Abstract

The mouse is the most commonly used model species in biomedical research. Just as human physical and mental health are influenced by the commensal gut bacteria, mouse models of disease are influenced by the fecal microbiome (FM). The source of mice represents one of the strongest influences on the FM and can influence the phenotype of disease models. The FM influences behavior in mice leading to the hypothesis that mice of the same genetic background from different vendors, will have different behavioral phenotypes. To test this hypothesis, colonies of CD-1 mice, rederived via embryo transfer into surrogate dams from four different suppliers, were subjected to phenotyping assays assessing behavior and physiological parameters. Significant differences in behavior, growth rate, metabolism, and hematological parameters were observed. Collectively, these findings show the profound influence of supplier-origin FMs on host behavior and physiology in healthy, genetically similar, wild-type mice maintained in identical environments.

Ericsson et al. show that different vendors (suppliers of mouse strains) harbor distinct microbiomes, which drive distinct behavioral phenotypes when the genetics are fixed. They specifically focus on changes relating to exploratory and anxiety-related behavior, physiological phenotypic parameters, glucose metabolism, and blood leukocytes. They conclude by emphasizing that supplier-origin fecal microbiomes represent potential sources of poor experimental reproducibility and suggest means to optimize experimentation with mice and their microbiomes.

Details

Title
Supplier-origin mouse microbiomes significantly influence locomotor and anxiety-related behavior, body morphology, and metabolism
Author
Ericsson, Aaron C 1   VIAFID ORCID Logo  ; Hart, Marcia L 2 ; Kwan, Jessica 3 ; Lanoue, Louise 4 ; Bower, Lynette R 4 ; Araiza Renee 5   VIAFID ORCID Logo  ; Kent, Lloyd K, C 6   VIAFID ORCID Logo  ; Franklin, Craig L 1   VIAFID ORCID Logo 

 University of Missouri (MU), Department of Veterinary Pathobiology, College of Veterinary Medicine, University of Missouri Metagenomics Center (MUMC), Columbia, USA (GRID:grid.134936.a) (ISNI:0000 0001 2162 3504); MU Mutant Mouse Resource and Research Center (MU MMRRC), Columbia, USA (GRID:grid.134936.a) (ISNI:0000 0001 2162 3504) 
 IDEXX BioAnalytics, Columbia, USA (GRID:grid.497035.c) (ISNI:0000 0004 0409 7356) 
 University of California (UC), School of Veterinary Medicine, Davis, USA (GRID:grid.27860.3b) (ISNI:0000 0004 1936 9684) 
 Mouse Metabolic Phenotyping Center (MMPC) at UC Davis, Davis, USA (GRID:grid.27860.3b) (ISNI:0000 0004 1936 9684) 
 Mouse Metabolic Phenotyping Center (MMPC) at UC Davis, Davis, USA (GRID:grid.27860.3b) (ISNI:0000 0004 1936 9684); Mutant Mouse Resource and Research Center at UC Davis, Davis, USA (GRID:grid.27860.3b) (ISNI:0000 0004 1936 9684) 
 Mouse Metabolic Phenotyping Center (MMPC) at UC Davis, Davis, USA (GRID:grid.27860.3b) (ISNI:0000 0004 1936 9684); Mutant Mouse Resource and Research Center at UC Davis, Davis, USA (GRID:grid.27860.3b) (ISNI:0000 0004 1936 9684); UC Davis Mouse Biology Program (MBP), Davis, USA (GRID:grid.27860.3b) (ISNI:0000 0004 1936 9684); UC Davis, Department of Surgery, School of Medicine, Sacramento, USA (GRID:grid.27860.3b) (ISNI:0000 0004 1936 9684) 
Publication year
2021
Publication date
2021
Publisher
Nature Publishing Group
e-ISSN
23993642
Source type
Scholarly Journal
Language of publication
English
ProQuest document ID
2539746083
Copyright
© The Author(s) 2021. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.