Plaque Microbiome in Caries-Active and Caries-Free Teeth by Dentition

Author:

Bhaumik D.1,Salzman E.1,Davis E.1,Blostein F.1ORCID,Li G.2,Neiswanger K.3,Weyant R.J.4,Crout R.5,McNeil D.W.6ORCID,Marazita M.L.7,Foxman B.1ORCID

Affiliation:

1. Center of Molecular and Clinical Epidemiology of Infectious Diseases, Department of Epidemiology, University of Michigan School of Public Health, Ann Arbor, MI, USA

2. Department of Biostatistics, University of Michigan School of Public Health, Ann Arbor, MI, USA

3. Center for Craniofacial and Dental Genetics, University of Pittsburgh, Pittsburgh, PA, USA

4. Dental Public Health, School of Dental Medicine, University of Pittsburgh, Pittsburgh, PA, USA

5. Department of Periodontics, West Virginia University, Morgantown, WV, USA

6. Departments of Psychology and Dental Practice & Rural Health, and Center for Oral Health Research in Appalachia, West Virginia University, Morgantown, WV, USA

7. Center for Craniofacial and Dental Genetics, Department of Oral and Craniofacial Sciences; Department of Human Genetics, Graduate School of Public Health; Clinical and Translational Science, School of Medicine University of Pittsburgh, Pittsburgh, PA, USA

Abstract

Objective: Describe associations between dental caries and dental plaque microbiome, by dentition and family membership. Methods: This cross-sectional analysis included 584 participants in the Center for Oral Health Research in Appalachia Cohort 1 (COHRA1). We sequenced the 16S ribosomal RNA gene (V4 region) of frozen supragingival plaque, collected 10 y prior, from 185 caries-active (enamel and dentinal) and 565 caries-free (no lesions) teeth using the Illumina MiSeq platform. Sequences were filtered using the R DADA2 package and assigned taxonomy using the Human Oral Microbiome Database. Results: Microbiomes of caries-active and caries-free teeth were most similar in primary dentition and least similar in permanent dentition, but caries-active teeth were significantly less diverse than caries-free teeth in all dentition types. Streptococcus mutans had greater relative abundance in caries-active than caries-free teeth in all dentition types ( P < 0.01), as did Veillonella dispar in primary and mixed dentition ( P < 0.01). Fusobacterium sp. HMT 203 had significantly higher relative abundance in caries-free than caries-active teeth in all dentition types ( P < 0.01). In a linear mixed model adjusted for confounders, the relative abundance of S. mutans was significantly greater in plaque from caries-active than caries-free teeth ( P < 0.001), and the relative abundance of Fusobacterium sp. HMT 203 was significantly lower in plaque from caries-active than caries-free teeth ( P < 0.001). Adding an effect for family improved model fit for Fusobacterium sp. HMT 203 but not S. mutans. Conclusions: The diversity of supragingival plaque composition from caries-active and caries-free teeth changed with dentition, but S. mutans was positively and Fusobacterium sp. HMT 203 was negatively associated with caries regardless of dentition. There was a strong effect of family on the associations of Fusobacterium sp. HMT 203 with the caries-free state, but this was not true for S. mutans and the caries-active state. Knowledge Transfer Statement: Patients’ and dentists’ concerns about transmission of bacteria within families causing caries should be tempered by the evidence that some shared bacteria may contribute to good oral health.

Funder

National Institute of Dental and Craniofacial Research

Publisher

SAGE Publications

Subject

General Dentistry

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