Susceptibility of Enterococcus faecalis and Propionibacterium acnes to antimicrobial photodynamic therapy

• Autor(a) principal: de Annunzio, Sarah Raquel [UNESP]
• Data de Publicação: 2018
• Outros Autores: de Freitas, Laura Marise [UNESP], Blanco, Ana Lígia [UNESP], da Costa, Mardoqueu Martins, Carmona-Vargas, Christian C., de Oliveira, Kleber Thiago, Fontana, Carla Raquel [UNESP]
• Tipo de documento: Artigo
• Idioma: eng
• Título da fonte: Repositório Institucional da UNESP
• Texto Completo: http://dx.doi.org/10.1016/j.jphotobiol.2017.11.035; http://hdl.handle.net/11449/170499
• topic: Antimicrobial photodynamic therapy; Chlorin-e6; Curcumin; Enterococcus faecalis; Methylene blue; Propionibacterium acnes

Bacterial resistance to available antibiotics nowadays is a global threat leading researchers around the world to study new treatment modalities for infections. Antimicrobial photodynamic therapy (aPDT) has been considered an effective and promising therapeutic alternative in this scenario. Briefly, this therapy is based on the activation of a non-toxic photosensitizing agent, known as photosensitizer (PS), by light at a specific wavelength generating cytotoxic singlet oxygen and free radicals. Virtually all studies related to aPDT involve a huge screening to identify ideal PS concentration and light dose combinations, a laborious and time-consuming process that is hardly disclosed in the literature. Herein, we describe an antimicrobial Photodynamic Therapy (aPDT) study against Enterococcus faecalis and Propionibacterium acnes employing methylene blue, chlorin-e6 or curcumin as PS. Similarities and discrepancies between the two bacterial species were pointed out in an attempt to speed up and facilitate futures studies against those clinical relevant strains. Susceptibility tests were performed by the broth microdilution method. Our results demonstrate that aPDT mediated by the three above-mentioned PS was effective in eliminating both gram-positive bacteria, although P. acnes showed remarkably higher susceptibility to aPDT when compared to E. faecalis. PS uptake assays revealed that P. acnes is 80 times more efficient than E. faecalis in internalizing all three PS molecules. Our results evidence that the cell wall structure is not a limiting feature when predicting bacterial susceptibility to aPDT treatment.