奥兰诺芬
铜绿假单胞菌
毒力
生物膜
群体感应
微生物学
粘菌素
化学
抗生素
毒力因子
生物
细菌
生物化学
免疫学
基因
遗传学
类风湿性关节炎
作者
Joey Kuok Hoong Yam,L.Z.W. Tan,Ziyan Hong,May Margarette Santillan Salido,Bau Yi Woo,Adeline Mei Hui Yong,Casandra Ai Zhu Tan,Sam Fong Yau Li,Liang Yang,Michael Givskov,Shu‐Sin Chng
标识
DOI:10.1016/j.bmc.2023.117167
摘要
Pseudomonas aeruginosa is widely attributed as the leading cause of hospital-acquired infections. Due to intrinsic antibiotic resistance mechanisms and the ability to form biofilms, P. aeruginosa infections are challenging to treat. P. aeruginosa employs multiple virulence mechanisms to establish infections, many of which are controlled by the global virulence regulator Vfr. An attractive strategy to combat P. aeruginosa infections is thus the use of anti-virulence compounds. Here, we report the discovery that FDA-approved drug auranofin attenuates virulence pathways in P. aeruginosa, including quorum sensing (QS) and Type IV pili (TFP). We show that auranofin acts via multiple targets, one of which being Vfr. Consistent with inhibition of QS and TFP expression, we show that auranofin attenuates biofilm maturation, and when used in combination with colistin, displays strong synergy in eradicating P. aeruginosa biofilms. Auranofin may have immediate applications as an anti-virulence drug against P. aeruginosa infections.
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