一种以6-磷酸葡萄糖胺合成酶为靶点的优化氨基吡咯衍生物抑制耐甲氧西林金黄色葡萄球菌。

IF 10.4 1区 化学 Q1 CHEMISTRY, MULTIDISCIPLINARY
ACS Central Science Pub Date : 2024-10-25 eCollection Date: 2024-11-27 DOI:10.1021/acscentsci.4c01167
Fusheng Guo, Fan Xiao, Hao Song, Xiaoyong Li, Yaxin Xiao, Yong Qin, Xiaoguang Lei
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引用次数: 0

摘要

耐甲氧西林金黄色葡萄球菌(MRSA)是引起临床感染的常见病原菌,已成为世界上最重要的耐药菌之一。迫切需要开发基于新型作用模式的新型抗生素来对抗日益严重的MRSA感染。Marinopyrrole A (MA)是2008年从海洋链霉菌中提取的天然产物,具有独特的双吡咯化学骨架,对MRSA具有较强的抗菌活性。然而,它的作用方式仍然是难以捉摸的。在此,我们开发了一种优化的MA衍生物MA- d1,并应用化学蛋白质组学方法发现MA- d1通过直接靶向6-磷酸葡萄糖胺合成酶(GlmS)来破坏细菌细胞壁的生物合成来发挥其抗mrsa活性。计算和实验研究表明,MA-D1在一个新的结合口袋中与GlmS的关键R381和E382残基相互作用。此外,MA-D1对MRSA治疗的耐药频率较低,对耐利奈唑胺、万古霉素或替可普宁的MRSA菌株也很敏感。MA-D1在多种动物模型中也显示出体内抗生素疗效。该研究表明,靶向GlmS开发一类新的抗生素来控制MRSA病原体感染具有很大的潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
An Optimized Marinopyrrole A Derivative Targets 6-Phosphoglucosamine Synthetase to Inhibit Methicillin-Resistant Staphylococcus aureus.

Methicillin-resistant Staphylococcus aureus (MRSA) is a common pathogenic bacterium that causes clinical infection and has become one of the most prominent antibiotic-resistant bacteria in the world. There is a pressing need to develop new antibiotics based on novel modes of action to combat increasingly severe MRSA infection. Marinopyrrole A (MA), a natural product extracted from marine Streptomyces in 2008, has a unique bipyrrole chemical skeleton and shows potent antibacterial activity against MRSA. However, its mode of action is still elusive. Herein, we developed an optimized MA derivative, MA-D1, and applied a chemoproteomic approach to reveal that MA-D1 performs its anti-MRSA activity by directly targeting 6-phosphoglucosamine synthetase (GlmS) to cause the breakdown of bacterial cell wall biosynthesis. Computational and experimental studies showed that MA-D1 interacts with the key R381 and E382 residues of GlmS in a novel binding pocket. Furthermore, MA-D1 showed a low resistance frequency for MRSA treatment and was also sensitive against the linezolid-, vancomycin-, or teicoplanin-resistant MRSA strains. MA-D1 also showed in vivo antibiotic efficacy in multiple animal models. This study demonstrates the promising potential of targeting GlmS to develop a new class of antibiotics to control MRSA pathogen infection.

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来源期刊
ACS Central Science
ACS Central Science Chemical Engineering-General Chemical Engineering
CiteScore
25.50
自引率
0.50%
发文量
194
审稿时长
10 weeks
期刊介绍: ACS Central Science publishes significant primary reports on research in chemistry and allied fields where chemical approaches are pivotal. As the first fully open-access journal by the American Chemical Society, it covers compelling and important contributions to the broad chemistry and scientific community. "Central science," a term popularized nearly 40 years ago, emphasizes chemistry's central role in connecting physical and life sciences, and fundamental sciences with applied disciplines like medicine and engineering. The journal focuses on exceptional quality articles, addressing advances in fundamental chemistry and interdisciplinary research.
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