Exploration of membrane-active cephalosporin derivatives as potent antibacterial agents against Staphylococcus aureus biofilms and persisters

IF 5.9 2区 医学 Q1 CHEMISTRY, MEDICINAL European Journal of Medicinal Chemistry Pub Date : 2025-03-10 DOI:10.1016/j.ejmech.2025.117484
Shengcong Chen , Ye Qu , Ruirui Li , Maxwell Ampomah-Wireko , Hongtao Kong , Daran Li , Meng Wang , Chen Gao , Shangshang Qin , Jifeng Liu , Zhenya Wang , Muchen Zhang , En Zhang
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Abstract

Developing innovative antimicrobial agents is essential in the fight against drug-resistant bacteria, as well as biofilms and persistent bacteria. In this study, four series of amphiphilic cephalosporin derivatives were synthesized. Most of the compounds showed good activity against Gram-positive bacteria, among which membrane-active cephalosporin 15e showed high activity against Staphylococcus aureus. Furthermore, 15e can maintain antimicrobial activity in mammalian body fluids and does not develop detectable resistance. Antibacterial mechanism studies demonstrated that the compound 15e can destroy the bacterial cell membrane, causing leakage of intracellular nucleic acids and proteins. Moreover, it can also suppress bacterial metabolic activity and induce the accumulation of reactive oxygen species (ROS) in the bacteria. Of greater significance, compound 15e effectively prevented the formation of biofilms and eradicated established biofilms and persister cells. Notably, compound 15e exhibited potent in vivo antibacterial efficacy, which was better than cephalothin. These findings suggest that 15e has a potential to become a drug candidate for treating bacterial infections.

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探索膜活性头孢菌素衍生物作为抗金黄色葡萄球菌生物膜和顽固菌的强效抗菌剂
开发创新的抗菌剂对于对抗耐药细菌以及生物膜和持久性细菌至关重要。本研究合成了四个系列的两亲性头孢菌素衍生物。大部分化合物对革兰氏阳性菌具有良好的抑菌活性,其中膜活性头孢菌素15e对金黄色葡萄球菌具有较高的抑菌活性。此外,15e可以在哺乳动物体液中保持抗菌活性,不会产生可检测到的耐药性。抗菌机制研究表明,化合物15e可破坏细菌细胞膜,引起细胞内核酸和蛋白质的渗漏。此外,它还可以抑制细菌的代谢活性,诱导细菌体内活性氧(ROS)的积累。更重要的是,化合物15e有效地阻止了生物膜的形成,并根除了已形成的生物膜和持久性细胞。值得注意的是,化合物15e具有较强的体内抗菌作用,优于头孢菌素。这些发现表明,15e有可能成为治疗细菌感染的候选药物。
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来源期刊
CiteScore
11.70
自引率
9.00%
发文量
863
审稿时长
29 days
期刊介绍: The European Journal of Medicinal Chemistry is a global journal that publishes studies on all aspects of medicinal chemistry. It provides a medium for publication of original papers and also welcomes critical review papers. A typical paper would report on the organic synthesis, characterization and pharmacological evaluation of compounds. Other topics of interest are drug design, QSAR, molecular modeling, drug-receptor interactions, molecular aspects of drug metabolism, prodrug synthesis and drug targeting. The journal expects manuscripts to present the rational for a study, provide insight into the design of compounds or understanding of mechanism, or clarify the targets.
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