College of Pharmacy, Jinan University, Guangzhou 510632, P. R. China.
J Med Chem. 2024 Nov 14;67(21):18911-18929. doi: 10.1021/acs.jmedchem.4c01253. Epub 2024 Oct 23.
The release of virulence factors and biofilm formation by are pivotal drivers of its severe pathogenicity and antibiotic resistance. Based on our prior findings, cyclic di-GMP (c-di-GMP) G-quadruplex inducers are promising biofilm inhibitors and that quorum sensing systems are central regulators of virulence, we aimed to design and synthesize c-di-GMP G-quadruplex inducer-quorum sensing inhibitor hybrids. These hybrids were envisioned as bifunctional agents with both antibiofilm and antivirulence capabilities. Hybrids and , characterized by their quinoline and 3-indole rings, emerged as potent inhibitors. They achieve this dual action by inducing c-di-GMP G-quadruplex formation and disrupting the and signaling system. Additionally, hybrids and attenuated virulence factors and inhibited the motility phenotypes of . Furthermore, when tested in infection models, these hybrids, in combination with antibiotics such as tetracycline, improved survival rates, all while maintaining a favorable biosafety profile.
产毒因子的释放和生物膜的形成是其严重致病性和抗生素耐药性的关键驱动因素。基于我们之前的研究结果,环二鸟苷酸(c-di-GMP)G-四链体诱导剂是很有前途的生物膜抑制剂,而群体感应系统是毒力的中央调节器,我们旨在设计和合成 c-di-GMP G-四链体诱导剂-群体感应抑制剂杂合体。这些杂种被设想为具有双重功能的抗菌生物膜和抗病毒能力的药物。由喹啉和 3-吲哚环组成的杂种 和 表现出很强的抑制作用。它们通过诱导 c-di-GMP G-四链体形成和破坏 系统和 信号系统来实现这双重作用。此外,杂种 和 还能减弱毒力因子,并抑制 的运动表型。此外,当在 感染模型中进行测试时,这些杂种与四环素等抗生素联合使用,提高了存活率,同时保持了良好的生物安全性。