首页> 外文期刊>International journal of antimicrobial agents >Evaluation of the in vitro activities of ceftobiprole and comparators in staphylococcal colony or microtitre plate biofilm assays
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Evaluation of the in vitro activities of ceftobiprole and comparators in staphylococcal colony or microtitre plate biofilm assays

机译:评估头孢比普利和比较剂在葡萄球菌菌落或微量滴定板生物膜测定中的体外活性

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The aim of this study was to evaluate the in vitro efficacy of ceftobiprole and comparator antibiotics, either alone or in combination, in staphylococcal MBEC~(TM) (minimum biofilm eradication concentration) and colony biofilm assays at dilutions of the maximum free-drug plasma concentration attained during clinical use (fC_(max)). Staphylococci tested included meticillin-susceptible and meticillin-resistant Staphylococcus aureus (n = 6) and Staphylococcus epidermidis (n = 2). Relative to no-drug controls, after 7 days of exposure ceftobiprole concentrations from 1/4 fC_(max) to fC_(max) generally decreased CFUs in MBEC or colony biofilms of S. aureus isolates by ca. 1.5 log_(10) to ≥2.5 log_(10). Gentamicin reduced colony biofilm CFUs by ≥1.4 log_(10) at these concentrations with gentamicin-susceptible isolates. Following 7 days of exposure, vancomycin and rifampicin were ineffective as single agents or in combination in the colony model, but yielded CFU decreases from 0 to 5 log10 in the MBEC model. Treatment of biofilms with rifampicin for 7 days yielded rifampicin-resistant mutants, and the selection of rifampicin resistance was inhibited by co-treatment with ceftobiprole. Thus, ceftobiprole alone or in combination demonstrated promising activity against biofilms of meticillin-susceptible and -resistant staphylococci at clinically relevant concentrations. In contrast, vancomycin and rifampicin, two agents used clinically for the treatment of biofilm infections, tested separately or together gave inconsistent results and generally had little impact on cell viability.
机译:这项研究的目的是评估在最大自由药物血浆稀释度下,头孢比普利和比较抗生素(单独或联合使用)在葡萄球菌MBEC〜(TM)(最小生物膜清除浓度)和菌落生物膜测定中的体外功效。临床使用过程中达到的浓度(fC_(max))。所测试的葡萄球菌包括对甲氧西林敏感和耐甲氧西林的金黄色葡萄球菌(n = 6)和表皮葡萄球菌(n = 2)。相对于非药物对照组,暴露后7天,头孢比普罗浓度从1/4 fC_(max)降低至fC_(max)通常会使MBEC或金黄色葡萄球菌分离株的菌落生物膜中的CFU降低约20%。 1.5 log_(10)到≥2.5log_(10)。在这些浓度下,庆大霉素对庆大霉素敏感的分离物可使菌落生物膜CFU减少≥1.4log_(10)。暴露7天后,万古霉素和利福平作为单药或联合用药在菌落模型中无效,但在MBEC模型中,CFU从0下降到5 log10。用利福平处理生物膜7天产生了耐利福平的突变体,并且与头孢比普尔共同处理抑制了利福平抗性的选择。因此,在临床相关浓度下,单独或联合使用头孢托普罗对甲氧西林敏感和耐药葡萄球菌的生物膜表现出有希望的活性。相反,临床上用于治疗生物膜感染的两种药物万古霉素和利福平分别进行或一起测试,结果不一致,通常对细胞生存力影响很小。

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