Bacterial diversity in primary and secondary/persistent endodontic infections by Checkerboard DNA-DNA Hybridization technique

dc.contributor.authorEndo, Marcos Sergio
dc.contributor.authorCardoso, Erica Reginato
dc.contributor.authorPavan, Nair Narumi Orita
dc.contributor.authorde Morais, Carlos Alberto Herrero
dc.contributor.authorMartinho, Frederico Canato [UNESP]
dc.contributor.institutionUniversidade Estadual de Maringá (UEM)
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)
dc.date.accessioned2022-04-29T08:27:11Z
dc.date.available2022-04-29T08:27:11Z
dc.date.issued2017-01-01
dc.description.abstractIntroduction: One of the main advantages of the molecular diagnostic methods is detecting microorganisms using the bacterial DNA, leading to a more accurate microbial characterization. Objective: This paper aims to study the bacterial diversity present in primary and secondary/ persistent endodontic infections, comparing the profile of the existing microbial communities before and after endodontic therapy. Methods: Microbiological samples were collected using sterile/non-pyrogenic paper points in teeth with primary endodontic infections (n = 10) and teeth with persistent/secondary endodontic infections (n = 10), before (T1) and after endodontic therapy (T2). The presence and levels of 40 bacterial species in endodontic infections were investigated by checkerboard DNA-DNA hybridization. Results: In primary endodontic infections, higher levels of P. micra, F. nucleatum sp. nucleatum, S. constellatus, P. gingivalis, G. morbillorum, P. endodontalis, T. denticola, P. acnes, S. gordonii, S. mitis, V. parvula and C. rectus were found In T1. For T2, the most frequent bacteria were P. micra, S. oralis and P. acnes. The most frequent species found in T1, considering secondary endodontic infections group were: P. acnes, P. micra, S. constellatus, G. morbillorum, C. rectus, A. naeslundii, S. mitis and S. oralis. In T2, the most frequent species were E. faecalis and P. acnes. Conclusion: This study confirmed the distinctness of microbial communities in primary and secondary endodontic infections. Furthermore, clinical endodontic procedures were significantly effective in reducing the prevalence, the detection levels and bacterial diversity.en
dc.description.affiliationUniversidade Estadual de Maringá Departamento de Odontologia, área de Endodontia
dc.description.affiliationUniversidade Estadual de Maringá Programa de Pós-Graduação em Odontologia Integrada
dc.description.affiliationUniversidade Estadual Paulista Faculdade de Odontologia de São José dos Campos Departamento de Odontologia Restauradora
dc.description.affiliationUnespUniversidade Estadual Paulista Faculdade de Odontologia de São José dos Campos Departamento de Odontologia Restauradora
dc.format.extent61-66
dc.identifierhttp://dx.doi.org/10.14436/2358-2545.7.2.061-066.oar
dc.identifier.citationDental Press Endodontics, v. 7, n. 2, p. 61-66, 2017.
dc.identifier.doi10.14436/2358-2545.7.2.061-066.oar
dc.identifier.issn2178-3713
dc.identifier.scopus2-s2.0-85041951621
dc.identifier.urihttp://hdl.handle.net/11449/228504
dc.language.isoeng
dc.relation.ispartofDental Press Endodontics
dc.sourceScopus
dc.subjectBacteria
dc.subjectDental pulp cavity
dc.subjectEndodontics
dc.titleBacterial diversity in primary and secondary/persistent endodontic infections by Checkerboard DNA-DNA Hybridization techniqueen
dc.typeArtigo
unesp.campusUniversidade Estadual Paulista (Unesp), Instituto de Ciência e Tecnologia, São José dos Campospt
unesp.departmentOdontologia Restauradora - ICTpt

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