Altering the Intestinal Microbiota during a Critical Developmental Window Has Lasting Metabolic Consequences
Author(s) -
Laura M. Cox,
Shingo Yamanishi,
Jiho Sohn,
Alexander V. Alekseyenko,
Jacqueline M. Leung,
Ilseung Cho,
Sungheon Kim,
Huilin Li,
Zhan Gao,
Douglas Mahana,
Jorge Rodríguez,
Arlin B. Rogers,
Nicolas Robine,
P’ng Loke,
Martin J. Blaser
Publication year - 2014
Publication title -
cell
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 26.304
H-Index - 776
eISSN - 1097-4172
pISSN - 0092-8674
DOI - 10.1016/j.cell.2014.05.052
Subject(s) - biology , gut flora , phenotype , antibiotics , host (biology) , genetics , microbiology and biotechnology , immunology , gene
Acquisition of the intestinal microbiota begins at birth, and a stable microbial community develops from a succession of key organisms. Disruption of the microbiota during maturation by low-dose antibiotic exposure can alter host metabolism and adiposity. We now show that low-dose penicillin (LDP), delivered from birth, induces metabolic alterations and affects ileal expression of genes involved in immunity. LDP that is limited to early life transiently perturbs the microbiota, which is sufficient to induce sustained effects on body composition, indicating that microbiota interactions in infancy may be critical determinants of long-term host metabolic effects. In addition, LDP enhances the effect of high-fat diet induced obesity. The growth promotion phenotype is transferrable to germ-free hosts by LDP-selected microbiota, showing that the altered microbiota, not antibiotics per se, play a causal role. These studies characterize important variables in early-life microbe-host metabolic interaction and identify several taxa consistently linked with metabolic alterations. PAPERCLIP:
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