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海洋菌株NBUD24产生的蒽醌类化合物对耐甲氧西林金黄色葡萄球菌的抗菌及抗生物被膜活性

Antimicrobial and Antibiofilm Activity of Marine sp. NBUD24-Derived Anthraquinones Against MRSA.

作者信息

Yang Yuxin, Zhou Zhiyan, Huang Guobao, Yang Shuhua, Mao Ruoyu, Ding Lijian, Wang Xiao

机构信息

Health Science Center, Ningbo University, Ningbo 315211, China.

Gene Engineering Laboratory, Feed Research Institute, Chinese Academy of Agricultural Sciences, Beijing 100081, China.

出版信息

Mar Drugs. 2025 Jul 25;23(8):298. doi: 10.3390/md23080298.

Abstract

Antimicrobial resistance (AMR) has emerged as a global health crisis, with methicillin-resistant (MRSA) representing one of the most clinically significant multidrug-resistant pathogens. In this study, three structurally unique anthracycline derivatives-keto-ester (), 4-deoxy-ε-pyrromycinone (), and misamycin ()-were first isolated and characterized from the fermentation broth of the marine-derived NBUD24. These compounds exhibited notable antibacterial efficacy against MRSA, with minimum inhibitory concentrations (MICs) ranging from 16 to 32 µg/mL. Cytotoxicity assays confirmed their safety profile at therapeutic concentrations. The biofilm formation assay demonstrated that 4-deoxy-ε-pyrromycinone inhibited biofilm formation of MRSA ATCC43300, with an inhibition rate of 64.4%. Investigations of antibacterial mechanisms revealed that these compounds exert antibacterial effects primarily through disruption of bacterial cell wall integrity and destruction of DNA structure. These findings underscore the potential of marine-derived microbial metabolites as promising scaffolds for developing next-generation antimicrobial candidates to combat drug-resistant infections.

摘要

抗菌耐药性(AMR)已成为一场全球健康危机,耐甲氧西林金黄色葡萄球菌(MRSA)是临床上最重要的多重耐药病原体之一。在本研究中,首次从海洋来源的NBUD24发酵液中分离并鉴定出三种结构独特的蒽环类衍生物——酮酯()、4-脱氧-ε-吡咯霉素酮()和米萨霉素()。这些化合物对MRSA表现出显著的抗菌效果,最低抑菌浓度(MIC)范围为16至32µg/mL。细胞毒性试验证实了它们在治疗浓度下的安全性。生物膜形成试验表明,4-脱氧-ε-吡咯霉素酮抑制MRSA ATCC43300生物膜的形成,抑制率为64.4%。抗菌机制研究表明,这些化合物主要通过破坏细菌细胞壁完整性和破坏DNA结构发挥抗菌作用。这些发现强调了海洋来源的微生物代谢产物作为开发下一代抗微生物候选药物以对抗耐药感染的有前景支架的潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/64d8/12387178/d3f92ef7eeef/marinedrugs-23-00298-g001.jpg

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