Histatin 5 inhibits adhesion of C. albicans to Reconstructed Human Oral Epithelium
Autor(a) principal: | |
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Data de Publicação: | 2015 |
Outros Autores: | , , , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Institucional da UNESP |
Texto Completo: | http://dx.doi.org/10.3389/fmicb.2015.00885 http://hdl.handle.net/11449/160749 |
Resumo: | Candida albicans is the most pathogenic fungal species, commonly colonizing on human mucosal surfaces. As a polymorphic species, C. albicans is capable of switching between yeast and hyphal forms, causing an array of mucosal and disseminated infections with high mortality. While the yeast form is most commonly associated with systemic disease, the hyphae are more adept at adhering to and penetrating host tissue and are therefore frequently observed in mucosal fungal infections, most commonly oral candidiasis. The formation of a saliva-derived protein pellicle on the mucosa surface can provide protection against C. albicans on oral epithelial cells, and narrow information is available on the mucosal pellicle composition. Histatins are one of the most abundant salivary proteins and presents antifungal and antibacterial activities against many species of the oral microbiota, however, its presence has never been studied in oral mucosa pellicle. The objective of this study was to evaluate the potential of histatin 5 to protect the Human Oral Epithelium against C. albicans adhesion. Human Oral Epithelial Tissues (HOET) were incubated with PBS containing histatin 5 for 2 h, followed by incubation with C. albicans for 1 h at 37 degrees C. The tissues were then washed several times in PBS, transferred to fresh RPMI and incubated for 16 h at 37 degrees C at 5% CO2. HOET were then prepared for histopathological analysis using light microscopy. In addition, the TUNEL assay was employed to evaluate the apoptosis of epithelial cells using fluorescent microscopy. HOET pre-incubated with histatin 5 showed a lower rate of C. albicans growth and cell apoptosis when compared to the control groups (HOET alone and HOET incubated with C. albicans). The data suggest that the coating with histatin 5 is able to reduce C. albicans colonization on epithelial cell surfaces and also protect the basal cell layers from undergoing apoptosis. |
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Histatin 5 inhibits adhesion of C. albicans to Reconstructed Human Oral Epitheliumhistatinssalivary proteinsmucosal pellicleoral mucosaCandida albicansCandida albicans is the most pathogenic fungal species, commonly colonizing on human mucosal surfaces. As a polymorphic species, C. albicans is capable of switching between yeast and hyphal forms, causing an array of mucosal and disseminated infections with high mortality. While the yeast form is most commonly associated with systemic disease, the hyphae are more adept at adhering to and penetrating host tissue and are therefore frequently observed in mucosal fungal infections, most commonly oral candidiasis. The formation of a saliva-derived protein pellicle on the mucosa surface can provide protection against C. albicans on oral epithelial cells, and narrow information is available on the mucosal pellicle composition. Histatins are one of the most abundant salivary proteins and presents antifungal and antibacterial activities against many species of the oral microbiota, however, its presence has never been studied in oral mucosa pellicle. The objective of this study was to evaluate the potential of histatin 5 to protect the Human Oral Epithelium against C. albicans adhesion. Human Oral Epithelial Tissues (HOET) were incubated with PBS containing histatin 5 for 2 h, followed by incubation with C. albicans for 1 h at 37 degrees C. The tissues were then washed several times in PBS, transferred to fresh RPMI and incubated for 16 h at 37 degrees C at 5% CO2. HOET were then prepared for histopathological analysis using light microscopy. In addition, the TUNEL assay was employed to evaluate the apoptosis of epithelial cells using fluorescent microscopy. HOET pre-incubated with histatin 5 showed a lower rate of C. albicans growth and cell apoptosis when compared to the control groups (HOET alone and HOET incubated with C. albicans). The data suggest that the coating with histatin 5 is able to reduce C. albicans colonization on epithelial cell surfaces and also protect the basal cell layers from undergoing apoptosis.NSERCCIHRCFI-LOFFundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)CIHR New Investigator AwardUniv Western Ontario, Dept Biochem & Schulich Dent, Schulich Sch Med & Dent, London, ON N6A 5C1, CanadaUniv Estadual Paulista, Araraquara Dent Sch, Dept Dent Mat & Prosthodont, Sao Paulo, BrazilUniv Sao Paulo, Sch Dent, Sao Paulo, BrazilUniv Estadual Paulista, Inst Chem, Dept Biochem & Technol Chem, Sao Paulo, BrazilUniv Sao Paulo, Bauru Dent Sch, Dept Pediat Dent Orthodont & Publ Hlth, Bauru, BrazilUniv Estadual Paulista, Araraquara Dent Sch, Dept Dent Mat & Prosthodont, Sao Paulo, BrazilUniv Estadual Paulista, Inst Chem, Dept Biochem & Technol Chem, Sao Paulo, BrazilNSERC: 371813CIHR: 106657CIHR: 97577CFI-LOF: 25116FAPESP: 2011/23540-5FAPESP: 2011/23543-4FAPESP: 2013/15412-2CIHR New Investigator Award: 113166Frontiers Media SaUniv Western OntarioUniversidade Estadual Paulista (Unesp)Universidade de São Paulo (USP)Moffa, Eduardo B. [UNESP]Mussi, Maria C. M.Xiao, YizhiGarrido, Saulo S. [UNESP]Machado, Maria A. A. M.Giampaolo, Eunice T. [UNESP]Siqueira, Walter L.2018-11-26T16:16:34Z2018-11-26T16:16:34Z2015-08-28info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article7application/pdfhttp://dx.doi.org/10.3389/fmicb.2015.00885Frontiers In Microbiology. Lausanne: Frontiers Media Sa, v. 6, 7 p., 2015.1664-302Xhttp://hdl.handle.net/11449/16074910.3389/fmicb.2015.00885WOS:000360341400001WOS000360341400001.pdfWeb of Sciencereponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengFrontiers In Microbiologyinfo:eu-repo/semantics/openAccess2024-09-27T14:57:17Zoai:repositorio.unesp.br:11449/160749Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestrepositoriounesp@unesp.bropendoar:29462024-09-27T14:57:17Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false |
