Ericsson Aaron C, Davis J Wade, Spollen William, Bivens Nathan, Givan Scott, Hagan Catherine E, McIntosh Mark, Franklin Craig L
Department of Veterinary Pathobiology, University of Missouri, Columbia, Missouri, United States of America; Mutant Mouse Resource and Research Center, University of Missouri, Columbia, Missouri, United States of America; University of Missouri Metagenomics Center, University of Missouri, Columbia, Missouri, United States of America.
Department of Biostatistics, University of Missouri, Columbia, Missouri, United States of America.
PLoS One. 2015 Feb 12;10(2):e0116704. doi: 10.1371/journal.pone.0116704. eCollection 2015.
The commensal gut microbiota has been implicated as a determinant in several human diseases and conditions. There is mounting evidence that the gut microbiota of laboratory mice (Mus musculus) similarly modulates the phenotype of mouse models used to study human disease and development. While differing model phenotypes have been reported using mice purchased from different vendors, the composition and uniformity of the fecal microbiota in mice of various genetic backgrounds from different vendors is unclear. Using culture-independent methods and robust statistical analysis, we demonstrate significant differences in the richness and diversity of fecal microbial populations in mice purchased from two large commercial vendors. Moreover, the abundance of many operational taxonomic units, often identified to the species level, as well as several higher taxa, differed in vendor- and strain-dependent manners. Such differences were evident in the fecal microbiota of weanling mice and persisted throughout the study, to twenty-four weeks of age. These data provide the first in-depth analysis of the developmental trajectory of the fecal microbiota in mice from different vendors, and a starting point from which researchers may be able to refine animal models affected by differences in the gut microbiota and thus possibly reduce the number of animals required to perform studies with sufficient statistical power.
共生肠道微生物群被认为是多种人类疾病和病症的一个决定因素。越来越多的证据表明,实验室小鼠(小家鼠)的肠道微生物群同样会调节用于研究人类疾病和发育的小鼠模型的表型。虽然使用从不同供应商购买的小鼠报告了不同的模型表型,但来自不同供应商的各种遗传背景小鼠粪便微生物群的组成和一致性尚不清楚。通过使用非培养方法和强大的统计分析,我们证明了从两个大型商业供应商购买的小鼠粪便微生物种群的丰富度和多样性存在显著差异。此外,许多通常在物种水平鉴定的操作分类单元以及几个更高分类群的丰度,在供应商和品系依赖的方式上有所不同。这种差异在断奶小鼠的粪便微生物群中很明显,并在整个研究过程中持续存在,直至24周龄。这些数据首次对来自不同供应商的小鼠粪便微生物群的发育轨迹进行了深入分析,并为研究人员提供了一个起点,他们或许能够优化受肠道微生物群差异影响的动物模型,从而可能减少进行具有足够统计效力的研究所需的动物数量。