This study investigated the relationship between different vendors, production sites, and gut microbiome of mice, revealing significant differences among mice and changes in microbial profiles over time.
Animal models play a critical role in establishing causal relationships between gut microbiota and disease. The laboratory mouse is widely used to study the role of microbes in various disorders; however, differences between mouse vendors, genetic lineages and husbandry protocols have been shown to contribute to variation in phenotypes and to non-reproducibility of experimental results. We sought to understand how gut microbiome profiles of mice vary by vendor, vendor production facility and health status upon receipt into an academic facility and how they change over 12 weeks in the new environment. C57BL/6 mice were sourced from two different production sites for each of three different vendors. Mice were shipped to an academic research vivarium, and fresh-catch stool samples were collected from mice immediately from the shipping box upon receipt, and again after 2, 6 and 12 weeks in the new facility. Substantial variation in bacterial proportional abundance was observed among mice from each vendor at the time of receipt, but shared microbes accounted for most sequence reads. Vendor-specific microbes were generally of low abundance. Microbial profiles of mice from all vendors exhibited shifts over time, highlighting the importance of environmental conditions on microbial dynamics. Our results emphasize the need for continued efforts to account for sources of variation in animal models and understand how they contribute to experimental reproducibility. Long et al. examined the gut microbiome of C57BL/6 mice from two production sites of three different vendors upon receipt, and as the mice adapted to the new vivarium at the University of Connecticut Health Center. Bacterial proportional abundance varied among mice from each vendor, and mice from all vendors exhibited changes in microbial profiles over time. These findings support the need to consider the microbiome as a potential source of variation in mouse studies.
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