4.6 Article

Artemisia brevifolia Wall. Ex DC Enhances Cefixime Susceptibility by Reforming Antimicrobial Resistance

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ANTIBIOTICS-BASEL
卷 12, 期 10, 页码 -

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MDPI
DOI: 10.3390/antibiotics12101553

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RP-HPLC; cefixime; antibacterial susceptibility testing; Artemisia brevifolia; traditional medicine; plant extracts; antimicrobial activity; drug resistance; phytotherapy; bioactive compounds

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This study found that the combination of A. brevifolia and cefixime has the potential to inhibit antimicrobial resistance, effectively inhibiting the growth of resistant strains.
(1) Background: A possible solution to antimicrobial resistance (AMR) is synergism with plants like Artemisia brevifolia Wall. ex DC. (2) Methods: Phytochemical quantification of extracts (n-hexane (NH), ethyl acetate (EA), methanol (M), and aqueous (Aq)) was performed using RP-HPLC and chromogenic assays. Extracts were screened against resistant clinical isolates via disc diffusion, broth dilution, the checkerboard method, time-kill, and protein quantification assays. (3) Results: M extract had the maximum phenolic (15.98 +/- 0.1 mu g GAE/mgE) and flavonoid contents (9.93 +/- 0.5 mu g QE/mgE). RP-HPLC displayed the maximum polyphenols in the M extract. Secondary metabolite determination showed M extract to have the highest glycosides, alkaloids, and tannins. Preliminary resistance profiling indicated that selected isolates were resistant to cefixime (MIC 20-40 mu g/mL). Extracts showed moderate antibacterial activity (MIC 60-100 mu g/mL). The checkerboard method revealed a total synergy between EA extract and cefixime with 10-fold reductions in cefixime dose against resistant P. aeruginosa and MRSA. Moreover, A. brevifolia extracts potentiated the antibacterial effect of cefixime after 6 and 9 h. The synergistic combination was non- to slightly hemolytic and could inhibit bacterial protein in addition to cefixime disrupting the cell wall, thus making it difficult for bacteria to survive. (4) Conclusion: A. brevifolia in combination with cefixime has the potential to inhibit AMR.

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