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The bidirectional biological interplay between microbiome and viruses in periodontitis and type-2 diabetes mellitus
Periodontitis was an inflammatory disease associated with a dysbiosis of the oral flora characterized by a chronic sustained inflammation inducing the resorption of alveolar bone and leading to tooth loss. Type 2 diabetes mellitus (T2D) was a metabolic disease caused by impaired insulin action. The...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9483123/ https://www.ncbi.nlm.nih.gov/pubmed/36131931 http://dx.doi.org/10.3389/fimmu.2022.885029 |
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author | Tang, Boyu Yan, Caixia Shen, Xin Li, Yan |
author_facet | Tang, Boyu Yan, Caixia Shen, Xin Li, Yan |
author_sort | Tang, Boyu |
collection | PubMed |
description | Periodontitis was an inflammatory disease associated with a dysbiosis of the oral flora characterized by a chronic sustained inflammation inducing the resorption of alveolar bone and leading to tooth loss. Type 2 diabetes mellitus (T2D) was a metabolic disease caused by impaired insulin action. The oral microbiome played a crucial role in modulating both the innate and adaptive immune system during the trigger and exacerbation of periodontitis and T2D. The bidirectional relationship of T2D and periodontitis had been the focus of intensive research, but those were not well explored. In this commentary, an in-depth analysis of the changes of microbiome and bacterial metabolites in periodontitis with or without diabetes was described. The promotion of periodontitis to T2D might involve inflammatory factors/receptors, oxidative stress, microRNA and so on. The effect of diabetes on periodontitis might involve adipose factor pathway, AGE/RAGE and RANK/RANKL pathway etc. Generally, periodontitis and diabetes are closely related to the microecological-epithelial interaction, soft tissue degradation, bone coupling disorder, immune regulation and gene transcription. The viruses, including HBV, HCV, HSV-1, Coronavirus, HCMV, EBV, HIV, phageome and so on, played an important role in the development of T2D and periodontitis. An in-depth understanding of the relationship between microbiome and host was of great significance to clarify the bidirectional mechanisms, suggesting that the periodontitis or T2D remission will have a positive impact on the other. |
format | Online Article Text |
id | pubmed-9483123 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-94831232022-09-20 The bidirectional biological interplay between microbiome and viruses in periodontitis and type-2 diabetes mellitus Tang, Boyu Yan, Caixia Shen, Xin Li, Yan Front Immunol Immunology Periodontitis was an inflammatory disease associated with a dysbiosis of the oral flora characterized by a chronic sustained inflammation inducing the resorption of alveolar bone and leading to tooth loss. Type 2 diabetes mellitus (T2D) was a metabolic disease caused by impaired insulin action. The oral microbiome played a crucial role in modulating both the innate and adaptive immune system during the trigger and exacerbation of periodontitis and T2D. The bidirectional relationship of T2D and periodontitis had been the focus of intensive research, but those were not well explored. In this commentary, an in-depth analysis of the changes of microbiome and bacterial metabolites in periodontitis with or without diabetes was described. The promotion of periodontitis to T2D might involve inflammatory factors/receptors, oxidative stress, microRNA and so on. The effect of diabetes on periodontitis might involve adipose factor pathway, AGE/RAGE and RANK/RANKL pathway etc. Generally, periodontitis and diabetes are closely related to the microecological-epithelial interaction, soft tissue degradation, bone coupling disorder, immune regulation and gene transcription. The viruses, including HBV, HCV, HSV-1, Coronavirus, HCMV, EBV, HIV, phageome and so on, played an important role in the development of T2D and periodontitis. An in-depth understanding of the relationship between microbiome and host was of great significance to clarify the bidirectional mechanisms, suggesting that the periodontitis or T2D remission will have a positive impact on the other. Frontiers Media S.A. 2022-09-05 /pmc/articles/PMC9483123/ /pubmed/36131931 http://dx.doi.org/10.3389/fimmu.2022.885029 Text en Copyright © 2022 Tang, Yan, Shen and Li https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Immunology Tang, Boyu Yan, Caixia Shen, Xin Li, Yan The bidirectional biological interplay between microbiome and viruses in periodontitis and type-2 diabetes mellitus |
title | The bidirectional biological interplay between microbiome and viruses in periodontitis and type-2 diabetes mellitus |
title_full | The bidirectional biological interplay between microbiome and viruses in periodontitis and type-2 diabetes mellitus |
title_fullStr | The bidirectional biological interplay between microbiome and viruses in periodontitis and type-2 diabetes mellitus |
title_full_unstemmed | The bidirectional biological interplay between microbiome and viruses in periodontitis and type-2 diabetes mellitus |
title_short | The bidirectional biological interplay between microbiome and viruses in periodontitis and type-2 diabetes mellitus |
title_sort | bidirectional biological interplay between microbiome and viruses in periodontitis and type-2 diabetes mellitus |
topic | Immunology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9483123/ https://www.ncbi.nlm.nih.gov/pubmed/36131931 http://dx.doi.org/10.3389/fimmu.2022.885029 |
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