Strategy-based design for the identification of next generation β-lactam antibiotics that evade resistance from Gram-negative pathogens.

IF 7.3 2区 医学 Q1 PHARMACOLOGY & PHARMACY
Michio Kurosu, Iván Cheng-Sánchez, Mohammad M Aboulwafa, Amro Hanora, Mohamed K El-Ashrey, Ahmad M Abbas, Mahmoud A El Hassab, Moustafa A Tageldein, Francisco Sarabia
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Abstract

Introduction: β-Lactam antibiotics have defined antibacterial chemotherapy for over eight decades and remain indispensable for the treatment of bacterial infections. Despite their clinical success, escalating antimicrobial resistance, particularly among Gram-negative pathogens, continues to impair their efficacy. This challenge has shifted the field from scaffold discovery to strategy-driven innovation aimed at overcoming firmly established resistance mechanisms.

Areas covered: This review summarizes the current landscape of β-lactam antibiotic discovery and development, with particular emphasis on strategies designed to overcome resistance in Gram-negative pathogens. The authors discuss recent advances in β-lactam antibiotics and β-lactamase inhibitors, including clinically approved agents, compounds in late-stage clinical development, and emerging approaches targeting resistant pathogens. Furthermore, they highlight the key molecular determinants of resistance that undermine current β-lactam therapies and provide perspectives on emerging opportunities for the development of next-generation β-lactam antibiotics and β-lactamase inhibitors designed to retain activity against multidrug-resistant Gram-negative pathogens.

Expert opinion: Strategies to overcome resistance in Gram-negative bacteria have established a robust foundation for the development of next-generation β-lactam antibiotics. The integration of broad-spectrum β-lactamase inhibitors, novel PBP-targeting chemotypes, enhanced outer-membrane permeation, siderophore-mediated drug delivery, and structure-guided medicinal chemistry is expected to produce β-lactam agents with improved efficacy against multidrug-resistant Gram-negative pathogens.

基于策略的新一代β-内酰胺类抗生素的鉴定,以逃避革兰氏阴性病原体的耐药。
简介:β-内酰胺类抗生素已经定义了抗菌化疗超过80年,仍然是治疗细菌感染不可或缺的。尽管它们在临床取得了成功,但不断升级的抗菌素耐药性,特别是在革兰氏阴性病原体中,继续损害其疗效。这一挑战已经将该领域从支架发现转变为旨在克服牢固建立的抗性机制的策略驱动创新。涵盖领域:本文综述了β-内酰胺类抗生素发现和开发的现状,特别强调了克服革兰氏阴性病原体耐药性的策略。作者讨论了β-内酰胺类抗生素和β-内酰胺酶抑制剂的最新进展,包括临床批准的药物,后期临床开发的化合物,以及针对耐药病原体的新方法。此外,他们强调了破坏当前β-内酰胺治疗的耐药性的关键分子决定因素,并为开发下一代β-内酰胺抗生素和β-内酰胺酶抑制剂提供了新的机会,这些抑制剂旨在保持对多重耐药革兰氏阴性病原体的活性。专家意见:克服革兰氏阴性菌耐药的策略为开发下一代β-内酰胺类抗生素奠定了坚实的基础。结合广谱β-内酰胺酶抑制剂、新型pbp靶向化学型、增强的外膜渗透、铁载体介导的药物传递和结构引导的药物化学,有望生产出对多重耐药革兰氏阴性病原体具有更高疗效的β-内酰胺药物。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
10.20
自引率
1.60%
发文量
78
审稿时长
6-12 weeks
期刊介绍: Expert Opinion on Drug Discovery (ISSN 1746-0441 [print], 1746-045X [electronic]) is a MEDLINE-indexed, peer-reviewed, international journal publishing review articles on novel technologies involved in the drug discovery process, leading to new leads and reduced attrition rates. Each article is structured to incorporate the author’s own expert opinion on the scope for future development. The Editors welcome: Reviews covering chemoinformatics; bioinformatics; assay development; novel screening technologies; in vitro/in vivo models; structure-based drug design; systems biology Drug Case Histories examining the steps involved in the preclinical and clinical development of a particular drug The audience consists of scientists and managers in the healthcare and pharmaceutical industry, academic pharmaceutical scientists and other closely related professionals looking to enhance the success of their drug candidates through optimisation at the preclinical level.
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