Cargando…

The apical root canal system microbial communities determined by next-generation sequencing

The aim of this study was to explore the microbial communities of endodontic infections at their apical portion by 16S rRNA Illumina sequencing and delineate the core microbiome of root canal infections and that of their associated clinical symptomatology. Samples were collected from fifteen subject...

Descripción completa

Detalles Bibliográficos
Autores principales: de Brito, Luciana Carla Neves, Doolittle-Hall, Janet, Lee, Chun-Teh, Moss, Kevin, Bambirra Júnior, Wilson, Tavares, Warley Luciano Fonseca, Ribeiro Sobrinho, Antônio Paulino, Teles, Flávia Rocha Fonseca
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7331743/
https://www.ncbi.nlm.nih.gov/pubmed/32616783
http://dx.doi.org/10.1038/s41598-020-67828-3
_version_ 1783553394682626048
author de Brito, Luciana Carla Neves
Doolittle-Hall, Janet
Lee, Chun-Teh
Moss, Kevin
Bambirra Júnior, Wilson
Tavares, Warley Luciano Fonseca
Ribeiro Sobrinho, Antônio Paulino
Teles, Flávia Rocha Fonseca
author_facet de Brito, Luciana Carla Neves
Doolittle-Hall, Janet
Lee, Chun-Teh
Moss, Kevin
Bambirra Júnior, Wilson
Tavares, Warley Luciano Fonseca
Ribeiro Sobrinho, Antônio Paulino
Teles, Flávia Rocha Fonseca
author_sort de Brito, Luciana Carla Neves
collection PubMed
description The aim of this study was to explore the microbial communities of endodontic infections at their apical portion by 16S rRNA Illumina sequencing and delineate the core microbiome of root canal infections and that of their associated clinical symptomatology. Samples were collected from fifteen subjects presenting one tooth with a root canal infection, and their associated symptoms were recorded. Samples were collected from the apical third of roots using a #10 K file and then amplified using multiple displacement amplification and PCR-amplified with universal primers. Amplicons were sequenced (V3–V4 hypervariable region of the 16S rRNA gene) using MiSeq (Illumina, CA). The microbial composition of the samples was determined using QIIME and HOMINGS. Data were analyzed using t tests and ANOVA. A total of 1,038,656 good quality sequences were obtained, and OTUs were assigned to 10 bacterial phyla, led by Bacteroidetes (51.2%) and Firmicutes (27.1%), and 94 genera were represented primarily by Prevotella (17.9%) and Bacteroidaceae G-1 (14.3%). Symptomatic teeth were associated with higher levels of Porphyromonas (p < 0.05) and Prevotella. P. endodontalis and P. oris were present in both cores. The present study demonstrated the complexity of the root canal microbiome and the “common denominators” of root canal infections and identified taxa whose virulence properties should be further explored. The polymicrobial etiology of endodontic infections has long been established. However, few studies have focused on expanding the breadth and depth of coverage of microbiome-infected root canals at their apical portion.
format Online
Article
Text
id pubmed-7331743
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher Nature Publishing Group UK
record_format MEDLINE/PubMed
spelling pubmed-73317432020-07-06 The apical root canal system microbial communities determined by next-generation sequencing de Brito, Luciana Carla Neves Doolittle-Hall, Janet Lee, Chun-Teh Moss, Kevin Bambirra Júnior, Wilson Tavares, Warley Luciano Fonseca Ribeiro Sobrinho, Antônio Paulino Teles, Flávia Rocha Fonseca Sci Rep Article The aim of this study was to explore the microbial communities of endodontic infections at their apical portion by 16S rRNA Illumina sequencing and delineate the core microbiome of root canal infections and that of their associated clinical symptomatology. Samples were collected from fifteen subjects presenting one tooth with a root canal infection, and their associated symptoms were recorded. Samples were collected from the apical third of roots using a #10 K file and then amplified using multiple displacement amplification and