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Diurnal and eating-associated microbial patterns revealed via high-frequency saliva sampling

The oral microbiome is linked to oral and systemic health, but its fluctuation under frequent daily activities remains elusive. Here, we sampled saliva at 10- to 60-min intervals to track the high-resolution microbiome dynamics during the course of human activities. This dense time series data showe...

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Autores principales: Hu, Yichen, Amir, Amnon, Huang, Xiaochang, Li, Yan, Huang, Shi, Wolfe, Elaine, Weiss, Sophie, Knight, Rob, Xu, Zhenjiang Zech
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cold Spring Harbor Laboratory Press 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9248889/
https://www.ncbi.nlm.nih.gov/pubmed/35688483
http://dx.doi.org/10.1101/gr.276482.121
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author Hu, Yichen
Amir, Amnon
Huang, Xiaochang
Li, Yan
Huang, Shi
Wolfe, Elaine
Weiss, Sophie
Knight, Rob
Xu, Zhenjiang Zech
author_facet Hu, Yichen
Amir, Amnon
Huang, Xiaochang
Li, Yan
Huang, Shi
Wolfe, Elaine
Weiss, Sophie
Knight, Rob
Xu, Zhenjiang Zech
author_sort Hu, Yichen
collection PubMed
description The oral microbiome is linked to oral and systemic health, but its fluctuation under frequent daily activities remains elusive. Here, we sampled saliva at 10- to 60-min intervals to track the high-resolution microbiome dynamics during the course of human activities. This dense time series data showed that eating activity markedly perturbed the salivary microbiota, with tongue-specific Campylobacter concisus and Oribacterium sinus and dental plaque-specific Lautropia mirabilis, Rothia aeria, and Neisseria oralis increased after every meal in a temporal order. The observation was reproducible in multiple subjects and across an 11-mo period. The microbiome composition showed significant diurnal oscillation patterns at different taxonomy levels with Prevotella/Alloprevotella increased at night and Bergeyella HMT 206/Haemophilus slowly increased during the daytime. We also identified microbial co-occurring patterns in saliva that are associated with the intricate biogeography of the oral microbiome. Microbial source tracking analysis showed that the contributions of distinct oral niches to the salivary microbiome were dynamically affected by daily activities, reflecting the role of saliva in exchanging microbes with other oral sites. Collectively, our study provides insights into the temporal microbiome variation in saliva and highlights the need to consider daily activities and diurnal factors in design of oral microbiome studies.
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spelling pubmed-92488892022-12-01 Diurnal and eating-associated microbial patterns revealed via high-frequency saliva sampling Hu, Yichen Amir, Amnon Huang, Xiaochang Li, Yan Huang, Shi Wolfe, Elaine Weiss, Sophie Knight, Rob Xu, Zhenjiang Zech Genome Res Research The oral microbiome is linked to oral and systemic health, but its fluctuation under frequent daily activities remains elusive. Here, we sampled saliva at 10- to 60-min intervals to track the high-resolution microbiome dynamics during the course of human activities. This dense time series data showed that eating activity markedly perturbed the salivary microbiota, with tongue-specific Campylobacter concisus and Oribacterium sinus and dental plaque-specific Lautropia mirabilis, Rothia aeria, and Neisseria oralis increased after every meal in a temporal order. The observation was reproducible in multiple subjects and across an 11-mo period. The microbiome composition showed significant diurnal oscillation patterns at different taxonomy levels with Prevotella/Alloprevotella increased at night and Bergeyella HMT 206/Haemophilus slowly increased during the daytime. We also identified microbial co-occurring patterns in saliva that are associated with the intricate biogeography of the oral microbiome. Microbial source tracking analysis showed that the contributions of distinct oral niches to the salivary microbiome were dynamically affected by daily activities, reflecting the role of saliva in exchanging microbes with other oral sites. Collectively, our study provides insights into the temporal microbiome variation in saliva and highlights the need to consider daily activities and diurnal factors in design of oral microbiome studies. Cold Spring Harbor Laboratory Press 2022-06 /pmc/articles/PMC9248889/ /pubmed/35688483 http://dx.doi.org/10.1101/gr.276482.121 Text en © 2022 Hu et al.; Published by Cold Spring Harbor Laboratory Press https://creativecommons.org/licenses/by-nc/4.0/This article is distributed exclusively by Cold Spring Harbor Laboratory Press for the first six months after the full-issue publication date (see https://genome.cshlp.org/site/misc/terms.xhtml). After six months, it is available under a Creative Commons License (Attribution-NonCommercial 4.0 International), as described at http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) .
spellingShingle Research
Hu, Yichen
Amir, Amnon
Huang, Xiaochang
Li, Yan
Huang, Shi
Wolfe, Elaine
Weiss, Sophie
Knight, Rob
Xu, Zhenjiang Zech
Diurnal and eating-associated microbial patterns revealed via high-frequency saliva sampling
title Diurnal and eating-associated microbial patterns revealed via high-frequency saliva sampling
title_full Diurnal and eating-associated microbial patterns revealed via high-frequency saliva sampling
title_fullStr Diurnal and eating-associated microbial patterns revealed via high-frequency saliva sampling
title_full_unstemmed Diurnal and eating-associated microbial patterns revealed via high-frequency saliva sampling
title_short Diurnal and eating-associated microbial patterns revealed via high-frequency saliva sampling
title_sort diurnal and eating-associated microbial patterns revealed via high-frequency saliva sampling
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9248889/
https://www.ncbi.nlm.nih.gov/pubmed/35688483
http://dx.doi.org/10.1101/gr.276482.121
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