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Diversity of Enterococcus faecalis Genotypes from Multiple Oral Sites Associated with Endodontic Failure Using Repetitive Sequence-based Polymerase Chain Reaction and Arbitrarily Primed Polymerase Chain Reaction.
Delboni, Maraísa G; Gomes, Brenda P F A; Francisco, Priscila A; Teixeira, Fabrício B; Drake, David.
Afiliação
  • Delboni MG; College of Dentistry, Facid DeVry University, Teresina, Piauí, Brazil; Department of Restorative Dentistry, Endodontic Division, Piracicaba Dental School, State University of Campinas, Piracicaba, São Paulo, Brazil.
  • Gomes BP; Department of Restorative Dentistry, Endodontic Division, Piracicaba Dental School, State University of Campinas, Piracicaba, São Paulo, Brazil. Electronic address: bpgomes@unicamp.br.
  • Francisco PA; Department of Restorative Dentistry, Endodontic Division, Piracicaba Dental School, State University of Campinas, Piracicaba, São Paulo, Brazil.
  • Teixeira FB; Department of Endodontics, Dows Institute for Dental Research, College of Dentistry, University of Iowa, Iowa City, Iowa.
  • Drake D; Department of Endodontics, Dows Institute for Dental Research, College of Dentistry, University of Iowa, Iowa City, Iowa.
J Endod ; 43(3): 377-382, 2017 Mar.
Article em En | MEDLINE | ID: mdl-28131414
ABSTRACT

INTRODUCTION:

The aim of this study was to evaluate the diversity and similarity of Enterococcus faecalis genotype isolates from multiple oral sites using repetitive sequence-based polymerase chain reaction and arbitrarily primed polymerase chain reaction (AP-PCR).

METHODS:

Forty-two endodontically treated teeth with apical periodontitis were selected. A total of 126 microbial samples were collected from 3 different sites (saliva, pulp chamber, and root canals, all n = 42) during the nonsurgical retreatment procedures. After growth on m-Enterococcus agar, the colonies were isolated, characterized as gram-positive catalase negative cocci, and identified using an API 20 Strep kit (bioMérieux, Marcy-l'Etoile, France). Seventy-four colonies from 10 patients were confirmed as E. faecalis by polymerase chain reaction (16S ribosomal RNA). Repetitive sequence-based polymerase chain reactions using ERIC and AP-PCR using RW3A primers were performed in all 74 colonies. Fingerprints were analyzed and separated into genotypic groups based on the Dice coefficient percentage of similarity (82% or greater) as determined by ERIC reproducibility assays involving E. faecalis controls.

RESULTS:

Seven different E. faecalis genotypes (GTs) (GT1 = 27%, GT2 = 17.6%, GT3 = 1.3%, GT4 = 18.9%, GT5 = 9.5%, GT6 = 14.9%, and GT7 = 10.8%) were observed in different subjects and oral sites associated with endodontic failure. Remarkably, in 4 of 5 patients, the same GTs present in the infected root canals were also isolated from either the pulp chamber or the saliva samples. In particular, GT6 was detected in all 3 oral sites of patient 37.

CONCLUSIONS:

E. faecalis GTs isolated from saliva, the pulp chamber, and the root canal were similar using the Rep-PCR and AP-PCR methods. These findings suggest that coronal microleakage is a conceivable cause of endodontic failure.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Periodontite Periapical / Saliva / Reação em Cadeia da Polimerase / Enterococcus faecalis / Dente não Vital / Cavidade Pulpar / Genótipo Idioma: En Ano de publicação: 2017 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Periodontite Periapical / Saliva / Reação em Cadeia da Polimerase / Enterococcus faecalis / Dente não Vital / Cavidade Pulpar / Genótipo Idioma: En Ano de publicação: 2017 Tipo de documento: Article