Beukes Derylize, du Preez Ilse, Loots Du Toit
Human Metabolomics, North-West University, Private Bag X6001, Box 269, Potchefstroom, South Africa.
Methods Mol Biol. 2019;1859:121-131. doi: 10.1007/978-1-4939-8757-3_6.
Over the past 10 years, the number of metabolomics based publications in the available scientific literature has exponentially grown, a large portion of which describing new biomarkers better elucidating microbial disease mechanisms and improved diagnostics and treatment thereof. Here, we describe a metabolomics method for extracting the total metabolome (all compounds present in the microbial cell irrespective of the compound class), for analysis in a single analytical run using only one analytical instrument. This method includes disruption of robust microbial cell walls, and the precipitation of proteins and cell debris using a combination of mechanical methods and solvents. These extracts are subsequently derivatized, in order to improve the volatility of polar compounds for efficient gas chromatography-mass spectrometry (GC-MS) analysis. This methodology can be applied to all microbes, including those with robust cell walls, such as M. tuberculosis. To date, the biomarkers identified using this approach have led to improved tuberculosis (TB) diagnostics, improved TB treatment approaches, and better understanding of host-microbe interactions and associated mycobacterial genomics.
在过去10年里,现有科学文献中基于代谢组学的出版物数量呈指数级增长,其中很大一部分描述了新的生物标志物,能更好地阐明微生物致病机制以及改进其诊断和治疗方法。在此,我们描述了一种代谢组学方法,用于提取总代谢组(微生物细胞中存在的所有化合物,无论其化合物类别如何),以便仅使用一台分析仪器在一次分析运行中进行分析。该方法包括破坏坚固的微生物细胞壁,以及使用机械方法和溶剂的组合沉淀蛋白质和细胞碎片。随后对这些提取物进行衍生化处理,以提高极性化合物的挥发性,便于进行高效气相色谱 - 质谱(GC - MS)分析。这种方法可应用于所有微生物,包括那些具有坚固细胞壁的微生物,如结核分枝杆菌。迄今为止,使用这种方法鉴定出的生物标志物已带来了改进的结核病(TB)诊断、改进的TB治疗方法,以及对宿主 - 微生物相互作用和相关分枝杆菌基因组学的更好理解。