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Genome-scale resources in the infant gut symbiont Bifidobacterium breve reveal genetic determinants of colonization and host-microbe interactions
Department of Bioengineering, Stanford University, CA, Stanford, United States.
Department of Bioengineering, Stanford University, CA, Stanford, United States.
Department of Genetics, Stanford University, CA, Stanford, United States.
Department of Bioengineering, Stanford University, CA, Stanford, United States.
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2025 (English)In: Cell, ISSN 0092-8674, E-ISSN 1097-4172, Vol. 188, no 7, p. 2003-2021.e19Article in journal (Refereed) Published
Abstract [en]

Bifidobacteria represent a dominant constituent of human gut microbiomes during infancy, influencing nutrition, immune development, and resistance to infection. Despite interest in bifidobacteria as a live biotic therapy, our understanding of colonization, host-microbe interactions, and the health-promoting effects of bifidobacteria is limited. To address these major knowledge gaps, we used a large-scale genetic approach to create a mutant fitness compendium in Bifidobacterium breve. First, we generated a high-density randomly barcoded transposon insertion pool and used it to determine fitness requirements during colonization of germ-free mice and chickens with multiple diets and in response to hundreds of in vitro perturbations. Second, to enable mechanistic investigation, we constructed an ordered collection of insertion strains covering 1,462 genes. We leveraged these tools to reveal community- and diet-specific requirements for colonization and to connect the production of immunomodulatory molecules to growth benefits. These resources will catalyze future investigations of this important beneficial microbe.

Place, publisher, year, edition, pages
Cell Press, 2025. Vol. 188, no 7, p. 2003-2021.e19
Keywords [en]
bifidobacteria, functional genomics, genome-scale metabolic reconstruction, genome-scale ordered mutant collection, glucose-phosphate stress, indole-3-lactic acid, infant microbiome, metabolomics, microbiome assembly, RB-TnSeq
National Category
Microbiology
Identifiers
URN: urn:nbn:se:umu:diva-237160DOI: 10.1016/j.cell.2025.02.010PubMedID: 40068681Scopus ID: 2-s2.0-86000591622OAI: oai:DiVA.org:umu-237160DiVA, id: diva2:1952080
Funder
Swedish Research CouncilKnut and Alice Wallenberg FoundationThe Kempe FoundationsAvailable from: 2025-04-14 Created: 2025-04-14 Last updated: 2025-04-14Bibliographically approved

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Nieckarz, MartaCava, Felipe

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Molecular Infection Medicine Sweden (MIMS)Umeå Centre for Microbial Research (UCMR)Department of Molecular Biology (Faculty of Medicine)
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