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Oral Phenotype and Salivary Microbiome of Individuals With Papillon–Lefèvre Syndrome

Papillon–Lefèvre syndrome (PLS) is an autosomal recessive rare disease, main characteristics of which include palmoplantar hyperkeratosis and premature edentulism due to advanced periodontitis (formerly aggressive periodontitis). This study aimed to characterize the oral phenotype, including salivar...

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Autores principales: Lettieri, Giulia Melo, Santiago, Luander Medrado, Lettieri, Giancarlo Crosara, Borges, Luiz Gustavo dos Anjos, Marconatto, Letícia, de Oliveira, Laudimar Alves, Damé-Teixeira, Nailê, Salles, Loise Pedrosa
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8427699/
https://www.ncbi.nlm.nih.gov/pubmed/34513733
http://dx.doi.org/10.3389/fcimb.2021.720790
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author Lettieri, Giulia Melo
Santiago, Luander Medrado
Lettieri, Giancarlo Crosara
Borges, Luiz Gustavo dos Anjos
Marconatto, Letícia
de Oliveira, Laudimar Alves
Damé-Teixeira, Nailê
Salles, Loise Pedrosa
author_facet Lettieri, Giulia Melo
Santiago, Luander Medrado
Lettieri, Giancarlo Crosara
Borges, Luiz Gustavo dos Anjos
Marconatto, Letícia
de Oliveira, Laudimar Alves
Damé-Teixeira, Nailê
Salles, Loise Pedrosa
author_sort Lettieri, Giulia Melo
collection PubMed
description Papillon–Lefèvre syndrome (PLS) is an autosomal recessive rare disease, main characteristics of which include palmoplantar hyperkeratosis and premature edentulism due to advanced periodontitis (formerly aggressive periodontitis). This study aimed to characterize the oral phenotype, including salivary parameters, and the salivary microbiome of three PLS sisters, comparatively. Two sisters were toothless (PLSTL1 and PLSTL2), and one sister had most of the teeth in the oral cavity (PLST). Total DNA was extracted from the unstimulated saliva, and the amplicon sequencing of the 16S rRNA gene fragment was performed in an Ion PGM platform. The amplicon sequence variants (ASVs) were obtained using the DADA2 pipeline, and the taxonomy was assigned using the SILVA v.138. The main phenotypic characteristics of PLS were bone loss and premature loss of primary and permanent dentition. The PLST sister presented advanced periodontitis with gingival bleeding and suppuration, corresponding to the advanced periodontitis as a manifestation of systemic disease, stage IV, grade C. All three PLS sisters presented hyposalivation as a possible secondary outcome of the syndrome. Interestingly, PLST salivary microbiota was dominated by the uncultured bacteria Bacterioidales (F0058), Fusobacterium, Treponema, and Sulfophobococcus (Archaea domain). Streptococcus, Haemophilus, and Caldivirga (Archaea) dominated the microbiome of the PLSTL1 sister, while the PLSTL2 had higher abundances of Lactobacillus and Porphyromonas. This study was the first to show a high abundance of organisms belonging to the Archaea domain comprising a core microbiome in human saliva. In conclusion, a PLST individual does have a microbiota different from that of the periodontitis’ aggressiveness previously recognized. Due to an ineffective cathepsin C, the impairment of neutrophils probably provided a favorable environment for the PLS microbiome. The interactions of Bacteroidales F0058, Caldivirga, and Sulfophobococcus with the microbial consortium of PLS deserves future investigation. Traditional periodontal therapy is not efficient in PLS patients. Unraveling the PLS microbiome is essential in searching for appropriate treatment and avoiding early tooth loss.
