Isoelectric Focusing Fractionation Method for Signal Enhancement in Detection of Inactivated Biological Agents Using Matrix-Assisted Laser Desorption/Ionization Mass Spectrometry
Language English Country Germany Media print-electronic
Document type Journal Article
Grant support
VI20172020069
Ministry of the Interior of the Czech Republic
NU22-05-00110
Ministry of Health of the Czech Republic
RVO:68081715
Czech Academy of Sciences of the Czech Republic
PubMed
39748447
PubMed Central
PMC11865691
DOI
10.1002/elps.202400052
Knihovny.cz E-resources
- Keywords
- biological agents, chip, fractionation, isoelectric focusing, pathogenic bacteria, whole cell separation,
- MeSH
- Bacteria * chemistry isolation & purification drug effects MeSH
- Isoelectric Focusing methods MeSH
- Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization * methods MeSH
- Publication type
- Journal Article MeSH
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 H2O2 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 × 105 colony forming units per mL for inactivated B. anthracis.
Institute of Analytical Chemistry of the Czech Academy of Sciences Brno Czech Republic
National Institute for Nuclear Chemical and Biological Protection Kamenna Czech Republic
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