Department of Immunology, University Medicine Greifswald, Germany.
Charles River, Research and Professional Services, Wilmington, MA, United States.
Int J Med Microbiol. 2018 Aug;308(6):598-606. doi: 10.1016/j.ijmm.2017.11.006. Epub 2017 Nov 20.
We previously reported that laboratory mice from all global vendors are frequently colonized with Staphylococcus aureus (S. aureus). Genotyping of a snap sample of murine S. aureus isolates from Charles River, US, showed that mice were predominantly colonized with methicillin-sensitive CC88 strains. Here, we expanded our view and investigated whether laboratory mice from other global animal facilities are colonized with similar strains or novel S. aureus lineages, and whether the murine S. aureus isolates show features of host adaptation. In total, we genotyped 230 S. aureus isolates from various vendor facilities of laboratory mice around the globe (Charles River facilities in the USA, Canada, France, and Germany; another US facility) and university- or company-associated breeding facilities in Germany, China and New Zealand. Spa typing was performed to analyse the clonal relationship of the isolates. Moreover, multiplex PCRs were performed for human-specific virulence factors, the immune-evasion cluster (IEC) and superantigen genes (SAg). We found a total of 58 different spa types that clustered into 15 clonal complexes (CCs). Three of these S. aureus lineages had spread globally among laboratory mice and accounted for three quarters of the isolates: CC1 (13.5%), CC15 (14.3%), and CC88 (47.0%). Compared to human colonizing isolates of the same lineages, the murine isolates frequently lacked IEC genes and SAg genes on mobile genetic elements, implying long-term adaptation to the murine host. In conclusion, laboratory mice from various vendors are colonized with host-adapted S. aureus-strains of a few lineages, predominantly the CC88 lineage. S. aureus researchers must be cautioned that S. aureus colonization might be a relevant confounder in infection and vaccination studies and are therefore advised to screen their mice before experimentation.
我们之前曾报道,来自全球所有供应商的实验小鼠经常定植有金黄色葡萄球菌(S. aureus)。对来自美国 Charles River 的鼠源金黄色葡萄球菌分离株的即时样本进行基因分型显示,小鼠主要定植有耐甲氧西林敏感 CC88 株。在此,我们扩大了研究范围,调查了来自其他全球动物设施的实验小鼠是否定植有类似的菌株或新型金黄色葡萄球菌谱系,以及这些鼠源金黄色葡萄球菌分离株是否具有宿主适应性特征。总共,我们对来自全球各地不同供应商的实验小鼠(美国、加拿大、法国和德国的 Charles River 设施;另一家美国设施)和德国、中国和新西兰的大学或公司相关繁殖设施的 230 株金黄色葡萄球菌分离株进行了基因分型。葡萄球菌蛋白 A (spa)分型用于分析分离株的克隆关系。此外,还进行了多重 PCR 检测用于人类特异性毒力因子、免疫逃避簇(IEC)和超抗原基因(SAg)。我们发现了总共 58 种不同的 spa 型,这些 spa 型聚类为 15 个克隆复合体(CC)。其中三种金黄色葡萄球菌谱系在实验小鼠中已经在全球范围内传播,占分离株的四分之三:CC1(13.5%)、CC15(14.3%)和 CC88(47.0%)。与相同谱系的定植于人类的分离株相比,鼠源分离株经常缺乏可移动遗传元件上的 IEC 基因和 SAg 基因,这意味着它们长期适应于鼠宿主。总之,来自不同供应商的实验小鼠定植有少数几个谱系的宿主适应金黄色葡萄球菌菌株,主要是 CC88 谱系。金黄色葡萄球菌研究人员必须注意,金黄色葡萄球菌定植可能是感染和疫苗接种研究中的一个相关混杂因素,因此建议在实验前筛选他们的小鼠。