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Periodontal disease severity is associated to pathogenic consortia comprising putative and candidate periodontal pathogens
Based on a holistic concept of polymicrobial etiology, we have hypothesized that putative and candidate periodontal pathogens are more frequently detected in consortia than alone in advanced forms of periodontal diseases (PD). OBJECTIVE: To correlate specific consortia of periodontal pathogens with...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Faculdade De Odontologia De Bauru - USP
2023
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9828885/ https://www.ncbi.nlm.nih.gov/pubmed/36629716 http://dx.doi.org/10.1590/1678-7757-2022-0359 |
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author | ARAÚJO, Lélia Lima LOURENÇO, Talita Gomes Baêta COLOMBO, Ana Paula Vieira |
author_facet | ARAÚJO, Lélia Lima LOURENÇO, Talita Gomes Baêta COLOMBO, Ana Paula Vieira |
author_sort | ARAÚJO, Lélia Lima |
collection | PubMed |
description | Based on a holistic concept of polymicrobial etiology, we have hypothesized that putative and candidate periodontal pathogens are more frequently detected in consortia than alone in advanced forms of periodontal diseases (PD). OBJECTIVE: To correlate specific consortia of periodontal pathogens with clinical periodontal status and severity of periodontitis. METHODOLOGY: Subgingival biofilm was obtained from individuals with periodontal health (113, PH), gingivitis (91, G), and periodontitis (209, P). Genomic DNA was purified and the species Aggregatibacter actinomycetemcomitans (Aa), Aa JP2-like strain, Porphyromonas gingivalis (Pg), Dialister pneumosintes (Dp), and Filifactor alocis (Fa) were detected by PCR. Configural frequency and logistic regression analyses were performed to correlate microbial consortia and PD. RESULTS: Aa + Pg in the presence of Dp (phi=0.240; χ(2)=11.9, p<0.01), as well as Aa JP2 + Dp + Fa (phi=0.186, χ(2)=4.6, p<0.05) were significantly more associated in advanced stages of P. The consortium Aa + Fa + Dp was strongly associated with deep pocketing and inflammation (p<0.001). The best predictors of disease severity (80% accuracy) included older age (OR 1.11 [95% CI 1.07 – 1.15], p<0.001), Black/African-American ancestry (OR 1.89 [95% CI 1.19 – 2.99], p=0.007), and high frequency of Aa + Pg + Dp (OR 3.04 [95% CI 1.49 – 6.22], p=0.002). CONCLUSION: Specific microbial consortia of putative and novel periodontal pathogens, associated with demographic parameters, correlate with severe periodontitis, supporting the multifactorial nature of PD. |
format | Online Article Text |
id | pubmed-9828885 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Faculdade De Odontologia De Bauru - USP |
record_format | MEDLINE/PubMed |
spelling | pubmed-98288852023-01-13 Periodontal disease severity is associated to pathogenic consortia comprising putative and candidate periodontal pathogens ARAÚJO, Lélia Lima LOURENÇO, Talita Gomes Baêta COLOMBO, Ana Paula Vieira J Appl Oral Sci Original Article Based on a holistic concept of polymicrobial etiology, we have hypothesized that putative and candidate periodontal pathogens are more frequently detected in consortia than alone in advanced forms of periodontal diseases (PD). OBJECTIVE: To correlate specific consortia of periodontal pathogens with clinical periodontal status and severity of periodontitis. METHODOLOGY: Subgingival biofilm was obtained from individuals with periodontal health (113, PH), gingivitis (91, G), and periodontitis (209, P). Genomic DNA was purified and the species Aggregatibacter actinomycetemcomitans (Aa), Aa JP2-like strain, Porphyromonas gingivalis (Pg), Dialister pneumosintes (Dp), and Filifactor alocis (Fa) were detected by PCR. Configural frequency and logistic regression analyses were performed to correlate microbial consortia and PD. RESULTS: Aa + Pg in the presence of Dp (phi=0.240; χ(2)=11.9, p<0.01), as well as Aa JP2 + Dp + Fa (phi=0.186, χ(2)=4.6, p<0.05) were significantly more associated in advanced stages of P. The consortium Aa + Fa + Dp was strongly associated with deep pocketing and inflammation (p<0.001). The best predictors of disease severity (80% accuracy) included older age (OR 1.11 [95% CI 1.07 – 1.15], p<0.001), Black/African-American ancestry (OR 1.89 [95% CI 1.19 – 2.99], p=0.007), and high frequency of Aa + Pg + Dp (OR 3.04 [95% CI 1.49 – 6.22], p=0.002). CONCLUSION: Specific microbial consortia of putative and novel periodontal pathogens, associated with demographic parameters, correlate with severe periodontitis, supporting the multifactorial nature of PD. Faculdade De Odontologia De Bauru - USP 2023-01-06 /pmc/articles/PMC9828885/ /pubmed/36629716 http://dx.doi.org/10.1590/1678-7757-2022-0359 Text en https://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article ARAÚJO, Lélia Lima LOURENÇO, Talita Gomes Baêta COLOMBO, Ana Paula Vieira Periodontal disease severity is associated to pathogenic consortia comprising putative and candidate periodontal pathogens |
title | Periodontal disease severity is associated to pathogenic consortia comprising putative and candidate periodontal pathogens
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title_full | Periodontal disease severity is associated to pathogenic consortia comprising putative and candidate periodontal pathogens
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title_fullStr | Periodontal disease severity is associated to pathogenic consortia comprising putative and candidate periodontal pathogens
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title_full_unstemmed | Periodontal disease severity is associated to pathogenic consortia comprising putative and candidate periodontal pathogens
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title_short | Periodontal disease severity is associated to pathogenic consortia comprising putative and candidate periodontal pathogens
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title_sort | periodontal disease severity is associated to pathogenic consortia comprising putative and candidate periodontal pathogens |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9828885/ https://www.ncbi.nlm.nih.gov/pubmed/36629716 http://dx.doi.org/10.1590/1678-7757-2022-0359 |
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