Department of Dermatology, Southwest Hospital, Third Military Medical University (Army Medical University), Chongqing, 400030, China.
Department of Microbiology,Third Military Medical University (Army Medical University), Chongqing, 400030, China.
Photodiagnosis Photodyn Ther. 2022 Sep;39:102900. doi: 10.1016/j.pdpdt.2022.102900. Epub 2022 May 5.
Photodynamic therapy (PDT) is an effective method to inactivate microorganisms which is based on reactive oxygen species (ROS) generated by photosensitizer and light at certain wavelength. Exposure to sub-lethal dose of PDT (sPDT) could activate the regulatory systems in the surviving bacteria in response to oxidative stress. This study aimed to evaluate the effect of sPDT on efflux pump and biofilm formation in Staphylococcus aureus (S. aureus), which are two important virulence related factors.
Different light irradiation time and toluidine blue O (TBO) concentrations were tested to select a sPDT in methicillin-susceptible and methicillin-resistant S. aureus (MSSA and MRSA). Efflux function was evaluated with EtBr efflux experiment. Biofilm formation was evaluated by crystal violet staining. Gene expressions of norA, norB, sepA, mepA and mdeA following sPDT were analyzed with real-time PCR.
Sub-lethal PDT was set at 40 J/cm associated with 0.5 μM TBO. Efflux function was significantly inhibited in both strains. The average expression levels of mdeA and mepA in MSSA and MRSA were increased by (3.09, 1.77, 1.57) and (3,44, 1.59, 6.29) fold change respectively, norB and sepA were decreased by (3.77, 6.14) and (3.02, 3.47) fold change respectively. Expression level of norA was decreased by 5.44-fold change in MSSA but increased by 2.80-fold change in MRSA. Biofilm formation in both strains was impeded.
TBO-mediated sPDT could inhibit efflux pump function, alter efflux pump encoding gene expression levels and retard biofilm formation in MSSA and MRSA. Therefore, sPDT is proposed as a potential adjuvant therapy for infections.
光动力疗法(PDT)是一种基于光敏剂和特定波长光产生的活性氧(ROS)来灭活微生物的有效方法。亚致死剂量 PDT(sPDT)的暴露会激活存活细菌中的调节系统,以应对氧化应激。本研究旨在评估 sPDT 对金黄色葡萄球菌(S. aureus)中两种重要毒力相关因素外排泵和生物膜形成的影响。
测试了不同的光照射时间和甲苯胺蓝 O(TBO)浓度,以选择对甲氧西林敏感和耐甲氧西林金黄色葡萄球菌(MSSA 和 MRSA)的 sPDT。用 EtBr 外排实验评估外排功能。用结晶紫染色评估生物膜形成。用实时 PCR 分析 sPDT 后 norA、norB、sepA、mepA 和 mdeA 的基因表达。
亚致死 PDT 设定为 40 J/cm 与 0.5 μM TBO 相关。两种菌株的外排功能均受到显著抑制。MSSA 和 MRSA 中 mdeA 和 mepA 的平均表达水平分别增加了 3.09、1.77、1.57 倍和 3.44、1.59、6.29 倍,norB 和 sepA 分别减少了 3.77、6.14 倍和 3.02、3.47 倍。MSSA 中 norA 的表达水平降低了 5.44 倍,但 MRSA 中 norA 的表达水平增加了 2.80 倍。两种菌株的生物膜形成均受到抑制。
TBO 介导的 sPDT 可抑制外排泵功能,改变外排泵编码基因的表达水平,延缓 MSSA 和 MRSA 生物膜的形成。因此,sPDT 可作为感染的潜在辅助治疗方法。