Photodynamic therapy of oral Candida infection in a mouse model

Detalhes bibliográficos
Autor(a) principal: Freire, Fernanda [UNESP]
Data de Publicação: 2016
Outros Autores: Ferraresi, Cleber, Jorge, Antonio Olavo C. [UNESP], Hamblin, Michael R.
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNESP
Texto Completo: http://dx.doi.org/10.1016/j.jphotobiol.2016.03.049
http://hdl.handle.net/11449/172854
Resumo: Species of the fungal genus Candida, can cause oral candidiasis especially in immunosuppressed patients. Many studies have investigated the use of photodynamic therapy (PDT) to kill fungi in vitro, but this approach has seldom been reported in animal models of infection. This study investigated the effects of PDT on Candida albicans as biofilms grown in vitro and also in an immunosuppressed mouse model of oral candidiasis infection. We used a luciferase-expressing strain that allowed non-invasive monitoring of the infection by bioluminescence imaging. The phenothiazinium salts, methylene blue (MB) and new methylene blue (NMB) were used as photosensitizers (PS), combined or not with potassium iodide (KI), and red laser (660 nm) at four different light doses (10 J, 20 J, 40 J and 60 J). The best in vitro log reduction of CFU/ml on biofilm grown cells was: MB plus KI with 40 J (2.31 log; p < 0.001); and NMB without KI with 60 J (1.77 log; p < 0.001). These conditions were chosen for treating the in vivo model of oral Candida infection. After 5 days of treatment the disease was practically eradicated, especially using MB plus KI with 40 J. This study suggests that KI can potentiate PDT of fungal infection using MB (but not NMB) and could be a promising new approach for the treatment of oral candidiasis.
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spelling Photodynamic therapy of oral Candida infection in a mouse modelAbbreviations PDT photodynamic therapyKI potassium iodideMB methylene blueNMB new methylene bluePS photosensitizersSpecies of the fungal genus Candida, can cause oral candidiasis especially in immunosuppressed patients. Many studies have investigated the use of photodynamic therapy (PDT) to kill fungi in vitro, but this approach has seldom been reported in animal models of infection. This study investigated the effects of PDT on Candida albicans as biofilms grown in vitro and also in an immunosuppressed mouse model of oral candidiasis infection. We used a luciferase-expressing strain that allowed non-invasive monitoring of the infection by bioluminescence imaging. The phenothiazinium salts, methylene blue (MB) and new methylene blue (NMB) were used as photosensitizers (PS), combined or not with potassium iodide (KI), and red laser (660 nm) at four different light doses (10 J, 20 J, 40 J and 60 J). The best in vitro log reduction of CFU/ml on biofilm grown cells was: MB plus KI with 40 J (2.31 log; p < 0.001); and NMB without KI with 60 J (1.77 log; p < 0.001). These conditions were chosen for treating the in vivo model of oral Candida infection. After 5 days of treatment the disease was practically eradicated, especially using MB plus KI with 40 J. This study suggests that KI can potentiate PDT of fungal infection using MB (but not NMB) and could be a promising new approach for the treatment of oral candidiasis.Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)Wellman Center for Photomedicine Massachusetts General HospitalDepartment of Biosciences and Oral Diagnosis Institute of Science and Technology Universidade Estadual Paulista (UNESP) São José Dos CamposDepartment of Dermatology Harvard Medical SchoolHarvard-MIT Division of Health Sciences and TechnologyDepartment of Biosciences and Oral Diagnosis Institute of Science and Technology Universidade Estadual Paulista (UNESP) São José Dos CamposFAPESP: 2014/25772-9Massachusetts General HospitalUniversidade Estadual Paulista (Unesp)Harvard Medical SchoolHarvard-MIT Division of Health Sciences and TechnologyFreire, Fernanda [UNESP]Ferraresi, CleberJorge, Antonio Olavo C. [UNESP]Hamblin, Michael R.2018-12-11T17:02:26Z2018-12-11T17:02:26Z2016-06-01info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article161-168application/pdfhttp://dx.doi.org/10.1016/j.jphotobiol.2016.03.049Journal of Photochemistry and Photobiology B: Biology, v. 159, p. 161-168.1873-26821011-1344http://hdl.handle.net/11449/17285410.1016/j.jphotobiol.2016.03.0492-s2.0-849639976522-s2.0-84963997652.pdfScopusreponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengJournal of Photochemistry and Photobiology B: Biology0,698info:eu-repo/semantics/openAccess2023-11-12T06:08:50Zoai:repositorio.unesp.br:11449/172854Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462024-08-05T17:26:03.745565Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false
dc.title.none.fl_str_mv Photodynamic therapy of oral Candida infection in a mouse model
title Photodynamic therapy of oral Candida infection in a mouse model
spellingShingle Photodynamic therapy of oral Candida infection in a mouse model
Freire, Fernanda [UNESP]
Abbreviations PDT photodynamic therapy
KI potassium iodide
MB methylene blue
NMB new methylene blue
PS photosensitizers
title_short Photodynamic therapy of oral Candida infection in a mouse model
title_full Photodynamic therapy of oral Candida infection in a mouse model
title_fullStr Photodynamic therapy of oral Candida infection in a mouse model
title_full_unstemmed Photodynamic therapy of oral Candida infection in a mouse model
title_sort Photodynamic therapy of oral Candida infection in a mouse model
author Freire, Fernanda [UNESP]
author_facet Freire, Fernanda [UNESP]
Ferraresi, Cleber
Jorge, Antonio Olavo C. [UNESP]
Hamblin, Michael R.
