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两种联合β-内酰胺酶抑制剂对耐碳青霉烯鲍曼不动杆菌的体外和体内评价

In vitro and in vivo evaluation of two combined β-lactamase inhibitors against carbapenem-resistant Acinetobacter baumannii.

作者信息

Domínguez Andrea Vila, Panadero Irene Molina, Smani Younes

机构信息

Instituto de Biomedicina de Sevilla (IBiS), Hospital Universitario Virgen del Rocío/CSIC, Universidad de Seville, Seville, Spain.

Centro Andaluz de Biología del Desarrollo, Universidad Pablo de Olavide/Consejo Superior de Investigaciones Científicas/Junta de Andalucía, Sevilla, Spain.

出版信息

Eur J Clin Microbiol Infect Dis. 2023 Nov;42(11):1317-1325. doi: 10.1007/s10096-023-04664-z. Epub 2023 Sep 15.

Abstract

The objective of this study was to evaluate the in vitro and in vivo efficacy of clavulanic acid (C/A) in combination with tazobactam against clinical strains of carbapenem-resistant Acinetobacter baumannii. The MIC of 24 clinical strains of A. baumannii was determined, and a checkerboard assay and time-kill curve analysis were performed in selected strains to determine the synergy between C/A and tazobactam. The efficacy of C/A in monotherapy and in combination with tazobactam was evaluated in vitro in cell culture experiments and in a murine peritoneal sepsis model. The C/A and C/A plus tazobactam MIC were 128 and <1 mg/L, respectively. The checkerboard assay showed that tazobactam (4 and 8 mg/L) demonstrated synergy with C/A against A. baumannii Ab40, an OXA-24 producer strain, and Ab293, a lacking OXA β-lactamase strain. The time-kill curve assay showed both bactericidal and synergistic effects against Ab40 and Ab293, with C/A 1xMIC and tazobactam (4 and 8 mg/L) at 24 h. In the murine peritoneal sepsis model with Ab293 strain, the combination of C/A and tazobactam reduced bacterial loads in tissues and blood by 2 and 4 log CFU/g or mL compared with C/A alone. Combining C/A with tazobactam could be considered as a potential alternative strategy to treat A. baumannii in some cases, and future work with more strains is needed to confirm this possibility.

摘要

本研究的目的是评估克拉维酸(C/A)与他唑巴坦联合使用对耐碳青霉烯鲍曼不动杆菌临床菌株的体外和体内疗效。测定了24株鲍曼不动杆菌临床菌株的最低抑菌浓度(MIC),并对选定菌株进行棋盘法测定和时间杀菌曲线分析,以确定C/A与他唑巴坦之间的协同作用。在细胞培养实验和小鼠腹腔败血症模型中对C/A单药治疗以及与他唑巴坦联合治疗的疗效进行了体外评估。C/A和C/A加他唑巴坦的MIC分别为128和<1mg/L。棋盘法测定表明,他唑巴坦(4和8mg/L)与C/A联合对一株产OXA-24的鲍曼不动杆菌Ab40菌株和一株缺乏OXAβ-内酰胺酶的Ab293菌株具有协同作用。时间杀菌曲线分析表明,在24小时时,C/A 1xMIC与他唑巴坦(4和8mg/L)联合对Ab40和Ab293具有杀菌和协同作用。在Ab293菌株的小鼠腹腔败血症模型中,与单独使用C/A相比,C/A与他唑巴坦联合使用可使组织和血液中的细菌载量分别降低2和4个对数CFU/g或mL。在某些情况下,将C/A与他唑巴坦联合使用可被视为治疗鲍曼不动杆菌的一种潜在替代策略,未来需要对更多菌株开展研究以证实这种可能性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ae8a/10587209/e4a01f75885c/10096_2023_4664_Fig1_HTML.jpg

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