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头孢他啶-阿维巴坦和氨曲南能否克服肠杆菌科细菌中金属β-内酰胺酶介导的β-内酰胺耐药性?

Can Ceftazidime-Avibactam and Aztreonam Overcome β-Lactam Resistance Conferred by Metallo-β-Lactamases in Enterobacteriaceae?

作者信息

Marshall Steven, Hujer Andrea M, Rojas Laura J, Papp-Wallace Krisztina M, Humphries Romney M, Spellberg Brad, Hujer Kristine M, Marshall Emma K, Rudin Susan D, Perez Federico, Wilson Brigid M, Wasserman Ronald B, Chikowski Linda, Paterson David L, Vila Alejandro J, van Duin David, Kreiswirth Barry N, Chambers Henry F, Fowler Vance G, Jacobs Michael R, Pulse Mark E, Weiss William J, Bonomo Robert A

机构信息

Louis Stokes Cleveland Department of Veterans Affairs Medical Center, Cleveland, Ohio, USA.

Department of Medicine, Case Western Reserve University School of Medicine, Cleveland, Ohio, USA.

出版信息

Antimicrob Agents Chemother. 2017 Mar 24;61(4). doi: 10.1128/AAC.02243-16. Print 2017 Apr.

Abstract

Based upon knowledge of the hydrolytic profile of major β-lactamases found in Gram-negative bacteria, we tested the efficacy of the combination of ceftazidime-avibactam (CAZ-AVI) with aztreonam (ATM) against carbapenem-resistant enteric bacteria possessing metallo-β-lactamases (MBLs). Disk diffusion and agar-based antimicrobial susceptibility testing were initially performed to determine the efficacy of a unique combination of CAZ-AVI and ATM against 21 representative isolates with a complex molecular background that included , , , , , and combinations thereof. Time-kill assays were conducted, and the efficacy of this combination was assessed in a murine neutropenic thigh infection model. By disk diffusion assay, all 21 isolates were resistant to CAZ-AVI alone, and 19/21 were resistant to ATM. The activity of CAZ-AVI in combination with ATM against diverse possessing MBLs was demonstrated in 17/21 isolates, where the zone of inhibition was ≥21 mm. All isolates demonstrated a reduction in CAZ-AVI agar dilution MICs with the addition of ATM. At 2 h, time-kill assays demonstrated a ≥4-log-CFU decrease for all groups that had CAZ-AVI with ATM (8 μg/ml) added, compared to the group treated with CAZ-AVI alone. In the murine neutropenic thigh infection model, an almost 4-log-CFU reduction was noted at 24 h for CAZ-AVI (32 mg/kg every 8 h [q8h]) plus ATM (32 mg/kg q8h) versus CAZ-AVI (32 mg/kg q8h) alone. The data presented herein require us to carefully consider this new therapeutic combination to treat infections caused by MBL-producing .

摘要

基于对革兰氏阴性菌中主要β-内酰胺酶水解特性的了解,我们测试了头孢他啶-阿维巴坦(CAZ-AVI)与氨曲南(ATM)联合用药对携带金属β-内酰胺酶(MBLs)的耐碳青霉烯类肠道细菌的疗效。最初进行了纸片扩散法和基于琼脂的抗菌药敏试验,以确定CAZ-AVI和ATM的独特组合对21株具有复杂分子背景的代表性菌株的疗效,这些菌株包括 、 、 、 、 及其组合。进行了时间杀菌试验,并在小鼠中性粒细胞减少大腿感染模型中评估了该组合的疗效。通过纸片扩散试验,所有21株菌株单独对CAZ-AVI耐药,21株中有19株对ATM耐药。在21株中有17株显示出CAZ-AVI与ATM联合对多种携带MBLs的菌株具有活性,其抑菌圈≥21 mm。添加ATM后,所有菌株的CAZ-AVI琼脂稀释最低抑菌浓度(MIC)均降低。在2小时时,时间杀菌试验表明,与单独使用CAZ-AVI治疗的组相比,添加了CAZ-AVI与ATM(8 μg/ml)的所有组的菌落形成单位(CFU)减少了≥4个对数。在小鼠中性粒细胞减少大腿感染模型中,与单独使用CAZ-AVI(每8小时32 mg/kg [q8h])相比,CAZ-AVI(32 mg/kg q8h)加ATM(32 mg/kg q8h)在24小时时CFU减少了近4个对数。本文提供的数据要求我们仔细考虑这种新的治疗组合,以治疗由产MBL的 引起的感染。

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