Synergistic Activities of Colistin with Tigecycline Combination Against Clinical Isolates of Carbapenemresistant Acinetobacter baumannii

S. Sitaruno, W. Santimaleeworagun, S. Leelasupasri
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Abstract

OBJECTIVES: To determine in vitro antimicrobial susceptibility and synergistic activity of colistin in combination with tigecycline against clinical strains of carbapenem- resistant Acinetobacter baumannii (CRAB). MATERIAL AND METHODS: Colistin and tigecycline minimum inhibitory concentrations (MICs) of 12-clinical CRAB isolates were determined by broth microdilution. Checkerboard testing was performed to assess the interaction of the colistin-tigecycline combination. Fractional inhibitory concentration indexes (ΣFIC) in the range of 0.5 to 1.0, > 1.0 to < 4.0 and ≥ 4.0 are considered as additive, indifferent, and antagonistic effects, respectively. RESULTS: All CRAB isolates were susceptible to colistin. Three out of 12 CRABs were susceptible to tigecycline based on a pharmacokinetic-pharmacodynamics (PK-PD) breakpoint (MICs ≤ 0.25 μg/mL). The MIC of both antimicrobials was decreased in most of the CRAB isolates in the checkerboard synergy testing. The interaction of colistin and tigecycline combination revealed both additive and indifferent effects in five and seven of the 12-CRAB isolates, respectively. Neither synergism nor antagonism of colistin and tigecycline combination was demonstrated. CONCLUSION: No synergistic effect between colistin and tigecycline against CRAB isolates was detected. However, the combination of these two drugs is likely to result in a decrease in the MIC of both drugs. Further studies with a larger sample to determine the in vitro synergistic activity of colistin and tigecycline combination are required. Keywords: in vitro, synergism, tigecycline, colistin, checkerboard method DOI: 10.31524/bkkmedj.2019.02.005
大肠杆菌素与替加环素联合对临床分离的碳青霉烯耐药性鲍曼不动杆菌的协同作用
目的:测定粘菌素联合替加环素对临床耐药的鲍曼不动杆菌(CRAB)的体外抗菌敏感性和协同活性。材料和方法:用肉汤微量稀释法测定12株临床CRAB分离株的粘菌素和替加环素的最低抑菌浓度。进行棋盘格测试以评估粘菌素-替加环素组合的相互作用。在0.5至1.0、>1.0至<4.0和≥4.0范围内的部分抑制浓度指数(∑FIC)分别被认为是相加作用、无影响作用和拮抗作用。结果:所有CRAB分离株均对粘菌素敏感。基于药代动力学-药效学(PK-PD)断点(MICs≤0.25μg/mL),12个CRAB中有3个对替加环素敏感。在棋盘协同试验中,大多数CRAB分离株的两种抗菌药物的MIC均降低。粘菌素和替加环素组合的相互作用分别在12个CRAB分离株中的5个和7个中显示出相加和无差异的作用。粘菌素和替加环素的组合既没有协同作用也没有拮抗作用。结论:粘菌素和替加环素对CRAB分离株无协同作用。然而,这两种药物的组合可能会导致两种药物MIC的降低。需要用更大的样本进行进一步的研究,以确定粘菌素和替加环素组合的体外协同活性。关键词:体外,增效作用,替加环素,粘菌素,棋盘格法DOI:10.31524/bkkmedj.2019.02.005
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