PCR-amplified with universal primers. Amplicons were sequenced (V3–V4 hypervariable region of the 16S rRNA gene) using MiSeq (Illumina, CA). The microbial composition of the samples was determined using QIIME and HOMINGS. Data were analyzed using t tests and ANOVA. A total of 1,038,656 good quality sequences were obtained, and OTUs were assigned to 10 bacterial phyla, led by Bacteroidetes (51.2%) and Firmicutes (27.1%), and 94 genera were represented primarily by Prevotella (17.9%) and Bacteroidaceae G-1 (14.3%). Symptomatic teeth were associated with higher levels of Porphyromonas (p < 0.05) and Prevotella. P. endodontalis and P. oris were present in both cores. The present study demonstrated the complexity of the root canal microbiome and the “common denominators” of root canal infections and identified taxa whose virulence properties should be further explored. The polymicrobial etiology of endodontic infections has long been established. However, few studies have focused on expanding the breadth and depth of coverage of microbiome-infected root canals at their apical portion. Nature Publishing Group UK 2020-07-02 /pmc/articles/PMC7331743/ /pubmed/32616783 http://dx.doi.org/10.1038/s41598-020-67828-3 Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
de Brito, Luciana Carla Neves
Doolittle-Hall, Janet
Lee, Chun-Teh
Moss, Kevin
Bambirra Júnior, Wilson
Tavares, Warley Luciano Fonseca
Ribeiro Sobrinho, Antônio Paulino
Teles, Flávia Rocha Fonseca
The apical root canal system microbial communities determined by next-generation sequencing
title The apical root canal system microbial communities determined by next-generation sequencing
title_full The apical root canal system microbial communities determined by next-generation sequencing
title_fullStr The apical root canal system microbial communities determined by next-generation sequencing
title_full_unstemmed The apical root canal system microbial communities determined by next-generation sequencing
title_short The apical root canal system microbial communities determined by next-generation sequencing
title_sort apical root canal system microbial communities determined by next-generation sequencing
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7331743/
https://www.ncbi.nlm.nih.gov/pubmed/32616783
http://dx.doi.org/10.1038/s41598-020-67828-3
work_keys_str_mv AT debritolucianacarlaneves theapicalrootcanalsystemmicrobialcommunitiesdeterminedbynextgenerationsequencing
AT doolittlehalljanet theapicalrootcanalsystemmicrobialcommunitiesdeterminedbynextgenerationsequencing
AT leechunteh theapicalrootcanalsystemmicrobialcommunitiesdeterminedbynextgenerationsequencing
AT mosskevin theapicalrootcanalsystemmicrobialcommunitiesdeterminedbynextgenerationsequencing
AT bambirrajuniorwilson theapicalrootcanalsystemmicrobialcommunitiesdeterminedbynextgenerationsequencing
AT tavareswarleylucianofonseca theapicalrootcanalsystemmicrobialcommunitiesdeterminedbynextgenerationsequencing
AT ribeirosobrinhoantoniopaulino theapicalrootcanalsystemmicrobialcommunitiesdeterminedbynextgenerationsequencing
AT telesflaviarochafonseca theapicalrootcanalsystemmicrobialcommunitiesdeterminedbynextgenerationsequencing
AT debritolucianacarlaneves apicalrootcanalsystemmicrobialcommunitiesdeterminedbynextgenerationsequencing
AT doolittlehalljanet apicalrootcanalsystemmicrobialcommunitiesdeterminedbynextgenerationsequencing
AT leechunteh apicalrootcanalsystemmicrobialcommunitiesdeterminedbynextgenerationsequencing
AT mosskevin apicalrootcanalsystemmicrobialcommunitiesdeterminedbynextgenerationsequencing
AT bambirrajuniorwilson apicalrootcanalsystemmicrobialcommunitiesdeterminedbynextgenerationsequencing
AT tavareswarleylucianofonseca apicalrootcanalsystemmicrobialcommunitiesdeterminedbynextgenerationsequencing
AT ribeirosobrinhoantoniopaulino apicalrootcanalsystemmicrobialcommunitiesdeterminedbynextgenerationsequencing
AT telesflaviarochafonseca apicalrootcanalsystemmicrobialcommunitiesdeterminedbynextgenerationsequencing