Inhibition of gold nanoparticles (AuNPs) on pathogenic biofilm formation and invasion to host cells

被引:146
作者
Yu, Qilin [1 ]
Li, Jianrong [1 ]
Zhang, Yueqi [1 ]
Wang, Yufan [2 ]
Liu, Lu [3 ]
Li, Mingchun [1 ]
机构
[1] Nankai Univ, Dept Microbiol, Key Lab Mol Microbiol & Technol, Minist Educ, Tianjin 300071, Peoples R China
[2] Tianjin Third Cent Hosp, Clin Lab, Tianjin, Peoples R China
[3] Nankai Univ, Coll Environm Sci & Engn, Tianjin Key Lab Environm Remediat & Pollut Contro, Tianjin 300071, Peoples R China
基金
中国博士后科学基金; 中国国家自然科学基金;
关键词
BLOOD-STREAM INFECTIONS; CANDIDA-ALBICANS; VIRULENCE; DISEASE; NANOMATERIALS; CYTOTOXICITY; BEHAVIOR; SIZE;
D O I
10.1038/srep26667
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Owing to the growing infectious diseases caused by eukaryotic and prokaryotic pathogens, it is urgent to develop novel antimicrobial agents against clinical pathogenic infections. Biofilm formation and invasion into the host cells are vital processes during pathogenic colonization and infection. In this study, we tested the inhibitory effect of Au nanoparticles (AuNPs) on pathogenic growth, biofilm formation and invasion. Interestingly, although the synthesized AuNPs had no significant toxicity to the tested pathogens, Candida albicans and Pseudomonas aeruginosa, the nanoparticles strongly inhibited pathogenic biofilm formation and invasion to dental pulp stem cells (DPSCs). Further investigations revealed that AuNPs abundantly bound to the pathogen cells, which likely contributed to their inhibitory effect on biofilm formation and invasion. Moreover, treatment of AuNPs led to activation of immune response-related genes in DPSCs, which may enhance the activity of host immune system against the pathogens. Zeta potential analysis and polyethylene glycol (PEG)/polyethyleneimine (PEI) coating tests further showed that the interaction between pathogen cells and AuNPs is associated with electrostatic attractions. Our findings shed novel light on the application of nanomaterials in fighting against clinical pathogens, and imply that the traditional growth inhibition test is not the only way to evaluate the drug effect during the screening of antimicrobial agents.
引用
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页数:14
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