Nashat Melissa A, Ricart Arbona Rodolfo J, Lepherd Michelle L, Santagostino Sara F, Livingston Robert S, Riedel Elyn R, Lipman Neil S
Tri-Institutional Training Program in Laboratory Animal Medicine and Science, Memorial Sloan Kettering Cancer Center, Weill Cornell Medicine, and The Rockefeller University, New York, New York.
Tri-Institutional Training Program in Laboratory Animal Medicine and Science, Memorial Sloan Kettering Cancer Center, Weill Cornell Medicine, and The Rockefeller University, New York, New York, Center for Comparative Medicine and Pathology, Memorial Sloan Kettering Cancer Center, Weill Cornell Medicine, and The Rockefeller University, New York, New York.
J Am Assoc Lab Anim Sci. 2018 Sep 1;57(5):483-497. doi: 10.30802/AALAS-JAALAS-18-000003. Epub 2018 Sep 5.
Demodex musculi is a prostigmatid follicular mite that has rarely been reported in laboratory mice. Although prevalence of this species has not been assessed formally, we have found that many imported mouse strains from noncommercial sources harbor Demodex mites. To assess whether an acaricide can be used to eradicate this mite, infested immunocompromised mice were provided ivermectin-compounded (12 ppm) feed without restriction for 8 wk (n = 10), were treated topically with moxidectin and imidacloprid (MI; 3 and 13 mg/kg, respectively) weekly for 8 wk (n = 10), or remained untreated (n = 10). Mice were confirmed to be mite-infested before treatment and were tested after treatment by using fur plucks (FP), deep skin scrapes (DSS), and PCR analysis of fur swabs. In addition, the presence of mites was confirmed through skin biopsies at 2 study endpoints (1 wk [n = 5] and 12 wk [ n = 5] after treatment). Samples collected before treatment and from untreated mice were positive for D. musculi at all time points and by all test modalities. After treatment, all ivermectin-treated animals remained infested, whereas mice treated with MI were repeatedly negative by all test modalities. An additional shortened treatment trial revealed that 4 wk of MI (n = 7) was insufficient to eradicate mites. Neither treatment produced any evidence of adverse effects according to hematology, serum chemistry parameters, behavior, body weight, and histopathology. Of the 70 PCR assays performed in treated mice, 14 were positive when FP+DSS was negative. In 6 cases where PCR results were negative, 5 were positive by FP+DSS and a single sample was positive on skin biopsy. Although PCR analysis has a high detection rate for D. musculi, FP+DSS can further enhance the detection rate. In conclusion, topical MI administered for 8 consecutive weeks can safely eradicate D. musculi from an immunocompromised mouse strain.
肌蠕形螨是一种前气门目毛囊螨,在实验室小鼠中鲜有报道。尽管尚未对该物种的流行情况进行正式评估,但我们发现许多来自非商业来源的进口小鼠品系都携带蠕形螨。为了评估杀螨剂是否可用于根除这种螨虫,我们为受感染的免疫受损小鼠提供了含伊维菌素(12 ppm)的饲料,不限量喂食8周(n = 10),每周对其进行一次莫昔克丁和吡虫啉(MI;分别为3和13 mg/kg)的局部治疗,持续8周(n = 10),或不进行治疗(n = 10)。在治疗前确认小鼠感染螨虫,并在治疗后通过拔毛(FP)、深部皮肤刮片(DSS)以及毛发拭子的PCR分析进行检测。此外,在2个研究终点(治疗后1周[n = 5]和12周[n = 5])通过皮肤活检确认螨虫的存在。治疗前采集的样本以及未治疗小鼠的样本在所有时间点通过所有检测方式均显示肌蠕形螨呈阳性。治疗后,所有接受伊维菌素治疗的动物仍受感染,而接受MI治疗的小鼠通过所有检测方式反复呈阴性。一项额外的缩短治疗试验表明,4周的MI治疗(n = 7)不足以根除螨虫。根据血液学、血清化学参数、行为、体重和组织病理学检查,两种治疗均未产生任何不良反应的证据。在对治疗后的小鼠进行的70次PCR检测中,当FP + DSS为阴性时,有14次呈阳性。在PCR结果为阴性的6个案例中,5个通过FP + DSS呈阳性,1个样本在皮肤活检时呈阳性。尽管PCR分析对肌蠕形螨的检测率很高,但FP + DSS可进一步提高检测率。总之,连续8周局部施用MI可安全地从免疫受损小鼠品系中根除肌蠕形螨。