IAME, UMR1137, INSERM and Université Paris Diderot, Sorbonne Paris Cité, Paris, France.
CHU de Caen, Service de Microbiologie, Caen, France.
J Antimicrob Chemother. 2018 Nov 1;73(11):3074-3080. doi: 10.1093/jac/dky283.
Alternative therapeutic regimens are urgently needed against carbapenemase-producing Enterobacteriaceae. Fosfomycin often remains active against KPC and OXA-48 producers, but emergence of resistance is a major limitation. Our aim was to determine whether the association of temocillin with fosfomycin might be useful to treat KPC- or OXA-48-producing Escherichia coli infections.
Isogenic derivatives of E. coli CFT073 with blaKPC-3- or blaOXA-48-harbouring plasmids (named CFT073-KPC-3 and CFT073-OXA-48, respectively) were used. The addition of temocillin to fosfomycin was tested using the chequerboard method and time-kill curves as well as in a fatal peritonitis murine model. Mice were treated for 24 h with fosfomycin alone or in combination with temocillin. Bacterial loads, before and after treatment, were determined in the peritoneal fluid and fosfomycin-resistant mutants were detected.
Temocillin MICs were 8, 32 and 256 mg/L for CFT073 (WT), CFT073-KPC-3 and CFT073-OXA-48, respectively. Fosfomycin MIC was 0.5 mg/L for all strains. The chequerboard experiments demonstrated synergy for all three strains. In time-kill curves, combining temocillin with fosfomycin was synergistic, bactericidal and prevented emergence of resistance for CFT073-pTOPO and CFT073-KPC-3, but not CFT073-OXA-48. In vivo, for the three strains, bacterial counts were lower in peritoneal fluid with the combination compared with fosfomycin alone (P < 0.001) and inhibited growth of resistant mutants in all cases.
The combination of fosfomycin and temocillin demonstrated a benefit in vitro and in vivo against E. coli strains producing KPC-3 or OXA-48-type carbapenemases. This combination prevented the emergence of fosfomycin resistance and proved to be more bactericidal than fosfomycin alone.
迫切需要针对产碳青霉烯酶肠杆菌科的替代治疗方案。磷霉素通常对 KPC 和 OXA-48 产生者保持活性,但出现耐药性是一个主要的限制。我们的目的是确定替莫西林与磷霉素联合使用是否可用于治疗产 KPC 或 OXA-48 的大肠埃希菌感染。
使用携带 blaKPC-3 或 blaOXA-48 质粒的大肠杆菌 CFT073 的同工酶衍生物(分别命名为 CFT073-KPC-3 和 CFT073-OXA-48)。使用棋盘法和时间杀伤曲线以及致命性腹膜炎小鼠模型测试替莫西林与磷霉素的联合作用。用磷霉素单独或与替莫西林联合治疗 24 小时。在腹膜液中测定治疗前后的细菌负荷,并检测耐磷霉素突变体。
替莫西林 MIC 分别为 8、32 和 256mg/L,用于 CFT073(WT)、CFT073-KPC-3 和 CFT073-OXA-48,磷霉素 MIC 为 0.5mg/L 用于所有菌株。棋盘实验表明所有三种菌株均具有协同作用。在时间杀伤曲线中,替莫西林与磷霉素联合使用对 CFT073-pTOPO 和 CFT073-KPC-3 具有协同、杀菌作用,并防止耐药突变体的出现,但对 CFT073-OXA-48 无效。在体内,对于三种菌株,与磷霉素单独使用相比,联合使用时腹膜液中的细菌计数较低(P<0.001),并且在所有情况下都抑制了耐药突变体的生长。
磷霉素与替莫西林联合使用在体外和体内对产 KPC-3 或 OXA-48 型碳青霉烯酶的大肠埃希菌菌株均具有获益。这种联合使用防止了磷霉素耐药性的出现,并证明比单独使用磷霉素更具杀菌作用。