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大肠埃希菌和铜绿假单胞菌中产 ESBLs 对头孢他啶/阿维巴坦和头孢洛扎/他唑巴坦组合的耐药性。

ESBLs and resistance to ceftazidime/avibactam and ceftolozane/tazobactam combinations in Escherichia coli and Pseudomonas aeruginosa.

机构信息

Emerging Antibiotic Resistance Unit, Medical and Molecular Microbiology, Department of Medicine, University of Fribourg, Fribourg, Switzerland.

Swiss National Reference Centre for Emerging Antibiotic Resistance, Fribourg, Switzerland.

出版信息

J Antimicrob Chemother. 2019 Jul 1;74(7):1934-1939. doi: 10.1093/jac/dkz149.

Abstract

OBJECTIVES

To evaluate the efficacy of the recently launched β-lactam/β-lactamase inhibitor combinations ceftazidime/avibactam and ceftolozane/tazobactam against ESBL-producing Escherichia coli and Pseudomonas aeruginosa strains.

METHODS

A series of ESBL-encoding genes (blaTEM, blaSHV, blaCTX-M, blaVEB, blaPER, blaGES and blaBEL) was cloned and expressed in E. coli or P. aeruginosa recipient strains. Cultures of E. coli TOP10 harbouring recombinant plasmids and therefore producing the different ESBLs tested were grown in order to perform measurements of catalytic activities, using benzylpenicillin, ceftazidime and ceftolozane as substrates. IC50s were additionally determined for clavulanic acid, tazobactam and avibactam.

RESULTS

We showed here an overall better activity of ceftazidime/avibactam compared with ceftolozane/tazobactam toward ESBL-producing E. coli and P. aeruginosa. Several ESBLs of the GES, PER and BEL types conferred resistance to ceftolozane/tazobactam in E. coli and P. aeruginosa. For GES-6 and PER-1 producers, resistance to ceftolozane/tazobactam could be explained by a high hydrolysis of ceftolozane and a low activity of tazobactam as an inhibitor. On the other hand, PER-producing P. aeruginosa also exhibited resistance to ceftazidime/avibactam.

CONCLUSIONS

Altogether, the results show that the ESBL PER-1, which is widespread worldwide, may be a source of resistance to both ceftolozane/tazobactam and ceftazidime/avibactam. Excellent activity of ceftazidime/avibactam was highlighted for both ESBL-producing E. coli and ESBL-producing P. aeruginosa.

摘要

目的

评估最近推出的β-内酰胺/β-内酰胺酶抑制剂组合头孢他啶/阿维巴坦和头孢唑肟/他唑巴坦对产 ESBL 的大肠埃希菌和铜绿假单胞菌菌株的疗效。

方法

一系列 ESBL 编码基因(blaTEM、blaSHV、blaCTX-M、blaVEB、blaPER、blaGES 和 blaBEL)被克隆并在大肠埃希菌或铜绿假单胞菌受体菌株中表达。培养携带重组质粒的大肠埃希菌 TOP10 菌株,因此产生了测试的不同 ESBL,使用苯唑西林、头孢他啶和头孢唑肟作为底物进行催化活性测量。还确定了克拉维酸、他唑巴坦和阿维巴坦的 IC50。

结果

我们在这里表明,头孢他啶/阿维巴坦对产 ESBL 的大肠埃希菌和铜绿假单胞菌的活性总体优于头孢唑肟/他唑巴坦。几种 GES、PER 和 BEL 类型的 ESBL 使大肠埃希菌和铜绿假单胞菌对头孢唑肟/他唑巴坦产生耐药性。对于 GES-6 和 PER-1 产生者,头孢唑肟/他唑巴坦的耐药性可以通过头孢唑肟的高水解和他唑巴坦作为抑制剂的低活性来解释。另一方面,产 PER 的铜绿假单胞菌也对头孢他啶/阿维巴坦产生耐药性。

结论

总的来说,结果表明,广泛分布于世界各地的 ESBL PER-1 可能是对头孢唑肟/他唑巴坦和头孢他啶/阿维巴坦都产生耐药性的来源。头孢他啶/阿维巴坦对产 ESBL 的大肠埃希菌和产 ESBL 的铜绿假单胞菌均表现出优异的活性。

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