Cultivable Anaerobic Microbiota of Infected Root Canals

Objective. Periapical periodontitis is an infectious and inflammatory disease of the periapical tissues caused by oral bacteria invading the root canal. In the present study, profiling of the microbiota in infected root canals was performed using anaerobic culture and molecular biological techniques...

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Main Authors: Takuichi Sato, Keiko Yamaki, Naoko Ishida, Kazuhiro Hashimoto, Yasuhisa Takeuchi, Megumi Shoji, Emika Sato, Junko Matsuyama, Hidetoshi Shimauchi, Nobuhiro Takahashi
Format: Article
Language:English
Published: Wiley 2012-01-01
Series:International Journal of Dentistry
Online Access:http://dx.doi.org/10.1155/2012/609689
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author Takuichi Sato
Keiko Yamaki
Naoko Ishida
Kazuhiro Hashimoto
Yasuhisa Takeuchi
Megumi Shoji
Emika Sato
Junko Matsuyama
Hidetoshi Shimauchi
Nobuhiro Takahashi
author_facet Takuichi Sato
Keiko Yamaki
Naoko Ishida
Kazuhiro Hashimoto
Yasuhisa Takeuchi
Megumi Shoji
Emika Sato
Junko Matsuyama
Hidetoshi Shimauchi
Nobuhiro Takahashi
author_sort Takuichi Sato
collection DOAJ
description Objective. Periapical periodontitis is an infectious and inflammatory disease of the periapical tissues caused by oral bacteria invading the root canal. In the present study, profiling of the microbiota in infected root canals was performed using anaerobic culture and molecular biological techniques for bacterial identification. Methods. Informed consent was obtained from all subjects (age ranges, 34–71 years). Nine infected root canals with periapical lesions from 7 subjects were included. Samples from infected root canals were collected, followed by anaerobic culture on CDC blood agar plates. After 7 days, colony forming units (CFU) were counted and isolated bacteria were identified by 16S rRNA gene sequencing. Results. The mean bacterial count (CFU) in root canals was (0.5±1.1)×106 (range 8.0×101–3.1×106), and anaerobic bacteria were predominant (89.8%). The predominant isolates were Olsenella (25.4%), Mogibacterium (17.7%), Pseudoramibacter (17.7%), Propionibacterium (11.9%) and Parvimonas (5.9%). Conclusion. The combination of anaerobic culture and molecular biological techniques makes it possible to analyze rapidly the microbiota in infected root canals. The overwhelming majority of the isolates from infected root canals were found to be anaerobic bacteria, suggesting that the environment in root canals is anaerobic and therefore support the growth of anaerobes.
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series International Journal of Dentistry
spelling doaj-art-66e1a394f8744d3697d0aeb476daac6f2025-02-03T06:06:10ZengWileyInternational Journal of Dentistry1687-87281687-87362012-01-01201210.1155/2012/609689609689Cultivable Anaerobic Microbiota of Infected Root CanalsTakuichi Sato0Keiko Yamaki1Naoko Ishida2Kazuhiro Hashimoto3Yasuhisa Takeuchi4Megumi Shoji5Emika Sato6Junko Matsuyama7Hidetoshi Shimauchi8Nobuhiro Takahashi9Division of Oral Ecology and Biochemistry, Tohoku University Graduate School of Dentistry, Sendai 980-8575, JapanDivision of Periodontology and Endodontology, Tohoku University Graduate School of Dentistry, Sendai 980-8575, JapanDivision of Advanced Prosthetic Dentistry, Tohoku University Graduate School of Dentistry, Sendai 980-8575, JapanDivision of Periodontology and Endodontology, Tohoku University Graduate School of Dentistry, Sendai 980-8575, JapanDivision of Advanced Prosthetic Dentistry, Tohoku University Graduate School of Dentistry, Sendai 980-8575, JapanDivision of Oral Ecology and Biochemistry, Tohoku University Graduate School of Dentistry, Sendai 980-8575, JapanDivision of Oral Ecology and Biochemistry, Tohoku University Graduate School of Dentistry, Sendai 980-8575, JapanDivision of Pediatric Dentistry, Niigata University Graduate School of Medical and Dental Sciences, Niigata 951-8514, JapanDivision of Periodontology and Endodontology, Tohoku University Graduate School of Dentistry, Sendai 980-8575, JapanDivision of Oral Ecology and Biochemistry, Tohoku University Graduate School of Dentistry, Sendai 980-8575, JapanObjective. Periapical periodontitis is an infectious and inflammatory disease of the periapical tissues caused by oral bacteria invading the root canal. In the present study, profiling of the microbiota in infected root canals was performed using anaerobic culture and molecular biological techniques for bacterial identification. Methods. Informed consent was obtained from all subjects (age ranges, 34–71 years). Nine infected root canals with periapical lesions from 7 subjects were included. Samples from infected root canals were collected, followed by anaerobic culture on CDC blood agar plates. After 7 days, colony forming units (CFU) were counted and isolated bacteria were identified by 16S rRNA gene sequencing. Results. The mean bacterial count (CFU) in root canals was (0.5±1.1)×106 (range 8.0×101–3.1×106), and anaerobic bacteria were predominant (89.8%). The predominant isolates were Olsenella (25.4%), Mogibacterium (17.7%), Pseudoramibacter (17.7%), Propionibacterium (11.9%) and Parvimonas (5.9%). Conclusion. The combination of anaerobic culture and molecular biological techniques makes it possible to analyze rapidly the microbiota in infected root canals. The overwhelming majority of the isolates from infected root canals were found to be anaerobic bacteria, suggesting that the environment in root canals is anaerobic and therefore support the growth of anaerobes.http://dx.doi.org/10.1155/2012/609689
spellingShingle Takuichi Sato
Keiko Yamaki
Naoko Ishida
Kazuhiro Hashimoto
Yasuhisa Takeuchi
Megumi Shoji
Emika Sato
Junko Matsuyama
Hidetoshi Shimauchi
Nobuhiro Takahashi
Cultivable Anaerobic Microbiota of Infected Root Canals
International Journal of Dentistry
title Cultivable Anaerobic Microbiota of Infected Root Canals
title_full Cultivable Anaerobic Microbiota of Infected Root Canals
title_fullStr Cultivable Anaerobic Microbiota of Infected Root Canals
title_full_unstemmed Cultivable Anaerobic Microbiota of Infected Root Canals
title_short Cultivable Anaerobic Microbiota of Infected Root Canals
title_sort cultivable anaerobic microbiota of infected root canals
url http://dx.doi.org/10.1155/2012/609689
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