Mechanical biofilm disruption causes microbial and immunological shifts in periodontitis patients

Abstract Periodontitis is characterized by subgingival biofilm dysbiosis, inflammation and tissue destruction. Current treatment involves mechanical biofilm disruption known as non-surgical periodontal therapy (NSPT). This study sought to characterise the impact of treatment on microbial diversity a...

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Main Authors: W. Johnston, B. T. Rosier, A. Artacho, M. Paterson, K. Piela, C. Delaney, J. L. Brown, G. Ramage, A. Mira, S. Culshaw
Format: Article
Language:English
Published: Nature Publishing Group 2021-05-01
Series:Scientific Reports
Online Access:https://doi.org/10.1038/s41598-021-89002-z
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spelling doaj-fcd48989555842a292e1041f8e92ab922021-05-09T11:32:17ZengNature Publishing GroupScientific Reports2045-23222021-05-0111111410.1038/s41598-021-89002-zMechanical biofilm disruption causes microbial and immunological shifts in periodontitis patientsW. Johnston0B. T. Rosier1A. Artacho2M. Paterson3K. Piela4C. Delaney5J. L. Brown6G. Ramage7A. Mira8S. Culshaw9Oral Sciences, Glasgow Dental Hospital and School, School of Medicine, Dentistry and Nursing, College of Medical, Veterinary and Life Sciences, University of GlasgowThe Foundation for the Promotion of Health and Biomedical Research (FISABIO)The Foundation for the Promotion of Health and Biomedical Research (FISABIO)Oral Sciences, Glasgow Dental Hospital and School, School of Medicine, Dentistry and Nursing, College of Medical, Veterinary and Life Sciences, University of GlasgowOral Sciences, Glasgow Dental Hospital and School, School of Medicine, Dentistry and Nursing, College of Medical, Veterinary and Life Sciences, University of GlasgowOral Sciences, Glasgow Dental Hospital and School, School of Medicine, Dentistry and Nursing, College of Medical, Veterinary and Life Sciences, University of GlasgowOral Sciences, Glasgow Dental Hospital and School, School of Medicine, Dentistry and Nursing, College of Medical, Veterinary and Life Sciences, University of GlasgowOral Sciences, Glasgow Dental Hospital and School, School of Medicine, Dentistry and Nursing, College of Medical, Veterinary and Life Sciences, University of GlasgowThe Foundation for the Promotion of Health and Biomedical Research (FISABIO)Oral Sciences, Glasgow Dental Hospital and School, School of Medicine, Dentistry and Nursing, College of Medical, Veterinary and Life Sciences, University of GlasgowAbstract Periodontitis is characterized by subgingival biofilm dysbiosis, inflammation and tissue destruction. Current treatment involves mechanical biofilm disruption known as non-surgical periodontal therapy (NSPT). This study sought to characterise the impact of treatment on microbial diversity and overall community, and the parallel impact on host inflammation in the oral cavity. Fourty-two periodontitis patients were included in this study, with periodontal clinical parameters, subgingival plaque and saliva samples collected at baseline and 90 days after treatment. Salivary cytokines were quantified, and subgingival plaque was analysed using 16S rRNA sequencing. After treatment, there were marked health-associated alterations in microbial composition and diversity, including differential abundance of 42 genera and 61 species. These changes were accompanied by substantial clinical improvement (pockets ≥ 5 mm, 27.50% to 9.00%, p < 0.001) and a decrease in salivary IL-1β (p < 0.001)—a putative marker of periodontal inflammation. Despite significant reductions in disease associated anaerobes, several genera (Fusobacterium, Prevotella, Tanenerella, Treponema) remained present and formed a distinct subnetwork associated with residual disease. Collectively, this study shows that current periodontal treatment results in partial restoration of a healthy microbial ecosystem, but features of biofilm dysbiosis and host inflammation remain in some patients, which were surprisingly independent of clinical response.https://doi.org/10.1038/s41598-021-89002-z
collection DOAJ
language English
format Article
sources DOAJ
author W. Johnston
B. T. Rosier
A. Artacho
M. Paterson
K. Piela
C. Delaney
J. L. Brown
G. Ramage
A. Mira
S. Culshaw
spellingShingle W. Johnston
B. T. Rosier
A. Artacho
M. Paterson
K. Piela
C. Delaney
J. L. Brown
G. Ramage
A. Mira
S. Culshaw
Mechanical biofilm disruption causes microbial and immunological shifts in periodontitis patients
Scientific Reports
author_facet W. Johnston
B. T. Rosier
A. Artacho
M. Paterson
K. Piela
C. Delaney
J. L. Brown
G. Ramage
A. Mira
S. Culshaw
author_sort W. Johnston
title Mechanical biofilm disruption causes microbial and immunological shifts in periodontitis patients
title_short Mechanical biofilm disruption causes microbial and immunological shifts in periodontitis patients
title_full Mechanical biofilm disruption causes microbial and immunological shifts in periodontitis patients
title_fullStr Mechanical biofilm disruption causes microbial and immunological shifts in periodontitis patients
title_full_unstemmed Mechanical biofilm disruption causes microbial and immunological shifts in periodontitis patients
title_sort mechanical biofilm disruption causes microbial and immunological shifts in periodontitis patients
publisher Nature Publishing Group
series Scientific Reports
issn 2045-2322
publishDate 2021-05-01
description Abstract Periodontitis is characterized by subgingival biofilm dysbiosis, inflammation and tissue destruction. Current treatment involves mechanical biofilm disruption known as non-surgical periodontal therapy (NSPT). This study sought to characterise the impact of treatment on microbial diversity and overall community, and the parallel impact on host inflammation in the oral cavity. Fourty-two periodontitis patients were included in this study, with periodontal clinical parameters, subgingival plaque and saliva samples collected at baseline and 90 days after treatment. Salivary cytokines were quantified, and subgingival plaque was analysed using 16S rRNA sequencing. After treatment, there were marked health-associated alterations in microbial composition and diversity, including differential abundance of 42 genera and 61 species. These changes were accompanied by substantial clinical improvement (pockets ≥ 5 mm, 27.50% to 9.00%, p < 0.001) and a decrease in salivary IL-1β (p < 0.001)—a putative marker of periodontal inflammation. Despite significant reductions in disease associated anaerobes, several genera (Fusobacterium, Prevotella, Tanenerella, Treponema) remained present and formed a distinct subnetwork associated with residual disease. Collectively, this study shows that current periodontal treatment results in partial restoration of a healthy microbial ecosystem, but features of biofilm dysbiosis and host inflammation remain in some patients, which were surprisingly independent of clinical response.
url https://doi.org/10.1038/s41598-021-89002-z
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