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Streptococcus mutans supernatant affects the virulence of Candida albicans

dc.contributor.authorGarcia, Maíra Terra [UNESP]
dc.contributor.authordos Santos, Jéssica Diane [UNESP]
dc.contributor.authordo Carmo, Paulo Henrique Fonseca [UNESP]
dc.contributor.authorMendes, Gabriela Vieira [UNESP]
dc.contributor.authorde Oliveira, Jonatas Rafael
dc.contributor.authorde Oliveira, Luciane Dias [UNESP]
dc.contributor.authorJunqueira, Juliana Campos [UNESP]
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)
dc.contributor.institutionSchool of Medicine
dc.date.accessioned2025-04-29T18:57:29Z
dc.date.issued2024-03-01
dc.description.abstractCandida albicans causes a variety of clinical manifestations through multiple virulence factors that act simultaneously to overcome the immune system and invade the host tissues. Owing to the limited number of antifungal agents available, new candidiasis therapeutic strategies are required. Previous studies have demonstrated that the metabolites produced by Streptococcus mutans lead to a decrease in the number of Candida cells. Here, for the first time, we evaluated whether the C. albicans cells that survived the pretreatment with S. mutans supernatant can modify their virulence factors and their capability to infect Galleria mellonella larvae. Streptococcus mutans supernatant (SM-S) was obtained by filtering the culture supernatant of this bacterium. Then, C. albicans cells were pretreated with SM-S for 24 h, and the surviving cells were evaluated using in vitro and in vivo assays. The C. albicans pretreated with SM-S showed a significant inhibition of hyphal growth, an altered adhesion pattern, and an impaired capability to form biofilms; however, its proteolytic activity was not affected. In the in vivo assays, C. albicans cells previously exposed to SM-S exhibited a reduced ability to infect G. mellonella and a higher amount of circulating hemocytes. Thus, SM-S could inhibit important virulence factors of C. albicans, which may contribute to the development of new candidiasis therapeutic strategies.en
dc.description.affiliationDepartment of Biosciences and Oral Diagnosis São Paulo State University (UNESP) Institute of Science and Technology, Av. Engenheiro Francisco José Longo, 777, SP
dc.description.affiliationAnhembi Morumbi University School of Medicine, Av. Deputado Benedito Matarazzo, 6709, SP
dc.description.affiliationUnespDepartment of Biosciences and Oral Diagnosis São Paulo State University (UNESP) Institute of Science and Technology, Av. Engenheiro Francisco José Longo, 777, SP
dc.format.extent365-374
dc.identifierhttp://dx.doi.org/10.1007/s42770-023-01198-6
dc.identifier.citationBrazilian Journal of Microbiology, v. 55, n. 1, p. 365-374, 2024.
dc.identifier.doi10.1007/s42770-023-01198-6
dc.identifier.issn1678-4405
dc.identifier.issn1517-8382
dc.identifier.scopus2-s2.0-85178217742
dc.identifier.urihttps://hdl.handle.net/11449/301196
dc.language.isoeng
dc.relation.ispartofBrazilian Journal of Microbiology
dc.sourceScopus
dc.subjectAntifungal metabolites
dc.subjectCandida albicans
dc.subjectCandidiasis
dc.subjectGalleria mellonella
dc.subjectStreptococcus mutans
dc.subjectVirulence factors
dc.titleStreptococcus mutans supernatant affects the virulence of Candida albicansen
dc.typeArtigopt
dspace.entity.typePublication
unesp.author.orcid0000-0002-1193-2909[1]
unesp.author.orcid0000-0003-0769-2938[2]
unesp.author.orcid0000-0003-3186-885X[3]
unesp.author.orcid0000-0003-1600-8560[4]
unesp.author.orcid0000-0003-2398-6506[5]
unesp.author.orcid0000-0001-9956-7768[6]
unesp.author.orcid0000-0001-6646-6856[7]
unesp.campusUniversidade Estadual Paulista (UNESP), Instituto de Ciência e Tecnologia, São José dos Campospt

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