Format

Send to

Choose Destination
Front Microbiol. 2017 Feb 23;8:196. doi: 10.3389/fmicb.2017.00196. eCollection 2017.

Variable Colonization after Reciprocal Fecal Microbiota Transfer between Mice with Low and High Richness Microbiota.

Author information

1
University of Missouri Metagenomics Center, University of MissouriColumbia, MO, USA; University of Missouri Mutant Mouse Resource and Research Center, University of MissouriColumbia, MO, USA; Comparative Metagenomics Laboratory, Department of Veterinary Pathobiology, University of MissouriColumbia, MO, USA.
2
Comparative Metagenomics Laboratory, Department of Veterinary Pathobiology, University of Missouri Columbia, MO, USA.
3
University of Missouri Mutant Mouse Resource and Research Center, University of MissouriColumbia, MO, USA; Comparative Metagenomics Laboratory, Department of Veterinary Pathobiology, University of MissouriColumbia, MO, USA.

Abstract

Several associations have been made between characteristics of the resident gut microbiota and human health and disease susceptibility. Animal models provide the means to test these correlations prospectively and evaluate causality. Experimental fecal microbiota transfer (FMT), or the intentional transplantation of gut microbes into recipient mice depleted of their autochthonous microbes with antibiotics, is a commonly used method of testing these relationships. The true completeness of microbial transfer through such procedures is poorly documented in the literature, particularly in the context of reciprocal transfer of microbes between recipient and donor mice harboring microbial populations of differing richness and diversity. Moreover, it is unclear whether the use of frozen fecal contents or cecal contents would confer any difference in the outcomes of transfer. Herein, groups of mice colonized with distinct gut microbiota of differing richness and composition were used in a reciprocal FMT study, with different groups receiving transfer of material prepared from fresh cecal contents, fresh feces, or frozen feces. Targeted 16S rRNA gene amplicon sequencing was used at intervals throughout the study to characterize the microbiota. Notably, despite comparable depletion of the microbiota in recipient mice prior to transfer, donor-specific taxa reliably colonized recipients only when relatively rich donor material was transferred to mice originally colonized with a simpler microbiota. It is unclear whether these differences were due to differences in the endogenous recipient microbiota or host factors induced in early life by microbial factors. These findings are of practical import for researchers using FMT to prospectively assess the influence of the gut microbiota in mouse models, and to those studying host-microbial interactions and their influence on gut barrier function.

KEYWORDS:

16S rRNA gene; colonization resistance; fecal microbiota transfer; microbiome; mouse; richness

Supplemental Content

Full text links

Icon for Frontiers Media SA Icon for PubMed Central
Loading ...
Support Center