Antibacterial photodynamic therapy mediated by 5-aminolevulinic acid on methicillin-resistant Staphylococcus aureus

被引:27
作者
Huan, Jianhua [1 ]
Guo, Mingquan [2 ]
Jin, Shengkai [3 ]
Wu, Minfeng [1 ]
Yang, Chen [3 ]
Zhang, Guolong [3 ]
Wang, Peiru [3 ]
Ji, Jie [3 ]
Zeng, Qingyu [3 ]
Wang, Xiuli [3 ]
Wang, Hongwei [1 ]
机构
[1] Fudan Univ, Huadong Hosp, Dept Dermatol, Shanghai 200040, Peoples R China
[2] Fudan Univ, Shanghai Publ Hlth Clin Ctr, Shanghai Inst Bacteriophage & Drug Resistance, Shanghai 201514, Peoples R China
[3] Tongji Univ, Sch Med, Shanghai Skin Dis Hosp, Shanghai, Peoples R China
基金
中国国家自然科学基金;
关键词
Drug resistance; Staphylococcus aureus; MRSA; 5-aminolevulinic acid; Photodynamic therapy; Antimicrobial Photdynamic Therapy; IN-VITRO; ANTIMICROBIAL CHEMOTHERAPY; CANDIDA-ALBICANS; INACTIVATION; BIOFILMS; INFECTIONS; CHAIN;
D O I
10.1016/j.pdpdt.2019.09.008
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The emergence of drug-resistant bacteria, such as methicillin-resistant Staphylococcus aureus (MRSA), has brought great difficulties to clinical treatment. Antibacterial photodynamic therapy (aPDT) is a new non-antibiotic treatment strategy for a variety of drug-resistant bacteria. However, there are few studies on the antimicrobial mechanism of a PDT mediated by 5-aminolevulinic acid (ALA-PDT) for MRSA. In this study, we observed the bactericidal effect of ALA-PDT on MRSA. We found that ALA-PDT had the strongest bactericidal effect when ALA was at 0.05 mM, and the bactericidal activity of aPDT increased with the increase of light dose. MRSA was almost completely eliminated at 0.05 mM and 384 Jcm(-2). In addition, the bactericidal morphology was also observed under a fluorescence microscope using a LIVE/DEAD (R) BacLighe (TM) Bacterial Viability Kit and an electron microscope. It was also found that proteins and DNA were damaged by ALA-PDT. Finally, the transcription level of the specific gene of MRSA, nuc, was decreased by 0.74-fold (P < 0.05) after ALA-PDT treatment by qRT-PCR analysis. The findings suggest that ALA-PDT can effectively inhibit MRSA by damaging cell membrane, cytoplasm, proteins and nucleic acid.
引用
收藏
页码:330 / 337
页数:8
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