Horká Marie, Karásek Pavel, Roth Michal, Růžička Filip
Czech Academy of Sciences, Institute of Analytical Chemistry, v. v. i., Veveří 97, 602 00, Brno, Czech Republic.
The Department of Microbiology, Faculty of Medicine, Masaryk University, Kamenice 53/5, 625 00, Brno, Czech Republic.
Anal Bioanal Chem. 2018 Jan;410(1):167-175. doi: 10.1007/s00216-017-0706-y. Epub 2017 Oct 23.
The transient isotachophoretic stacking and sweeping was used for the on-line large-volume sample pre-concentration of bacteria, Escherichia coli and Staphylococcus aureus cells (methicillin-susceptible or methicillin-resistant), in the initial stage of micellar electrokinetic chromatography using a non-ionogenic surfactant or of capillary electrophoresis, respectively. These procedures were employed in single-piece fused silica capillary etched with supercritical water with two different internal diameter segments featuring different inner surface roughness. Large volumes (maximum 2.8 μL) of the high conductivity sample matrices, physiological saline solution, urine or blood (with purification step), spiked with examined cells were injected into the wider end of a capillary with an inlet inner diameter 195 μm. This novel on-line combination of preconcentration strategies for cells produced an up to 680-fold increase in sensitivity for E. coli or S. aureus cells. The average calculated resolutions, R, for five selected methicillin-susceptible or methicillin-resistant strains were found to be 6.3 for the agar-cultivated and 14.9 for the blood-incubated cells. A low number of bacteria similar to those in clinical samples were also tested. The modified surface roughness step helped to significantly narrow the cell zones and to increase resolution. The migration velocities of E. coli agar-cultivated and blood-incubated cells were approximately the same as those of S. aureus, probably due to the minimal differences in their surface properties. This procedure, on-line pre-concentration and separation of bacteria, is rapid and provides good reproducibility and repeatability.
在胶束电动色谱的初始阶段,分别使用非离子表面活性剂或毛细管电泳,采用瞬态等速电泳堆积和扫集技术,对细菌、大肠杆菌和金黄色葡萄球菌细胞(甲氧西林敏感或耐药)进行在线大体积样品预浓缩。这些操作在经超临界水蚀刻的单件熔融石英毛细管中进行,该毛细管具有两个内径不同且内表面粗糙度不同的段。将大量(最大2.8 μL)高电导率样品基质(生理盐水溶液、尿液或经过净化步骤的血液),加入检测细胞后,注入内径为195 μm的毛细管较宽一端。这种用于细胞的预浓缩策略的新型在线组合,使大肠杆菌或金黄色葡萄球菌细胞的灵敏度提高了680倍。对于五种选定的甲氧西林敏感或耐药菌株,计算得到的平均分辨率R,琼脂培养的细胞为6.3,血液培养的细胞为14.9。还测试了与临床样本中数量相似的少量细菌。表面粗糙度的改变步骤有助于显著缩小细胞区带并提高分辨率。大肠杆菌琼脂培养和血液培养细胞的迁移速度与金黄色葡萄球菌的迁移速度大致相同,这可能是由于它们表面性质的差异极小。这种细菌在线预浓缩和分离程序快速,具有良好的重现性和重复性。