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Saliva microbiome alterations in dental fluorosis population
BACKGROUND: We aimed to explore saliva microbiome alterations in dental fluorosis population. METHODS: The prevalence of dental fluorosis was examined in 957 college students. Dean’s fluorosis index was used to evaluate the dental fluorosis status. Changes in the composition of the salivary microbio...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Taylor & Francis
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9946311/ https://www.ncbi.nlm.nih.gov/pubmed/36844898 http://dx.doi.org/10.1080/20002297.2023.2180927 |
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author | Liu, Shanshan Song, Qiangsheng Zhang, Chenchen Li, Mengwan Li, Zhenzhen Liu, Yudong Xu, Li Xie, Xiaofei Zhao, Lili Zhang, Rongxiu Wang, Qinglong Zeng, Guojin Zhang, Yifan Zhang, Kai |
author_facet | Liu, Shanshan Song, Qiangsheng Zhang, Chenchen Li, Mengwan Li, Zhenzhen Liu, Yudong Xu, Li Xie, Xiaofei Zhao, Lili Zhang, Rongxiu Wang, Qinglong Zeng, Guojin Zhang, Yifan Zhang, Kai |
author_sort | Liu, Shanshan |
collection | PubMed |
description | BACKGROUND: We aimed to explore saliva microbiome alterations in dental fluorosis population. METHODS: The prevalence of dental fluorosis was examined in 957 college students. Dean’s fluorosis index was used to evaluate the dental fluorosis status. Changes in the composition of the salivary microbiome were assessed in a subset of these patients (100 healthy controls, 100 dental fluorosis patients). RESULTS: Dental fluorosis affected 47% of the student sample, and incidence was unrelated to gender. Compared with healthy controls, the microbiota of patients with dental fluorosis exhibited increased diversity, with increased abundance of Treponema lecithinolyticum, Vibrio metschnikovii, Cupriavidus pauculus, Pseudomonas, Pseudomonadaceae, Pseudomonadales, and decreased abundance of Streptococcus mutans, Streptococcus sanguinis, Gemella, and Staphylococcales. Function analyses showed increases in arginine biosynthesis in patients affected by dental fluorosis, together with reductions in amino sugar and nucleotide sugar metabolism, fructose and mannose metabolism, and starch and sucrose metabolism. CONCLUSIONS: These results suggest that there are striking differences in salivary microbiome between healthy controls and dental fluorosis patients. Dental fluorosis may contribute to periodontitis and systemic lung diseases. There is a need for cohort studies to determine whether altering the salivary microbiota in dental fluorosis patients can alter the development of oral or systemic diseases. |
format | Online Article Text |
id | pubmed-9946311 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Taylor & Francis |
record_format | MEDLINE/PubMed |
spelling | pubmed-99463112023-02-23 Saliva microbiome alterations in dental fluorosis population Liu, Shanshan Song, Qiangsheng Zhang, Chenchen Li, Mengwan Li, Zhenzhen Liu, Yudong Xu, Li Xie, Xiaofei Zhao, Lili Zhang, Rongxiu Wang, Qinglong Zeng, Guojin Zhang, Yifan Zhang, Kai J Oral Microbiol Original Article BACKGROUND: We aimed to explore saliva microbiome alterations in dental fluorosis population. METHODS: The prevalence of dental fluorosis was examined in 957 college students. Dean’s fluorosis index was used to evaluate the dental fluorosis status. Changes in the composition of the salivary microbiome were assessed in a subset of these patients (100 healthy controls, 100 dental fluorosis patients). RESULTS: Dental fluorosis affected 47% of the student sample, and incidence was unrelated to gender. Compared with healthy controls, the microbiota of patients with dental fluorosis exhibited increased diversity, with increased abundance of Treponema lecithinolyticum, Vibrio metschnikovii, Cupriavidus pauculus, Pseudomonas, Pseudomonadaceae, Pseudomonadales, and decreased abundance of Streptococcus mutans, Streptococcus sanguinis, Gemella, and Staphylococcales. Function analyses showed increases in arginine biosynthesis in patients affected by dental fluorosis, together with reductions in amino sugar and nucleotide sugar metabolism, fructose and mannose metabolism, and starch and sucrose metabolism. CONCLUSIONS: These results suggest that there are striking differences in salivary microbiome between healthy controls and dental fluorosis patients. Dental fluorosis may contribute to periodontitis and systemic lung diseases. There is a need for cohort studies to determine whether altering the salivary microbiota in dental fluorosis patients can alter the development of oral or systemic diseases. Taylor & Francis 2023-02-20 /pmc/articles/PMC9946311/ /pubmed/36844898 http://dx.doi.org/10.1080/20002297.2023.2180927 Text en © 2023 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Liu, Shanshan Song, Qiangsheng Zhang, Chenchen Li, Mengwan Li, Zhenzhen Liu, Yudong Xu, Li Xie, Xiaofei Zhao, Lili Zhang, Rongxiu Wang, Qinglong Zeng, Guojin Zhang, Yifan Zhang, Kai Saliva microbiome alterations in dental fluorosis population |
title | Saliva microbiome alterations in dental fluorosis population |
title_full | Saliva microbiome alterations in dental fluorosis population |
title_fullStr | Saliva microbiome alterations in dental fluorosis population |
title_full_unstemmed | Saliva microbiome alterations in dental fluorosis population |
title_short | Saliva microbiome alterations in dental fluorosis population |
title_sort | saliva microbiome alterations in dental fluorosis population |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9946311/ https://www.ncbi.nlm.nih.gov/pubmed/36844898 http://dx.doi.org/10.1080/20002297.2023.2180927 |
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