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氨曲南与新开发的β-内酰胺酶抑制剂联合应用对产金属β-内酰胺酶的多重耐药肠杆菌科细菌和铜绿假单胞菌的体外活性。

In vitro activity of aztreonam in combination with newly developed β-lactamase inhibitors against MDR Enterobacterales and Pseudomonas aeruginosa producing metallo-β-lactamases.

作者信息

Le Terrier Christophe, Nordmann Patrice, Poirel Laurent

机构信息

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

Division of Intensive Care Unit, University Hospitals of Geneva, Geneva, Switzerland.

出版信息

J Antimicrob Chemother. 2022 Dec 23;78(1):101-107. doi: 10.1093/jac/dkac360.

Abstract

OBJECTIVES

To evaluate the in vitro activity of aztreonam in combination with novel β-lactamase inhibitors, namely avibactam, nacubactam, taniborbactam and zidebactam, against MDR MBL-producing Enterobacterales and Pseudomonas aeruginosa clinical isolates.

METHODS

MIC values of aztreonam, aztreonam/β-lactam inhibitor but also cefiderocol as comparator were determined for 64 and 39 clinical Enterobacterales or P. aeruginosa isolates, respectively, producing representative MBLs, i.e. derivatives of NDM (n = 64), VIM (n = 32), IMP (n = 8) and SPM (n = 2). MICs were also determined for Escherichia coli TOP10 and P. aeruginosa PAO1 harbouring recombinant plasmids producing the different β-lactamases under isogenic backgrounds (n = 22 and n = 11, respectively). Fifty percent inhibitory concentrations were additionally determined for the abovementioned β-lactamase inhibitors using β-lactamase crude extracts.

RESULTS

The susceptibility rate for aztreonam was 17.1% among MBL-producing Enterobacterales, while it was very high with aztreonam/zidebactam (98.4%), and to a lower extent with aztreonam/nacubactam (84.4%) and aztreonam/taniborbactam (75%), compared with aztreonam/avibactam (70.3%) and cefiderocol (39.1%). Among MBL-producing P. aeruginosa isolates, the susceptibility rates were 53.8% with aztreonam, 66.7% with aztreonam/nacubactam and aztreonam/taniborbactam combinations, and 69.2% with aztreonam/avibactam, aztreonam/zidebactam and cefiderocol.

CONCLUSIONS

Altogether, these results showed that combinations including aztreonam and novel β-lactamase inhibitors, such as zidebactam, nacubactam or taniborbactam, have a very significant in vitro activity against MDR MBL-producing Enterobacterales clinical isolates, the aztreonam/zidebactam combination being the best option. On the other hand, aztreonam/zidebactam is equivalent to aztreonam/avibactam and cefiderocol among MBL-producing P. aeruginosa isolates.

摘要

目的

评估氨曲南联合新型β-内酰胺酶抑制剂阿维巴坦、那库巴坦、他尼硼巴坦和齐德巴坦对产超广谱β-内酰胺酶(MBL)的多重耐药肠杆菌科细菌和铜绿假单胞菌临床分离株的体外活性。

方法

分别测定了64株和39株产代表性MBL(即NDM衍生物(n = 64)、VIM衍生物(n = 32)、IMP衍生物(n = 8)和SPM衍生物(n = 2))的临床肠杆菌科细菌或铜绿假单胞菌分离株对氨曲南、氨曲南/β-内酰胺酶抑制剂以及作为对照的头孢地尔的最低抑菌浓度(MIC)值。还测定了在同基因背景下携带产生不同β-内酰胺酶的重组质粒的大肠杆菌TOP10和铜绿假单胞菌PAO1的MIC值(分别为n = 22和n = 11)。使用β-内酰胺酶粗提物额外测定了上述β-内酰胺酶抑制剂的50%抑制浓度。

结果

在产MBL的肠杆菌科细菌中,氨曲南的敏感率为17.1%,而氨曲南/齐德巴坦的敏感率非常高(98.4%),氨曲南/那库巴坦(84.4%)和氨曲南/他尼硼巴坦(75%)的敏感率相对较低,相比之下氨曲南/阿维巴坦(70.3%)和头孢地尔(39.1%)。在产MBL的铜绿假单胞菌分离株中,氨曲南的敏感率为53.8%,氨曲南/那库巴坦和氨曲南/他尼硼巴坦组合的敏感率为66.7%,氨曲南/阿维巴坦、氨曲南/齐德巴坦和头孢地尔的敏感率为69.2%。

结论

总体而言,这些结果表明,包括氨曲南和新型β-内酰胺酶抑制剂(如齐德巴坦、那库巴坦或他尼硼巴坦)的联合用药对产MBL的多重耐药肠杆菌科细菌临床分离株具有非常显著的体外活性,氨曲南/齐德巴坦组合是最佳选择。另一方面,在产MBL的铜绿假单胞菌分离株中,氨曲南/齐德巴坦与氨曲南/阿维巴坦和头孢地尔相当。

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