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Large variations in clinical antibiotic activity against Staphylococcus aureus Staphylococcus aureus biofilms of periprosthetic joint infection isolates

机译:对葡萄球菌金黄色葡萄球菌葡萄球菌的临床抗生素活性的大变异性Periprositth接合感染分离物的葡萄球菌生物膜

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ABSTRACT Staphylococcus aureus biofilms have a high tolerance to antibiotics, making the treatment of periprosthetic joint infection (PJI) challenging. From a clinical perspective, bacteria from surgical specimens are cultured in a planktonic state to determine antibiotic sensitivity. However, S. aureus exists primarily as established biofilms in PJI. To address this dichotomy, we developed a prospective registry of total knee and hip arthroplasty PJI S. aureus isolates to quantify the activity of clinically important antibiotics against isolates grown as biofilms. S. aureus planktonic minimum inhibitory concentration (MIC) and minimum bactericidal concentration (MBC) were assessed using clinical laboratory standard index assays for 10 antibiotics (cefazolin, clindamycin, vancomycin, rifampin, linezolid, nafcillin, gentamicin, trimethoprim/sulfamethoxazole, doxycycline, and daptomycin). Mature biofilms of each strain were grown in vitro, after which biofilm MIC (MBIC) and biofilm MBC (MBBC) were determined. Overall, isolates grown as biofilms displayed larger variations in antibiotic MICs as compared to planktonic MIC values. Only rifampin, doxycycline, and daptomycin had measurable biofilm MIC values across all S. aureus isolates tested. Biofilm MBC observations complemented biofilm MIC observations; rifampin, doxycycline, and daptomycin were the only antibiotics with measurable biofilm MBC values. 90% of S. aureus biofilms could be killed by rifampin, 50% by doxycycline, and only 15% by daptomycin. Biofilm formation increased bacterial antibiotic tolerance nonspecifically across all antibiotics, in both MSSA and MRSA samples. Rifampin and doxycycline were the most effective antibiotics at killing established S. aureus biofilms. ? 2019 Orthopaedic Research Society. Published by Wiley Periodicals, Inc. J Orthop Res 37:1604–1609, 2019.
机译:摘要金黄色葡萄球菌生物膜对抗生素具有高耐受性,使治疗有骨质增长感染(PJI)具有挑战性。从临床的角度来看,来自外科手术标本的细菌在浮躁状态下培养以确定抗生素敏感性。然而,S.UUREUS主要存在于PJI中的已成立的生物膜。为了解决这一二分法,我们开发了一个预期的膝关节和髋关节置换术PJI S. aureus的预期登记术,分离植物,以量化临床重要抗生素对生物膜生长的分离物的活动。使用临床实验室标准指数测定来评估金黄色葡萄球菌的最小抑制浓度(MIC)和最小杀菌浓度(MBC)(Cefazolin,Clindamycin,万古霉素,利福平,Linezolid,Nafcillin,庆大霉素,三甲基丙醇/磺胺甲恶唑,强霉素和达达霉素)。在体外生长每个菌株的成熟生物膜,之后测定生物膜MIC(MBIC)和生物膜MBC(MBBC)。总体而言,与浮游生物麦克风值相比,随着生物膜的分离物在抗生素MIC中显示出更大的抗生素MIC的变化。只有利福平,强霉素和达达霉素在所有S. aureus分离物中都有可测量的生物膜MIC值。 Biofilm MBC观察结果补充了生物膜MIC观察;利福平,十二胞环素和达达霉素是唯一具有可测量的生物膜MBC值的抗生素。 90%的S.UUREUS生物膜可以被利福平,50%由十氧环菌杀死,达达霉素仅为15%。生物膜形成在MSSA和MRSA样品中,在所有抗生素中增加了细菌抗生素耐受性。利福平和强力环素是杀死成立的S. aureus Biofilms的最有效的抗生素。还2019年骨科研究会。由Wiley Hearyicals,Inc.J Orthop Res 37:1604-1609,2019出版。

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