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Identification of Specific Anaerobic Bacteria in Endodontic Infections of Primary Teeth—A PCR Study
INTRODUCTION: Invasion of microorganisms and their multiplication in root canals (RCs) results in endodontic infections of primary teeth. Acute and chronic inflammation may be present in the periapical area and are based on the amount and virulence of microorganisms, especially anaerobic bacteria pr...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Jaypee Brothers Medical Publishers
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6710938/ https://www.ncbi.nlm.nih.gov/pubmed/31496562 http://dx.doi.org/10.5005/jp-journals-10005-1573 |
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author | Thimmegowda, Umapathy Thomas, Joseph Bilichodmath, Shivaprasad Preethi, Naveena |
author_facet | Thimmegowda, Umapathy Thomas, Joseph Bilichodmath, Shivaprasad Preethi, Naveena |
author_sort | Thimmegowda, Umapathy |
collection | PubMed |
description | INTRODUCTION: Invasion of microorganisms and their multiplication in root canals (RCs) results in endodontic infections of primary teeth. Acute and chronic inflammation may be present in the periapical area and are based on the amount and virulence of microorganisms, especially anaerobic bacteria present in the RC. To identify microorganisms very precisely in endodontic infections, polymerase chain reaction (PCR) is used. AIM: The aim of the present study is to identify the specific anaerobic bacteria like Porphyromonas gingivalis, Prevotella intermedia, and Actinomyces naeslundii in the RCs of primary teeth using real-time PCR. METHODOLOGY: Fifteen subjects aged 3–8 years who had endodontic infections in primary molars were selected. The cases who had been selected did not receive any endodontic treatment and antibiotics within 3 months, and children with systemic diseases were not included. SAMPLE COLLECTION: Samples were taken by placing absorbent paper points into the largest canals of maxillary and mandibular molars for 60 seconds and are then transferred to a sterile Eppendorf tube with tris-hydochloride EDTA (TE) buffer. The samples were stored at −80°C. All samples were subjected to PCR analysis. RESULT: The specific anaerobes detected in the samples were A. naeslundii (93.3%), Prevotella intermedia (53.3%), and Porphyromonas gingivalis (13.3%). CONCLUSION: The results suggested a high bacterial diversity in the RCs of infected primary teeth. HOW TO CITE THIS ARTICLE: Thimmegowda U, Thomas J, et al. Identification of Specific Anaerobic Bacteria in Endodontic Infections of Primary Teeth—A PCR Study. Int J Clin Pediatr Dent 2019;12(1):1–4. |
format | Online Article Text |
id | pubmed-6710938 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Jaypee Brothers Medical Publishers |
record_format | MEDLINE/PubMed |
spelling | pubmed-67109382019-09-06 Identification of Specific Anaerobic Bacteria in Endodontic Infections of Primary Teeth—A PCR Study Thimmegowda, Umapathy Thomas, Joseph Bilichodmath, Shivaprasad Preethi, Naveena Int J Clin Pediatr Dent Original Article INTRODUCTION: Invasion of microorganisms and their multiplication in root canals (RCs) results in endodontic infections of primary teeth. Acute and chronic inflammation may be present in the periapical area and are based on the amount and virulence of microorganisms, especially anaerobic bacteria present in the RC. To identify microorganisms very precisely in endodontic infections, polymerase chain reaction (PCR) is used. AIM: The aim of the present study is to identify the specific anaerobic bacteria like Porphyromonas gingivalis, Prevotella intermedia, and Actinomyces naeslundii in the RCs of primary teeth using real-time PCR. METHODOLOGY: Fifteen subjects aged 3–8 years who had endodontic infections in primary molars were selected. The cases who had been selected did not receive any endodontic treatment and antibiotics within 3 months, and children with systemic diseases were not included. SAMPLE COLLECTION: Samples were taken by placing absorbent paper points into the largest canals of maxillary and mandibular molars for 60 seconds and are then transferred to a sterile Eppendorf tube with tris-hydochloride EDTA (TE) buffer. The samples were stored at −80°C. All samples were subjected to PCR analysis. RESULT: The specific anaerobes detected in the samples were A. naeslundii (93.3%), Prevotella intermedia (53.3%), and Porphyromonas gingivalis (13.3%). CONCLUSION: The results suggested a high bacterial diversity in the RCs of infected primary teeth. HOW TO CITE THIS ARTICLE: Thimmegowda U, Thomas J, et al. Identification of Specific Anaerobic Bacteria in Endodontic Infections of Primary Teeth—A PCR Study. Int J Clin Pediatr Dent 2019;12(1):1–4. Jaypee Brothers Medical Publishers 2019 /pmc/articles/PMC6710938/ /pubmed/31496562 http://dx.doi.org/10.5005/jp-journals-10005-1573 Text en Copyright © 2019; Jaypee Brothers Medical Publishers (P) Ltd. This work is licensed under a Creative Commons Attribution 4.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Original Article Thimmegowda, Umapathy Thomas, Joseph Bilichodmath, Shivaprasad Preethi, Naveena Identification of Specific Anaerobic Bacteria in Endodontic Infections of Primary Teeth—A PCR Study |
title | Identification of Specific Anaerobic Bacteria in Endodontic Infections of Primary Teeth—A PCR Study |
title_full | Identification of Specific Anaerobic Bacteria in Endodontic Infections of Primary Teeth—A PCR Study |
title_fullStr | Identification of Specific Anaerobic Bacteria in Endodontic Infections of Primary Teeth—A PCR Study |
title_full_unstemmed | Identification of Specific Anaerobic Bacteria in Endodontic Infections of Primary Teeth—A PCR Study |
title_short | Identification of Specific Anaerobic Bacteria in Endodontic Infections of Primary Teeth—A PCR Study |
title_sort | identification of specific anaerobic bacteria in endodontic infections of primary teeth—a pcr study |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6710938/ https://www.ncbi.nlm.nih.gov/pubmed/31496562 http://dx.doi.org/10.5005/jp-journals-10005-1573 |
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