Characterization and Potentiating Effects of the Ethanolic Extracts of the Red Seaweed Gracillaria sp. on the Activity of Carbenicillin against Vibrios .
Wen-Jung LuYa-Chin TsuiChun-Ju ChangPang-Hung HsuMei-Ying HuangMargaret LaiYu-Wei LianChia-Lin ChenHong-Ting Victor LinPublished in: ACS omega (2022)
β-lactam-resistant Vibrio strains are a significant clinical problem, and β-lactamase inhibitors are generally coadministered with β-lactam drugs to control drug-resistant bacteria. Seaweed is a rich source of natural bioactive compounds; however, their potential as β-lactamase inhibitors against bacterial pathogens remains unknown. Herein, we evaluated the potential β-lactamase inhibitory effect of the ethanolic extracts of the red seaweed Gracilaria sp. (GE) against four Vibrio strains. The minimum inhibitory concentration, half-maximal inhibitory concentration, checkerboard assay results, and time-kill study results indicate that GE has limited antibacterial activity but can potentiate the activity of the β-lactam antibiotic carbenicillin against Vibrio parahemolyticus and V . cholerae . We overexpressed and purified recombinant metallo-β-lactamase, VarG, from V . cholerae for in vitro studies and observed that adding GE reduced the carbenicillin and nitrocefin degradation by VarG by 20% and 60%, respectively. Angiotensin I-converting enzyme inhibition studies demonstrated that GE did not inhibit VarG via metal chelation. Toxicity assays indicated that GE exhibited mild toxicity against human cells. Through gas chromatography and mass spectrometry, we showed that GE comprises alkaloids, phenolic compounds, terpenoids, terpenes, and halogenated aromatic compounds. This study revealed that extracts of the red seaweed Gracillaria sp. can potentially inhibit β-lactamase activity.
Keyphrases
- gram negative
- multidrug resistant
- escherichia coli
- drug resistant
- mass spectrometry
- klebsiella pneumoniae
- gas chromatography
- acinetobacter baumannii
- biofilm formation
- liquid chromatography
- high throughput
- tandem mass spectrometry
- high resolution mass spectrometry
- high resolution
- angiotensin ii
- solid phase extraction