细菌细胞中的铁代谢:从生理意义到一类新的抗菌药物

A. Kozlov, A. Lyamin, A. V. Zhestkov, O. Gusyakova, A. Khaliulin
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引用次数: 2

摘要

由洋葱伯克霍尔德菌复合菌引起的呼吸道感染并发症是囊性纤维化患者死亡的主要原因。天然和获得性耐药机制允许洋葱伯克霍尔德菌复合病原体适应常规抗生素治疗的条件,这就需要使用具有替代作用机制的抗菌药物。对铁在细菌代谢中的重要作用以及从环境中获取铁的方法的研究,促成了一种新的抗生素——头孢菌素的开发。在头孢地醇的结构中,形成了一个类似铁载体的片段,铁载体是一种螯合分子,确保铁离子运输到微生物的内部环境中。一种独特的机制,在科学文献中被描述为“特洛伊木马”,允许抗生素分子与铁载体结合,有效地渗透到细菌细胞中,发挥杀菌作用。因此,头孢地罗可用于治疗由洋葱伯克霍尔德菌复合体(包括耐多药菌株)引起的囊性纤维化患者肺部的感染性并发症。此外,头孢地罗的活性谱允许使用这种抗生素治疗由医院内的革兰氏阴性细菌引起的感染,如肠杆菌、不动杆菌、假单胞菌和窄养单胞菌。
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Iron metabolism in bacterial cells: from physiological significance to a new class of antimicrobial agents
Infectious complications in the respiratory tract caused by microorganisms from the Burkholderia cepacia complex are the main cause of death among patients with cystic fibrosis. Natural and acquired resistance mechanisms allow Burkholderia cepacia complex pathogens to adapt to the conditions of regular antibiotic therapy, which necessitates the use of antibacterial drugs with an alternative mechanism of action. Studies on the importance of iron as an essential factor in the metabolism of bacteria and methods of its acquisition from the environment contributed to the development of a new antibiotic from a number of cephalosporins – cefiderocol. In the structure of cefiderocol, a fragment is formed that imitates siderophores – chelating molecules that ensure the transport of iron ions into the internal environment of the microorganism. A unique mechanism, described in the scientific literature as a “Trojan horse”, allows antibiotic molecules conjugated with siderophores to effectively penetrate into the bacterial cell, exerting a bactericidal effect. Thus, cefiderocol can be used to treat infectious complications in the lungs of patients with cystic fibrosis caused by bacteria from the Burkholderia cepacia complex, including multidrug-resistant strains. In addition, the spectrum of activity of cefiderocol allows the use of this antibiotic in the treatment of infections caused by nosocomial gram-negative bacteria such as Enterobacterales, Acinetobacter, Pseudomonas and Stenotrophomonas.
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