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Inactivation of Streptococcus mutans genes lytST and dltAD impairs its pathogenicity in vivo

dc.contributor.authorCastillo Pedraza, Midian C. [UNESP]
dc.contributor.authorRosalen, Pedro L.
dc.contributor.authorCastilho, Aline Rogéria Freire de
dc.contributor.authorFreires, Irlan de Almeida
dc.contributor.authorde Sales Leite, Luana [UNESP]
dc.contributor.authorFaustoferri, Roberta C.
dc.contributor.authorQuivey Jr, Robert G.
dc.contributor.authorKlein, Marlise I. [UNESP]
dc.contributor.institutionUniversidade Estadual Paulista (Unesp)
dc.contributor.institutionUniversidade Estadual de Campinas (UNICAMP)
dc.contributor.institutionUniversity of Rochester
dc.date.accessioned2019-10-06T15:43:30Z
dc.date.available2019-10-06T15:43:30Z
dc.date.issued2019-01-01
dc.description.abstractBackground: Streptococcus mutans orchestrates the development of a biofilm that causes dental caries in the presence of dietary sucrose, and, in the bloodstream, S. mutans can cause systemic infections. The development of a cariogenic biofilm is dependent on the formation of an extracellular matrix rich in exopolysaccharides, which contains extracellular DNA (eDNA) and lipoteichoic acids (LTAs). While the exopolysaccharides are virulence markers, the involvement of genes linked to eDNA and LTAs metabolism in the pathogenicity of S. mutans remains unclear. Objective and Design: In this study, a parental strain S. mutans UA159 and derivative strains carrying single gene deletions were used to investigate the role of eDNA (ΔlytS and ΔlytT), LTA (ΔdltA and ΔdltD), and insoluble exopolysaccharides (ΔgtfB) in virulence in a rodent model of dental caries (rats) and a systemic infection model (Galleria mellonella larvae). Results: Fewer carious lesions were observed on smooth and sulcal surfaces of enamel and dentin of the rats infected with ∆lytS, ∆dltD, and ΔgtfB (vs. the parental strain). Moreover, strains carrying gene deletions prevented the killing of larvae (vs. the parental strain). Conclusions: Altogether, these findings indicate that inactivation of lytST and dltAD impaired S. mutans cariogenicity and virulence in vivo.en
dc.description.affiliationDepartment of Dental Materials and Prosthodontics Sao Paulo State University (Unesp) School of Dentistry
dc.description.affiliationDepartment of Physiological Sciences Piracicaba Dental School University of Campinas–UNICAMP
dc.description.affiliationDepartment of Pediatric Dentistry Piracicaba Dental School University of Campinas–UNICAMP
dc.description.affiliationCenter for Oral Biology University of Rochester
dc.description.affiliationUnespDepartment of Dental Materials and Prosthodontics Sao Paulo State University (Unesp) School of Dentistry
dc.identifierhttp://dx.doi.org/10.1080/20002297.2019.1607505
dc.identifier.citationJournal of Oral Microbiology, v. 11, n. 1, 2019.
dc.identifier.doi10.1080/20002297.2019.1607505
dc.identifier.issn2000-2297
dc.identifier.scopus2-s2.0-85065714274
dc.identifier.urihttp://hdl.handle.net/11449/187666
dc.language.isoeng
dc.relation.ispartofJournal of Oral Microbiology
dc.rights.accessRightsAcesso aberto
dc.sourceScopus
dc.subjectdental caries
dc.subjecteDNA
dc.subjectExopolysaccharides
dc.subjectlipoteichoic acids
dc.subjectoxidative stress
dc.subjectsystemic infection
dc.titleInactivation of Streptococcus mutans genes lytST and dltAD impairs its pathogenicity in vivoen
dc.typeArtigo
dspace.entity.typePublication
unesp.author.orcid0000-0003-0812-4027[2]
unesp.author.orcid0000-0003-4704-6973[3]
unesp.author.orcid0000-0002-1079-6941[4]
unesp.author.orcid0000-0001-8204-838X[7]
unesp.author.orcid0000-0002-7916-1557[8]

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