Charuchaibovorn Sarit, Sanprasert Vivornpun, Nuchprayoon Surang
Medical Sciences Program, Faculty of Medicine, Chulalongkorn University, Bangkok 10330, Thailand.
Lymphatic Filariasis and Tropical Medicine Research Unit, Chulalongkorn Medical Research Center, Faculty of Medicine, Chulalongkorn University, Bangkok 10330, Thailand.
Pathogens. 2019 Feb 5;8(1):21. doi: 10.3390/pathogens8010021.
Strongyloidiasis is life-threatening disease which is mainly caused by infection. Autoinfection of the parasite results in long-lasting infection and fatal conditions, hyperinfection and dissemination (primarily in immunosuppressed hosts). However, mechanisms of autoinfection and biology remain largely unknown. Rodent models including mice and rats are not susceptible to the human isolate of . Variations in susceptibility of the human isolate of are found in dogs. and infections in rats are an alternative model without the ability to cause autoinfection. The absence of appropriate model for the human isolate of strongyloidiasis hampers a better understanding of human strongyloidiasis. We demonstrated the maintenance of the human isolate of the life cycle in the Mongolian gerbil (). The human isolate of caused a patent infection in immunosuppressed gerbils, more than 18 months. The mean number of recovery adult parasitic worms were 120 ± 23 (1.2% of the initial dose) and L1s were 12,500 ± 7,500 after day 28 post-inoculation (p.i.). The prepatent period was 9⁻14 days. Mild diarrhoea was found in gerbils carrying a high number of adult parasitic worms. Our findings provided a promising model for studying biology and searching new alternative drugs against the parasites. Further studies about the hyperinfection and dissemination would be performed.
粪类圆线虫病是一种主要由感染引起的危及生命的疾病。寄生虫的自身感染会导致持续感染和致命状况、超感染和播散(主要发生在免疫抑制宿主中)。然而,自身感染机制和生物学特性在很大程度上仍不清楚。包括小鼠和大鼠在内的啮齿动物模型对人源粪类圆线虫分离株不敏感。在犬类中发现了人源粪类圆线虫分离株易感性的差异。大鼠感染粪类圆线虫和巴西日圆线虫是一种不能引起自身感染的替代模型。缺乏适合人源粪类圆线虫病的模型阻碍了对人类粪类圆线虫病的更好理解。我们证明了人源粪类圆线虫生命周期在蒙古沙鼠中的维持。人源粪类圆线虫在免疫抑制的沙鼠中引起了超过18个月的显性感染。接种后第28天(p.i.),回收的成虫寄生蠕虫平均数量为120±23(初始剂量的1.2%),L1幼虫为12,500±7,500。潜伏期为9至14天。在携带大量成虫寄生蠕虫的沙鼠中发现了轻度腹泻。我们的研究结果为研究生物学特性和寻找抗寄生虫的新替代药物提供了一个有前景的模型。将对超感染和播散进行进一步研究。