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解锁氨基糖苷类抗生素对铜绿假单胞菌的增强疗效。

Unlocking Enhanced Efficacy of Aminoglycoside Antibiotics Against Pseudomonas aeruginosa.

作者信息

Tawiah Patrick Ofori, Sultana Sadia, Dahl Jan-Ulrik

机构信息

School of Biological Sciences, Microbiology, Illinois State University, Normal, Illinois, USA.

出版信息

Microb Biotechnol. 2025 Jun;18(6):e70174. doi: 10.1111/1751-7915.70174.

Abstract

Infectious diseases continue to be a global health burden. Among the major human pathogens is the Gram-negative bacterium Pseudomonas aeruginosa, which is particularly due to its wide range of drug resistance mechanisms. Aminoglycosides, which have long been used in treating pseudomonal infections, are increasingly undermined by resistance. This opinion article discusses the use and challenges of aminoglycosides against P. aeruginosa and highlights recent strategies that enhance aminoglycoside efficacy. These include combinational therapies, metabolic stimulants/adjuvants, silver, and more recently developed derivatives such as AGXX, many of which have been reported to potentiate the cytotoxic effects of aminoglycosides and re-sensitise aminoglycoside-resistant strains. While these findings pave the way for future therapies, the clinical relevance of many in vitro studies remains to be investigated.

摘要

传染病仍然是全球健康负担。革兰氏阴性菌铜绿假单胞菌是主要的人类病原体之一,这尤其归因于其广泛的耐药机制。长期以来用于治疗铜绿假单胞菌感染的氨基糖苷类药物,正越来越多地受到耐药性的影响。这篇观点文章讨论了氨基糖苷类药物针对铜绿假单胞菌的应用及挑战,并强调了提高氨基糖苷类药物疗效的最新策略。这些策略包括联合疗法、代谢刺激剂/佐剂、银,以及最近开发的衍生物如AGXX,其中许多已被报道可增强氨基糖苷类药物的细胞毒性作用并使耐氨基糖苷类菌株重新敏感。虽然这些发现为未来的治疗铺平了道路,但许多体外研究的临床相关性仍有待研究。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d44a/12124998/7d7a8b28a0ee/MBT2-18-e70174-g002.jpg

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