铁载体的产生及其作为治疗剂的作用

Ayaz Ahmed, S. Kazmi
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引用次数: 0

摘要

铁载体是铁螯合剂,是细菌在生长所需的缺铁条件下产生的。因此,铁载体可以作为一种载体,将药物引导到细菌中并杀死它们。本研究旨在筛选不同细菌在缺铁培养基中产生的铁载体及其杀死耐药细菌的协同能力。用氮铬S (CAS)法测定缺铁条件下的铁载体。采用肉汤微量稀释法和棋盘法测定所选药物或未食子儿茶素没食子酸酯(EGCG)单独或与合成铁载体联合使用的抗菌性能。结果表明,在缺乏铁的条件下,所有被试微生物都产生了铁载体,CAS琼脂板上的橙色晕带证明了这一点。革兰氏阴性菌比革兰氏阳性菌(13-15mm)产生更多的铁载体,其细菌带抑制为17-22mm,橙色反映。与抗生素和EGCG相比,乙酰羟肟酸(aHa;合成铁载体(1500 ~ 6500µg/ml)无抗菌作用。aHa与四环素、头孢曲松、EGCG (FIC指数<0.5)对伤寒葡萄球菌、耐甲氧西林和敏感金黄色葡萄球菌、大肠杆菌的协同作用明显。总之,铁载体可能被认为是设计针对新出现的抗菌素耐药病原体的不同联合治疗的潜在候选者。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Siderophore Production and its Role as Therapeutic Agent
Siderophores are iron chelators, which are produced by bacteria under iron-deficient conditions required for their growth. Therefore, siderophores can be used as a carrier to direct drugs into the bacteria and kill them. The present study was designed to screen siderophore production using different bacteria using an iron-deficient medium and its synergistic capability to kill drug-resistant bacteria. Siderophore under iron-deprived condition was evaluated by chrome azurol S (CAS) assay. Whereas, broth micro-dilution method and checkerboard assay were used to determine the antimicrobial properties of selected drugs or epigallocatechin gallate (EGCG) individually or in combination with synthetic siderophore. Results demonstrated that the entire tested microorganisms produced siderophore under the iron-deprived condition as evidenced by orange halo zones in CAS agar plates.  Gram-negative bacteria produced more siderophores as reflected by orange color with bacterial zone inhibition of 17-22mm as compared to Gram-positive bacteria (13-15mm). As compared to antibiotics and EGCG, acetohydroxamic acid (aHa; synthetic siderophore) showed no antibacterial properties (1500 - 6500 µg/ml). The synergism of aHa with tetracycline, ceftriaxone, and EGCG (FIC index <0.5) against S. typhi, methicillin-resistant and sensitive Staphylococcus aureus, and E. coli were evident. In conclusion, siderophore may be considered a potential candidate to design different combination therapy against emerging antimicrobial-resistant pathogens.
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