Ware Michael W, Villegas Eric N
US Environmental Protection Agency, National Exposure Research Laboratory, 26 W. Martin Luther King Drive, Cincinnati, OH, 45268, United States.
US Environmental Protection Agency, National Exposure Research Laboratory, 26 W. Martin Luther King Drive, Cincinnati, OH, 45268, United States.
Vet Parasitol. 2019 Apr;268:32-35. doi: 10.1016/j.vetpar.2019.02.010. Epub 2019 Mar 5.
This study developed and evaluated Giardia duodenalis cyst propagation using a dexamethasone immunosuppressed CF-1 mouse model as an alternative to a previously described Mongolian gerbil model. The CF-1 mouse model shed significantly more cysts per animal during a 16-18 h collection period compared to the gerbil (averages: 7.8 × 10 cysts/CF-1 mouse and 2.5 × 10 cysts/gerbil). In addition, the patency period for this model differed from both G. muris in mice and G. duodenalis in gerbils in that cysts were shed continuously for over 20 days. Results further showed that the β-giardin gene sequences from gerbil derived and mouse derived G. duodenalis were identical, after 34 serial passages through the CF-1 mouse model. Overall, the CF-1 mouse model produced higher concentrations of cysts per animal, and were genetically and phenotypically stable based on β-giardin gene sequences.
本研究开发并评估了使用地塞米松免疫抑制的CF-1小鼠模型来繁殖十二指肠贾第鞭毛虫囊肿,以此替代先前描述的蒙古沙鼠模型。与沙鼠相比,CF-1小鼠模型在16 - 18小时的收集期内,每只动物排出的囊肿显著更多(平均值:7.8×10个囊肿/CF-1小鼠和2.5×10个囊肿/沙鼠)。此外,该模型的排囊期与小鼠体内的鼠贾第鞭毛虫和沙鼠体内的十二指肠贾第鞭毛虫均不同,因为囊肿持续排出超过20天。结果还表明,在通过CF-1小鼠模型连续传代34次后,来自沙鼠和小鼠的十二指肠贾第鞭毛虫的β-贾第蛋白基因序列是相同的。总体而言,CF-1小鼠模型每只动物产生的囊肿浓度更高,并且基于β-贾第蛋白基因序列在遗传和表型上是稳定的。