Suppr超能文献

两种新型天然产物,即切氏萜类化合物B和切氏萜类化合物B裂环酸甲酯,对铜绿假单胞菌的多方面抗病原活性

Multifaceted Antipathogenic Activity of Two Novel Natural Products, Chermesiterpenoid B and Chermesiterpenoid B Seco Acid Methyl Ester, Against Pseudomonas aeruginosa.

作者信息

Li Dan-Dan, Wang Ying, Li Huiyan, Niu Wen-Xin, Hong Jongki, Jung Jee H, Lee Joon-Hee

机构信息

College of Pharmacy, Pusan National University, Busan, Republic of Korea.

Research Institute for Drug Development, Pusan National University, Busan, Republic of Korea.

出版信息

Microb Biotechnol. 2025 Feb;18(2):e70101. doi: 10.1111/1751-7915.70101.

Abstract

Pseudomonas aeruginosa is an opportunistic human pathogen that causes both acute and chronic infections due to its virulence factors, biofilm formation and the ability to suppress the host immune system. Quorum sensing (QS) plays a key role in regulating these pathogenic traits and also downregulates the expression of peroxisome proliferator-activated receptor-γ (PPAR-γ) in host cells. In this study, we isolated two novel natural products from the jellyfish-derived fungus Penicillium chermesinum, chermesiterpenoid B (Che B) seco acid methyl ester (Che B ester) and Che B. Both compounds act as partial agonists of PPAR-γ and exhibit anti-QS activity. Che B ester and Che B were found to inhibit biofilm formation, reduce the production of proteases and decrease the infectivity of P. aeruginosa, all without affecting bacterial growth. In host cells, Che B ester and Che B reduced P. aeruginosa-induced inflammation by activating PPAR-γ. This multifaceted function makes these compounds promising candidates for developing new antipathogenic agents against bacterial infections with few side effects.

摘要

铜绿假单胞菌是一种机会性人类病原体,由于其毒力因子、生物膜形成以及抑制宿主免疫系统的能力,可导致急性和慢性感染。群体感应(QS)在调节这些致病特性中起关键作用,并且还下调宿主细胞中过氧化物酶体增殖物激活受体-γ(PPAR-γ)的表达。在本研究中,我们从水母来源的真菌短柄青霉中分离出两种新型天然产物,短柄萜类化合物B(Che B)癸二酸甲酯(Che B酯)和Che B。这两种化合物均作为PPAR-γ的部分激动剂,并表现出抗群体感应活性。发现Che B酯和Che B可抑制生物膜形成、减少蛋白酶的产生并降低铜绿假单胞菌的感染性,且所有这些均不影响细菌生长。在宿主细胞中,Che B酯和Che B通过激活PPAR-γ减轻铜绿假单胞菌诱导的炎症。这种多方面的功能使这些化合物成为开发具有很少副作用的新型抗细菌感染致病药物的有前景的候选物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fad0/11815713/db8fe7e719fc/MBT2-18-e70101-g008.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验