Department of Pharmaceutical Microbiology, Faculty of Pharmacy, Istanbul University, Istanbul, Turkey.
Department of Infectious Diseases and Clinical Microbiology, School of Medicine, Istanbul Medipol University, Istanbul, Turkey.
Infect Dis (Lond). 2020 Sep;52(9):616-624. doi: 10.1080/23744235.2020.1767803. Epub 2020 May 19.
This study aims to analyse the effect of ceftazidime-avibactam plus various antibiotics against multidrug-resistant (MDR) isolated from Intensive Care Units. 40 non-duplicate . isolates were screened for their MICs of ceftazidime, ceftazidime-avibactam, colistin, levofloxacin, doripenem and tobramycin. MICs were determined by the broth microdilution method. The bactericidal activities of ceftazidime-avibactam compared to studied antibiotics were also determined by time-kill curve assays both at 1xMIC and at 4xMIC against carbapenemase-producing or -not producing six colistin-nonsusceptible MDR clinical strains of . Additionally, synergistic interactions were investigated by the time-kill curve assay. The MIC values for ceftazidime, ceftazidime-avibactam, colistin, levofloxacin, doripenem and tobramycin against MDR isolates were found to be >256, 64, 8, 64, 128, and >256 mg/L, respectively. The minimum bactericidal concentration values for those antibiotics were also >256, 64, 16, 128, 256, and >256 mg/L, respectively. While doripenem, tobramycin and levofloxacin were bactericidal (>3 log killing) against the 2/6, 3/6 and 1/6 isolates at 4xMIC concentrations, respectively, levofloxacin and tobramycin were bactericidal against only one isolate (1/6) at 1xMIC concentrations at 24 h. The synergistic interactions of these antimicrobial agents were also achieved with ceftazidime/avibactam + colistin (4/6), ceftazidime/avibactam + tobramycin (3/6), and ceftazidime/avibactam + levofloxacin (3/6) combinations. No antagonism was observed against studied strains. The findings of this study suggest that ceftazidime/avibactam with colistin, or tobramycin, were effective against colistin-nonsusceptible strains. This combination therapy could be an alternative antibiotic therapy for resistant strains.
本研究旨在分析头孢他啶-阿维巴坦联合各种抗生素对重症监护病房(ICU)分离的多药耐药(MDR)的作用。筛选了 40 株非重复的. 分离株,以测定其头孢他啶、头孢他啶-阿维巴坦、多粘菌素、左氧氟沙星、多尼培南和妥布霉素的 MIC。采用肉汤微量稀释法测定 MIC。通过时间杀伤曲线试验,还测定了头孢他啶-阿维巴坦与研究抗生素相比对产碳青霉烯酶和不产碳青霉烯酶的 6 株多粘菌素不敏感的 MDR 临床株的杀菌活性,分别在 1xMIC 和 4xMIC 下。此外,还通过时间杀伤曲线试验研究了协同作用。发现头孢他啶、头孢他啶-阿维巴坦、多粘菌素、左氧氟沙星、多尼培南和妥布霉素对 MDR 分离株的 MIC 值分别为 >256、64、8、64、128 和 >256mg/L。这些抗生素的最低杀菌浓度值也分别为 >256、64、16、128、256 和 >256mg/L。虽然多尼培南、妥布霉素和左氧氟沙星在 4xMIC 浓度下对 2/6、3/6 和 1/6 分离株的杀菌作用(>3 log 杀灭),但左氧氟沙星和妥布霉素在 1xMIC 浓度下仅对 1/6 分离株在 24 小时时有杀菌作用。这些抗菌药物的协同作用也在头孢他啶/阿维巴坦+多粘菌素(4/6)、头孢他啶/阿维巴坦+妥布霉素(3/6)和头孢他啶/阿维巴坦+左氧氟沙星(3/6)组合中实现。对研究菌株未观察到拮抗作用。本研究结果表明,头孢他啶/阿维巴坦联合多粘菌素或妥布霉素对多粘菌素不敏感的菌株有效。这种联合治疗可能是治疗耐药菌株的一种替代抗生素治疗方法。