Cargando…

Oxidative stress in the oral cavity is driven by individual-specific bacterial communities

The term “bacterial dysbiosis” is being used quite extensively in metagenomic studies, however, the identification of harmful bacteria often fails due to large overlap between the bacterial species found in healthy volunteers and patients. We hypothesized that the pathogenic oral bacteria are indivi...

Descripción completa

Detalles Bibliográficos
Autores principales: Džunková, Mária, Martinez-Martinez, Daniel, Gardlík, Roman, Behuliak, Michal, Janšáková, Katarína, Jiménez, Nuria, Vázquez-Castellanos, Jorge F., Martí, Jose Manuel, D’Auria, Giuseppe, Bandara, H. M. H. N., Latorre, Amparo, Celec, Peter, Moya, Andrés
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6258756/
https://www.ncbi.nlm.nih.gov/pubmed/30510769
http://dx.doi.org/10.1038/s41522-018-0072-3
_version_ 1783374551248273408
author Džunková, Mária
Martinez-Martinez, Daniel
Gardlík, Roman
Behuliak, Michal
Janšáková, Katarína
Jiménez, Nuria
Vázquez-Castellanos, Jorge F.
Martí, Jose Manuel
D’Auria, Giuseppe
Bandara, H. M. H. N.
Latorre, Amparo
Celec, Peter
Moya, Andrés
author_facet Džunková, Mária
Martinez-Martinez, Daniel
Gardlík, Roman
Behuliak, Michal
Janšáková, Katarína
Jiménez, Nuria
Vázquez-Castellanos, Jorge F.
Martí, Jose Manuel
D’Auria, Giuseppe
Bandara, H. M. H. N.
Latorre, Amparo
Celec, Peter
Moya, Andrés
author_sort Džunková, Mária
collection PubMed
description The term “bacterial dysbiosis” is being used quite extensively in metagenomic studies, however, the identification of harmful bacteria often fails due to large overlap between the bacterial species found in healthy volunteers and patients. We hypothesized that the pathogenic oral bacteria are individual-specific and they correlate with oxidative stress markers in saliva which reflect the inflammatory processes in the oral cavity. Temporally direct and lagged correlations between the markers and bacterial taxa were computed individually for 26 volunteers who provided saliva samples during one month (21.2 ± 2.7 samples/volunteer, 551 samples in total). The volunteers’ microbiomes differed significantly by their composition and also by their degree of microbiome temporal variability and oxidative stress markers fluctuation. The results showed that each of the marker-taxa pairs can have negative correlations in some volunteers while positive in others. Streptococcus mutans, which used to be associated with caries before the metagenomics era, had the most prominent correlations with the oxidative stress markers, however, these correlations were not confirmed in all volunteers. The importance of longitudinal samples collections in correlation studies was underlined by simulation of single sample collections in 1000 different combinations which produced contradictory results. In conclusion, the distinct intra-individual correlation patterns suggest that different bacterial consortia might be involved in the oxidative stress induction in each human subject. In the future, decreasing cost of DNA sequencing will allow to analyze multiple samples from each patient, which might help to explore potential diagnostic applications and understand pathogenesis of microbiome-associated oral diseases.
format Online
Article
Text
id pubmed-6258756
institution National Center for Biotechnology Information
language English
publishDate 2018
publisher Nature Publishing Group UK
record_format MEDLINE/PubMed
spelling pubmed-62587562018-12-03 Oxidative stress in the oral cavity is driven by individual-specific bacterial communities Džunková, Mária Martinez-Martinez, Daniel Gardlík, Roman Behuliak, Michal Janšáková, Katarína Jiménez, Nuria Vázquez-Castellanos, Jorge F. Martí, Jose Manuel D’Auria, Giuseppe Bandara, H. M. H. N. Latorre, Amparo Celec, Peter Moya, Andrés NPJ Biofilms Microbiomes Article The term “bacterial dysbiosis” is being used quite extensively in metagenomic studies, however, the identification of harmful bacteria often fails due to large overlap between the bacterial species found in healthy volunteers and patients. We hypothesized that the