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对治疗过程中对头孢洛扎/他唑巴坦产生耐药性的广泛耐药铜绿假单胞菌分离株中的 AmpC β-内酰胺酶突变进行表征。

Characterization of AmpC β-lactamase mutations of extensively drug-resistant Pseudomonas aeruginosa isolates that develop resistance to ceftolozane/tazobactam during therapy.

机构信息

Servicio de Microbiología, Hospital Universitario Miguel Servet, IIS Aragón, Zaragoza, Spain.

Servicio de Microbiología, Hospital Universitario Miguel Servet, IIS Aragón, Zaragoza, Spain.

出版信息

Enferm Infecc Microbiol Clin (Engl Ed). 2020 Dec;38(10):474-478. doi: 10.1016/j.eimc.2020.01.017. Epub 2020 Mar 3.

Abstract

INTRODUCTION

We characterized AmpC β-lactamase mutations that resulted in ceftolozane/tazobactam resistance in extensively drug-resistant (XDR) Pseudomonas aeruginosa isolates recovered from patients treated with this agent from June 2016 to December 2018.

METHODS

Five pairs of ceftolozane/tazobactam susceptible/resistant P. aeruginosa XDR isolates were included among a total of 49 patients treated. Clonal relationship among isolates was first evaluated by pulsed-field gel electrophoresis (PFGE). Multilocus sequence typing (MLST) was further performed. AmpC mutations were investigated by PCR amplification of the blaPDC gene followed by sequencing.

RESULTS

The ST175 high-risk clone was detected in four of the pairs of isolates and the ST1182 in the remaining one. All resistant isolates showed a mutation in AmpC: T96I in two of the isolates, and E247K, G183V, and a deletion of 19 amino acids (G229-E247) in the other three. The G183V mutation had not been described before. The five isolates resistant to ceftolozane/tazobactam showed cross-resistance to ceftazidime/avibactam and lower MICs of imipenem and piperacillin/tazobactam than the susceptible isolates.

CONCLUSIONS

Ceftolozane/tazobactam resistance was associated in all of the cases with AmpC mutations, including a novel mutation (G183V) not previously described. There is a vital need for surveillance and characterization of emerging ceftolozane/tazobactam resistance, in order to preserve this valuable antipseudomonal agent.

摘要

简介

我们对 2016 年 6 月至 2018 年 12 月期间接受该药物治疗的患者中分离出的广泛耐药(XDR)铜绿假单胞菌的 AmpC β-内酰胺酶突变进行了特征分析,这些突变导致头孢洛扎/他唑巴坦耐药。

方法

在总共 49 名接受治疗的患者中,包括 5 对头孢洛扎/他唑巴坦敏感/耐药的 XDR 铜绿假单胞菌分离株。首先通过脉冲场凝胶电泳(PFGE)评估分离株之间的克隆关系。进一步进行多位点序列分型(MLST)。通过扩增 blaPDC 基因并用测序法研究 AmpC 突变。

结果

在 4 对分离株中检测到高风险克隆 ST175,在其余一对中检测到 ST1182。所有耐药分离株均显示 AmpC 突变:2 个分离株为 T96I,另外 3 个为 E247K、G183V 和 19 个氨基酸缺失(G229-E247)。以前没有描述过 G183V 突变。对头孢洛扎/他唑巴坦耐药的 5 个分离株对头孢他啶/阿维巴坦显示交叉耐药,且对亚胺培南和哌拉西林/他唑巴坦的 MIC 较低。

结论

在所有情况下,头孢洛扎/他唑巴坦耐药均与 AmpC 突变相关,包括以前未描述的新突变(G183V)。迫切需要监测和描述新兴的头孢洛扎/他唑巴坦耐药性,以保护这种有价值的抗假单胞菌药物。

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