Transient colonizing microbes promote gut dysbiosis and functional impairmentUniversité Clermont Auvergne, INRAE, UMR 454 MEDIS, 28 place Henri Dunant, F-63000, Clermont-Ferrand, France, 28 place Henri Dunant.
Centre for Host-Microbiome Interactions, Faculty of Dentistry, Oral & Craniofacial Sciences, King’s College London, SE1 9RT, London, UK.
Department of Bio and Brain Engineering, KAIST, 291 Daehak-ro, Yuseong-gu, 305-701, Daejeon, Republic of Korea.
University Paris-Saclay, INRAE, MetaGenoPolis, 78350, Jouy-en-Josas, France.
Centre for Host-Microbiome Interactions, Faculty of Dentistry, Oral & Craniofacial Sciences, King’s College London, SE1 9RT, London, UK.
University Paris-Saclay, INRAE, MetaGenoPolis, 78350, Jouy-en-Josas, France.
University Paris-Saclay, INRAE, MetaGenoPolis, 78350, Jouy-en-Josas, France.
Centre for Translational Microbiome Research, Department of Microbiology, Tumour and Cell Biology, Karolinska Institutet, SE-171 77, Stockholm, Sweden.
Centre for Translational Microbiome Research, Department of Microbiology, Tumour and Cell Biology, Karolinska Institutet, SE-171 77, Stockholm, Sweden.
Centre for Translational Microbiome Research, Department of Microbiology, Tumour and Cell Biology, Karolinska Institutet, SE-171 77, Stockholm, Sweden.
Centre for Translational Microbiome Research, Department of Microbiology, Tumour and Cell Biology, Karolinska Institutet, SE-171 77, Stockholm, Sweden.
Department of Bio and Brain Engineering, KAIST, 291 Daehak-ro, Yuseong-gu, 305-701, Daejeon, Republic of Korea.
Centre for Host-Microbiome Interactions, Faculty of Dentistry, Oral & Craniofacial Sciences, King’s College London, SE1 9RT, London, UK.
Université Clermont Auvergne, INRAE, UMR 454 MEDIS, 28 place Henri Dunant, F-63000, Clermont-Ferrand, France, 28 place Henri Dunant.
Centre for Host-Microbiome Interactions, Faculty of Dentistry, Oral & Craniofacial Sciences, King’s College London, SE1 9RT, London, UK.
University Paris-Saclay, INRAE, MetaGenoPolis, 78350, Jouy-en-Josas, France.
University Paris-Saclay, INRAE, MetaGenoPolis, 78350, Jouy-en-Josas, France.
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2024 (English)In: npj Biofilms and Microbiomes, E-ISSN 2055-5008, Vol. 10, no 1, article id 80Article in journal (Refereed) Published
Abstract [en]
Species composition of the healthy adult gut microbiota tends to be stable over time. Destabilization of the gut microbiome under the influence of different factors is the main driver of the microbial dysbiosis and subsequent impacts on host physiology. Here, we used metagenomics data from a Swedish longitudinal cohort, to determine the stability of the gut microbiome and uncovered two distinct microbial species groups; persistent colonizing species (PCS) and transient colonizing species (TCS). We validated the continuation of this grouping, generating gut metagenomics data for additional time points from the same Swedish cohort. We evaluated the existence of PCS/TCS across different geographical regions and observed they are globally conserved features. To characterize PCS/TCS phenotypes, we performed bioreactor fermentation with faecal samples and metabolic modeling. Finally, using chronic disease gut metagenome and other multi-omics data, we identified roles of TCS in microbial dysbiosis and link with abnormal changes to host physiology.
Place, publisher, year, edition, pages
Springer Nature , 2024. Vol. 10, no 1, article id 80
National Category
Microbiology Bioinformatics and Computational Biology
Identifiers
URN: urn:nbn:se:kth:diva-353444DOI: 10.1038/s41522-024-00561-1ISI: 001307255800001PubMedID: 39245657Scopus ID: 2-s2.0-85203264308OAI: oai:DiVA.org:kth-353444DiVA, id: diva2:1899119
Note
QC 20240926
2024-09-192024-09-192025-02-05Bibliographically approved