Inbred Mouse Populations Exhibit Intergenerational Changes in Intestinal Microbiota Composition and Function Following Introduction to a Facility

被引:18
作者
Choo, Jocelyn M. [1 ]
Trim, Paul J. [2 ]
Leong, Lex E. X. [1 ]
Abell, Guy C. J. [3 ]
Brune, Carly [4 ]
Jeffries, Nicole [4 ]
Wesselingh, Steve [1 ]
Dear, T. N. [1 ]
Snel, Marten F. [2 ]
Rogers, Geraint B. [1 ,3 ]
机构
[1] South Australian Hlth & Med Res Inst, Infect & Immun Theme, Adelaide, SA, Australia
[2] South Australian Hlth & Med Res Inst, Nutr & Metab Theme, Lysosomal Dis Res Unit, Adelaide, SA, Australia
[3] Flinders Univ S Australia, Sch Med, Adelaide, SA, Australia
[4] South Australian Hlth & Med Res Inst, Bioresources Facil, Adelaide, SA, Australia
关键词
C57BL/6J inbred mice; mice generations; fecal microbiota; fecal metabolome; microbiome variation; CHAIN FATTY-ACIDS; GUT MICROBIOTA; LABORATORY MICE; FECAL FLORA; INFLAMMATION; METABOLISM; CELLS; IMMUNITY; BACTERIA; COLITIS;
D O I
10.3389/fmicb.2017.00608
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Inbred mice are used to investigate many aspects of human physiology, including susceptibility to disease and response to therapies. Despite increasing evidence that the composition and function of the murine intestinal microbiota can substantially influence a broad range of experimental outcomes, relatively little is known about microbiome dynamics within experimental mouse populations. We investigated changes in the intestinal microbiome between C57BL/6J mice spanning six generations (assessed at generations 1, 2, 3, and 6), following their introduction to a stringently controlled facility. Fecal microbiota composition and function were assessed by 16S rRNA gene amplicon sequencing and liquid chromatography mass spectrometry, respectively. Significant divergence of the intestinal microbiota between founder and second generation mice, as well as continuing inter-generational variance, was observed. Bacterial taxa whose relative abundance changed significantly through time included Akkermansia, Turicibacter, and Bifidobacterium (p < 0.05), all of which are recognized as having the potential to substantially influence host physiology. Shifts in microbiota composition were mirrored by corresponding differences in the fecal metabolome (r = 0.57, p = 0.0001), with notable differences in levels of tryptophan pathway metabolites and amino acids, including glutamine, glutamate and aspartate. We related the magnitude of changes in the intestinal microbiota and metabolome characteristics during acclimation to those observed between populations housed in separate facilities, which differed in regards to husbandry, barrier conditions and dietary intake. The microbiome variance reported here has implications for experimental reproducibility, and as a consequence, experimental design and the interpretation of research outcomes across wide range of contexts.
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