Enhancing activity of antibiotics against Staphylococcus aureus: Zanthoxylum capense constituents and derivatives

被引:23
作者
Cabral, Vanessa [1 ]
Luo, Xuan [1 ]
Junqueira, Elisabete [2 ]
Costa, Sofia S. [2 ,3 ]
Mulhovo, Silva [4 ]
Duarte, Aida [1 ]
Couto, Isabel [2 ,3 ]
Viveiros, Miguel [2 ,5 ]
Ferreira, Maria-Jose U. [1 ]
机构
[1] Univ Lisbon, Fac Pharm, Res Inst Med iMed ULisboa, P-1649003 Lisbon, Portugal
[2] Univ Nova Lisboa, Inst Higiene & Med Trop, Unidade Microbiol Med, Grp Microbacterias, P-1349008 Lisbon, Portugal
[3] Univ Nova Lisboa, Ctr Recursos Microbiol CREM, P-2829516 Caparica, Portugal
[4] Univ Pedag, Fac Ciencias Nat & Matemat, Ctr Estudos Mocambicanos & Etnociecias CEMES, Maputo 21402161, Mozambique
[5] Univ Nova Lisboa, Inst Higiene & Med Trop, Ctr Malaria & Outras Daencas Trop CMDT, P-1349008 Lisbon, Portugal
关键词
Bacterial resistance; Phenylpropanoids; Benzophenanthridine alkaloids; Staphylococcus aureus; Zanthoxylum capense; EFFLUX PUMPS; RESISTANCE; ANTIMICROBIALS; TRITERPENOIDS; COMBAT; PLANTS; ROOTS;
D O I
10.1016/j.phymed.2015.02.003
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Six compounds (1-6), isolated from the methanol extract of the roots of the African medicinal plant Zanthoxylum capense Thunb. (Rutaceae), and seven ester derivatives (7-13) were evaluated for their antibacterial activities and modulatory effects on the MIC of antibiotics (erythromycin, oxacillin, and tetracycline) and ethidium bromide (EtBr) against a Staphylococcus aureus reference strain (ATCC 6538). Using the same model, compounds 1-13 were also assessed for their potential as efflux pump inhibitors by a fluorometric assay that measures the accumulation of the broad range efflux pump substrate EtBr. Compounds 8 and 11 were further evaluated for their antibacterial, modulatory and EtBr accumulation effects against four additional S. aureus strains, which included two clinical methicillin-resistant S. aureus (MRSA) strains. Compounds (1-13) have not shown antibacterial activity at the concentration ranges tested. When evaluated against S. (wrens ATCC 6538, oxychelerythrine (1) a benzophenanthridine alkaloid, showed the highest modulatory activity enhancing the susceptibility of this strain to all the tested antibiotics from two to four-fold. Ailanthoidiol diacetate (8) and ailanthoidiol di-2-ethylbutanoate (11) were also good modulators when combined with EtBr, increasing the bacteria susceptibility by four and two-fold, respectively. In the EtBr accumulation assay, using ATCC 6533 strain, the phenylpropanoid (+)-ailanthoidiol (6) and most of its ester derivatives (8 11) exhibited higher activity than the positive control verapamil. The highest effects were found for compounds Sand 11 that also increased the accumulation of EtBr, using S:. (wrens ATCC 25923 as model. Furthermore, both compounds (8, 11) were able to enhance the ciprofloxacin activity against the MRSA clinical strains tested, causing a reduction of the antibiotic MIC values from two to four-fold. The EtBr accumulation assay revealed that this modulation activity was not due to an inhibition of efflux pumps mechanism. These results suggested that Z. capense constituents may be valuable as leads for restoring antibiotic activity against MRSA strains. (C) 2015 Elsevier GmbH. All rights reserved.
引用
收藏
页码:469 / 476
页数:8
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