LEPABE - Laboratory for Process Engineering, Environment, Biotechnology and Energy, Faculty of Engineering, University of Porto, Rua Dr. Roberto Frias, 4200-465 Porto, Portugal; CIQUP - Department of Chemistry and Biochemistry, Faculty of Sciences, University of Porto, Rua do Campo Alegre, 4169-007 Porto, Portugal.
LEPABE - Laboratory for Process Engineering, Environment, Biotechnology and Energy, Faculty of Engineering, University of Porto, Rua Dr. Roberto Frias, 4200-465 Porto, Portugal.
J Adv Res. 2022 Jul;39:89-101. doi: 10.1016/j.jare.2021.10.010. Epub 2021 Nov 1.
Bacterial infections involving multidrug-resistant Gram-negative bacteria have become critically involved in the current antibiotic crisis. This, together with the bacterial evolution ability, prioritizes the discovery of new antibiotics. Research on microbial iron acquisition pathways and metabolites, particularly siderophores, has highlighted hopeful aspects for the design of advanced antimicrobial approaches. Moreover, exploiting siderophores machinery to treat diseases associated with iron overload and cancer is of additional interest for the therapeutic arena.
This review highlights and provides a renewed perspective on the evolutionary path of siderophores, from primordial siderophores to new iron chelating agents, stimulating the field to build on the past and shape the future.
The effectiveness of siderophore-mimicking antibiotics appears to be high and selective for Gram-negative pathogens, rendering multidrug-resistant (MDR) bacteria susceptible to killing. Herein, cefiderocol, a new siderophore antibiotic, is well positioned in the clinic to treat MDR infections instigated by Gram-negative bacteria, particularly urinary tract infections and pneumonia. This siderophore has a mode of action based on a "Trojan horse" strategy, using the iron uptake systems for efficient bacterial penetration and killing. Recent progress has also been achieved concerning new iron chelating compounds to treat diseases associated with iron overload and cancer. Though these compounds still face great challenges for a clinical application, their promising results open up new doors for the design and development of innovative iron chelating compounds, taking benefit from the structurally diverse nature of siderophores.
涉及多重耐药革兰氏阴性菌的细菌感染已成为当前抗生素危机的关键问题。再加上细菌的进化能力,这就优先需要发现新的抗生素。对微生物铁获取途径和代谢物(尤其是铁载体)的研究为设计先进的抗菌方法提供了有希望的方面。此外,利用铁载体机制来治疗与铁过载和癌症相关的疾病,在治疗领域具有额外的意义。
本文重点介绍并提供了铁载体进化途径的新视角,从原始铁载体到新型铁螯合剂,激发了该领域在过去的基础上构建未来的灵感。
铁载体模拟抗生素的有效性似乎很高,对革兰氏阴性病原体具有选择性,使多药耐药(MDR)细菌容易被杀死。在此,新型铁载体抗生素头孢他啶在临床上具有良好的定位,可以治疗由革兰氏阴性细菌引起的 MDR 感染,特别是尿路感染和肺炎。这种铁载体的作用机制基于“特洛伊木马”策略,利用铁摄取系统进行有效的细菌穿透和杀伤。最近在治疗与铁过载和癌症相关的疾病的新型铁螯合化合物方面也取得了进展。尽管这些化合物在临床应用方面仍面临巨大挑战,但它们有前景的结果为设计和开发创新的铁螯合化合物开辟了新的途径,利用铁载体的结构多样性从中受益。