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Artonin I inhibits multidrug resistance in S taphylococcus aureus and potentiates the action of inactive antibiotics in vitro
Author(s) -
Farooq S.,
Wahab A.T.,
Fozing C.D.A.,
Rahman A.U.,
Choudhary M. Iqbal
Publication year - 2014
Publication title -
journal of applied microbiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.889
H-Index - 156
eISSN - 1365-2672
pISSN - 1364-5072
DOI - 10.1111/jam.12595
Subject(s) - efflux , ethidium bromide , staphylococcus aureus , antibiotics , multiple drug resistance , microbiology and biotechnology , antimicrobial , minimum inhibitory concentration , mechanism of action , chemistry , biology , pharmacology , in vitro , biochemistry , bacteria , dna , genetics
Aims The emergence of multidrug‐resistant ( MDR ) S taphylococcus aureus is a challenge for the treatment of infections. We report here the antimicrobial activity of artonin I against MDR S taph. aureus, its mechanism of reversal of resistance and synergistic effects by combinational therapy. Methods and Results Artonin I, a flavonoid obtained from M orus mesozygia Stapf., inhibited the bacterial efflux pump and induced depolarization of the cell membrane. To study the dose‐dependent production of reactive oxygen species in MDR cells by artonin I, lucigenin chemiluminescence assay was employed. Reversal of multidrug resistance by artonin I, in combination with antibiotics, was measured by a fractional inhibitory concentration index assay. The effect of artonin I on ultrastructural features was studied by microscopy. Artonin I increased the penetration of ethidium bromide by blocking the efflux mechanism. It also helped anionic probe Di BAC 4 (3) to bind with the lipid‐rich cellular components by causing depolarization of the cell membrane. Artonin I reversed multidrug resistance and increased the susceptibility of existing antibiotics by lowering their minimum inhibitory concentrations ( MIC s). Conclusions Artonin I was identified both as a new antibacterial agent and a helper molecule to potentiate the action of otherwise inactive antibiotics. Significance and Impact of the Study Artonin I can be developed as potential antimicrobial and resistance reversal agent.