Standardized Complex Gut Microbiomes Influence Fetal Growth, Food Intake, and Adult Body Weight in Outbred Mice

Obesity places a tremendous burden on individual health and the healthcare system. The gut microbiome (GM) influences host metabolism and behaviors affecting body weight (BW) such as feeding. The GM of mice varies between suppliers and significantly influences BW. We sought to determine whether GM-a...

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Main Authors: Christa N. Cheatham, Kevin L. Gustafson, Zachary L. McAdams, Giedre M. Turner, Rebecca A. Dorfmeyer, Aaron C. Ericsson
Format: Article
Language:English
Published: MDPI AG 2023-02-01
Series:Microorganisms
Subjects:
Online Access:https://www.mdpi.com/2076-2607/11/2/484
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author Christa N. Cheatham
Kevin L. Gustafson
Zachary L. McAdams
Giedre M. Turner
Rebecca A. Dorfmeyer
Aaron C. Ericsson
author_facet Christa N. Cheatham
Kevin L. Gustafson
Zachary L. McAdams
Giedre M. Turner
Rebecca A. Dorfmeyer
Aaron C. Ericsson
author_sort Christa N. Cheatham
collection DOAJ
description Obesity places a tremendous burden on individual health and the healthcare system. The gut microbiome (GM) influences host metabolism and behaviors affecting body weight (BW) such as feeding. The GM of mice varies between suppliers and significantly influences BW. We sought to determine whether GM-associated differences in BW are associated with differences in intake, fecal energy loss, or fetal growth. Pair-housed mice colonized with a low or high microbial richness GM were weighed, and the total and BW-adjusted intake were measured at weaning and adulthood. Pups were weighed at birth to determine the effects of the maternal microbiome on fetal growth. Fecal samples were collected to assess the fecal energy loss and to characterize differences in the microbiome. The results showed that supplier-origin microbiomes were associated with profound differences in fetal growth and excessive BW-adjusted differences in intake during adulthood, with no detected difference in fecal energy loss. Agreement between the features of the maternal microbiome associated with increased birth weight here and in recent human studies supports the value of this model to investigate the mechanisms by which the maternal microbiome regulates offspring growth and food intake.
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spelling doaj.art-513af5d80e054a66a23dfbc7a7f6eea32023-11-16T22:16:32ZengMDPI AGMicroorganisms2076-26072023-02-0111248410.3390/microorganisms11020484Standardized Complex Gut Microbiomes Influence Fetal Growth, Food Intake, and Adult Body Weight in Outbred MiceChrista N. Cheatham0Kevin L. Gustafson1Zachary L. McAdams2Giedre M. Turner3Rebecca A. Dorfmeyer4Aaron C. Ericsson5Comparative Medicine Program, Department of Veterinary Pathobiology, University of Missouri (MU), Columbia, MO 65201, USAComparative Medicine Program, Department of Veterinary Pathobiology, University of Missouri (MU), Columbia, MO 65201, USAMolecular Pathogenesis and Therapeutics Program, University of Missouri (MU), Columbia, MO 65201, USAMutant Mouse Resource and Research Center, University of Missouri (MU), Columbia, MO 65201, USAMutant Mouse Resource and Research Center, University of Missouri (MU), Columbia, MO 65201, USAComparative Medicine Program, Department of Veterinary Pathobiology, University of Missouri (MU), Columbia, MO 65201, USAObesity places a tremendous burden on individual health and the healthcare system. The gut microbiome (GM) influences host metabolism and behaviors affecting body weight (BW) such as feeding. The GM of mice varies between suppliers and significantly influences BW. We sought to determine whether GM-associated differences in BW are associated with differences in intake, fecal energy loss, or fetal growth. Pair-housed mice colonized with a low or high microbial richness GM were weighed, and the total and BW-adjusted intake were measured at weaning and adulthood. Pups were weighed at birth to determine the effects of the maternal microbiome on fetal growth. Fecal samples were collected to assess the fecal energy loss and to characterize differences in the microbiome. The results showed that supplier-origin microbiomes were associated with profound differences in fetal growth and excessive BW-adjusted differences in intake during adulthood, with no detected difference in fecal energy loss. Agreement between the features of the maternal microbiome associated with increased birth weight here and in recent human studies supports the value of this model to investigate the mechanisms by which the maternal microbiome regulates offspring growth and food intake.https://www.mdpi.com/2076-2607/11/2/484microbiomemousebirth weightbody weightintake
spellingShingle Christa N. Cheatham
Kevin L. Gustafson
Zachary L. McAdams
Giedre M. Turner
Rebecca A. Dorfmeyer
Aaron C. Ericsson
Standardized Complex Gut Microbiomes Influence Fetal Growth, Food Intake, and Adult Body Weight in Outbred Mice
Microorganisms
microbiome
mouse
birth weight
body weight
intake
title Standardized Complex Gut Microbiomes Influence Fetal Growth, Food Intake, and Adult Body Weight in Outbred Mice
title_full Standardized Complex Gut Microbiomes Influence Fetal Growth, Food Intake, and Adult Body Weight in Outbred Mice
title_fullStr Standardized Complex Gut Microbiomes Influence Fetal Growth, Food Intake, and Adult Body Weight in Outbred Mice
title_full_unstemmed Standardized Complex Gut Microbiomes Influence Fetal Growth, Food Intake, and Adult Body Weight in Outbred Mice
title_short Standardized Complex Gut Microbiomes Influence Fetal Growth, Food Intake, and Adult Body Weight in Outbred Mice
title_sort standardized complex gut microbiomes influence fetal growth food intake and adult body weight in outbred mice
topic microbiome
mouse
birth weight
body weight
intake
url https://www.mdpi.com/2076-2607/11/2/484
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