Hinokitiol Selectively Enhances the Antibacterial Activity of Tetracyclines against Staphylococcus aureus.

IF 3.8 2区 生物学 Q2 MICROBIOLOGY
Chun-Yan Le, Yu-Jian Ye, Jian Xu, Lei Li, Xi-Qing Feng, Ni-Pi Chen, Bing-Qi Zhu, Zhi-Shan Ding, Chao-Dong Qian
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引用次数: 1

Abstract

The increasing prevalence of antibiotic resistance causes an urgent need for alternative agents to combat drug-resistant bacterial pathogens. Plant-derived compounds are promising candidates for the treatment of infections caused by antibiotic-resistant bacteria. Hinokitiol (β-thujaplicin), a natural tropolone derivative found in the heartwood of cupressaceous plants, has been widely used in oral and skin care products as an antimicrobial agent. The aim of this work was to study the synergy potential of hinokitiol with antibiotics against Staphylococcus aureus, which is an extremely successful opportunistic pathogen capable of causing nosocomial and community-acquired infections worldwide. The MIC was determined by the broth microdilution method, and the effect of combinations was evaluated through fractional inhibitory concentration indices (FICI). The mechanism behind this synergy was also investigated by using fluorescence spectroscopy and high-performance liquid chromatography (HPLC). The MICs of hinokitiol alone against most S. aureus strains were 32 μg/mL. Selectively synergistic activities (FICIs of ≤0.5) were observed for combinations of this phytochemical with tetracyclines against all tested strains of S. aureus. Importantly, hinokitiol at 1 μg/mL completely or partially reversed tetracycline resistance in staphylococcal isolates. The increased accumulation of tetracycline inside S. aureus in the presence of hinokitiol was observed. In addition, hinokitiol promoted the uptake of ethidium bromide (EB) in bacterial cells without membrane depolarization, suggesting that it may be an efflux pump inhibitor. IMPORTANCE The disease caused by S. aureus is a public health issue due to the continuing emergence of drug-resistant strains, particularly methicillin-resistant S. aureus (MRSA). Tetracyclines, one of the old classes of antimicrobials, have been used for the treatment of infections caused by S. aureus. However, the increased resistance to tetracyclines together with their toxicity have limited their use in the clinic. Here, we demonstrated that the combination of hinokitiol and tetracyclines displayed synergistic antibacterial activity against S. aureus, including tetracycline-resistant strains and MRSA, offering a potential alternative approach for the treatment of infections caused by this bacterium.

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Hinokitiol选择性增强四环素类药物对金黄色葡萄球菌的抗菌活性。
抗生素耐药性的日益普遍导致迫切需要替代药物来对抗耐药细菌病原体。植物来源的化合物是治疗抗生素耐药性细菌引起的感染的有希望的候选药物。Hinokitiol(β-thujaplicin)是一种在紫铜科植物心材中发现的天然原松衍生物,作为一种抗菌剂,已广泛应用于口腔和皮肤护理产品中。这项工作的目的是研究hinokiol与抗生素对金黄色葡萄球菌的协同作用潜力,金黄色葡萄菌是一种非常成功的机会致病菌,能够在全球范围内引起医院和社区获得性感染。用肉汤微量稀释法测定MIC,并用部分抑制浓度指数(FICI)评价组合的效果。还通过荧光光谱和高效液相色谱(HPLC)研究了这种协同作用背后的机制。单独使用hinokitol对大多数金黄色葡萄球菌菌株的MIC为32 μg/mL。选择性协同活动 ≤0.5)针对所有测试的金黄色葡萄球菌菌株观察到该植物化学物质与四环素的组合。重要的是,1 μg/mL完全或部分逆转葡萄球菌分离株对四环素的耐药性。观察到四环素在金黄色葡萄球菌内的积累在hinokitol存在下增加。此外,hinokitiol在没有膜去极化的情况下促进了细菌细胞对溴化乙锭(EB)的摄取,这表明它可能是一种外排泵抑制剂。重要性金黄色葡萄球菌引起的疾病是一个公共卫生问题,因为耐药菌株的持续出现,特别是耐甲氧西林金黄色葡萄菌(MRSA)。四环素是一种古老的抗菌药物,已被用于治疗金黄色葡萄球菌引起的感染。然而,对四环素类药物耐药性的增加及其毒性限制了其在临床上的应用。在这里,我们证明了hinokitol和四环素类药物的组合对金黄色葡萄球菌表现出协同抗菌活性,包括四环素耐药性菌株和MRSA,为治疗这种细菌引起的感染提供了一种潜在的替代方法。
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来源期刊
Microbiology spectrum
Microbiology spectrum Biochemistry, Genetics and Molecular Biology-Genetics
CiteScore
3.20
自引率
5.40%
发文量
1800
期刊介绍: Microbiology Spectrum publishes commissioned review articles on topics in microbiology representing ten content areas: Archaea; Food Microbiology; Bacterial Genetics, Cell Biology, and Physiology; Clinical Microbiology; Environmental Microbiology and Ecology; Eukaryotic Microbes; Genomics, Computational, and Synthetic Microbiology; Immunology; Pathogenesis; and Virology. Reviews are interrelated, with each review linking to other related content. A large board of Microbiology Spectrum editors aids in the development of topics for potential reviews and in the identification of an editor, or editors, who shepherd each collection.
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