dc.title.none.fl_str_mv |
Histatin 5 inhibits adhesion of C. albicans to Reconstructed Human Oral Epithelium |
title |
Histatin 5 inhibits adhesion of C. albicans to Reconstructed Human Oral Epithelium |
spellingShingle |
Histatin 5 inhibits adhesion of C. albicans to Reconstructed Human Oral Epithelium Moffa, Eduardo B. [UNESP] histatins salivary proteins mucosal pellicle oral mucosa Candida albicans |
title_short |
Histatin 5 inhibits adhesion of C. albicans to Reconstructed Human Oral Epithelium |
title_full |
Histatin 5 inhibits adhesion of C. albicans to Reconstructed Human Oral Epithelium |
title_fullStr |
Histatin 5 inhibits adhesion of C. albicans to Reconstructed Human Oral Epithelium |
title_full_unstemmed |
Histatin 5 inhibits adhesion of C. albicans to Reconstructed Human Oral Epithelium |
title_sort |
Histatin 5 inhibits adhesion of C. albicans to Reconstructed Human Oral Epithelium |
author |
Moffa, Eduardo B. [UNESP] |
author_facet |
Moffa, Eduardo B. [UNESP] Mussi, Maria C. M. Xiao, Yizhi Garrido, Saulo S. [UNESP] Machado, Maria A. A. M. Giampaolo, Eunice T. [UNESP] Siqueira, Walter L. |
author_role |
author |
author2 |
Mussi, Maria C. M. Xiao, Yizhi Garrido, Saulo S. [UNESP] Machado, Maria A. A. M. Giampaolo, Eunice T. [UNESP] Siqueira, Walter L. |
author2_role |
author author author author author author |
dc.contributor.none.fl_str_mv |
Univ Western Ontario Universidade Estadual Paulista (Unesp) Universidade de São Paulo (USP) |
dc.contributor.author.fl_str_mv |
Moffa, Eduardo B. [UNESP] Mussi, Maria C. M. Xiao, Yizhi Garrido, Saulo S. [UNESP] Machado, Maria A. A. M. Giampaolo, Eunice T. [UNESP] Siqueira, Walter L. |
dc.subject.por.fl_str_mv |
histatins salivary proteins mucosal pellicle oral mucosa Candida albicans |
topic |
histatins salivary proteins mucosal pellicle oral mucosa Candida albicans |
description |
Candida albicans is the most pathogenic fungal species, commonly colonizing on human mucosal surfaces. As a polymorphic species, C. albicans is capable of switching between yeast and hyphal forms, causing an array of mucosal and disseminated infections with high mortality. While the yeast form is most commonly associated with systemic disease, the hyphae are more adept at adhering to and penetrating host tissue and are therefore frequently observed in mucosal fungal infections, most commonly oral candidiasis. The formation of a saliva-derived protein pellicle on the mucosa surface can provide protection against C. albicans on oral epithelial cells, and narrow information is available on the mucosal pellicle composition. Histatins are one of the most abundant salivary proteins and presents antifungal and antibacterial activities against many species of the oral microbiota, however, its presence has never been studied in oral mucosa pellicle. The objective of this study was to evaluate the potential of histatin 5 to protect the Human Oral Epithelium against C. albicans adhesion. Human Oral Epithelial Tissues (HOET) were incubated with PBS containing histatin 5 for 2 h, followed by incubation with C. albicans for 1 h at 37 degrees C. The tissues were then washed several times in PBS, transferred to fresh RPMI and incubated for 16 h at 37 degrees C at 5% CO2. HOET were then prepared for histopathological analysis using light microscopy. In addition, the TUNEL assay was employed to evaluate the apoptosis of epithelial cells using fluorescent microscopy. HOET pre-incubated with histatin 5 showed a lower rate of C. albicans growth and cell apoptosis when compared to the control groups (HOET alone and HOET incubated with C. albicans). The data suggest that the coating with histatin 5 is able to reduce C. albicans colonization on epithelial cell surfaces and also protect the basal cell layers from undergoing apoptosis. |
publishDate |
2015 |
dc.date.none.fl_str_mv |
2015-08-28 2018-11-26T16:16:34Z 2018-11-26T16:16:34Z |
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/10.3389/fmicb.2015.00885 Frontiers In Microbiology. Lausanne: Frontiers Media Sa, v. 6, 7 p., 2015. 1664-302X http://hdl.handle.net/11449/160749 10.3389/fmicb.2015.00885 WOS:000360341400001 WOS000360341400001.pdf |
url |
http://dx.doi.org/10.3389/fmicb.2015.00885 http://hdl.handle.net/11449/160749 |
identifier_str_mv |
Frontiers In Microbiology. Lausanne: Frontiers Media Sa, v. 6, 7 p., 2015. 1664-302X 10.3389/fmicb.2015.00885 WOS:000360341400001 WOS000360341400001.pdf |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
Frontiers In Microbiology |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
7 application/pdf |
dc.publisher.none.fl_str_mv |
Frontiers Media Sa |
publisher.none.fl_str_mv |
Frontiers Media Sa |
dc.source.none.fl_str_mv |
Web of Science 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 |
repositoriounesp@unesp.br |
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1813546485489336320 |