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通过青霉素结合蛋白修饰介导的ESKAPE病原体中的β-内酰胺耐药性:综述

β-Lactam Resistance in ESKAPE Pathogens Mediated Through Modifications in Penicillin-Binding Proteins: An Overview.

作者信息

Sethuvel Dhiviya Prabaa Muthuirulandi, Bakthavatchalam Yamuna Devi, Karthik Maruthan, Irulappan Madhumathi, Shrivastava Rahul, Periasamy Hariharan, Veeraraghavan Balaji

机构信息

Department of Clinical Microbiology, Christian Medical College, Vellore, 632004, India.

Wockhardt Research Centre, Aurangabad, India.

出版信息

Infect Dis Ther. 2023 Mar;12(3):829-841. doi: 10.1007/s40121-023-00771-8. Epub 2023 Mar 6.

Abstract

Bacteria acquire β-lactam resistance through a multitude of mechanisms among which production of β-lactamases (enzymes that hydrolyze β-lactams) is the most common, especially in Gram-negatives. Structural changes in the high-molecular-weight, essential penicillin-binding proteins (PBPs) are widespread in Gram-positives and increasingly reported in Gram-negatives. PBP-mediated resistance is largely achieved by accumulation of mutation(s) resulting in reduced binding affinities of β-lactams. Herein, we discuss PBP-mediated resistance among ESKAPE pathogens that cause diverse hospital- and community-acquired infections globally.

摘要

细菌通过多种机制获得β-内酰胺抗性,其中β-内酰胺酶(水解β-内酰胺的酶)的产生最为常见,尤其是在革兰氏阴性菌中。高分子量必需青霉素结合蛋白(PBPs)的结构变化在革兰氏阳性菌中广泛存在,在革兰氏阴性菌中的报道也越来越多。PBP介导的抗性主要是通过积累突变导致β-内酰胺的结合亲和力降低来实现的。在此,我们讨论了在全球范围内引起各种医院获得性和社区获得性感染的ESKAPE病原体中PBP介导的抗性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d81d/10017896/26fcda953c46/40121_2023_771_Fig1_HTML.jpg

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