Meta-analysis of the human upper respiratory tract microbiome reveals robust taxonomic associations with health and disease.


Journal

BMC biology
ISSN: 1741-7007
Titre abrégé: BMC Biol
Pays: England
ID NLM: 101190720

Informations de publication

Date de publication:
23 Apr 2024
Historique:
received: 02 09 2023
accepted: 15 04 2024
medline: 24 4 2024
pubmed: 24 4 2024
entrez: 23 4 2024
Statut: epublish

Résumé

The human upper respiratory tract (URT) microbiome, like the gut microbiome, varies across individuals and between health and disease states. However, study-to-study heterogeneity in reported case-control results has made the identification of consistent and generalizable URT-disease associations difficult. In order to address this issue, we assembled 26 independent 16S rRNA gene amplicon sequencing data sets from case-control URT studies, with approximately 2-3 studies per respiratory condition and ten distinct conditions covering common chronic and acute respiratory diseases. We leveraged the healthy control data across studies to investigate URT associations with age, sex, and geographic location, in order to isolate these associations from health and disease states. We found several robust genus-level associations, across multiple independent studies, with either health or disease status. We identified disease associations specific to a particular respiratory condition and associations general to all conditions. Ultimately, we reveal robust associations between the URT microbiome, health, and disease, which hold across multiple studies and can help guide follow-up work on potential URT microbiome diagnostics and therapeutics.

Sections du résumé

BACKGROUND BACKGROUND
The human upper respiratory tract (URT) microbiome, like the gut microbiome, varies across individuals and between health and disease states. However, study-to-study heterogeneity in reported case-control results has made the identification of consistent and generalizable URT-disease associations difficult.
RESULTS RESULTS
In order to address this issue, we assembled 26 independent 16S rRNA gene amplicon sequencing data sets from case-control URT studies, with approximately 2-3 studies per respiratory condition and ten distinct conditions covering common chronic and acute respiratory diseases. We leveraged the healthy control data across studies to investigate URT associations with age, sex, and geographic location, in order to isolate these associations from health and disease states.
CONCLUSIONS CONCLUSIONS
We found several robust genus-level associations, across multiple independent studies, with either health or disease status. We identified disease associations specific to a particular respiratory condition and associations general to all conditions. Ultimately, we reveal robust associations between the URT microbiome, health, and disease, which hold across multiple studies and can help guide follow-up work on potential URT microbiome diagnostics and therapeutics.

Identifiants

pubmed: 38654335
doi: 10.1186/s12915-024-01887-0
pii: 10.1186/s12915-024-01887-0
doi:

Substances chimiques

RNA, Ribosomal, 16S 0

Types de publication

Journal Article Meta-Analysis Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

93

Informations de copyright

© 2024. The Author(s).

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Auteurs

Nick Quinn-Bohmann (N)

Institute for Systems Biology, Seattle, WA, 98109, USA. nbohmann@gmail.com.
Molecular Engineering Graduate Program, University of Washington, Seattle, WA, 98195, USA. nbohmann@gmail.com.

Jose A Freixas-Coutin (JA)

Reckitt Health US LLC, 1 Philips Pkwy, Montvale, NJ, 07645, USA.

Jin Seo (J)

Reckitt Health US LLC, 1 Philips Pkwy, Montvale, NJ, 07645, USA.

Ruth Simmons (R)

Reckitt Benckiser Healthcare Ltd, 105 Bath Road, Slough, Berkshire, SL1 3UH, UK.

Christian Diener (C)

Institute for Systems Biology, Seattle, WA, 98109, USA.

Sean M Gibbons (SM)

Institute for Systems Biology, Seattle, WA, 98109, USA. sgibbons@isbscience.org.
Molecular Engineering Graduate Program, University of Washington, Seattle, WA, 98195, USA. sgibbons@isbscience.org.
Department of Bioengineering, University of Washington, Seattle, WA, 98195, USA. sgibbons@isbscience.org.
Department of Genome Sciences, University of Washington, Seattle, WA, 98195, USA. sgibbons@isbscience.org.
eScience Institute, University of Washington, Seattle, WA, 98195, USA. sgibbons@isbscience.org.

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