Maxillofacial Injury and Disease Department, Naval, Medical Research Unit San Antonio, JBSA-Fort Sam Houston, TX.
Maxillofacial Injury and Disease Department, Naval, Medical Research Unit San Antonio, JBSA-Fort Sam Houston, TX.
Nanomedicine. 2019 Aug;20:102018. doi: 10.1016/j.nano.2019.102018. Epub 2019 May 22.
The growing prevalence of biofilm-associated multi-drug resistant (MDR) bacteria necessitates the innovation of non-traditional approaches to improve the effectiveness of mainstay antibiotics. Here, we evaluated the use of gold nanoparticle (GNP)-targeted pulsed laser therapy to enhance antibiotic efficacy against in vitro methicillin-resistant Staphylococcus aureus (MRSA) and MDR Pseudomonas aeruginosa biofilms. Treatment with antibody-conjugated GNPs followed by nanosecond-pulsed laser irradiation at 532 nm (~1.0 J/cm) dispersed 96-99% of the biofilms relative to controls. GNP-targeted laser therapy combined with gentamicin or amikacin caused a synergistic 4- and 5-log reduction in the viability of MRSA and P. aeruginosa biofilms, respectively, whereas GNP-targeted laser therapy or antibiotics alone decreased biofilm viability by only ~1 log. Notably, GNP-targeted laser therapy was able to increase the antibiotic susceptibility of the biofilms to the level of drug sensitivity observed in planktonic MRSA and P. aeruginosa cultures, further indicating effective biofilm dispersal via this novel approach.
生物膜相关的多药耐药(MDR)细菌的日益流行,需要创新非传统方法来提高主要抗生素的效果。在这里,我们评估了金纳米颗粒(GNP)靶向脉冲激光治疗在增强抗药性金黄色葡萄球菌(MRSA)和多药耐药铜绿假单胞菌生物膜体外抗生素功效的应用。与对照组相比,用抗体偶联的 GNP 处理,然后用 532nm(~1.0J/cm)纳秒脉冲激光照射,分散了 96-99%的生物膜。GNP 靶向激光治疗联合庆大霉素或阿米卡星分别导致 MRSA 和铜绿假单胞菌生物膜的活力协同减少 4-5 个对数级,而 GNP 靶向激光治疗或单独使用抗生素仅使生物膜活力减少约 1 个对数级。值得注意的是,GNP 靶向激光治疗能够增加生物膜对抗生素的敏感性,使其达到浮游 MRSA 和铜绿假单胞菌培养物中观察到的药物敏感性水平,这进一步表明通过这种新方法能够有效分散生物膜。