| Literature DB >> 33820995 |
Micheál Mac Aogáin1, Jayanth Kumar Narayana1, Pei Yee Tiew1,2, Nur A'tikah Binte Mohamed Ali1, Valerie Fei Lee Yong1, Tavleen Kaur Jaggi1, Albert Yick Hou Lim3, Holly R Keir4, Alison J Dicker4, Kai Xian Thng1, Akina Tsang1, Fransiskus Xaverius Ivan1, Mau Ern Poh5, Martina Oriano6,7, Stefano Aliberti6,7, Francesco Blasi6,7, Teck Boon Low8, Thun How Ong2, Brian Oliver9,10, Yan Hui Giam4, Augustine Tee8, Mariko Siyue Koh2, John Arputhan Abisheganaden3, Krasimira Tsaneva-Atanasova11, James D Chalmers4, Sanjay H Chotirmall12.
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.Entities:
Year: 2021 PMID: 33820995 DOI: 10.1038/s41591-021-01289-7
Source DB: PubMed Journal: Nat Med ISSN: 1078-8956 Impact factor: 53.440