Literature DB >> 32385883

The role of the microbiota in periodontal disease.

Mike A Curtis1, Patricia I Diaz2, Thomas E Van Dyke3.   

Abstract

The last decade has witnessed unparalleled advances in our understanding of the complexity of the oral microbiome and the compositional changes that occur in subgingival biofilms in the transition from health to gingivitis and to destructive periodontal disease. The traditional view, which has held sway for the last 2 decades, that disease is characterized by the outgrowth of a consortium, or consortia, of a limited number of potentially pathogenic organisms, has given way to an alternative paradigm. In this new view, the microbiological changes associated with disease represent whole-scale alterations to the overall microbial population structure and to the functional properties of the entire community. Thus, and in common with other microbially mediated diseases of the gastrointestinal tract, the normally balanced, symbiotic, and generally benign commensal microbiome of the tooth-associated biofilm undergoes dysbiosis to a potentially deleterious microbiota. Coincident with progress in defining the microbiology of these diseases, there have been equally important advances in our understanding of the inflammatory systems of the periodontal tissues, their control, and how inflammation may contribute both to the development of dysbiosis and, in a deregulated state, the destructive disease process. One can therefore speculate that the inflammatory response and the periodontal microbiome are in a bidirectional balance in oral health and a bidirectional imbalance in periodontitis. However, despite these clear insights into both sides of the host/microbe balance in periodontal disease, there remain several unresolved issues concerning the role of the microbiota in disease. These include, but are not limited to, the factors which determine progression from gingivitis to periodontitis in a proportion of the population, whether dysbiosis causes disease or results from disease, and the molecular details of the microbial stimulus responsible for driving the destructive inflammatory response. Further progress in resolving these issues may provide significant benefit to diagnosis, treatment, and prevention.
© 2020 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd.

Entities:  

Keywords:  destructive periodontal disease; dysbiosis; gingivitis; inflammatory response; periodontal microbiota

Mesh:

Year:  2020        PMID: 32385883     DOI: 10.1111/prd.12296

Source DB:  PubMed          Journal:  Periodontol 2000        ISSN: 0906-6713            Impact factor:   7.589


  88 in total

1.  A thermosensitive gel with an active hyaluronic acid ingredient that contains an octenidine preservation system as an adjunct to scaling and root planning: a randomized prospective clinical study.

Authors:  Hirsch Ariel; Adrian Kahn; Ziv-On Hila; Sculean Anton; Gadoth Natan; Roni Kolerman
Journal:  Clin Oral Investig       Date:  2022-01-08       Impact factor: 3.573

Review 2.  The role of oral bacteria in inflammatory bowel disease.

Authors:  Emily Read; Michael A Curtis; Joana F Neves
Journal:  Nat Rev Gastroenterol Hepatol       Date:  2021-08-16       Impact factor: 46.802

3.  Loss of Neutrophil Homing to the Periodontal Tissues Modulates the Composition and Disease Potential of the Oral Microbiota.

Authors:  A Hashim; A Alsam; M A Payne; J Aduse-Opoku; M A Curtis; S Joseph
Journal:  Infect Immun       Date:  2021-09-07       Impact factor: 3.441

4.  Oral microbiome interactions with gingival gene expression patterns for apoptosis, autophagy and hypoxia pathways in progressing periodontitis.

Authors:  Jeffrey L Ebersole; Sreenatha S Kirakodu; Octavio A Gonzalez
Journal:  Immunology       Date:  2021-01-04       Impact factor: 7.397

Review 5.  Oral-Gut Microbiome Axis in Gastrointestinal Disease and Cancer.

Authors:  Se-Young Park; Byeong-Oh Hwang; Mihwa Lim; Seung-Ho Ok; Sun-Kyoung Lee; Kyung-Soo Chun; Kwang-Kyun Park; Yinling Hu; Won-Yoon Chung; Na-Young Song
Journal:  Cancers (Basel)       Date:  2021-04-28       Impact factor: 6.639

6.  Using Oral Microbiota Data to Design a Short Sucrose Intake Index.

Authors:  Anders Esberg; Linda Eriksson; Pamela Hasslöf; Simon Haworth; Pernilla Lif Holgerson; Ingegerd Johansson
Journal:  Nutrients       Date:  2021-04-21       Impact factor: 5.717

7.  A cocoa (Theobroma cacao L.) extract impairs the growth, virulence properties, and inflammatory potential of Fusobacterium nucleatum and improves oral epithelial barrier function.

Authors:  Amel Ben Lagha; Patricia Maquera Huacho; Daniel Grenier
Journal:  PLoS One       Date:  2021-05-24       Impact factor: 3.240

8.  SMDI: An Index for Measuring Subgingival Microbial Dysbiosis.

Authors:  T Chen; P D Marsh; N N Al-Hebshi
Journal:  J Dent Res       Date:  2021-08-25       Impact factor: 6.116

9.  Calprotectin (S100A8/A9) Is an Innate Immune Effector in Experimental Periodontitis.

Authors:  Karen F Johnstone; Yuping Wei; Peter D Bittner-Eddy; Gerrit W Vreeman; Ian A Stone; Jonathan B Clayton; Cavan S Reilly; Travis B Walbon; Elisa N Wright; Susan L Hoops; William S Boyle; Massimo Costalonga; Mark C Herzberg
Journal:  Infect Immun       Date:  2021-06-07       Impact factor: 3.441

10.  Differential Response of Oral Mucosal and Gingival Cells to Corynebacterium durum, Streptococcus sanguinis, and Porphyromonas gingivalis Multispecies Biofilms.

Authors:  Ulrike Redanz; Sylvio Redanz; Puthalayai Treerat; Sivaraman Prakasam; Li-Jung Lin; Justin Merritt; Jens Kreth
Journal:  Front Cell Infect Microbiol       Date:  2021-07-01       Impact factor: 5.293

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.