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spelling pubmed-84276992021-09-10 Oral Phenotype and Salivary Microbiome of Individuals With Papillon–Lefèvre Syndrome Lettieri, Giulia Melo Santiago, Luander Medrado Lettieri, Giancarlo Crosara Borges, Luiz Gustavo dos Anjos Marconatto, Letícia de Oliveira, Laudimar Alves Damé-Teixeira, Nailê Salles, Loise Pedrosa Front Cell Infect Microbiol Cellular and Infection Microbiology Papillon–Lefèvre syndrome (PLS) is an autosomal recessive rare disease, main characteristics of which include palmoplantar hyperkeratosis and premature edentulism due to advanced periodontitis (formerly aggressive periodontitis). This study aimed to characterize the oral phenotype, including salivary parameters, and the salivary microbiome of three PLS sisters, comparatively. Two sisters were toothless (PLSTL1 and PLSTL2), and one sister had most of the teeth in the oral cavity (PLST). Total DNA was extracted from the unstimulated saliva, and the amplicon sequencing of the 16S rRNA gene fragment was performed in an Ion PGM platform. The amplicon sequence variants (ASVs) were obtained using the DADA2 pipeline, and the taxonomy was assigned using the SILVA v.138. The main phenotypic characteristics of PLS were bone loss and premature loss of primary and permanent dentition. The PLST sister presented advanced periodontitis with gingival bleeding and suppuration, corresponding to the advanced periodontitis as a manifestation of systemic disease, stage IV, grade C. All three PLS sisters presented hyposalivation as a possible secondary outcome of the syndrome. Interestingly, PLST salivary microbiota was dominated by the uncultured bacteria Bacterioidales (F0058), Fusobacterium, Treponema, and Sulfophobococcus (Archaea domain). Streptococcus, Haemophilus, and Caldivirga (Archaea) dominated the microbiome of the PLSTL1 sister, while the PLSTL2 had higher abundances of Lactobacillus and Porphyromonas. This study was the first to show a high abundance of organisms belonging to the Archaea domain comprising a core microbiome in human saliva. In conclusion, a PLST individual does have a microbiota different from that of the periodontitis’ aggressiveness previously recognized. Due to an ineffective cathepsin C, the impairment of neutrophils probably provided a favorable environment for the PLS microbiome. The interactions of Bacteroidales F0058, Caldivirga, and Sulfophobococcus with the microbial consortium of PLS deserves future investigation. Traditional periodontal therapy is not efficient in PLS patients. Unraveling the PLS microbiome is essential in searching for appropriate treatment and avoiding early tooth loss. Frontiers Media S.A. 2021-08-26 /pmc/articles/PMC8427699/ /pubmed/34513733 http://dx.doi.org/10.3389/fcimb.2021.720790 Text en Copyright © 2021 Lettieri, Santiago, Lettieri, Borges, Marconatto, de Oliveira, Damé-Teixeira and Salles 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 Cellular and Infection Microbiology
Lettieri, Giulia Melo
Santiago, Luander Medrado
Lettieri, Giancarlo Crosara
Borges, Luiz Gustavo dos Anjos
Marconatto, Letícia
de Oliveira, Laudimar Alves
Damé-Teixeira, Nailê
Salles, Loise Pedrosa
Oral Phenotype and Salivary Microbiome of Individuals With Papillon–Lefèvre Syndrome
title Oral Phenotype and Salivary Microbiome of Individuals With Papillon–Lefèvre Syndrome
title_full Oral Phenotype and Salivary Microbiome of Individuals With Papillon–Lefèvre Syndrome
title_fullStr Oral Phenotype and Salivary Microbiome of Individuals With Papillon–Lefèvre Syndrome
title_full_unstemmed Oral Phenotype and Salivary Microbiome of Individuals With Papillon–Lefèvre Syndrome
title_short Oral Phenotype and Salivary Microbiome of Individuals With Papillon–Lefèvre Syndrome
title_sort oral phenotype and salivary microbiome of individuals with papillon–lefèvre syndrome
topic Cellular and Infection Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8427699/
https://www.ncbi.nlm.nih.gov/pubmed/34513733
http://dx.doi.org/10.3389/fcimb.2021.720790
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