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Characterization of the oral microbiome of children with type 1 diabetes in the acute and chronic phases
BACKGROUND AND AIM: The relationship between the oral microbiota and type 1 diabetes (T1D) remains unclear. We aimed to evaluate the variations in the oral microbiome in T1D and identify potentially associated bacterial factors. METHODS: We performed high-throughput sequencing of the V3-V4 area of t...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Taylor & Francis
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9291685/ https://www.ncbi.nlm.nih.gov/pubmed/35859767 http://dx.doi.org/10.1080/20002297.2022.2094048 |
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author | Yuan, Xiaoxiao Wu, Jin Chen, Ruimin Chen, Zhihong Su, Zhe Ni, Jinwen Zhang, Miaoying Sun, Chengjun Zhang, Fengwei Liu, Yefei He, Junlin Zhang, Lei Luo, Feihong Wang, Ruirui |
author_facet | Yuan, Xiaoxiao Wu, Jin Chen, Ruimin Chen, Zhihong Su, Zhe Ni, Jinwen Zhang, Miaoying Sun, Chengjun Zhang, Fengwei Liu, Yefei He, Junlin Zhang, Lei Luo, Feihong Wang, Ruirui |
author_sort | Yuan, Xiaoxiao |
collection | PubMed |
description | BACKGROUND AND AIM: The relationship between the oral microbiota and type 1 diabetes (T1D) remains unclear. We aimed to evaluate the variations in the oral microbiome in T1D and identify potentially associated bacterial factors. METHODS: We performed high-throughput sequencing of the V3-V4 area of the 16S rRNA gene to profile the oral bacterial composition of 47 healthy children (CON group), 46 children with new-onset T1D in the acute phase (NT1D group), and 10 children with T1D in the chronic phase receiving insulin treatment (CT1D group). Multivariate statistical analysis of sequencing data was performed. RESULTS: Compared to the CON group, the NT1D group was characterized by decreased diversity and increased abundance of genera harboring opportunistic pathogens, while this trend was partially reversed in the CT1D group. Differential genera between groups could distinguish the NT1D group from the CON group (AUC = 0.933) and CT1D group (AUC = 0.846), respectively. Moreover, T1D-enriched genera were closely correlated with HbA1c, FBG and WBCs levels. CONCLUSION: Our results showed that the acute phase of T1D was characterized by oral microbiota dysbiosis, which could be partially ameliorated via glycemic control. The possible role of oral microbiota dysbiosis on oral health and systemic metabolic status in T1D warrants further mechanistic investigation. |
format | Online Article Text |
id | pubmed-9291685 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Taylor & Francis |
record_format | MEDLINE/PubMed |
spelling | pubmed-92916852022-07-19 Characterization of the oral microbiome of children with type 1 diabetes in the acute and chronic phases Yuan, Xiaoxiao Wu, Jin Chen, Ruimin Chen, Zhihong Su, Zhe Ni, Jinwen Zhang, Miaoying Sun, Chengjun Zhang, Fengwei Liu, Yefei He, Junlin Zhang, Lei Luo, Feihong Wang, Ruirui J Oral Microbiol Original Article BACKGROUND AND AIM: The relationship between the oral microbiota and type 1 diabetes (T1D) remains unclear. We aimed to evaluate the variations in the oral microbiome in T1D and identify potentially associated bacterial factors. METHODS: We performed high-throughput sequencing of the V3-V4 area of the 16S rRNA gene to profile the oral bacterial composition of 47 healthy children (CON group), 46 children with new-onset T1D in the acute phase (NT1D group), and 10 children with T1D in the chronic phase receiving insulin treatment (CT1D group). Multivariate statistical analysis of sequencing data was performed. RESULTS: Compared to the CON group, the NT1D group was characterized by decreased diversity and increased abundance of genera harboring opportunistic pathogens, while this trend was partially reversed in the CT1D group. Differential genera between groups could distinguish the NT1D group from the CON group (AUC = 0.933) and CT1D group (AUC = 0.846), respectively. Moreover, T1D-enriched genera were closely correlated with HbA1c, FBG and WBCs levels. CONCLUSION: Our results showed that the acute phase of T1D was characterized by oral microbiota dysbiosis, which could be partially ameliorated via glycemic control. The possible role of oral microbiota dysbiosis on oral health and systemic metabolic status in T1D warrants further mechanistic investigation. Taylor & Francis 2022-07-11 /pmc/articles/PMC9291685/ /pubmed/35859767 http://dx.doi.org/10.1080/20002297.2022.2094048 Text en © 2022 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 Yuan, Xiaoxiao Wu, Jin Chen, Ruimin Chen, Zhihong Su, Zhe Ni, Jinwen Zhang, Miaoying Sun, Chengjun Zhang, Fengwei Liu, Yefei He, Junlin Zhang, Lei Luo, Feihong Wang, Ruirui Characterization of the oral microbiome of children with type 1 diabetes in the acute and chronic phases |
title | Characterization of the oral microbiome of children with type 1 diabetes in the acute and chronic phases |
title_full | Characterization of the oral microbiome of children with type 1 diabetes in the acute and chronic phases |
title_fullStr | Characterization of the oral microbiome of children with type 1 diabetes in the acute and chronic phases |
title_full_unstemmed | Characterization of the oral microbiome of children with type 1 diabetes in the acute and chronic phases |
title_short | Characterization of the oral microbiome of children with type 1 diabetes in the acute and chronic phases |
title_sort | characterization of the oral microbiome of children with type 1 diabetes in the acute and chronic phases |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9291685/ https://www.ncbi.nlm.nih.gov/pubmed/35859767 http://dx.doi.org/10.1080/20002297.2022.2094048 |
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