Evaluation of Malondialdehyde Levels, Oxidative Stress and Host-Bacteria Interactions: Escherichia coli and Salmonella Derby.
Vardan TsaturyanArmen PoghosyanMichał ToczyłowskiAstghik Z PepoyanPublished in: Cells (2022)
Either extracts, cell-free suspensions or bacterial suspensions are used to study bacterial lipid peroxidation processes. Along with gas chromatography-mass spectrometry, liquid chromatography-mass spectrometry, and several other strategies, the thiobarbituric acid test is used for the determination of malondialdehyde (MDA) as the basis for the commercial test kits and the colorimetric detection of lipid peroxidation. The aim of the current study was to evaluate lipid peroxidation processes levels in the suspensions, extracts and culture supernatants of Escherichia coli and Salmonella Derby strains. The dependence of the formation of thiobarbituric acid-reactive substances levels in the cell extracts, the suspensions and cell-free supernatants on bacterial species, and their concentration and growth phase were revealed. The effect of bacterial concentrations on MDA formation was also found to be more pronounced in bacterial suspensions than in extracts, probably due to the dynamics of MDA release into the intercellular space. This study highlights the possible importance of MDA determination in both cell-free suspensions and extracts, as well as in bacterial suspensions to elucidate the role of lipid peroxidation processes in bacterial physiology, bacteria-host interactions, as well as in host physiology.
Keyphrases
- cell free
- escherichia coli
- mass spectrometry
- oxidative stress
- liquid chromatography
- breast cancer cells
- fatty acid
- gas chromatography mass spectrometry
- gold nanoparticles
- single cell
- circulating tumor
- high resolution
- dna damage
- cell proliferation
- ms ms
- hydrogen peroxide
- bone marrow
- cell death
- klebsiella pneumoniae
- cell cycle arrest
- pseudomonas aeruginosa
- sensitive detection
- high resolution mass spectrometry
- multidrug resistant
- heat shock protein
- living cells
- capillary electrophoresis
- induced apoptosis