Toluidine blue O-induced photoinactivation inhibit the biofilm formation of methicillin-resistant Staphylococcus aureus

• Published in: Photodiagnosis and photodynamic therapy Vol. 39; p. 102902
• Main Authors: He, Yaxiong, Pang, Jiaying, Yang, Zengjun, Zheng, Mengxue, Yu, Yanlan, Liu, Zhiyong, Zhao, Baohua, Hu, Guangyun, Yin, Rui
• Format: Journal Article
• Language: English
• Published: Netherlands Elsevier B.V 01.09.2022
• Subjects: Biofilms; MRSA; Photodynamic antimicrobial chemotherapy; Photodynamic therapy; Toluidine blue O; Virulence; Biofilms; Photodynamic therapy; Toluidine blue O; Virulence; Photodynamic antimicrobial chemotherapy; MRSA
• ISSN: 1572-1000; 1873-1597
• DOI: 10.1016/j.pdpdt.2022.102902

•TBO-PDT can reduce the viability of MRSA mature biofilms via disrupting their EPS, cells and the three-dimensional structure.•TBO-PDT can inhibit the virulence factors of MRSA mature biofilms.•TBO-PDT prolongs the self-recovery of biofilm structure and function. Methicillin-resistant Staphylococcus aureus (MRSA) is resistant to conventional antimicrobial therapies, allowing for high morbidity and mortality. Photodynamic antimicrobial chemotherapy (PACT) is one method that combines visible harmless light with the optimum wavelength with photosensitizers or dyes, producing singlet oxygen (1O2) and reactive oxygen strains (ROS), making permanent damages to the target cells. The purpose of this research is to evaluate the suppression efficacy of toluidine blue O (TBO)-mediated PACT on mature MRSA biofilm in vitro. In this study, the 48 h mature biofilm of the multidrug-resistant Staphylococcus aureus strain MRSA252 was used. The photodynamic therapy (PDT) group was treated with different concentrations of TBO (0.5, 0.75, 1.0 or 1.25 µM) and different doses of red light (635 ± 5 nm wavelength; 30 or 50 J/cm2). The biofilms viability after PDT were evaluated by crystal violet (CV) staining assay and {2,3-bis(2-methoxy-4-nitro-5-sulfophenyl)-5-[(phenylamino)carbonyl]-2H-tetra-zolium hydroxide} (XTT) assay; meanwhile, the morphological changes were detected by confocal laser scanning microscopy (CLSM) and scanning electron microscopy (SEM), separately. Moreover, the biofilms virulence was evaluated by red blood cell (RBC) hemolysis assay and staphylococcal virulence factor enterotoxins A (SEA) detected by enzyme linked immunosorbent assay (ELISA). After PDT, the biofilm was re-cultured for extra 48 h. Its formation viability and virulence were detected again. All data were analyzed by ANOVAs followed by the Games Howell post hoc test (α = 0.05). The biofilm was inactivated about 2.3 log10 at 1.25 µM with 30 J/cm2 illumination, and 3.5 log10 with 50 J/cm2 after PDT (P<0.05). XTT assays demonstrated the viability of mature MRSA biofilms was reduced after PACT. PDT group shows a distinct reduction in RBC hemolysis rate and the concentration of SEA compared to the control groups. The morphological features of the biofilms showed great changes, such as shrinkage, fissure, fragmentation, and rarefaction after being treated by TBO-PDT and observed by SEM. The recovery of the structure and virulence of biofilm were suppressed after PDT. TBO-mediated PDT could destroy the biofilm structure, reduce its virulence and depress its self-recovery.