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In Vitro and In Vivo Synergistic Activities of Linezolid Combined with Subinhibitory Concentrations of Imipenem against Methicillin-Resistant Staphylococcus aureus

机译:利奈唑胺联合亚抑制浓度亚胺培南对耐甲氧西林金黄色葡萄球菌的体外和体内协同活性

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摘要

Indifference or moderate antagonism of linezolid combined with other antibiotics in vitro and in vivo have mainly been reported in the literature. We have assessed the in vitro activities of linezolid, alone or in combination with imipenem, against methicillin-resistant Staphylococcus aureus (MRSA) strains using the dynamic checkerboard and time-kill curve methods. Linezolid and low concentrations of imipenem had a synergistic effect, leading us to evaluate the in vivo antibacterial activity of the combination using the rabbit endocarditis experimental model. Two MRSA strains were used for in vivo experiments: one was a heterogeneous glycopeptide-intermediate clinical S. aureus strain isolated from blood cultures, and the other was the S. aureus COL reference strain. Animals infected with one of two MRSA strains were randomly assigned to one of the following treatments: no treatment (controls), linezolid (simulating a dose in humans of 10 mg/kg of body weight every 12 h), a constant intravenous infusion of imipenem (which allowed the steady-state concentration of about 1/32 the MIC of imipenem for each strain to be reached in serum), or the combination of both treatments. Linezolid and imipenem as monotherapies exhibited no bactericidal activity against either strain. The combination of linezolid plus imipenem showed in vivo bactericidal activity that corresponded to a decrease of at least 4.5 log CFU/g of vegetation compared to the counts for the controls. In conclusion, the combination exhibited synergistic and bactericidal activities against two MRSA strains after 5 days of treatment. The combination of linezolid plus imipenem appears to be promising for the treatment of severe MRSA infections and merits further investigations to explore the mechanism underlying the synergy between the two drugs.
机译:利奈唑胺与其他抗生素在体内和体外的冷漠或中度拮抗作用主要在文献中已有报道。我们使用动态棋盘和时间杀伤曲线方法评估了利奈唑胺单独或与亚胺培南联用对耐甲氧西林金黄色葡萄球菌(MRSA)菌株的体外活性。利奈唑胺和低浓度的亚胺培南具有协同作用,因此我们使用兔心内膜炎实验模型评估了该组合的体内抗菌活性。两种MRSA菌株用于体内实验:一种是从血液培养物中分离的异源糖肽中间临床金黄色葡萄球菌菌株,另一种是金黄色葡萄球菌COL参考菌株。将被两种MRSA菌株之一感染的动物随机分配至以下治疗方法之一:不进行治疗(对照),利奈唑胺(每12小时模拟人的剂量为10 mg / kg体重的剂量),亚胺培南的恒定静脉输注(这使得每种菌株在血清中的稳态浓度约为亚胺培南的MIC的1/32),或两种处理方式的组合。利奈唑胺和亚胺培南作为单一疗法对两种菌株均无杀菌活性。利奈唑胺加亚胺培南的组合显示体内杀菌活性,与对照相比,相当于减少了至少4.5 log CFU / g植被。总之,在治疗5天后,该组合物对两种MRSA菌株表现出协同和杀菌活性。利奈唑胺加亚胺培南的组合似乎有望用于治疗严重的MRSA感染,值得进一步研究以探索两种药物协同作用的潜在机制。

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