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Statherin-derived peptides as antifungal strategy against Candida albicans

dc.contributor.authorPellissari, Claudia Viviane Guimarães [UNESP]
dc.contributor.authorJorge, Janaina Habib [UNESP]
dc.contributor.authorMarin, Lina Maria
dc.contributor.authorSabino-Silva, Robinson
dc.contributor.authorSiqueira, Walter Luiz
dc.contributor.institutionUniversidade Estadual Paulista (Unesp)
dc.contributor.institutionUniversity of Saskatchewan
dc.contributor.institutionUniversidade Federal de Uberlândia (UFU)
dc.date.accessioned2021-06-25T10:55:22Z
dc.date.available2021-06-25T10:55:22Z
dc.date.issued2021-05-01
dc.description.abstractObjective: The aim of this in vitro study was to evaluate the effect of statherin and its naturally occurring peptides (DR9-2, DR9, GE-12, IT-32, GQ-19, IP-18) on Candida albicans metabolism and biofilm development. Design: After the killing assay, a peptide pellicle was formed on the bottom of a polystyrene plate at the IC50 of each peptide. Over the peptide pellicle, Candida albicans biofilm (48 h) was grown. The peptides antimicrobial activity after the peptides treatment was evaluated by alamarBlue, total biofilm biomass and colony forming units (CFU) counting. Results: The pellicle with statherin and the peptides (DR9-2, DR9, GE-12, IP-18, GQ-19) was able to reduce he viability of Candida albicans compared to the negative control. They also decreased cell proliferation by 20 % and total biomass. IT-32 showed the highest reduction in cell proliferation and biomass, which was similar to the positive control, histatin 5. Conclusions: These results suggest that the naturally occuring peptides from statherin are able to decrease Candida albicans colonization and biofilm proliferation.en
dc.description.affiliationDepartment of Dental Materials and Prosthodontics Araraquara Dental School São Paulo State University UNESP, 1680 Rua Humaitá
dc.description.affiliationCollege of Dentistry University of Saskatchewan, 105 Wiggins Road
dc.description.affiliationDepartment of Physiology Institute of Biomedical Sciences Federal University of Uberlandia, 3Q – 2121 Av. João Naves de Ávila
dc.description.affiliationUnespDepartment of Dental Materials and Prosthodontics Araraquara Dental School São Paulo State University UNESP, 1680 Rua Humaitá
dc.description.sponsorshipCanadian Institutes of Health Research
dc.description.sponsorshipFundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)
dc.description.sponsorshipIdCanadian Institutes of Health Research: # 106657
dc.description.sponsorshipIdFAPESP: # 2015/06016-1
dc.description.sponsorshipIdCanadian Institutes of Health Research: # 400347
dc.description.sponsorshipIdFAPESP: #2016/03847-2
dc.description.sponsorshipIdFAPESP: #2018/13904-9
dc.identifierhttp://dx.doi.org/10.1016/j.archoralbio.2021.105106
dc.identifier.citationArchives of Oral Biology, v. 125.
dc.identifier.doi10.1016/j.archoralbio.2021.105106
dc.identifier.issn1879-1506
dc.identifier.issn0003-9969
dc.identifier.scopus2-s2.0-85102487078
dc.identifier.urihttp://hdl.handle.net/11449/207449
dc.language.isoeng
dc.relation.ispartofArchives of Oral Biology
dc.sourceScopus
dc.subjectAntifungal activity
dc.subjectCandida albicans
dc.subjectStomatitis
dc.titleStatherin-derived peptides as antifungal strategy against Candida albicansen
dc.typeArtigopt
dspace.entity.typePublication
relation.isDepartmentOfPublication3936e2e2-946a-42ab-8b9d-9521513200fc
relation.isDepartmentOfPublication.latestForDiscovery3936e2e2-946a-42ab-8b9d-9521513200fc
relation.isOrgUnitOfPublicationca4c0298-cd82-48ee-a9c8-c97704bac2b0
relation.isOrgUnitOfPublication.latestForDiscoveryca4c0298-cd82-48ee-a9c8-c97704bac2b0
unesp.author.orcid0000-0002-9135-3455[2]
unesp.author.orcid0000-0003-2108-4656[3]
unesp.campusUniversidade Estadual Paulista (UNESP), Faculdade de Odontologia, Araraquarapt
unesp.departmentMateriais Odontológicos e Prótese - FOARpt

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