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The bacterial microbiome and metabolome in caries progression and arrest.
da Costa Rosa, Thamirys; de Almeida Neves, Aline; Azcarate-Peril, M Andrea; Divaris, Kimon; Wu, Di; Cho, Hunyong; Moss, Kevin; Paster, Bruce J; Chen, Tsute; B Freitas-Fernandes, Liana; Fidalgo, Tatiana K S; Tadeu Lopes, Ricardo; Valente, Ana Paula; R Arnold, Roland; de Aguiar Ribeiro, Apoena.
Afiliación
  • da Costa Rosa T; Department of Pediatric Dentistry, Fluminense Federal University, Nova Friburgo, Brazil.
  • de Almeida Neves A; Department of Pediatric Dentistry, Rio de Janeiro Federal University, Brazil.
  • Azcarate-Peril MA; Centre for Oral Clinical and Translational Sciences, King's College London, London, UK.
  • Divaris K; Microbiome Core Facility, University of North Carolina School of Medicine, Chapel Hill, USA.
  • Wu D; Department of Medicine, Division of Gastroenterology and Hepatology, School of Medicine, University of North Carolina, Chapel Hill, USA.
  • Cho H; Division of Pediatric and Public Health, Adams School of Dentistry, University of North Carolina, Chapel Hill, USA.
  • Moss K; Department of Epidemiology, Gillings School of Global Public Health, University of North Carolina, Chapel Hill, USA.
  • Paster BJ; Division of Oral and Craniofacial Health Sciences, School of Dentistry, University of North Carolina, Chapel Hill, USA.
  • Chen T; Department of Biostatistics, Gillings School of Global Public Health, University of North Carolina, Chapel Hill, USA.
  • B Freitas-Fernandes L; Department of Biostatistics, Gillings School of Global Public Health, University of North Carolina, Chapel Hill, USA.
  • Fidalgo TKS; Division of Oral and Craniofacial Health Sciences, School of Dentistry, University of North Carolina, Chapel Hill, USA.
  • Tadeu Lopes R; Department of Microbiology, Forsyth Institute, Cambridge, USA.
  • Valente AP; Department of Oral Medicine, Infection and Immunity, Harvard School of Dental Medicine, Boston, USA.
  • R Arnold R; Department of Microbiology, Forsyth Institute, Cambridge, USA.
  • de Aguiar Ribeiro A; Department of Pediatric Dentistry, Rio de Janeiro Federal University, Brazil.
J Oral Microbiol ; 13(1): 1886748, 2021 Jun 16.
Article en En | MEDLINE | ID: mdl-34188775
Aim: This in vivo experimental study investigated bacterial microbiome and metabolome longitudinal changes associated with enamel caries lesion progression and arrest. Methods: We induced natural caries activity in three caries-free volunteers prior to four premolar extractions for orthodontic reasons. The experimental model included placement of a modified orthodontic band on smooth surfaces and a mesh on occlusal surfaces. We applied the caries-inducing protocol for 4- and 6-weeks, and subsequently promoted caries lesion arrest via a 2-week toothbrushing period. Lesions were verified clinically and quantitated via micro-CT enamel density measurements. The biofilm microbial composition was determined via 16S rRNA gene Illumina sequencing and NMR spectrometry was used for metabolomics. Results: Biofilm maturation and caries lesion progression were characterized by an increase in Gram-negative anaerobes, including Veillonella and Prevotella. Streptococcus was associated caries lesion progression, while a more equal distribution of Streptococcus, Bifidobacterium, Atopobium, Prevotella, Veillonella, and Saccharibacteria (TM7) characterized arrest. Lactate, acetate, pyruvate, alanine, valine, and sugars were more abundant in mature biofilms compared to newly formed biofilms. Conclusions: These longitudinal bacterial microbiome and metabolome results provide novel mechanistic insights into the role of the biofilm in caries progression and arrest and offer promising candidate biomarkers for validation in future studies.
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Texto completo: 1 Base de datos: MEDLINE Tipo de estudio: Guideline Idioma: En Revista: J Oral Microbiol Año: 2021 Tipo del documento: Article

Texto completo: 1 Base de datos: MEDLINE Tipo de estudio: Guideline Idioma: En Revista: J Oral Microbiol Año: 2021 Tipo del documento: Article