Low‐gainer diet‐induced obese microbiota transplanted mice exhibit increased fighting

Author:

Junker Mentzel Caroline M.1,Hui Yan2,Hammerich Tanja Maria Stentoft2,Klug‐Dambmann Malene2,Liu Yi2,Zachariassen Line Fisker1ORCID,Hansen Lars Hestbjerg3,Aslampaloglou Antonios2,Kiersgaard Maria4,Nielsen Dennis Sandris2,Hansen Axel Kornerup1ORCID,Krych Lukasz2ORCID

Affiliation:

1. Section for Experimental Animals Models, Department of Veterinary and Animal Sciences, Faculty of Health Science University of Copenhagen Frederiksberg Denmark

2. Section for Microbiology and Fermentation, Department of Food Science, Faculty of Science University of Copenhagen Frederiksberg Denmark

3. Section for Microbial Ecology and Biotechnology, Department of Plant and Environmental Sciences, Faculty of Science University of Copenhagen Frederiksberg Denmark

4. Laboratory Animal Science Novo Nordisk A/S Måløv Denmark

Abstract

AbstractWeight gain variation is a great challenge in diet‐induced obesity studies since low‐gainer animals are of limited experimental value. The inbred C57BL/6 (B6) mice are frequently used models due to their genetic homogeneity and susceptibility to diet‐induced obesity (DIO). The aim of this study is to investigate if the gut microbiota (GM) influences the fraction of low weight gainers in DIO studies. A total of 100 male B6 mice (donor population) were fed a high‐fat diet for 14 weeks and divided into the study groups high gainer (HG) and low gainer (LG) based on their weight gain. Subsequently, fecal matter transplantation (FMT) was done on germ‐free B6 mice with GM from HG and LG donors (FMT population). LG (13.35 ± 2.5 g) and HG (25.52 ± 2.0 g) animals were identified by the weight gain from week 1 to week 12. Interestingly, the start weight of the LG (20.36 ± 1.4 g) and HG (21.59 ± 0.7 g) groups differed significantly. Transplanting LG or HG fecal matter to germ‐free mice resulted in significant differences in weight gain between HG and LG, as well as differences in serum leptin levels and epididymal fat pad weight. A clear LG‐specific GM composition could not be distinguished by 16S rRNA gene amplicon sequencing. Surprisingly, significantly more fighting was recorded in LG groups of both donor populations and when transplanted to germ‐free mice. The HG and LG phenotypes could be transferred to germ‐free mice. The increased fighting in the LG group in both studies suggests not only that the tendency to fight can be transferred by FMT in these mice, but also that fighting should be prevented in DIO studies to minimize the number of LG animals.

Publisher

Wiley

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