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对铜绿假单胞菌中导致头孢他啶/他唑巴坦耐药的突变所驱动的亚胺培南交叉耐药性的生化研究。

Biochemical Insights into Imipenem Collateral Susceptibility Driven by Mutations Conferring Ceftolozane/Tazobactam Resistance in Pseudomonas aeruginosa.

机构信息

Servicio de Microbiología, Hospital Universitario Son Espases, Instituto de Investigación Sanitaria Illes Balears (IdISBa), Palma de Mallorca, Spain.

Department of Microbiology, University of Manitoba, Winnipeg, Manitoba, Canada.

出版信息

Antimicrob Agents Chemother. 2023 Feb 16;67(2):e0140922. doi: 10.1128/aac.01409-22. Epub 2023 Jan 30.

Abstract

Several Pseudomonas aeruginosa AmpC mutants have emerged that exhibit enhanced activity against ceftazidime and ceftolozane, while also evading inhibition by avibactam. Interestingly, P. aeruginosa strains harboring these AmpC mutations fortuitously exhibit enhanced carbapenem susceptibility. This acquired susceptibility was investigated by comparing the degradation of imipenem by wild-type and cephalosporin-resistant AmpC. We show that cephalosporin-resistant AmpC enzymes lose their efficacy for hydrolyzing imipenem and suggest that this may be due to their increased flexibility and dynamics relative to the wild type.

摘要

几种铜绿假单胞菌 AmpC 突变体已经出现,它们对头孢他啶和头孢洛扎烷的活性增强,同时逃避了阿维巴坦的抑制。有趣的是,携带这些 AmpC 突变的铜绿假单胞菌菌株偶然表现出对碳青霉烯类药物的敏感性增强。通过比较野生型和头孢菌素耐药 AmpC 对亚胺培南的降解,研究了这种获得性敏感性。我们表明,头孢菌素耐药 AmpC 酶失去了水解亚胺培南的效力,这可能是由于它们相对于野生型的柔韧性和动力学增加所致。

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