 (IMS) 来定位宿主与定植微生物群相互作用产生的代谢物。这种方法补充了其他分子成像方法,因为分析物不需要事先知道,从而提供了非靶向分析的可能性。然后通过纳米解吸电喷雾电离傅里叶变换离子回旋共振-质谱 (nanoDESI FTICR-MS) 对胃肠道内的局部分子进行表面采样原位鉴定。鉴定出了包括胆固醇衍生脂质、聚糖和极性代谢物在内的多种结构类别的产物。通过培养中的细菌验证了微生物群进行的特定化学转化。本研究说明了如何将代谢物的非靶向空间特征应用于原位复杂生物学的分子剖析。