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Impact of different oral treatments on the composition of the supragingival plaque microbiome
BACKGROUND: Dental plaque consists of a diverse microbial community embedded in a complex structure of exopolysaccharides. Dental biofilms form a natural barrier against pathogens but lead to oral diseases in a dysbiotic state. OBJECTIVE: Using a metaproteome approach combined with a standard plaque...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Taylor & Francis
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9629129/ https://www.ncbi.nlm.nih.gov/pubmed/36338832 http://dx.doi.org/10.1080/20002297.2022.2138251 |
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author | Rabe, Alexander Gesell Salazar, Manuela Michalik, Stephan Kocher, Thomas Below, Harald Völker, Uwe Welk, Alexander |
author_facet | Rabe, Alexander Gesell Salazar, Manuela Michalik, Stephan Kocher, Thomas Below, Harald Völker, Uwe Welk, Alexander |
author_sort | Rabe, Alexander |
collection | PubMed |
description | BACKGROUND: Dental plaque consists of a diverse microbial community embedded in a complex structure of exopolysaccharides. Dental biofilms form a natural barrier against pathogens but lead to oral diseases in a dysbiotic state. OBJECTIVE: Using a metaproteome approach combined with a standard plaque-regrowth study, this pilot study examined the impact of different concentrations of lactoperoxidase (LPO) on early plaque formation, and active biological processes. DESIGN: Sixteen orally healthy subjects received four local treatments as a randomized single-blind study based on a cross-over design. Two lozenges containing components of the LPO-system in different concentrations were compared to a placebo and Listerine®. The newly formed dental plaque was analyzed by mass spectrometry (nLC-MS/MS). RESULTS: On average 1,916 metaproteins per sample were identified, which could be assigned to 116 genera and 1,316 protein functions. Listerine® reduced the number of metaproteins and their relative abundance, confirming the plaque inhibiting effect. The LPO-lozenges triggered mainly higher metaprotein abundances of early and secondary colonizers as well as bacteria associated with dental health but also periodontitis. Functional information indicated plaque biofilm growth. CONCLUSION: In conclusion, the mechanisms on plaque biofilm formation of Listerine® and the LPO-system containing lozenges are different. In contrast to Listerine®, the lozenges led to a higher bacterial diversity. |
format | Online Article Text |
id | pubmed-9629129 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Taylor & Francis |
record_format | MEDLINE/PubMed |
spelling | pubmed-96291292022-11-03 Impact of different oral treatments on the composition of the supragingival plaque microbiome Rabe, Alexander Gesell Salazar, Manuela Michalik, Stephan Kocher, Thomas Below, Harald Völker, Uwe Welk, Alexander J Oral Microbiol Original Article BACKGROUND: Dental plaque consists of a diverse microbial community embedded in a complex structure of exopolysaccharides. Dental biofilms form a natural barrier against pathogens but lead to oral diseases in a dysbiotic state. OBJECTIVE: Using a metaproteome approach combined with a standard plaque-regrowth study, this pilot study examined the impact of different concentrations of lactoperoxidase (LPO) on early plaque formation, and active biological processes. DESIGN: Sixteen orally healthy subjects received four local treatments as a randomized single-blind study based on a cross-over design. Two lozenges containing components of the LPO-system in different concentrations were compared to a placebo and Listerine®. The newly formed dental plaque was analyzed by mass spectrometry (nLC-MS/MS). RESULTS: On average 1,916 metaproteins per sample were identified, which could be assigned to 116 genera and 1,316 protein functions. Listerine® reduced the number of metaproteins and their relative abundance, confirming the plaque inhibiting effect. The LPO-lozenges triggered mainly higher metaprotein abundances of early and secondary colonizers as well as bacteria associated with dental health but also periodontitis. Functional information indicated plaque biofilm growth. CONCLUSION: In conclusion, the mechanisms on plaque biofilm formation of Listerine® and the LPO-system containing lozenges are different. In contrast to Listerine®, the lozenges led to a higher bacterial diversity. Taylor & Francis 2022-10-31 /pmc/articles/PMC9629129/ /pubmed/36338832 http://dx.doi.org/10.1080/20002297.2022.2138251 Text en © 2022 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Rabe, Alexander Gesell Salazar, Manuela Michalik, Stephan Kocher, Thomas Below, Harald Völker, Uwe Welk, Alexander Impact of different oral treatments on the composition of the supragingival plaque microbiome |
title | Impact of different oral treatments on the composition of the supragingival plaque microbiome |
title_full | Impact of different oral treatments on the composition of the supragingival plaque microbiome |
title_fullStr | Impact of different oral treatments on the composition of the supragingival plaque microbiome |
title_full_unstemmed | Impact of different oral treatments on the composition of the supragingival plaque microbiome |
title_short | Impact of different oral treatments on the composition of the supragingival plaque microbiome |
title_sort | impact of different oral treatments on the composition of the supragingival plaque microbiome |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9629129/ https://www.ncbi.nlm.nih.gov/pubmed/36338832 http://dx.doi.org/10.1080/20002297.2022.2138251 |
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