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A salivary metabolite signature that reflects gingival host-microbe interactions: instability predicts gingivitis susceptibility

Several proteins and peptides in saliva were shown to stimulate gingival wound repair, but the role of salivary metabolites in this process remains unexplored. In vitro gingival re-epithelialization kinetics were determined using unstimulated saliva samples from healthy individuals collected during...

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Autores principales: Fernandez-Gutierrez, Marcela M., Imangaliyev, Sultan, Prodan, Andrei, Loos, Bruno G., Keijser, Bart J. F., Kleerebezem, Michiel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7033112/
https://www.ncbi.nlm.nih.gov/pubmed/32080300
http://dx.doi.org/10.1038/s41598-020-59988-z
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author Fernandez-Gutierrez, Marcela M.
Imangaliyev, Sultan
Prodan, Andrei
Loos, Bruno G.
Keijser, Bart J. F.
Kleerebezem, Michiel
author_facet Fernandez-Gutierrez, Marcela M.
Imangaliyev, Sultan
Prodan, Andrei
Loos, Bruno G.
Keijser, Bart J. F.
Kleerebezem, Michiel
author_sort Fernandez-Gutierrez, Marcela M.
collection PubMed
description Several proteins and peptides in saliva were shown to stimulate gingival wound repair, but the role of salivary metabolites in this process remains unexplored. In vitro gingival re-epithelialization kinetics were determined using unstimulated saliva samples from healthy individuals collected during an experimental gingivitis study. Elastic net regression with stability selection identified a specific metabolite signature in a training dataset that was associated with the observed re-epithelialization kinetics and enabled its prediction for all saliva samples obtained in the clinical study. This signature encompassed ten metabolites, including plasmalogens, diacylglycerol and amino acid derivatives, which reflect enhanced host-microbe interactions. This association is in agreement with the positive correlation of the metabolite signature with the individual’s gingival bleeding index. Remarkably, intra-individual signature-variation over time was associated with elevated risk for gingivitis development. Unravelling how these metabolites stimulate wound repair could provide novel avenues towards therapeutic approaches in patients with impaired wound healing capacity.
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spelling pubmed-70331122020-02-27 A salivary metabolite signature that reflects gingival host-microbe interactions: instability predicts gingivitis susceptibility Fernandez-Gutierrez, Marcela M. Imangaliyev, Sultan Prodan, Andrei Loos, Bruno G. Keijser, Bart J. F. Kleerebezem, Michiel Sci Rep Article Several proteins and peptides in saliva were shown to stimulate gingival wound repair, but the role of salivary metabolites in this process remains unexplored. In vitro gingival re-epithelialization kinetics were determined using unstimulated saliva samples from healthy individuals collected during an experimental gingivitis study. Elastic net regression with stability selection identified a specific metabolite signature in a training dataset that was associated with the observed re-epithelialization kinetics and enabled its prediction for all saliva samples obtained in the clinical study. This signature encompassed ten metabolites, including plasmalogens, diacylglycerol and amino acid derivatives, which reflect enhanced host-microbe interactions. This association is in agreement with the positive correlation of the metabolite signature with the individual’s gingival bleeding index. Remarkably, intra-individual signature-variation over time was associated with elevated risk for gingivitis development. Unravelling how these metabolites stimulate wound repair could provide novel avenues towards therapeutic approaches in patients with impaired wound healing capacity. Nature Publishing Group UK 2020-02-20 /pmc/articles/PMC7033112/ /pubmed/32080300 http://dx.doi.org/10.1038/s41598-020-59988-z Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Fernandez-Gutierrez, Marcela M.
Imangaliyev, Sultan
Prodan, Andrei
Loos, Bruno G.
Keijser, Bart J. F.
Kleerebezem, Michiel
A salivary metabolite signature that reflects gingival host-microbe interactions: instability predicts gingivitis susceptibility
title A salivary metabolite signature that reflects gingival host-microbe interactions: instability predicts gingivitis susceptibility
title_full A salivary metabolite signature that reflects gingival host-microbe interactions: instability predicts gingivitis susceptibility
title_fullStr A salivary metabolite signature that reflects gingival host-microbe interactions: instability predicts gingivitis susceptibility
title_full_unstemmed A salivary metabolite signature that reflects gingival host-microbe interactions: instability predicts gingivitis susceptibility
title_short A salivary metabolite signature that reflects gingival host-microbe interactions: instability predicts gingivitis susceptibility
title_sort salivary metabolite signature that reflects gingival host-microbe interactions: instability predicts gingivitis susceptibility
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7033112/
https://www.ncbi.nlm.nih.gov/pubmed/32080300
http://dx.doi.org/10.1038/s41598-020-59988-z
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