TY - JOUR
T1 - Analysis of early childhood intestinal microbial dynamics in a continuous-flow bioreactor
AU - DIABIMMUNE Study Group
AU - Granato, Alessandra
AU - Renwick, Simone
AU - Yau, Christopher
AU - Kong, Tiffany
AU - Daigneault, Michelle C.
AU - Knip, Mikael
AU - Allen-Vercoe, Emma
AU - Danska, Jayne S.
N1 - Publisher Copyright:
© The Author(s) 2024.
PY - 2024/12
Y1 - 2024/12
N2 - Background: The human gut microbiota is inoculated at birth and undergoes a process of assembly and diversification during the first few years of life. Studies in mice and humans have revealed associations between the early-life gut microbiome and future susceptibility to immune and metabolic diseases. To resolve microbe and host contributing factors to early-life development and to disease states requires experimental platforms that support reproducible, longitudinal, and high-content analyses. Results: Here, we deployed a continuous single-stage chemostat culture model of the human distal gut to study gut microbiota from 18- to 24-month-old children integrating both culture-dependent and -independent methods. Chemostat cultures recapitulated multiple aspects of the fecal microbial ecosystem enabling investigation of relationships between bacterial strains and metabolic function, as well as a resource from which we isolated and curated a diverse library of early life bacterial strains. Conclusions: We report the reproducible, longitudinal dynamics of early-life bacterial communities cultured in an advanced model of the human gut providing an experimental approach and a characterized bacterial resource to support future investigations of the human gut microbiota in early childhood.
AB - Background: The human gut microbiota is inoculated at birth and undergoes a process of assembly and diversification during the first few years of life. Studies in mice and humans have revealed associations between the early-life gut microbiome and future susceptibility to immune and metabolic diseases. To resolve microbe and host contributing factors to early-life development and to disease states requires experimental platforms that support reproducible, longitudinal, and high-content analyses. Results: Here, we deployed a continuous single-stage chemostat culture model of the human distal gut to study gut microbiota from 18- to 24-month-old children integrating both culture-dependent and -independent methods. Chemostat cultures recapitulated multiple aspects of the fecal microbial ecosystem enabling investigation of relationships between bacterial strains and metabolic function, as well as a resource from which we isolated and curated a diverse library of early life bacterial strains. Conclusions: We report the reproducible, longitudinal dynamics of early-life bacterial communities cultured in an advanced model of the human gut providing an experimental approach and a characterized bacterial resource to support future investigations of the human gut microbiota in early childhood.
KW - Anexic isolation
KW - Bacterial metabolites
KW - Chemostat continuous culture
KW - Defined bacterial consortia
KW - Early childhood microbiome
U2 - 10.1186/s40168-024-01976-w
DO - 10.1186/s40168-024-01976-w
M3 - Article
C2 - 39639333
AN - SCOPUS:85211458174
SN - 2049-2618
VL - 12
JO - Microbiome
JF - Microbiome
IS - 1
M1 - 255
ER -