4.7 Article

Metabolomics Comparison of Drug-Resistant and Drug-Susceptible Pseudomonas aeruginosa Strain (Intra- and Extracellular Analysis)

期刊

出版社

MDPI
DOI: 10.3390/ijms221910820

关键词

Pseudomonas aeruginosa; metabolomics; antibiotic resistance; NMR spectroscopy

资金

  1. Statutory project of WUST
  2. Faculty of Chemistry
  3. Department of Biochemistry, Molecular Biology and Biotechnology (2021)

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The research compared the metabolisms of two P. aeruginosa strains, showing that the differences between drug-resistant and drug-susceptible strains mainly lie in the turnover of amino acids. This study provides valuable information to complement research on drug resistance in P. aeruginosa.
Pseudomonas aeruginosa is a common human pathogen belonging to the ESKAPE group. The multidrug resistance of bacteria is a considerable problem in treating patients and may lead to increased morbidity and mortality rate. The natural resistance in these organisms is caused by the production of specific enzymes and biofilm formation, while acquired resistance is multifactorial. Precise recognition of potential antibiotic resistance on different molecular levels is essential. Metabolomics tools may aid in the observation of the flux of low molecular weight compounds in biochemical pathways yielding additional information about drug-resistant bacteria. In this study, the metabolisms of two P. aeruginosa strains were compared-antibiotic susceptible vs. resistant. Analysis was performed on both intra- and extracellular metabolites. The H-1 NMR method was used together with multivariate and univariate data analysis, additionally analysis of the metabolic pathways with the FELLA package was performed. The results revealed the differences in P. aeruginosa metabolism of drug-resistant and drug-susceptible strains and provided direct molecular information about P. aeruginosa response for different types of antibiotics. The most significant differences were found in the turnover of amino acids. This study can be a valuable source of information to complement research on drug resistance in P. aeruginosa.

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