Integrative microbiomics in bronchiectasis exacerbations
Mac Aogáin, M
Narayana, JK
Tiew, PY
Ali, NABM
Yong, VFL
Jaggi, TK
Lim, AYH
Keir, HR
Dicker, AJ
Thng, KX
Tsang, A
Ivan, FX
Poh, ME
Oriano, M
Aliberti, S
Blasi, F
Low, TB
Ong, TH
Oliver, B
Giam, YH
Tee, A
Koh, MS
Abisheganaden, JA
Tsaneva-Atanasova, K
Chalmers, JD
Chotirmall, SH
- Publisher:
- Springer Science and Business Media LLC
- Publication Type:
- Journal Article
- Citation:
- Nature Medicine, 2021, 27, (4), pp. 688-699
- Issue Date:
- 2021-04-05
Open Access
Copyright Clearance Process
- Recently Added
- In Progress
- Open Access
This item is open access.
The embargo period expires on 1 Apr 2022
Full metadata record
Field | Value | Language |
---|---|---|
dc.contributor.author | Mac Aogáin, M | |
dc.contributor.author | Narayana, JK | |
dc.contributor.author | Tiew, PY | |
dc.contributor.author | Ali, NABM | |
dc.contributor.author | Yong, VFL | |
dc.contributor.author | Jaggi, TK | |
dc.contributor.author | Lim, AYH | |
dc.contributor.author | Keir, HR | |
dc.contributor.author | Dicker, AJ | |
dc.contributor.author | Thng, KX | |
dc.contributor.author | Tsang, A | |
dc.contributor.author | Ivan, FX | |
dc.contributor.author | Poh, ME | |
dc.contributor.author | Oriano, M | |
dc.contributor.author | Aliberti, S | |
dc.contributor.author | Blasi, F | |
dc.contributor.author | Low, TB | |
dc.contributor.author | Ong, TH | |
dc.contributor.author |
Oliver, B https://orcid.org/0000-0002-7122-9262 |
|
dc.contributor.author | Giam, YH | |
dc.contributor.author | Tee, A | |
dc.contributor.author | Koh, MS | |
dc.contributor.author | Abisheganaden, JA | |
dc.contributor.author | Tsaneva-Atanasova, K | |
dc.contributor.author | Chalmers, JD | |
dc.contributor.author | Chotirmall, SH | |
dc.date.accessioned | 2022-01-14T05:00:47Z | |
dc.date.available | 2021-02-16 | |
dc.date.available | 2022-01-14T05:00:47Z | |
dc.date.issued | 2021-04-05 | |
dc.identifier.citation | Nature Medicine, 2021, 27, (4), pp. 688-699 | |
dc.identifier.issn | 1078-8956 | |
dc.identifier.issn | 1546-170X | |
dc.identifier.uri | http://hdl.handle.net/10453/153117 | |
dc.description.abstract | Bronchiectasis, a progressive chronic airway disease, is characterized by microbial colonization and infection. We present an approach to the multi-biome that integrates bacterial, viral and fungal communities in bronchiectasis through weighted similarity network fusion ( https://integrative-microbiomics.ntu.edu.sg ). Patients at greatest risk of exacerbation have less complex microbial co-occurrence networks, reduced diversity and a higher degree of antagonistic interactions in their airway microbiome. Furthermore, longitudinal interactome dynamics reveals microbial antagonism during exacerbation, which resolves following treatment in an otherwise stable multi-biome. Assessment of the Pseudomonas interactome shows that interaction networks, rather than abundance alone, are associated with exacerbation risk, and that incorporation of microbial interaction data improves clinical prediction models. Shotgun metagenomic sequencing of an independent cohort validated the multi-biome interactions detected in targeted analysis and confirmed the association with exacerbation. Integrative microbiomics captures microbial interactions to determine exacerbation risk, which cannot be appreciated by the study of a single microbial group. Antibiotic strategies probably target the interaction networks rather than individual microbes, providing a fresh approach to the understanding of respiratory infection. | |
dc.format | Print-Electronic | |
dc.language | eng | |
dc.publisher | Springer Science and Business Media LLC | |
dc.relation.ispartof | Nature Medicine | |
dc.relation.isbasedon | 10.1038/s41591-021-01289-7 | |
dc.rights | info:eu-repo/semantics/embargoedAccess | |
dc.subject | 11 Medical and Health Sciences | |
dc.subject.classification | Immunology | |
dc.subject.mesh | Bronchiectasis | |
dc.subject.mesh | Disease Progression | |
dc.subject.mesh | Humans | |
dc.subject.mesh | Metagenomics | |
dc.subject.mesh | Microbial Interactions | |
dc.subject.mesh | Microbiota | |
dc.subject.mesh | Phylogeny | |
dc.subject.mesh | Humans | |
dc.subject.mesh | Bronchiectasis | |
dc.subject.mesh | Disease Progression | |
dc.subject.mesh | Phylogeny | |
dc.subject.mesh | Metagenomics | |
dc.subject.mesh | Microbial Interactions | |
dc.subject.mesh | Microbiota | |
dc.title | Integrative microbiomics in bronchiectasis exacerbations | |
dc.type | Journal Article | |
utslib.citation.volume | 27 | |
utslib.location.activity | United States | |
utslib.for | 11 Medical and Health Sciences | |
pubs.organisational-group | /University of Technology Sydney | |
pubs.organisational-group | /University of Technology Sydney/Faculty of Science | |
pubs.organisational-group | /University of Technology Sydney/Strength - CHT - Health Technologies | |
pubs.organisational-group | /University of Technology Sydney/Faculty of Science/School of Life Sciences | |
pubs.organisational-group | /University of Technology Sydney/Centre for Health Technologies (CHT) | |
utslib.copyright.status | open_access | * |
utslib.copyright.embargo | 2022-04-01T00:00:00+1000Z | |
dc.date.updated | 2022-01-14T05:00:38Z | |
pubs.issue | 4 | |
pubs.publication-status | Published | |
pubs.volume | 27 | |
utslib.citation.issue | 4 |
Abstract:
Bronchiectasis, a progressive chronic airway disease, is characterized by microbial colonization and infection. We present an approach to the multi-biome that integrates bacterial, viral and fungal communities in bronchiectasis through weighted similarity network fusion ( https://integrative-microbiomics.ntu.edu.sg ). Patients at greatest risk of exacerbation have less complex microbial co-occurrence networks, reduced diversity and a higher degree of antagonistic interactions in their airway microbiome. Furthermore, longitudinal interactome dynamics reveals microbial antagonism during exacerbation, which resolves following treatment in an otherwise stable multi-biome. Assessment of the Pseudomonas interactome shows that interaction networks, rather than abundance alone, are associated with exacerbation risk, and that incorporation of microbial interaction data improves clinical prediction models. Shotgun metagenomic sequencing of an independent cohort validated the multi-biome interactions detected in targeted analysis and confirmed the association with exacerbation. Integrative microbiomics captures microbial interactions to determine exacerbation risk, which cannot be appreciated by the study of a single microbial group. Antibiotic strategies probably target the interaction networks rather than individual microbes, providing a fresh approach to the understanding of respiratory infection.
Please use this identifier to cite or link to this item:
Download statistics for the last 12 months
Not enough data to produce graph