Rineh Ardeshir, Dolla Naveen K, Ball Anthony R, Magana Maria, Bremner John B, Hamblin Michael R, Tegos George P, Kelso Michael J
Illawarra Health and Medical Research Institute and School of Chemistry, University of Wollongong , Northfields Ave., Wollongong, New South Wales 2522, Australia.
Gliese 623B , Lowell, Massachusetts 01852, United States.
ACS Infect Dis. 2017 Oct 13;3(10):756-766. doi: 10.1021/acsinfecdis.7b00095. Epub 2017 Aug 17.
Antimicrobial photodynamic inactivation (aPDI) uses photosensitizers (PSs) and harmless visible light to generate reactive oxygen species (ROS) and kill microbes. Multidrug efflux systems can moderate the phototoxic effects of PSs by expelling the compounds from cells. We hypothesized that increasing intracellular concentrations of PSs by inhibiting efflux with a covalently attached efflux pump inhibitor (EPI) would enhance bacterial cell phototoxicity and reduce exposure of neighboring host cells to damaging ROS. In this study, we tested the hypothesis by linking NorA EPIs to methylene blue (MB) and examining the photoantimicrobial activity of the EPI-MB hybrids against the human pathogen methicillin-resistant Staphylococcus aureus (MRSA). Photochemical/photophysical and in vitro microbiological evaluation of 16 hybrids carrying four different NorA EPIs attached to MB via four linker types identified INF55-(Ac)en-MB 12 as a lead. Compound 12 showed increased uptake into S. aureus cells and enhanced aPDI activity and wound healing effects (relative to MB) in a murine model of an abrasion wound infected by MRSA. The study supports a new approach for treating localized multidrug-resistant MRSA infections and paves the way for wider exploration of the EPI-PS hybrid strategy in aPDI.
抗菌光动力灭活(aPDI)利用光敏剂(PSs)和无害可见光产生活性氧(ROS)来杀灭微生物。多药外排系统可通过将化合物排出细胞来减轻PSs的光毒性作用。我们推测,通过使用共价连接的外排泵抑制剂(EPI)抑制外排来增加细胞内PSs浓度,会增强细菌细胞的光毒性,并减少邻近宿主细胞暴露于具有损伤性的ROS中。在本研究中,我们通过将NorA EPI与亚甲蓝(MB)相连,并检测EPI-MB杂合物对人类病原体耐甲氧西林金黄色葡萄球菌(MRSA)的光抗菌活性,来验证这一假设。对16种通过四种连接子类型与MB相连的携带四种不同NorA EPI的杂合物进行光化学/光物理及体外微生物学评估,确定INF55-(Ac)en-MB 12为先导物。在由MRSA感染的擦伤伤口小鼠模型中,化合物12显示出进入金黄色葡萄球菌细胞的摄取增加,以及增强的aPDI活性和伤口愈合效果(相对于MB)。该研究支持了一种治疗局部多药耐药MRSA感染的新方法,并为在aPDI中更广泛地探索EPI-PS杂合策略铺平了道路。