Montonye Dan R, Ericsson Aaron C, Busi Susheel B, Lutz Cathleen, Wardwell Keegan, Franklin Craig L
Comparative Medicine Program, Department of Veterinary Pathobiology, University of Missouri, Columbia, MO, United States.
University of Missouri Metagenomics Center, University of Missouri, Columbia, MO, United States.
Front Microbiol. 2018 May 28;9:1085. doi: 10.3389/fmicb.2018.01085. eCollection 2018.
Using animal models, the gut microbiota has been shown to play a critical role in the health and disease of many organ systems. Unfortunately, animal model studies often lack reproducibility when performed at different institutions. Previous studies in our laboratory have shown that the gut microbiota of mice can vary with a number of husbandry factors leading us to speculate that differing environments may alter gut microbiota, which in turn may influence animal model phenotypes. As an extension of these studies, we hypothesized that the shipping of mice from a mouse producer to an institution will result in changes in the type, relative abundance, and functional composition of the gut microbiota. Furthermore, we hypothesized that mice will develop a microbiota unique to the institution and facility in which they are housed. To test these hypotheses, mice of two strains (C57BL/6J and BALB/cJ), two age groups (4 week and 8 week old), and originating from two types of housing (research animal facility under conventional housing and production facilities under maximum barrier housing) were obtained from The Jackson Laboratory. Fecal samples were collected the day prior to shipping, immediately upon arrival, and then on days 2, 5, 7, and weeks 2, 4, and 9 post-arrival. Following the first post-arrival fecal collection, mice were separated into 2 groups and housed at different facilities at our institution while keeping their caging, diet, and husbandry practices the same. DNA was extracted from the collected fecal pellets and 16S rRNA amplicons were sequenced in order to characterize the type and relative abundance of gut bacteria. Principal component analysis (PCA) and permutational multivariate analysis of variance (PERMANOVA) demonstrated that both the shipping and the institution and facility in which mice were housed altered the gut microbiota. Phylogenetic investigation of communities by reconstruction of unobserved states (PICRUSt) predicted differences in functional composition in the gut microbiota of mice based on time of acclimation.
利用动物模型已表明,肠道微生物群在许多器官系统的健康与疾病中起着关键作用。不幸的是,动物模型研究在不同机构进行时往往缺乏可重复性。我们实验室之前的研究表明,小鼠的肠道微生物群会因多种饲养因素而有所不同,这使我们推测不同的环境可能会改变肠道微生物群,进而可能影响动物模型的表型。作为这些研究的延伸,我们假设将小鼠从生产商运至某机构会导致肠道微生物群的类型、相对丰度和功能组成发生变化。此外,我们假设小鼠会形成其所处机构和设施特有的微生物群。为验证这些假设,从杰克逊实验室获取了两种品系(C57BL/6J和BALB/cJ)、两个年龄组(4周龄和8周龄)且源自两种饲养环境(传统饲养条件下的研究动物设施和最大屏障饲养条件下的生产设施)的小鼠。在运输前一天、抵达时立即以及抵达后第2天、第5天、第7天以及第2周、第4周和第9周采集粪便样本。在首次抵达后粪便采集后,将小鼠分为两组,安置在我们机构的不同设施中,同时保持其笼具、饮食和饲养方式相同。从采集的粪便颗粒中提取DNA,并对16S rRNA扩增子进行测序,以表征肠道细菌的类型和相对丰度。主成分分析(PCA)和置换多元方差分析(PERMANOVA)表明,运输以及小鼠所处的机构和设施均改变了肠道微生物群。通过重建未观察状态进行群落系统发育研究(PICRUSt)预测了基于适应时间的小鼠肠道微生物群功能组成差异。