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Updated: Feb 4, 2026

Tick Microbiome Characterization by Next-Generation 16S rRNA Amplicon Sequencing
Published on: August 25, 2018
Root Canal Microbiome in Patients Undergoing Antineoplastic Therapy: A Next-generation Sequencing Study
Kaline Romeiro1, José F Siqueira2, Isabela N Rôças2
1Postgraduate Program in Dentistry, University of Grande Rio (UNIGRANRIO), Rio de Janeiro, Rio de Janeiro, Brazil; Division of Dentistry, Pelópidas Silveira Hospital, Recife, Pernambuco, Brazil; Department of Endodontics, Faculty of Dentistry, Facol University Center (UNIFACOL), Vitória de Santo Antão, Pernambuco, Brazil.
Introduction:
This study compared the intracanal microbiome of teeth with apical periodontitis in oncologic and healthy patients using 16S rRNA gene-based next generation sequencing.
Methods:
Root canal samples were taken from 46 teeth with pulp necrosis and primary apical periodontitis (23 from oncologic patients and 23 from healthy controls). DNA was extracted and sequenced using the Illumina MiSeq platform targeting the V3-V4 region of the 16S rRNA gene. Bioinformatics processing was conducted using QIIME2 and DADA2. Alpha and beta diversity analyses, genus-level abundance comparisons, and indicator species analyses were performed.
Results:
After quality filtering, 3,307,822 sequence reads were retained, averaging 68,912.96 reads/sample, and resulting in 3,241 unique amplicon sequence variants. Oncologic patients exhibited significantly higher bacterial richness (P = .01), while Shannon diversity showed no significant difference between groups. Beta diversity analysis (Bray-Curtis, MDS stress = 0.14) did not reveal significant differences between groups. Indicator species analysis identified some specific taxa more associated with oncologic patients, including the candidate endodontic pathogens Prevotella, Selenomonas, Alloprevotella, Rothia, and Fretibacterium.
Conclusions:
The root canal microbiome of oncologic patients with apical periodontitis was broadly similar to that of healthy controls. The oncologic group showed higher species richness, but no significant differences in the overall bacterial diversity or community structure.
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