Isothermal microcalorimetry vs checkerboard assay to evaluate in-vitro synergism of meropenem–amikacin and meropenem–colistin combinations against multi-drug-resistant Gram-negative pathogens

美罗培南 粘菌素 阿米卡星 鲍曼不动杆菌 微生物学 肺炎克雷伯菌 磷霉素 铜绿假单胞菌 肉汤微量稀释 不动杆菌 碳青霉烯 抗菌剂 抗生素 医学 生物 最小抑制浓度 大肠杆菌 抗生素耐药性 细菌 生物化学 基因 遗传学
作者
Alberto Antonelli,Marco Coppi,Chaitanya Tellapragada,Badrul Hasan,Ainhize Maruri-Aransolo,Desirèe Gijón,Fabio Morecchiato,Corné de Vogel,Annelies Verbon,Willem J. B. van Wamel,Kasper Nørskov Kragh,Niels Frimodt‐Møller,Rafael Cantón,Christian G. Giske,Gian María Rossolini
出处
期刊:International Journal of Antimicrobial Agents [Elsevier BV]
卷期号:60 (4): 106668-106668 被引量:8
标识
DOI:10.1016/j.ijantimicag.2022.106668
摘要

To evaluate the activity of meropenem-amikacin and meropenem-colistin combinations with checkerboard broth microdilution (CKBM) compared with isothermal microcalorimetry (ITMC) assays against a multi-centric collection of multi-drug-resistant Gram-negative clinical isolates; and to compare the fractional inhibitory concentration (FIC) index and time to results of CKBM and ITMC.A collection of 333 multi-drug-resistant Gram-negative clinical isolates showing reduced susceptibility to meropenem (121 Klebsiella pneumoniae, 14 Escherichia coli, 130 Pseudomonas aeruginosa and 68 Acinetobacter baumannii) isolated from different centres (Florence, Madrid, Rotterdam and Stockholm) was included in the study. The antimicrobial activity of meropenem-amikacin and meropenem-colistin combinations was evaluated with CKBM and ITMC. FIC index results were interpreted as synergistic/additive and indifferent for values ≤0.5/0.51, respectively. Whole-genome sequencing data of a subset of strains were used to evaluate their clonality.In total, 254 and 286 strains were tested with meropenem-colistin and meropenem-amikacin combinations with ITMC and CKBM, respectively. Synergistic/additive effects were observed for 46 strains (20 K. pneumoniae, four E. coli, 22 P. aeruginosa) and 20 strains (three K. pneumoniae, 11 P. aeruginosa and six A. baumannii) with meropenem-amikacin and meropenem-colistin combinations, respectively, with CKBM. ITMC showed good concordance with CKBM, with 89.5% and 92.2% of cases interpreted within the same FIC index category for meropenem-amikacin and meropenem-colistin combinations, respectively. Most of the synergistic/additive effects were detected within 6 h by ITMC.ITMC showed very good concordance with CKBM against a large collection of multi-drug-resistant Gram-negative clinical isolates, and could be implemented for the rapid evaluation of in-vitro activity of antimicrobial combinations.

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