新开发的重氮双环辛烷、硼酸衍生物和青霉素基砜类 β-内酰胺酶抑制剂对广谱 AmpC β-内酰胺酶的相对抑制活性。

IF 4.1 2区 医学 Q2 MICROBIOLOGY Antimicrobial Agents and Chemotherapy Pub Date : 2024-10-04 DOI:10.1128/aac.00775-24
Christophe Le Terrier, Patrik Mlynarcik, Mustafa Sadek, Patrice Nordmann, Laurent Poirel
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引用次数: 0

摘要

评估了重氮双环辛烷(阿维巴坦、雷贝他坦、齐德巴坦、那库巴坦、杜鲁巴坦)、硼酸衍生物(伐博巴坦、他尼博巴坦、Xeruborbactam)和青霉素基砜衍生物恩美唑巴坦对几种固有和获得性 C 类 β-内酰胺酶的相对抑制活性。与伐博巴坦和恩美唑巴坦相比,他尼巴坦、xeruborbactam 和所有二氮杂双环辛烷对大多数 AmpC 酶都表现出了有效的活性。值得注意的是,杜洛巴坦的抑制作用最为明显。有趣的是,鲍曼不动杆菌的染色体 AmpC 是对新开发的 β-内酰胺酶抑制剂最不敏感的酶。
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Relative inhibitory activities of newly developed diazabicyclooctanes, boronic acid derivatives, and penicillin-based sulfone β-lactamase inhibitors against broad-spectrum AmpC β-lactamases.

The relative inhibitory activities of diazabicyclooctanes (avibactam, relebactam, zidebactam, nacubactam, durlobactam), boronic acid derivatives (vaborbactam, taniborbactam, xeruborbactam), and penicillin-based sulfone derivative enmetazobactam were evaluated against several intrinsic and acquired class C β-lactamases. By contrast to vaborbactam and enmetazobactam, taniborbactam, xeruborbactam, and all diazabicyclooctanes demonstrated effective activities against most AmpC enzymes. Notably, durlobactam exhibited the most pronounced inhibitory effect. Interstingly, the chromosomal AmpC of Acinetobacter baumannii was the least sensitive enzyme to the newly developed β-lactamase inhibitors.

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来源期刊
CiteScore
10.00
自引率
8.20%
发文量
762
审稿时长
3 months
期刊介绍: Antimicrobial Agents and Chemotherapy (AAC) features interdisciplinary studies that build our understanding of the underlying mechanisms and therapeutic applications of antimicrobial and antiparasitic agents and chemotherapy.
期刊最新文献
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