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Evaluation of microbiome in primary and permanent dentition in grade C periodontitis in young individuals.
Koo, Sungeun Stephanie; Fernandes, Jussara G; Li, Lu; Huang, Hong; Aukhil, Ikramuddin; Harrison, Peter; Diaz, Patricia I; Shaddox, Luciana M.
Afiliación
  • Koo SS; Department of Periodontology, School of Dental Medicine, University of Connecticut, Farmington, Connecticut, USA.
  • Fernandes JG; Department of Oral Health Practice, Periodontology Division and Center for Oral Health Research, College of Dentistry, University of Kentucky, Lexington, Kentucky, USA.
  • Li L; Department of Oral Biology, School of Dental Medicine, University at Buffalo, State University of New York, Buffalo, New York, USA.
  • Huang H; UB Microbiome Center, University at Buffalo, State University of New York, Buffalo, New York, USA.
  • Aukhil I; Department of Periodontology, College of Dentistry, University of Florida, Gainesville, Florida, USA.
  • Harrison P; Department of Periodontology, College of Dentistry, University of Florida, Gainesville, Florida, USA.
  • Diaz PI; Department of Periodontology, College of Dentistry, University of Florida, Gainesville, Florida, USA.
  • Shaddox LM; Department of Periodontology, School of Dental Science, Trinity College Dublin, Dublin, Ireland.
J Periodontol ; 95(7): 650-661, 2024 Jul.
Article en En | MEDLINE | ID: mdl-38476115
ABSTRACT

BACKGROUND:

The aim of the present study was to evaluate the subgingival microbiome in patients with grade C molar-incisor pattern periodontitis (C-MIP) affecting the primary or permanent dentitions.

METHODS:

DNA was isolated from subgingival biofilm samples from diseased and healthy sites from 45 C-MIP patients and subjected to phylogenetic microarray analysis. C-MIP sites were compared between children affected in the primary to those affected in the permanent dentitions. Within-subject differences between C-MIP-affected sites and dentition-matched healthy sites were also evaluated.

RESULTS:

C-MIP sites of subjects affected in the primary dentition showed partially overlapping but distinct microbial communities from C-MIP permanent dentition sites (p < 0.05). Differences were due to increased levels in primary C-MIP sites of certain species of the genera Capnocytophaga and Leptotrichia, while C-MIP permanent dentition sites showed higher prevalence of Filifactor alocis. Aggregatibacter actinomycetemcomitans (Aa) was among species seen in high prevalence and levels in both primary and permanent C-MIP sites. Moreover, both permanent and primary C-MIP sites showed distinct microbial communities when compared to dentition-matched healthy sites in the same subject (p < 0.01).

CONCLUSIONS:

Primary and permanent teeth with C-MIP showed a dysbiotic microbiome, with children affected in the primary dentition showing a distinct profile from those affected in the permanent dentition. However, Aa was enriched in both primary and permanent diseased sites, confirming that this microorganism is implicated in C-MIP in both dentitions.
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Texto completo: 1 Base de datos: MEDLINE Asunto principal: Periodontitis / Diente Primario / Aggregatibacter actinomycetemcomitans / Biopelículas / Dentición Permanente / Microbiota Idioma: En Revista: J Periodontol Año: 2024 Tipo del documento: Article

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Periodontitis / Diente Primario / Aggregatibacter actinomycetemcomitans / Biopelículas / Dentición Permanente / Microbiota Idioma: En Revista: J Periodontol Año: 2024 Tipo del documento: Article