TY - JOUR
T1 - Genome-scale resources in the infant gut symbiont Bifidobacterium breve reveal genetic determinants of colonization and host-microbe interactions
AU - Shiver, Anthony L.
AU - Sun, Jiawei
AU - Culver, Rebecca
AU - Violette, Arvie
AU - Wynter, Char
AU - Nieckarz, Marta
AU - Mattiello, Samara Paula
AU - Sekhon, Prabhjot Kaur
AU - Bottacini, Francesca
AU - Friess, Lisa
AU - Carlson, Hans K.
AU - Wong, Daniel P.G.H.
AU - Higginbottom, Steven
AU - Weglarz, Meredith
AU - Wang, Weigao
AU - Knapp, Benjamin D.
AU - Guiberson, Emma
AU - Sanchez, Juan
AU - Huang, Po Hsun
AU - Garcia, Paulo A.
AU - Buie, Cullen R.
AU - Good, Benjamin H.
AU - DeFelice, Brian
AU - Cava, Felipe
AU - Scaria, Joy
AU - Sonnenburg, Justin L.
AU - Van Sinderen, Douwe
AU - Deutschbauer, Adam M.
AU - Huang, Kerwyn Casey
N1 - Publisher Copyright:
© 2025 Elsevier Inc.
PY - 2025/4/3
Y1 - 2025/4/3
N2 - 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.
AB - 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.
KW - bifidobacteria
KW - functional genomics
KW - genome-scale metabolic reconstruction
KW - genome-scale ordered mutant collection
KW - glucose-phosphate stress
KW - indole-3-lactic acid
KW - infant microbiome
KW - metabolomics
KW - microbiome assembly
KW - RB-TnSeq
UR - https://www.scopus.com/pages/publications/86000591622
U2 - 10.1016/j.cell.2025.02.010
DO - 10.1016/j.cell.2025.02.010
M3 - Article
C2 - 40068681
AN - SCOPUS:86000591622
SN - 0092-8674
VL - 188
SP - 2003-2021.e19
JO - Cell
JF - Cell
IS - 7
ER -