Evidence map›Paper›PMID 39963317›Full record

ArticleFrontiers in oral health2025

Whole-genome amplification as a tool to improve bacterial detection by PCR in microbiological samples after endodontic treatment.

Gabriela Ceccon Chianca, Caroline Corrêa Fendeler, Sérgio Pinto Chaves Junior, Gabriella Lorena Dias Pereira, Helvécio Cardoso Corrêa Póvoa, Lívia Azeredo Alves Antunes, Leonardo Santos Antunes, Natalia Lopes Pontes Póvoa Iorio

Abstract read
In one paragraph

Article in Frontiers in oral health, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors.

Gabriela Ceccon Chianca *Experimental and Applied Microbiology Laboratory, Nova Friburgo Institute of Health, Universidade Federal Fluminense (UFF), Nova Friburgo, Rio de Janeiro, Brazil.
Caroline Corrêa Fendeler *Experimental and Applied Microbiology Laboratory, Nova Friburgo Institute of Health, Universidade Federal Fluminense (UFF), Nova Friburgo, Rio de Janeiro, Brazil.
Sérgio Pinto Chaves JuniorExperimental and Applied Microbiology Laboratory, Nova Friburgo Institute of Health, Universidade Federal Fluminense (UFF), Nova Friburgo, Rio de Janeiro, Brazil.
Gabriella Lorena Dias PereiraExperimental and Applied Microbiology Laboratory, Nova Friburgo Institute of Health, Universidade Federal Fluminense (UFF), Nova Friburgo, Rio de Janeiro, Brazil.
Helvécio Cardoso Corrêa PóvoaExperimental and Applied Microbiology Laboratory, Nova Friburgo Institute of Health, Universidade Federal Fluminense (UFF), Nova Friburgo, Rio de Janeiro, Brazil.
Lívia Azeredo Alves AntunesGraduate Program in Dentistry, Nova Friburgo Institute of Health, UFF, Nova Friburgo, Rio de Janeiro, Brazil.
Leonardo Santos AntunesGraduate Program in Dentistry, Nova Friburgo Institute of Health, UFF, Nova Friburgo, Rio de Janeiro, Brazil.
Natalia Lopes Pontes Póvoa IorioExperimental and Applied Microbiology Laboratory, Nova Friburgo Institute of Health, Universidade Federal Fluminense (UFF), Nova Friburgo, Rio de Janeiro, Brazil.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Microorganisms have an important role in the pathogenesis of endodontic disease. Significant advances have been made to increase the sensitivity of microbial detection, identification and enumeration in endodontic samples. The aim of the present study is to compare culture and whole-genome amplification (WGA) followed by PCR assays in the detection of bacteria before and after chemical mechanical preparation (CMP) of root canals. Methods: Ten uniradicular teeth with primary endodontic infections were analyzed. Microbiological samples were collected before and after CMP using paper points, which were separated into two groups: (i) culture assay samples were plated onto Brucella agar with 5% defibrinated sheep's blood, menadione and hemin and incubated anaerobically for 14 days at 36°C; (ii) DNA was extracted from molecular assay samples and subject to WGA by isothermal strand displacement with Phi29 DNA polymerase followed by PCR to determine the presence of bacteria. Results: In both assays, samples before CMP showed the presence of bacteria in all 10 teeth. After CMP, however, bacterial detection differed in the assays performed ( Conclusion: The combination of WGA followed by PCR increased the detection of microorganisms from root canal samples after endodontic treatment using NaOCl as a CMP irrigant. So this combination of techniques can represent an important tool to improve the detection of microorganisms in endodontic research.

Indexed as

bacteriadental pulp necrosismicrobiologynucleic acid amplification techniquespolymerase chain reaction

Identifiers

PMID39963317
PMCPMC11830671

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.