Efflux inhibitory activity of flavonoids from Chromolaena odorata against selected methicillin-resistant Staphylococcus aureus (MRSA) isolates

被引:12
|
作者
Johari, Saiful Azmi [1 ]
Kiong, Ling Sui [2 ]
Mohtar, Mastura [1 ]
Isa, Mazurah Mohamed [1 ]
Man, Salbiah [2 ]
Mustafa, Shuhaimi [3 ]
Ali, Abdul Manaf [4 ]
机构
[1] Forest Res Inst Malaysia FRIM, Antimicrobial Lab, Bioact Programme, Nat Prod Div, Selangor, Malaysia
[2] Forest Res Inst Malaysia FRIM, Nat Prod Div, Phytochem Programme, Selangor, Malaysia
[3] Univ Putra Malaysia UPM, Fac Biotechnol & Biomol Sci, Selangor, Malaysia
[4] Univ Sultan Zainal Abidin UniSZA, Fac Agr & Biotechnol, Kuala Terengganu, Malaysia
来源
AFRICAN JOURNAL OF MICROBIOLOGY RESEARCH | 2012年 / 6卷 / 27期
关键词
Chromolaena odorata; methicillin-resistant Staphylococcus aureus (MRSA); multidrug-resistant (MDR); efflux pump inhibitor; minimum inhibitory concentration (MIC) assay; MULTIDRUG-RESISTANCE; GENES; PUMP; SUSCEPTIBILITY; LEVOFLOXACIN; NORFLOXACIN; MODULATORS; BERBERINE; PLANT;
D O I
10.5897/AJMR12.126
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Ten flavonoid compounds isolated from the methanolic extract of a tropical weed plant, Chromolaena odorata leaves were tested against three multidrug-resistant (MDR) methicillin-resistant Staphylococcus aureus (MRSA) isolates with active efflux properties. Only low inhibitory potential were detected through the preliminary evaluation as indicated by their respective minimum inhibitory concentration (MIC) value. These results justify the need to conduct subsequent evaluation namely the efflux inhibitory potential assay. Ethidium bromide (EtBr) and reserpine were used as the standard efflux substrate and efflux inhibitor, respectively while S. aureus ATCC 25923 was used as the reference strain. Three flavonoid compounds namely eriodictyol-7,4'-dimethyl ether, naringenin-4'-methyl ether and 2'4-dihydroxy-4'5'6'-trimethoxychalcone showed high efflux inhibitory activity with four to eight fold reduction of EtBr MIC value, hence suggesting their potential to be develop into efflux inhibitors for MRSA.
引用
收藏
页码:5631 / 5635
页数:5
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