Li Haotian, Zhu Xiaojing, Zhang Xing, Dong Changjiang
School of Pharmaceutical Sciences, Wuhan University, Wuhan, China.
Key Laboratory of Combinatorial Biosynthesis and Drug Discovery, Ministry of Education and School of Pharmaceutical Sciences, Wuhan University, Wuhan, China.
Front Microbiol. 2024 Aug 15;15:1447485. doi: 10.3389/fmicb.2024.1447485. eCollection 2024.
Developing antibiotic adjuvants is an effective strategy to combat antimicrobial resistance (AMR). The envelope of Gram-negative bacteria (GNB) is a barrier to prevent the entry of antibiotics, making it an attractive target for novel antibiotic and adjuvant development.
In this study, we identified Caspofungin acetate (CAS) as an antibiotic adjuvant against GNB in the repurposing screen of 3,158 FDA-approved drugs. Checkerboard assays suggested that CAS could enhance the antimicrobial activity of rifampin or colistin against various GNB strains , Moreover, larvae infection model also indicated that CAS significantly potentiated the efficacy of rifampin against multidrug-resistant 72 strain . Most importantly, resistance development assay showed that CAS was less susceptible to accelerating the resistance development of drug-sensitive strain MG1655. Functional studies and RNA-seq analysis confirmed that the mechanisms by which CAS enhanced the antimicrobial activities of antibiotics were involved in permeabilizing the bacterial cell envelope, disrupting proton motive force and inhibiting bacterial biofilm formation. Additionally, it has been found that PgaC is the CAS target and enzymatic assay has confirmed the inhibition activity.
Our results illustrate the feasibility of CAS as an antibiotic adjuvant against GNB, which is an alternative strategy of anti-infection.
开发抗生素佐剂是对抗抗菌药物耐药性(AMR)的有效策略。革兰氏阴性菌(GNB)的包膜是防止抗生素进入的屏障,使其成为新型抗生素和佐剂开发的有吸引力的靶点。
在本研究中,我们在对3158种FDA批准药物的重新筛选中确定醋酸卡泊芬净(CAS)为针对GNB的抗生素佐剂。棋盘法试验表明,CAS可增强利福平或黏菌素对各种GNB菌株的抗菌活性。此外,幼虫感染模型也表明,CAS显著增强了利福平对多重耐药72菌株的疗效。最重要的是,耐药性发展试验表明,CAS不太容易加速药物敏感菌株MG1655的耐药性发展。功能研究和RNA测序分析证实,CAS增强抗生素抗菌活性的机制涉及使细菌细胞膜通透性增加、破坏质子动力势和抑制细菌生物膜形成。此外,已发现PgaC是CAS的靶点,酶活性测定证实了其抑制活性。
我们的结果说明了CAS作为针对GNB的抗生素佐剂的可行性,这是一种抗感染的替代策略。