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Antibiofilm Activity and Synergistic Inhibition of Staphylococcus aureus Biofilms by Bactericidal Protein P128 in Combination with Antibiotics

机译:杀菌蛋白P128与抗生素联合使用对金黄色葡萄球菌生物膜的抗生物膜活性和协同抑制作用

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摘要

P128 is an antistaphylococcal protein, comprising a cell wall-degrading enzymatic region and a Staphylococcus-specific binding region, which possesses specific and potent bactericidal activity against sensitive and drug-resistant strains of Staphylococcus aureus. To explore P128's ability to kill S. aureus in a range of environments relevant to clinical infection, we investigated the anti-S. aureus activity of P128 alone and in combination with standard-of-care antibiotics on planktonic and biofilm-embedded cells. P128 was found to have potent antibiofilm activity on preformed S. aureus biofilms as detected by CFU reduction and a colorimetric minimum biofilm inhibitory concentration (MBIC) assay. Scanning electron microscopic images of biofilms formed on the surfaces of microtiter plates and on catheters showed that P128 at low concentrations could destroy the biofilm structure and lyse the cells. When it was tested in combination with antibiotics which are known to be poor inhibitors of S. aureus in biofilms, such as vancomycin, gentamicin, ciprofloxacin, linezolid, and daptomycin, P128 showed highly synergistic antibiofilm activity that resulted in much reduced MBIC values for P128 and the individual antibiotics. The synergistic effect was seen for both sensitive and resistant isolates of S. aureus. Additionally, in an in vitro mixed-biofilm model mimicking the wound infection environment, P128 was able to prevent biofilm formation by virtue of its anti-Staphylococcus activity. The potent S. aureus biofilm-inhibiting activity of P128 both alone and in combination with antibiotics is an encouraging sign for the development of P128 for treatment of complicated S. aureus infections involving biofilms.
机译:P128是抗葡萄球菌蛋白,包括细胞壁降解酶区和葡萄球菌特异性结合区,该结合区具有针对金黄色葡萄球菌敏感和耐药菌株的特异性和有效的杀菌活性。为了探索P128在与临床感染相关的一系列环境中杀死金黄色葡萄球菌的能力,我们调查了抗S抗体。单独的P128以及与护理标准抗生素联合使用时对浮游生物和生物膜包埋细胞的金黄色葡萄球菌活性。通过CFU还原和比色最小生物膜抑制浓度(MBIC)分析检测到,发现P128对预先形成的金黄色葡萄球菌生物膜具有有效的抗生物膜活性。扫描在微量滴定板表面和导管上形成的生物膜的电子显微镜图像显示,低浓度的P128可能破坏生物膜结构并裂解细胞。当与已知在生物膜中对金黄色葡萄球菌的抑制作用较弱的抗生素(例如万古霉素,庆大霉素,环丙沙星,利奈唑胺和达托霉素)组合使用时,P128显示出高度协同的抗生物膜活性,导致P128的MBIC值大大降低以及个别抗生素。对于金黄色葡萄球菌的敏感性和抗性分离株均观察到协同作用。此外,在模仿伤口感染环境的体外混合生物膜模型中,P128凭借其抗葡萄球菌活性能够阻止生物膜形成。 P128单独或与抗生素联合使用均具有强大的抑制金黄色葡萄球菌生物膜的活性,这是开发用于治疗涉及生物膜的复杂金黄色葡萄球菌感染的P128的令人鼓舞的迹象。

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