Issue 11, 2024

Metal chelation as an antibacterial strategy for Pseudomonas aeruginosa and Acinetobacter baumannii

Abstract

It is estimated that by 2050, bacterial infections will cause 1.8 million more deaths than cancer annually, and the current lack of antibiotic drug discovery is only exacerbating the crisis. Two pathogens in particular, Gram-negative bacteria A. baumannii and P. aeruginosa, are of grave concern because of their heightened multi-drug resistance due to a dense, impermeable outer membrane. However, targeting specific cellular processes may prove successful in overcoming bacterial resistance. This review will concentrate on a novel approach to combatting pathogenicity by disarming bacteria through the disruption of metal homeostasis to reduce virulence and enhance antibiotic uptake. The varying levels of success in bringing metallophores to clinical trials, with currently only one FDA-approved siderophore antibiotic to date, will also be detailed.

Graphical abstract: Metal chelation as an antibacterial strategy for Pseudomonas aeruginosa and Acinetobacter baumannii

Article information

Article type
Review Article
Submitted
24 Jul 2024
Accepted
23 Sep 2024
First published
24 Sep 2024
This article is Open Access
Creative Commons BY license

RSC Chem. Biol., 2024,5, 1083-1096

Metal chelation as an antibacterial strategy for Pseudomonas aeruginosa and Acinetobacter baumannii

M. M. Golden, A. C. Heppe, C. L. Zaremba and W. M. Wuest, RSC Chem. Biol., 2024, 5, 1083 DOI: 10.1039/D4CB00175C

This article is licensed under a Creative Commons Attribution 3.0 Unported Licence. You can use material from this article in other publications without requesting further permissions from the RSC, provided that the correct acknowledgement is given.

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