Athamneh A I M, Alajlouni R A, Wallace R S, Seleem M N, Senger R S
Department of Biological Systems Engineering, Virginia Tech, Blacksburg, Virginia, USA.
Antimicrob Agents Chemother. 2014;58(3):1302-14. doi: 10.1128/AAC.02098-13. Epub 2013 Dec 2.
Identifying the mechanism of action of new potential antibiotics is a necessary but time-consuming and costly process. Phenotypic profiling has been utilized effectively to facilitate the discovery of the mechanism of action and molecular targets of uncharacterized drugs. In this research, Raman spectroscopy was used to profile the phenotypic response of Escherichia coli to applied antibiotics. The use of Raman spectroscopy is advantageous because it is noninvasive, label free, and prone to automation, and its results can be obtained in real time. In this research, E. coli cultures were subjected to three times the MICs of 15 different antibiotics (representing five functional antibiotic classes) with known mechanisms of action for 30 min before being analyzed by Raman spectroscopy (using a 532-nm excitation wavelength). The resulting Raman spectra contained sufficient biochemical information to distinguish between profiles induced by individual antibiotics belonging to the same class. The collected spectral data were used to build a discriminant analysis model that identified the effects of unknown antibiotic compounds on the phenotype of E. coli cultures. Chemometric analysis showed the ability of Raman spectroscopy to predict the functional class of an unknown antibiotic and to identify individual antibiotics that elicit similar phenotypic responses. Results of this research demonstrate the power of Raman spectroscopy as a cellular phenotypic profiling methodology and its potential impact on antibiotic drug development research.
确定新型潜在抗生素的作用机制是一个必要但耗时且成本高昂的过程。表型分析已被有效利用,以促进对未表征药物的作用机制和分子靶点的发现。在本研究中,拉曼光谱用于分析大肠杆菌对应用抗生素的表型反应。使用拉曼光谱具有优势,因为它是非侵入性的、无需标记且易于自动化,并且其结果可以实时获得。在本研究中,在通过拉曼光谱(使用532nm激发波长)分析之前,将大肠杆菌培养物用15种不同抗生素(代表五种功能抗生素类别)的三倍最低抑菌浓度处理30分钟,这些抗生素具有已知的作用机制。所得的拉曼光谱包含足够的生化信息,以区分同一类别的个别抗生素所诱导的谱型。收集的光谱数据用于建立判别分析模型,该模型可识别未知抗生素化合物对大肠杆菌培养物表型的影响。化学计量分析表明,拉曼光谱能够预测未知抗生素的功能类别,并识别引起相似表型反应的个别抗生素。本研究结果证明了拉曼光谱作为一种细胞表型分析方法的强大功能及其对抗生素药物开发研究的潜在影响。