Photodynamic therapy of oral Candida infection in a mouse model
Autor(a) principal: | |
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Data de Publicação: | 2016 |
Outros Autores: | , , |
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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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 |
|
_version_ |
1808128810994892800 |