Histatin 5 inhibits adhesion of C. albicans to Reconstructed Human Oral Epithelium

Detalhes bibliográficos
Autor(a) principal: Moffa, Eduardo B. [UNESP]
Data de Publicação: 2015
Outros Autores: Mussi, Maria C. M., Xiao, Yizhi, Garrido, Saulo S. [UNESP], Machado, Maria A. A. M., Giampaolo, Eunice T. [UNESP], Siqueira, Walter L.
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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spelling 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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