Duša Filip, Šalplachta Jiří, Horká Marie, Lunerová Kamila, Čermáková Veronika, Dřevínek Michal, Kubíček Oldřich
Institute of Analytical Chemistry of the Czech Academy of Sciences, Brno, Czech Republic.
National Institute for Nuclear, Chemical and Biological Protection, Kamenna, Czech Republic.
Electrophoresis. 2025 Feb;46(3-4):212-220. doi: 10.1002/elps.202400052. Epub 2025 Jan 2.
Timely identification of highly pathogenic bacteria is crucial for efficient mitigation of the connected harmful health effects. Matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI-TOF MS) of intact cells enables fast identification of the microorganisms based on their mass spectrometry protein fingerprint profiles. However, the MALDI-TOF MS examination must be preceded by a time-demanding cultivation of the native bacteria to isolate representative cell samples to obtain indicative fingerprints. Isoelectric focusing (IEF) is capable of separating bacterial cells according to their isoelectric point while effectively removing other non-focusing compounds from sample matrix. In this work, we present a divergent-flow IEF chip (DF-IEF chip) fractionation as an alternative way for sample clean-up and concentration of bacterial cells to prepare samples usable for following MALDI-TOF MS analysis without the need of time-demanding cultivation. By means of DF-IEF chip method, we processed four species of highly pathogenic bacteria (Bacillus anthracis, Brucella abortus, Burkholderia mallei, and Yersinia pestis) inactivated with HO vapors or by heat treatment at 62.5°C for 24 h. The DF-IEF chip method continually separated and concentrated the inactivated bacterial cells for subsequent detection using MALDI-TOF MS. The content of the inactivated bacteria in the DF-IEF chip fractions was evaluated with the MS analysis, where inactivated Y. pestis was found to be the most efficiently focusing species. Sensitivity analysis showed limits as low as 2 × 10 colony forming units per mL for inactivated B. anthracis.
及时识别高致病性细菌对于有效减轻相关有害健康影响至关重要。完整细胞的基质辅助激光解吸/电离飞行时间质谱(MALDI-TOF MS)能够根据微生物的质谱蛋白质指纹图谱快速识别它们。然而,在进行MALDI-TOF MS检测之前,必须对天然细菌进行耗时的培养,以分离代表性细胞样本,从而获得指示性指纹图谱。等电聚焦(IEF)能够根据细菌细胞的等电点对其进行分离,同时有效地从样品基质中去除其他非聚焦化合物。在这项工作中,我们提出了一种分流IEF芯片(DF-IEF芯片)分级分离方法,作为样品净化和浓缩细菌细胞的替代方法,以便制备可用于后续MALDI-TOF MS分析的样品,而无需耗时的培养。通过DF-IEF芯片方法,我们处理了四种用HO蒸汽或在62.5°C下热处理24小时灭活的高致病性细菌(炭疽芽孢杆菌、流产布鲁氏菌、鼻疽伯克霍尔德菌和鼠疫耶尔森菌)。DF-IEF芯片方法持续分离和浓缩灭活的细菌细胞,以便随后使用MALDI-TOF MS进行检测。通过质谱分析评估了DF-IEF芯片级分中灭活细菌的含量,其中发现灭活的鼠疫耶尔森菌是聚焦效率最高的物种。灵敏度分析表明,灭活的炭疽芽孢杆菌的检测限低至每毫升2×10个菌落形成单位。