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Effects of antimicrobial photodynamic therapy with photodithazine® on methicillin-resistant Staphylococcus aureus (MRSA): Studies in biofilms and experimental model with Galleria mellonella

dc.contributor.authorSouza, Beatriz Müller N
dc.contributor.authorMiñán, Alejandro Guillermo
dc.contributor.authorBrambilla, Isabelle Ribeiro
dc.contributor.authorPinto, Juliana Guerra
dc.contributor.authorGarcia, Maíra Terra [UNESP]
dc.contributor.authorJunqueira, Juliana Campos [UNESP]
dc.contributor.authorFerreira-Strixino, Juliana
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)pt
dc.date.accessioned2026-07-23T11:33:30Z
dc.date.issued2024-02-03
dc.description.abstractStaphylococcus aureus infections are a severe health problem due to the high mortality rate. Conventional treatment of these infections is via the administration of antibiotics. However, its indiscriminate use can select resistant microorganisms. Thus, it is necessary to develop alternatives for antibiotic therapy. Antimicrobial Photodynamic Therapy (aPDT), a therapeutic method that associates a photosensitizer (PS), a light source with adequate wavelength to the PS, interacts with molecular oxygen generating reactive oxygen species responsible for cell inactivation, is a viable alternative. This work aimed to analyze, in vitro and in vivo, the action of aPDT with PS Photodithazine® (PDZ) on the methicillin-resistant S. aureus (MRSA) strain. In the in vitro method, the S. aureus biofilm was incubated with PDZ at 50 and 75 μg.mL<sup>-1</sup> for 15 min, adopting the light dose of 25, 50, and 100 J/cm<sup>2</sup>. In addition, PS interaction, formation of reactive oxygen species (ROS), bacterial metabolism, adhesion, bacterial viability, and biofilm structure were evaluated by scanning electron microscopy. Subsequently, the strain was inoculated into models of Galleria mellonella, and the survival curve, health scale, blood cell analysis, and CFU/mL of S. aureus in the hemolymph were analyzed after aPDT. In the in vitro results, bacterial reduction was observed in the different PDZ concentrations, highlighting the parameters of 75 μg.mL<sup>-1</sup> of PDZ and 100 J/cm<sup>2</sup>. As for in vivo results, aPDT increased survival and stimulated the immune system of G. mellonella infected by S. aureus. aPDT proved effective in both models, demonstrating its potential as an alternative therapy in treating MRSA bacterial infections.
dc.description.affiliationPhotobiology Applied to Health (PhotoBioS Lab), Universidade do Vale do Paraíba (UNIVAP), São José dos Campos, São Paulo, Brazil.
dc.description.affiliationInstituto de Investigaciones Fisicoquímicas Teóricas y Aplicadas, Facultad de Ciencias Exactas, Universidad Nacional de La Plata, La Plata 1900, Argentina. Electronic address: agminan@inifta.unlp.edu.ar.
dc.description.affiliationPhotobiology Applied to Health (PhotoBioS Lab), Universidade do Vale do Paraíba (UNIVAP), São José dos Campos, São Paulo, Brazil. Electronic address: juguerra@univap.br.
dc.description.affiliationDepartment of Biosciences and Oral Diagnosis, Universidade Estadual Paulista (Unesp), Institute of Science and Technology (ICT), São José dos Campos, São Paulo, Brazil.
dc.description.affiliationDepartment of Biosciences and Oral Diagnosis, Universidade Estadual Paulista (Unesp), Institute of Science and Technology (ICT), São José dos Campos, São Paulo, Brazil. Electronic address: juliana.junqueira@unesp.br.
dc.description.affiliationPhotobiology Applied to Health (PhotoBioS Lab), Universidade do Vale do Paraíba (UNIVAP), São José dos Campos, São Paulo, Brazil. Electronic address: juferreira@univap.br.
dc.description.affiliationUnespDepartment of Biosciences and Oral Diagnosis, Universidade Estadual Paulista (Unesp), Institute of Science and Technology (ICT), São José dos Campos, São Paulo, Brazil.
dc.description.affiliationUnespDepartment of Biosciences and Oral Diagnosis, Universidade Estadual Paulista (Unesp), Institute of Science and Technology (ICT), São José dos Campos, São Paulo, Brazil. Electronic address: juliana.junqueira@unesp.br.
dc.identifierhttps://app.dimensions.ai/details/publication/pub.1168530228
dc.identifier.dimensionspub.1168530228
dc.identifier.doi10.1016/j.jphotobiol.2024.112860
dc.identifier.issn1011-1344
dc.identifier.issn1873-2682
dc.identifier.orcid0000-0001-8864-8415
dc.identifier.orcid0000-0002-7356-1576
dc.identifier.orcid0000-0002-1193-2909
dc.identifier.orcid0000-0001-6646-6856
dc.identifier.orcid0000-0001-7128-6817
dc.identifier.pmid38330692
dc.identifier.urihttps://hdl.handle.net/11449/328449
dc.publisherElsevier
dc.relation.ispartofJournal of Photochemistry and Photobiology B Biology; v. 252; p. 112860
dc.rights.accessRightsAcesso restritopt
dc.rights.sourceRightsclosed
dc.sourceDimensions
dc.titleEffects of antimicrobial photodynamic therapy with photodithazine® on methicillin-resistant Staphylococcus aureus (MRSA): Studies in biofilms and experimental model with Galleria mellonella
dc.typeArtigopt
dspace.entity.typePublication
relation.isOrgUnitOfPublicationc73b286a-b5fa-4312-a7ec-62f987e7b514
relation.isOrgUnitOfPublication.latestForDiscoveryc73b286a-b5fa-4312-a7ec-62f987e7b514
unesp.campusUniversidade Estadual Paulista (UNESP), Instituto de Ciência e Tecnologia, São José dos Campospt

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