Nistelberger Rebecca, Gibler Patrizia, Barones Lisa, Absenger Arno, Kral-Pointner Julia B, Salzmann Manuel, Hartmann Boris, Podesser Bruno K, Hohensinner Phillip J, Plasenzotti Roberto
Medical University of Vienna Core Facility, Medical University of Vienna, 1090 Vienna, Austria.
Ludwig Boltzmann Institute for Cardiovascular Research, 1090 Vienna, Austria.
Animals (Basel). 2025 Jun 11;15(12):1725. doi: 10.3390/ani15121725.
The composition of the gut microbiome, defined by environmental factors, significantly affects research outcomes, with variations observed across animal facilities. Efforts to standardize led to the definition of the 'Altered Schaedler flora' (ASF), comprising eight bacterial groups. Our data highlights the variability of ASF under pathogen contact. Feces from two wild-type strains ( and mice) with and without proven infection was collected in two different animal facilities and analyzed. The data show a significant difference in the quantity (either reduction or increase) of the eight ASF bacterial groups when comparing infected and non-infected mice across different housing areas (SPF-specific pathogen-free, quarantine, and conventional-experimental areas) within a facility, as well as in comparison to another facility. Furthermore, strain-specific differences are also evident, with certain ASF groups showing a reduction in quantity at one facility but an increase at the other, comparing the same housing area. Comparative studies across facilities confirmed the necessity of baseline determination for accurate ASF analysis. Performing ASF analysis, facilitated by in-house qPCR (quantitative polymerase chain reaction) kits, offers prompt and precise microbiome profiling, enhancing experimental accuracy and health monitoring in animal research settings.
由环境因素定义的肠道微生物群组成会显著影响研究结果,不同动物设施之间存在差异。标准化的努力导致了“改变的 Schaedler 菌群”(ASF)的定义,其由八个细菌组组成。我们的数据突出了病原体接触下 ASF 的变异性。在两个不同的动物设施中收集了来自两种野生型菌株(和小鼠)有或无确诊感染的粪便并进行分析。数据显示,在同一设施内不同饲养区域(无特定病原体的 SPF 区域、隔离区域和常规实验区域)比较感染和未感染小鼠时,以及与另一个设施相比时,八个 ASF 细菌组的数量(减少或增加)存在显著差异。此外,菌株特异性差异也很明显,在相同饲养区域进行比较时,某些 ASF 组在一个设施中数量减少而在另一个设施中数量增加。跨设施的比较研究证实了进行基线测定以准确分析 ASF 的必要性。使用内部定量聚合酶链反应(qPCR)试剂盒进行 ASF 分析,可提供快速准确的微生物群分析,提高动物研究环境中的实验准确性和健康监测水平。