List Karoline Knudsen, Kolpen Mette, Kragh Kasper Nørskov, Charbon Godefroid, Radmer Stine, Hansen Frank, Løbner-Olesen Anders, Frimodt-Møller Niels, Hertz Frederik Boetius
Department of Clinical Microbiology, Rigshospitalet, DK-2100 Copenhagen, Denmark.
Costerton Biofilm Center, Department of Immunology and Microbiology, University of Copenhagen, DK-2200 Copenhagen, Denmark.
Antibiotics (Basel). 2022 Sep 20;11(10):1280. doi: 10.3390/antibiotics11101280.
Background: Carbapenemase-producing Klebsiella pneumoniae and Escherichia coli have become a significant global health challenge. This has created an urgent need for new treatment modalities. We evaluated the efficacy of mecillinam in combination with either avibactam or ceftazidime/avibactam against carbapenemase-producing clinical isolates. Materials and methods: Nineteen MDR clinical isolates of K. pneumoniae and E. coli were selected for the presence of blaKPC, blaNDM, blaOXA or blaIMP based on whole-genome sequencing and phenotypic susceptibility testing. We tested the synergy between mecillinam and avibactam or ceftazidime/avibactam. We used time−kill studies in vitro and a mouse peritonitis/sepsis model to confirm the synergistic effect. We investigated avibactam’s impact on mecillinam´s affinity for penicillin-binding proteins with a Bocillin assay, and cell changes with phase-contrast and confocal laser scanning microscopy. Results: Mecillinam combined with ceftazidime/avibactam or avibactam substantially reduced MICs (from up to >256 µg/mL to <0.0016 µg/mL) for 17/18 strains. Significant log-CFU reductions were confirmed in time−kill and in vivo experiments. The Bocillin assay did not reveal changes. Conclusion: Mecillinam in combination with avibactam or ceftazidime/avibactam has a notable effect on most types of CPEs, both in vitro and in vivo. The mecillinam/avibactam combination treatment could be a new efficient antibiotic treatment against multi-drug-resistant carbapenemase-producing Gram-negative pathogens.
产碳青霉烯酶的肺炎克雷伯菌和大肠杆菌已成为全球重大的健康挑战。这迫切需要新的治疗方式。我们评估了美西林与阿维巴坦或头孢他啶/阿维巴坦联合使用对产碳青霉烯酶临床分离株的疗效。
基于全基因组测序和表型药敏试验,选择了19株携带blaKPC、blaNDM、blaOXA或blaIMP的肺炎克雷伯菌和大肠杆菌多重耐药临床分离株。我们测试了美西林与阿维巴坦或头孢他啶/阿维巴坦之间的协同作用。我们使用体外时间杀菌研究和小鼠腹膜炎/脓毒症模型来确认协同效应。我们通过博西灵试验研究了阿维巴坦对美西林与青霉素结合蛋白亲和力的影响,并通过相差显微镜和共聚焦激光扫描显微镜观察细胞变化。
美西林与头孢他啶/阿维巴坦或阿维巴坦联合使用可使17/18株菌株的最低抑菌浓度大幅降低(从高达>256μg/mL降至<0.0016μg/mL)。在时间杀菌和体内实验中均证实了显著的对数菌落形成单位减少。博西灵试验未发现变化。
美西林与阿维巴坦或头孢他啶/阿维巴坦联合使用在体外和体内对大多数类型的产碳青霉烯酶肠杆菌科细菌均有显著效果。美西林/阿维巴坦联合治疗可能是一种针对多重耐药产碳青霉烯酶革兰氏阴性病原体的新型高效抗生素治疗方法。