author_role author
author2 Ferraresi, Cleber
Jorge, Antonio Olavo C. [UNESP]
Hamblin, Michael R.
author2_role author
author
author
dc.contributor.none.fl_str_mv Massachusetts General Hospital
Universidade Estadual Paulista (Unesp)
Harvard Medical School
Harvard-MIT Division of Health Sciences and Technology
dc.contributor.author.fl_str_mv Freire, Fernanda [UNESP]
Ferraresi, Cleber
Jorge, Antonio Olavo C. [UNESP]
Hamblin, Michael R.
dc.subject.por.fl_str_mv Abbreviations PDT photodynamic therapy
KI potassium iodide
MB methylene blue
NMB new methylene blue
PS photosensitizers
topic Abbreviations PDT photodynamic therapy
KI potassium iodide
MB methylene blue
NMB new methylene blue
PS photosensitizers
description Species of the fungal genus Candida, can cause oral candidiasis especially in immunosuppressed patients. Many studies have investigated the use of photodynamic therapy (PDT) to kill fungi in vitro, but this approach has seldom been reported in animal models of infection. This study investigated the effects of PDT on Candida albicans as biofilms grown in vitro and also in an immunosuppressed mouse model of oral candidiasis infection. We used a luciferase-expressing strain that allowed non-invasive monitoring of the infection by bioluminescence imaging. The phenothiazinium salts, methylene blue (MB) and new methylene blue (NMB) were used as photosensitizers (PS), combined or not with potassium iodide (KI), and red laser (660 nm) at four different light doses (10 J, 20 J, 40 J and 60 J). The best in vitro log reduction of CFU/ml on biofilm grown cells was: MB plus KI with 40 J (2.31 log; p < 0.001); and NMB without KI with 60 J (1.77 log; p < 0.001). These conditions were chosen for treating the in vivo model of oral Candida infection. After 5 days of treatment the disease was practically eradicated, especially using MB plus KI with 40 J. This study suggests that KI can potentiate PDT of fungal infection using MB (but not NMB) and could be a promising new approach for the treatment of oral candidiasis.
publishDate 2016
dc.date.none.fl_str_mv 2016-06-01
2018-12-11T17:02:26Z
2018-12-11T17:02:26Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://dx.doi.org/10.1016/j.jphotobiol.2016.03.049
Journal of Photochemistry and Photobiology B: Biology, v. 159, p. 161-168.
1873-2682
1011-1344
http://hdl.handle.net/11449/172854
10.1016/j.jphotobiol.2016.03.049
2-s2.0-84963997652
2-s2.0-84963997652.pdf
url http://dx.doi.org/10.1016/j.jphotobiol.2016.03.049
http://hdl.handle.net/11449/172854
identifier_str_mv Journal of Photochemistry and Photobiology B: Biology, v. 159, p. 161-168.
1873-2682
1011-1344
10.1016/j.jphotobiol.2016.03.049
2-s2.0-84963997652
2-s2.0-84963997652.pdf
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Journal of Photochemistry and Photobiology B: Biology
0,698
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv 161-168
application/pdf
dc.source.none.fl_str_mv Scopus
reponame:Repositório Institucional da UNESP
instname:Universidade Estadual Paulista (UNESP)
instacron:UNESP
instname_str Universidade Estadual Paulista (UNESP)
instacron_str UNESP
institution UNESP
reponame_str Repositório Institucional da UNESP
collection Repositório Institucional da UNESP
repository.name.fl_str_mv Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)
repository.mail.fl_str_mv
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