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Photodynamic and Antibiotic Therapy Impair the Pathogenesis of Enterococcus faecium in a Whole Animal Insect Model

dc.contributor.authorChibebe Junior, José [UNESP]
dc.contributor.authorFuchs, Beth B.
dc.contributor.authorSabino, Caetano P.
dc.contributor.authorJunqueira, Juliana Campos [UNESP]
dc.contributor.authorJorge, Antonio O. C. [UNESP]
dc.contributor.authorRibeiro, Martha S.
dc.contributor.authorGilmore, Michael S.
dc.contributor.authorRice, Louis B.
dc.contributor.authorTegos, George P.
dc.contributor.authorHamblin, Michael R.
dc.contributor.authorMylonakis, Eleftherios
dc.contributor.institutionUniversidade Estadual Paulista (Unesp)
dc.contributor.institutionMassachusetts General Hospital
dc.contributor.institutionFaculty of Pindamonhangaba
dc.contributor.institutionNuclear and Energy Research Institute
dc.contributor.institutionHarvard Medical School
dc.contributor.institutionBrown University
dc.contributor.institutionUniversity of New Mexico
dc.contributor.institutionMassachusetts Institute of Technology (MIT)
dc.date.accessioned2014-05-27T11:28:27Z
dc.date.available2014-05-27T11:28:27Z
dc.date.issued2013-02-14
dc.description.abstractEnterococcus faecium has emerged as one of the most important pathogens in healthcare-associated infections worldwide due to its intrinsic and acquired resistance to many antibiotics, including vancomycin. Antimicrobial photodynamic therapy (aPDT) is an alternative therapeutic platform that is currently under investigation for the control and treatment of infections. PDT is based on the use of photoactive dye molecules, widely known as photosensitizer (PS). PS, upon irradiation with visible light, produces reactive oxygen species that can destroy lipids and proteins causing cell death. We employed Galleria mellonella (the greater wax moth) caterpillar fatally infected with E. faecium to develop an invertebrate host model system that can be used to study the antimicrobial PDT (alone or combined with antibiotics). In the establishment of infection by E. faecium in G. mellonella, we found that the G. mellonella death rate was dependent on the number of bacterial cells injected into the insect hemocoel and all E. faecium strains tested were capable of infecting and killing G. mellonella. Antibiotic treatment with ampicillin, gentamicin or the combination of ampicillin and gentamicin prolonged caterpillar survival infected by E. faecium (P = 0.0003, P = 0.0001 and P = 0.0001, respectively). In the study of antimicrobial PDT, we verified that methylene blue (MB) injected into the insect followed by whole body illumination prolonged the caterpillar survival (P = 0.0192). Interestingly, combination therapy of larvae infected with vancomycin-resistant E. faecium, with antimicrobial PDT followed by vancomycin, significantly prolonged the survival of the caterpillars when compared to either antimicrobial PDT (P = 0.0095) or vancomycin treatment alone (P = 0.0025), suggesting that the aPDT made the vancomycin resistant E. faecium strain more susceptible to vancomycin action. In summary, G. mellonella provides an invertebrate model host to study the antimicrobial PDT and to explore combinatorial aPDT-based treatments.en
dc.description.affiliationDepartment of Biosciences and Oral Diagnosis Univ Estadual Paulista/UNESP, São José dos Campos, São Paulo
dc.description.affiliationDivision of Infectious Diseases Massachusetts General Hospital, Boston, MA
dc.description.affiliationDepartment of Restorative Dentistry Faculty of Pindamonhangaba, Pindamonhangaba, São Paulo
dc.description.affiliationWellman Center for Photomedicine Massachusetts General Hospital, Boston, MA
dc.description.affiliationCenter for Lasers and Applications Nuclear and Energy Research Institute, São Paulo, São Paulo
dc.description.affiliationMassachusetts Eye and Ear Infirmary Harvard Medical School, Boston, MA
dc.description.affiliationWarren Alpert Medical School Brown University/Rhode Island and Miriam Hospitals, Providence, RI
dc.description.affiliationDepartment of Dermatology Harvard Medical School, Boston, MA
dc.description.affiliationDepartment of Pathology and Center for Molecular Discovery University of New Mexico, Albuquerque, NM
dc.description.affiliationDivision of Health Sciences and Technology Harvard-Massachusetts Institute of Technology, Cambridge, MA
dc.description.affiliationUnespDepartment of Biosciences and Oral Diagnosis Univ Estadual Paulista/UNESP, São José dos Campos, São Paulo
dc.identifierhttp://dx.doi.org/10.1371/journal.pone.0055926
dc.identifier.citationPLoS ONE, v. 8, n. 2, 2013.
dc.identifier.doi10.1371/journal.pone.0055926
dc.identifier.file2-s2.0-84874006080.pdf
dc.identifier.issn1932-6203
dc.identifier.lattes0322020541055900
dc.identifier.scopus2-s2.0-84874006080
dc.identifier.urihttp://hdl.handle.net/11449/74593
dc.identifier.wosWOS:000315602700027
dc.language.isoeng
dc.relation.ispartofPLOS ONE
dc.relation.ispartofjcr2.766
dc.relation.ispartofsjr1,164
dc.rights.accessRightsAcesso aberto
dc.sourceScopus
dc.subjectampicillin
dc.subjectgentamicin
dc.subjectmethylene blue
dc.subjectphenothiazinium
dc.subjectphotosensitizing agent
dc.subjectstreptomycin
dc.subjectunclassified drug
dc.subjectvancomycin
dc.subjectantibiotic resistance
dc.subjectantibiotic sensitivity
dc.subjectantibiotic therapy
dc.subjectbacterial strain
dc.subjectcaterpillar
dc.subjectcombination chemotherapy
dc.subjectcontrolled study
dc.subjectdrug efficacy
dc.subjectdrug response
dc.subjectenterococcal infection
dc.subjectEnterococcus faecium
dc.subjectGalleria mellonella
dc.subjectin vivo study
dc.subjectinfection control
dc.subjectnonhuman
dc.subjectpathogenesis
dc.subjectphotodynamic therapy
dc.subjectsurvival rate
dc.subjectvancomycin resistant Enterococcus
dc.subjectAnimals
dc.subjectAnti-Bacterial Agents
dc.subjectDisease Models, Animal
dc.subjectGram-Positive Bacterial Infections
dc.subjectMethylene Blue
dc.subjectMoths
dc.subjectPhotochemotherapy
dc.subjectPhotosensitizing Agents
dc.titlePhotodynamic and Antibiotic Therapy Impair the Pathogenesis of Enterococcus faecium in a Whole Animal Insect Modelen
dc.typeArtigo
dcterms.licensehttp://www.plos.org/open-access/
dspace.entity.typePublication
unesp.author.lattes0322020541055900
unesp.author.lattes0053567153623569[5]
unesp.author.orcid0000-0002-1747-6158[5]
unesp.campusUniversidade Estadual Paulista (UNESP), Instituto de Ciência e Tecnologia, São José dos Campospt
unesp.departmentBiociências e Diagnóstico Bucal - ICTpt

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