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Salivary microbiome and metabolome analysis of severe early childhood caries

BACKGROUND: Severe early childhood caries (SECC) is an inflammatory disease with complex pathology. Although changes in the oral microbiota and metabolic profile of patients with SECC have been identified, the salivary metabolites and the relationship between oral bacteria and biochemical metabolism...

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Autores principales: Li, Kai, Wang, Jinmei, Du, Ning, Sun, Yanjie, Sun, Qi, Yin, Weiwei, Li, Huiying, Meng, Lingqiang, Liu, Xuecong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9850820/
https://www.ncbi.nlm.nih.gov/pubmed/36658579
http://dx.doi.org/10.1186/s12903-023-02722-8
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author Li, Kai
Wang, Jinmei
Du, Ning
Sun, Yanjie
Sun, Qi
Yin, Weiwei
Li, Huiying
Meng, Lingqiang
Liu, Xuecong
author_facet Li, Kai
Wang, Jinmei
Du, Ning
Sun, Yanjie
Sun, Qi
Yin, Weiwei
Li, Huiying
Meng, Lingqiang
Liu, Xuecong
author_sort Li, Kai
collection PubMed
description BACKGROUND: Severe early childhood caries (SECC) is an inflammatory disease with complex pathology. Although changes in the oral microbiota and metabolic profile of patients with SECC have been identified, the salivary metabolites and the relationship between oral bacteria and biochemical metabolism remains unclear. We aimed to analyse alterations in the salivary microbiome and metabolome of children with SECC as well as their correlations. Accordingly, we aimed to explore potential salivary biomarkers in order to gain further insight into the pathophysiology of dental caries. METHODS: We collected 120 saliva samples from 30 children with SECC and 30 children without caries. The microbial community was identified through 16S ribosomal RNA (rRNA) gene high-throughput sequencing. Additionally, we conducted non-targeted metabolomic analysis through ultra-high-performance liquid chromatography combined with quadrupole time-of-flight mass spectrometry to determine the relative metabolite levels and their correlation with the clinical caries status. RESULTS: There was a significant between-group difference in 8 phyla and 32 genera in the microbiome. Further, metabolomic and enrichment analyses revealed significantly altered 32 salivary metabolites in children with dental caries, which involved pathways such as amino acid metabolism, pyrimidine metabolism, purine metabolism, ATP-binding cassette transporters, and cyclic adenosine monophosphate signalling pathway. Moreover, four in vivo differential metabolites (2-benzylmalate, epinephrine, 2-formaminobenzoylacetate, and 3-Indoleacrylic acid) might be jointly applied as biomarkers (area under the curve = 0.734). Furthermore, the caries status was correlated with microorganisms and metabolites. Additionally, Spearman's correlation analysis of differential microorganisms and metabolites revealed that Veillonella, Staphylococcus, Neisseria, and Porphyromonas were closely associated with differential metabolites. CONCLUSION: This study identified different microbial communities and metabolic profiles in saliva, which may be closely related to caries status. Our findings could inform future strategies for personalized caries prevention, detection, and treatment. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12903-023-02722-8.
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spelling pubmed-98508202023-01-20 Salivary microbiome and metabolome analysis of severe early childhood caries Li, Kai Wang, Jinmei Du, Ning Sun, Yanjie Sun, Qi Yin, Weiwei Li, Huiying Meng, Lingqiang Liu, Xuecong BMC Oral Health Research BACKGROUND: Severe early childhood caries (SECC) is an inflammatory disease with complex pathology. Although changes in the oral microbiota and metabolic profile of patients with SECC have been identified, the salivary metabolites and the relationship between oral bacteria and biochemical metabolism remains unclear. We aimed to analyse alterations in the salivary microbiome and metabolome of children with SECC as well as their correlations. Accordingly, we aimed to explore potential salivary biomarkers in order to gain further insight into the pathophysiology of dental caries. METHODS: We collected 120 saliva samples from 30 children with SECC and 30 children without caries. The microbial community was identified through 16S ribosomal RNA (rRNA) gene high-throughput sequencing. Additionally, we conducted non-targeted metabolomic analysis through ultra-high-performance liquid chromatography combined with quadrupole time-of-flight mass spectrometry to determine the relative metabolite levels and their correlation with the clinical caries status. RESULTS: There was a significant between-group difference in 8 phyla and 32 genera in the microbiome. Further, metabolomic and enrichment analyses revealed significantly altered 32 salivary metabolites in children with dental caries, which involved pathways such as amino acid metabolism, pyrimidine metabolism, purine metabolism, ATP-binding cassette transporters, and cyclic adenosine monophosphate signalling pathway. Moreover, four in vivo differential metabolites (2-benzylmalate, epinephrine, 2-formaminobenzoylacetate, and 3-Indoleacrylic acid) might be jointly applied as biomarkers (area under the curve = 0.734). Furthermore, the caries status was correlated with microorganisms and metabolites. Additionally, Spearman's correlation analysis of differential microorganisms and metabolites revealed that Veillonella, Staphylococcus, Neisseria, and Porphyromonas were closely associated with differential metabolites. CONCLUSION: This study identified different microbial communities and metabolic profiles in saliva, which may be closely related to caries status. Our findings could inform future strategies for personalized caries prevention, detection, and treatment. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12903-023-02722-8. BioMed Central 2023-01-19 /pmc/articles/PMC9850820/ /pubmed/36658579 http://dx.doi.org/10.1186/s12903-023-02722-8 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Li, Kai
Wang, Jinmei
Du, Ning
Sun, Yanjie
Sun, Qi
Yin, Weiwei
Li, Huiying
Meng, Lingqiang
Liu, Xuecong
Salivary microbiome and metabolome analysis of severe early childhood caries
title Salivary microbiome and metabolome analysis of severe early childhood caries
title_full Salivary microbiome and metabolome analysis of severe early childhood caries
title_fullStr Salivary microbiome and metabolome analysis of severe early childhood caries
title_full_unstemmed Salivary microbiome and metabolome analysis of severe early childhood caries
title_short Salivary microbiome and metabolome analysis of severe early childhood caries
title_sort salivary microbiome and metabolome analysis of severe early childhood caries
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9850820/
https://www.ncbi.nlm.nih.gov/pubmed/36658579
http://dx.doi.org/10.1186/s12903-023-02722-8
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