FB2026_03 , released September 17, 2026
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Citation
Macêdo, N.S., de Sousa Silveira, Z., Cordeiro, P.P.M., Coutinho, H.D.M., Júnior, J.P.S., Júnior, L.J.Q., Siyadatpanah, A., Kim, B., da Cunha, F.A.B., da Silva, M.V. (2022). Inhibition of Staphylococcus aureus Efflux Pump by O-Eugenol and Its Toxicity in Drosophila melanogaster Animal Model.  Biomed Res. Int. 2022(): 1440996.
FlyBase ID
FBrf0254133
Publication Type
Research paper
Abstract
Efflux pumps are transmembrane proteins that expel drugs out of a bacterial cell contributing to microorganism drug resistance. Several studies addressing the use of natural products with medicinal properties have intensified given the above. Thus, the aim of the present study was to investigate the antibacterial activity and the O-eugenol potential in Staphylococcus aureus resistance reversal by efflux pump inhibition, as well as to evaluate its toxicity in the Drosophila melanogaster arthropod model. The broth microdilution method was used to determine the minimum inhibitory concentration (MIC) and the O-eugenol efflux pump inhibition. For the D. melanogaster toxicity assays, mortality and locomotor system damage were performed using the fumigation method. O-eugenol presented a MIC of 1024 μg/mL against S. aureus. The association of this compound with the antibiotic tetracycline demonstrated a synergistic effect (p < 0.0001), this also being observed when the antibiotic was associated with ethidium bromide (p < 0.0001); thus, these results may be attributable to an efflux pump inhibition. The D. melanogaster mortality and geotaxis assays revealed the compound is toxic, with an EC50 of 18 μg/mL within 48 hours of exposure. While we can conclude that the tested product has an efflux pump inhibitory effect, further studies are needed to elucidate its mechanisms of action, in addition to assays using other strains to verify whether the substance has the same inhibitory effect.
PubMed ID
PubMed Central ID
PMC9325621 (PMC) (EuropePMC)
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Secondary IDs
    Language of Publication
    English
    Additional Languages of Abstract
    Parent Publication
    Publication Type
    Journal
    Abbreviation
    Biomed Res. Int.
    Title
    BioMed research international
    ISBN/ISSN
    2314-6141 2314-6133
    Data From Reference
    Chemicals (5)
    Human Disease Models (1)