Cargando…

Long-term dynamics of the human oral microbiome during clinical disease progression

BACKGROUND: Oral microbiome dysbiosis is linked to overt inflammation of tooth-supporting tissues, leading to periodontitis, an oral condition that can cause tooth and bone loss. Microbiome dysbiosis has been described as a disruption in the symbiotic microbiota composition’s stability that could ad...

Descripción completa

Detalles Bibliográficos
Autores principales: Duran-Pinedo, Ana, Solbiati, Jose, Teles, Flavia, Teles, Ricardo, Zang, Yanping, Frias-Lopez, Jorge
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8572441/
https://www.ncbi.nlm.nih.gov/pubmed/34742306
http://dx.doi.org/10.1186/s12915-021-01169-z
_version_ 1784595216068509696
author Duran-Pinedo, Ana
Solbiati, Jose
Teles, Flavia
Teles, Ricardo
Zang, Yanping
Frias-Lopez, Jorge
author_facet Duran-Pinedo, Ana
Solbiati, Jose
Teles, Flavia
Teles, Ricardo
Zang, Yanping
Frias-Lopez, Jorge
author_sort Duran-Pinedo, Ana
collection PubMed
description BACKGROUND: Oral microbiome dysbiosis is linked to overt inflammation of tooth-supporting tissues, leading to periodontitis, an oral condition that can cause tooth and bone loss. Microbiome dysbiosis has been described as a disruption in the symbiotic microbiota composition’s stability that could adversely affect the host’s health status. However, the precise microbiome dynamics that lead to dysbiosis and the progression of the disease are largely unknown. The objective of our study was to investigate the long-term dynamics of periodontitis progression and its connection to dysbiosis. RESULTS: We studied three different teeth groups: sites that showed disease progression, sites that remained stable during the study, and sites that exhibited a cyclic deepening followed by spontaneous recovery. Time-series analysis revealed that communities followed a characteristic succession of bacteria clusters. Stable and fluctuating sites showed high asynchrony in the communities (i.e., different species responding dissimilarly through time) and a reordering of the communities where directional changes dominated (i.e., sample distance increases over time) in the stable sites but not in the fluctuating sites. Progressing sites exhibited low asynchrony and convergence (i.e., samples distance decreases over time). Moreover, new species were more likely to be recruited in stable samples if a close relative was not recruited previously. In contrast, progressing and fluctuating sites followed a neutral recruitment model, indicating that competition between closely related species is a significant component of species-species interactions in stable samples. Finally, periodontal treatment did not select similar communities but stabilized α-diversity, centered the abundance of different clusters to the mean, and increased community rearrangement. CONCLUSIONS: Here, we show that ecological principles can define dysbiosis and explain the evolution and outcomes of specific microbial communities of the oral microbiome in periodontitis progression. All sites showed an ecological succession in community composition. Stable sites were characterized by high asynchrony, a reordering of the communities where directional changes dominated, and new species were more likely to be recruited if a close relative was not recruited previously. Progressing sites were characterized by low asynchrony, community convergence, and a neutral model of recruitment. Finally, fluctuating sites were characterized by high asynchrony, community convergence, and a neutral recruitment model. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12915-021-01169-z.
format Online
Article
Text
id pubmed-8572441
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-85724412021-11-08 Long-term dynamics of the human oral microbiome during clinical disease progression Duran-Pinedo, Ana Solbiati, Jose Teles, Flavia Teles, Ricardo Zang, Yanping Frias-Lopez, Jorge BMC Biol Research Article BACKGROUND: Oral microbiome dysbiosis is linked to overt inflammation of tooth-supporting tissues, leading to periodontitis, an oral condition that can cause tooth and bone loss. Microbiome dysbiosis has been described as a disruption in the symbiotic microbiota composition’s stability that could adversely affect the host’s health status. However, the precise microbiome dynamics that lead to dysbiosis and the progression of the disease are largely unknown. The objective of our study was to investigate the long-term dynamics of periodontitis progression and its connection to dysbiosis. RESULTS: We studied three different teeth groups: sites that showed disease progression, sites that remained stable during the study, and sites that exhibited a cyclic deepening followed by spontaneous recovery. Time-series analysis revealed that communities followed a characteristic succession of bacteria clusters. Stable and fluctuating sites showed high asynchrony in the communities (i.e., different species responding dissimilarly through time) and a reordering of the communities where directional changes dominated (i.e., sample distance increases over time) in the stable sites but not in the fluctuating sites. Progressing sites exhibited low asynchrony and convergence (i.e., samples distance decreases over time). Moreover, new species were more likely to be recruited in stable samples if a close relative was not recruited previously. In contrast, progressing and fluctuating sites followed a neutral recruitment model, indicating that competition between closely related species is a significant component of species-species interactions in stable samples. Finally, periodontal treatment did not select similar communities but stabilized α-diversity, centered the abundance of different clusters to the mean, and increased community rearrangement. CONCLUSIONS: Here, we show that ecological principles can define dysbiosis and explain the evolution and outcomes of specific microbial communities of the oral microbiome in periodontitis progression. All sites showed an ecological succession in community composition. Stable sites were characterized by high asynchrony, a reordering of the communities where directional changes dominated, and new species were more likely to be recruited if a close relative was not recruited previously. Progressing sites were characterized by low asynchrony, community convergence, and a neutral model of recruitment. Finally, fluctuating sites were characterized by high asynchrony, community convergence, and a neutral recruitment model. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12915-021-01169-z. BioMed Central 2021-11-06 /pmc/articles/PMC8572441/ /pubmed/34742306 http://dx.doi.org/10.1186/s12915-021-01169-z Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research Article
Duran-Pinedo, Ana
Solbiati, Jose
Teles, Flavia
Teles, Ricardo
Zang, Yanping
Frias-Lopez, Jorge
Long-term dynamics of the human oral microbiome during clinical disease progression
title Long-term dynamics of the human oral microbiome during clinical disease progression
title_full Long-term dynamics of the human oral microbiome during clinical disease progression
title_fullStr Long-term dynamics of the human oral microbiome during clinical disease progression
title_full_unstemmed Long-term dynamics of the human oral microbiome during clinical disease progression
title_short Long-term dynamics of the human oral microbiome during clinical disease progression
title_sort long-term dynamics of the human oral microbiome during clinical disease progression
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8572441/
https://www.ncbi.nlm.nih.gov/pubmed/34742306
http://dx.doi.org/10.1186/s12915-021-01169-z
work_keys_str_mv AT duranpinedoana longtermdynamicsofthehumanoralmicrobiomeduringclinicaldiseaseprogression
AT solbiatijose longtermdynamicsofthehumanoralmicrobiomeduringclinicaldiseaseprogression
AT telesflavia longtermdynamicsofthehumanoralmicrobiomeduringclinicaldiseaseprogression
AT telesricardo longtermdynamicsofthehumanoralmicrobiomeduringclinicaldiseaseprogression
AT zangyanping longtermdynamicsofthehumanoralmicrobiomeduringclinicaldiseaseprogression
AT friaslopezjorge longtermdynamicsofthehumanoralmicrobiomeduringclinicaldiseaseprogression