Citrinin Is a Potential Quorum Sensing Inhibitor against Pseudomonas aeruginosa

被引:5
作者
Ji, Hongrui [1 ,2 ,3 ,4 ]
Zhao, Lu [1 ,2 ,3 ,4 ]
Lv, Kaiwen [1 ,2 ,3 ,4 ]
Zhang, Yuzhu [1 ,2 ,3 ,4 ]
Gao, Haibo [1 ,2 ,3 ,4 ]
Gong, Qianhong [1 ,2 ,3 ,4 ]
Yu, Wengong [1 ,2 ,3 ,4 ]
机构
[1] Ocean Univ China, Sch Med & Pharm, 5 Yushan Rd, Qingdao 266003, Peoples R China
[2] Qingdao Natl Lab Marine Sci & Technol, Lab Marine Drugs & Bioprod, 1 Wenhai Rd, Qingdao 266237, Peoples R China
[3] Ocean Univ China, Sch Med & Pharm, Chinese Minist Educ, Key Lab Marine Drugs, 5 Yushan Rd, Qingdao 266003, Peoples R China
[4] Ocean Univ China, Prov Key Lab Glycoscience & Glycotechnol, 5 Yushan Rd, Qingdao 266003, Peoples R China
基金
中国国家自然科学基金;
关键词
Pseudomonas aeruginosa; quorum sensing inhibitors; marine fungi; Penicillium sp; JH1; citrinin; BIOFILM FORMATION; BIOSYNTHESIS; MYCOTOXINS; PRODUCTS; ALGINATE;
D O I
10.3390/md21050296
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Pseudomonas aeruginosa is an opportunistic pathogen that infects patients by regulating virulence factors and biofilms through a quorum sensing (QS) system to protect itself from antibiotics and environmental stress. Therefore, the development of quorum sensing inhibitors (QSIs) is expected to become a new strategy for studying drug resistance to P. aeruginosa infections. Marine fungi are valuable resources for screening QSIs. A marine fungus, Penicillium sp. JH1, with anti-QS activity was isolated from the offshore waters of Qingdao (China), and citrinin, a novel QSI, was purified from secondary metabolites of this fungus. Citrinin could significantly inhibit the production of violacein in Chromobacterium violaceum CV12472 and the production of three virulence factors (elastase, rhamnolipid and pyocyanin) in P. aeruginosa PAO1. It could also inhibit the biofilm formation and motility of PAO1. In addition, citrinin downregulated the transcript levels of nine genes (lasI, rhlI, pqsA, lasR, rhlR, pqsR, lasB, rhlA and phzH) associated with QS. Molecular docking results showed that citrinin bound to PqsR and LasR with better affinity than the natural ligands. This study laid a foundation for the further study of the structure optimization and structure-activity relationship of citrinin.
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页数:15
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