pathogenic oral bacteria are individual-specific and they correlate with oxidative stress markers in saliva which reflect the inflammatory processes in the oral cavity. Temporally direct and lagged correlations between the markers and bacterial taxa were computed individually for 26 volunteers who provided saliva samples during one month (21.2 ± 2.7 samples/volunteer, 551 samples in total). The volunteers’ microbiomes differed significantly by their composition and also by their degree of microbiome temporal variability and oxidative stress markers fluctuation. The results showed that each of the marker-taxa pairs can have negative correlations in some volunteers while positive in others. Streptococcus mutans, which used to be associated with caries before the metagenomics era, had the most prominent correlations with the oxidative stress markers, however, these correlations were not confirmed in all volunteers. The importance of longitudinal samples collections in correlation studies was underlined by simulation of single sample collections in 1000 different combinations which produced contradictory results. In conclusion, the distinct intra-individual correlation patterns suggest that different bacterial consortia might be involved in the oxidative stress induction in each human subject. In the future, decreasing cost of DNA sequencing will allow to analyze multiple samples from each patient, which might help to explore potential diagnostic applications and understand pathogenesis of microbiome-associated oral diseases. Nature Publishing Group UK 2018-11-27 /pmc/articles/PMC6258756/ /pubmed/30510769 http://dx.doi.org/10.1038/s41522-018-0072-3 Text en © The Author(s) 2018 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
Džunková, Mária
Martinez-Martinez, Daniel
Gardlík, Roman
Behuliak, Michal
Janšáková, Katarína
Jiménez, Nuria
Vázquez-Castellanos, Jorge F.
Martí, Jose Manuel
D’Auria, Giuseppe
Bandara, H. M. H. N.
Latorre, Amparo
Celec, Peter
Moya, Andrés
Oxidative stress in the oral cavity is driven by individual-specific bacterial communities
title Oxidative stress in the oral cavity is driven by individual-specific bacterial communities
title_full Oxidative stress in the oral cavity is driven by individual-specific bacterial communities
title_fullStr Oxidative stress in the oral cavity is driven by individual-specific bacterial communities
title_full_unstemmed Oxidative stress in the oral cavity is driven by individual-specific bacterial communities
title_short Oxidative stress in the oral cavity is driven by individual-specific bacterial communities
title_sort oxidative stress in the oral cavity is driven by individual-specific bacterial communities
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6258756/
https://www.ncbi.nlm.nih.gov/pubmed/30510769
http://dx.doi.org/10.1038/s41522-018-0072-3
work_keys_str_mv AT dzunkovamaria oxidativestressintheoralcavityisdrivenbyindividualspecificbacterialcommunities
AT martinezmartinezdaniel oxidativestressintheoralcavityisdrivenbyindividualspecificbacterialcommunities
AT gardlikroman oxidativestressintheoralcavityisdrivenbyindividualspecificbacterialcommunities
AT behuliakmichal oxidativestressintheoralcavityisdrivenbyindividualspecificbacterialcommunities
AT jansakovakatarina oxidativestressintheoralcavityisdrivenbyindividualspecificbacterialcommunities
AT jimeneznuria oxidativestressintheoralcavityisdrivenbyindividualspecificbacterialcommunities
AT vazquezcastellanosjorgef oxidativestressintheoralcavityisdrivenbyindividualspecificbacterialcommunities
AT martijosemanuel oxidativestressintheoralcavityisdrivenbyindividualspecificbacterialcommunities
AT dauriagiuseppe oxidativestressintheoralcavityisdrivenbyindividualspecificbacterialcommunities
AT bandarahmhn oxidativestressintheoralcavityisdrivenbyindividualspecificbacterialcommunities
AT latorreamparo oxidativestressintheoralcavityisdrivenbyindividualspecificbacterialcommunities
AT celecpeter oxidativestressintheoralcavityisdrivenbyindividualspecificbacterialcommunities
AT moyaandres oxidativestressintheoralcavityisdrivenbyindividualspecificbacterialcommunities