Towne Justin W, Wagner April M, Griffin Kurt J, Buntzman Adam S, Frelinger Jeffrey A, Besselsen David G
University Animal Care, University of Arizona, Tucson, Arizona, USA.
Department of Immunobiology, University of Arizona, Tucson, Arizona, USA.
J Am Assoc Lab Anim Sci. 2014 Sep;53(5):517-22.
Multiple NOD. Cg-Prkdc(scid)Il2rg(tm1Wjl)Tg(HLA-A2.1)Enge/Sz (NSG/A2) transgenic mice maintained in a mouse barrier facility were submitted for necropsy to determine the cause of facial alopecia, tachypnea, dyspnea, and sudden death. Pneumonia and soft-tissue abscesses were observed, and Pasteurella pneumotropica biotype Jawetz was consistently isolated from the upper respiratory tract, lung, and abscesses. Epidemiologic investigation within the facility revealed presence of this pathogen in mice generated or rederived by the intramural Genetically Engineered Mouse Model (GEMM) Core but not in mice procured from several approved commercial vendors. Epidemiologic data suggested the infection originated from female or vasectomized male ND4 mice obtained from a commercial vendor and then comingled by the GEMM Core to induce pseudopregnancy in female mice for embryo implantation. Enrofloxacin delivered in drinking water (85 mg/kg body weight daily) for 14 d was sufficient to clear bacterial infection in normal, breeding, and immune-deficient mice without the need to change the antibiotic water source. This modified treatment regimen was administered to 2400 cages of mice to eradicate Pasteurella pneumotropica from the facility. Follow-up PCR testing for P. pneumotropica biotype Jawetz remained uniformly negative at 2, 6, 12, and 52 wk after treatment in multiple strains of mice that were originally infected. Together, these data indicate that enrofloxacin can eradicate P. pneumotropica from infected mice in a less labor-intensive approach that does not require breeding cessation and that is easily adaptable to the standard biweekly cage change schedule for individually ventilated cages.
将饲养在小鼠屏障设施中的多只NOD.Cg-Prkdc(scid)Il2rg(tm1Wjl)Tg(HLA-A2.1)Enge/Sz (NSG/A2)转基因小鼠进行尸检,以确定面部脱毛、呼吸急促、呼吸困难和猝死的原因。观察到肺炎和软组织脓肿,并且从鼻道、肺和脓肿中持续分离出嗜肺巴斯德杆菌生物型Jawetz。该设施内的流行病学调查显示,这种病原体存在于由校内基因工程小鼠模型(GEMM)核心产生或重新培育的小鼠中,但在从几家经批准的商业供应商采购的小鼠中未发现。流行病学数据表明,感染源自来一个商业供应商的雌性或输精管切除的雄性ND4小鼠,然后由GEMM核心将它们混养在一起,以诱导雌性小鼠假孕以便进行胚胎植入。在饮用水中添加恩诺沙星(每日85 mg/kg体重),持续14天,足以清除正常、繁殖和免疫缺陷小鼠中的细菌感染,而无需更换抗生素水源。将这种改良的治疗方案应用于2400笼小鼠,以从该设施中根除嗜肺巴斯德杆菌。在对最初感染的多株小鼠进行治疗后的2、6、12和52周,对嗜肺巴斯德杆菌生物型Jawetz的后续PCR检测结果始终为阴性。这些数据共同表明,恩诺沙星可以用一种劳动强度较小的方法从感染小鼠中根除嗜肺巴斯德杆菌,这种方法不需要停止繁殖,并且很容易适应独立通风笼具每两周更换一次笼具的标准时间表。