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当代临床分离株中对舒巴坦-多尼培南耐药的分子驱动因素。

Molecular drivers of resistance to sulbactam-durlobactam in contemporary clinical isolates of .

机构信息

Innoviva Specialty Therapeutics Inc., an affiliate of Entasis Therapeutics Inc. , Waltham, Massachusetts, USA.

Kemyth Biotech Co., Ltd. , Taipei City, Taiwan.

出版信息

Antimicrob Agents Chemother. 2023 Nov 15;67(11):e0066523. doi: 10.1128/aac.00665-23. Epub 2023 Oct 16.

Abstract
  • complex (ABC) causes severe infections that are difficult to treat due to pre-existing antibiotic resistance. Sulbactam-durlobactam (SUL-DUR) is a targeted β-lactam/β-lactamase inhibitor combination antibiotic designed to treat serious infections caused by , including multidrug- and carbapenem-resistant strains. In a recent global surveillance study of 5,032 ABC clinical isolates collected from 2016 to 2021, less than 2% of ABC isolates had SUL-DUR MIC values >4 µg/mL. Molecular characterization of these isolates confirmed the primary drivers of resistance are metallo-β-lactamases or penicillin-binding protein 3 (PBP3) mutations, as previously described. In addition, this study shows that certain common PBP3 variants, such as A515V, are insufficient to confer sulbactam resistance and that the efflux of durlobactam by AdeIJK is likely to play a role in a subset of strains.
摘要

(ABC)复合体导致严重感染,由于先前存在抗生素耐药性,这些感染难以治疗。舒巴坦-多鲁巴坦(SUL-DUR)是一种靶向β-内酰胺/β-内酰胺酶抑制剂联合抗生素,旨在治疗由 引起的严重感染,包括多药和碳青霉烯类耐药株。在最近一项对 2016 年至 2021 年期间收集的 5032 株 ABC 临床分离株的全球监测研究中,不到 2%的 ABC 分离株的 SUL-DUR MIC 值>4μg/ml。对这些分离株的分子特征分析证实,先前已描述的耐药主要驱动因素是金属β-内酰胺酶或青霉素结合蛋白 3(PBP3)突变。此外,这项研究表明,某些常见的 PBP3 变体,如 A515V,不足以赋予舒巴坦耐药性,并且 AdeIJK 对多鲁巴坦的外排可能在部分菌株中起作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7c90/10648852/779a3a910384/aac.00665-23.f001.jpg

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