Schad G A, Hellman M E, Muncey D W
Exp Parasitol. 1984 Jun;57(3):287-96. doi: 10.1016/0014-4894(84)90103-6.
Hyperinfective strongyloidiasis involving the threadworm , Strongyloides stercoralis, is well known in humans and primates. Although this nematode also frequently parasitizes dogs, canine hyperinfective strongyloidiasis has not been reported. To determine whether a fulminant pattern of nematode development can occur in dogs, and to test the S. stercoralis/dog system for suitability as a model for human hyperinfective and disseminated strongyloidiasis, five canine infections with a dog-derived strain of S. stercoralis were monitored by the quantitative recovery of larvae from feces. Even 3-month-old pups controlled their initial infections successfully, the number of larvae excreted declining to near zero in 90 days. Immunosuppressive treatment with prednisolone, prednisolone and azathiaprine , or niridazole resulted in a rapid return to former or greater intensities of infection, as judged by larval output. Only first stage ( rhabditiform ) larvae were passed in the feces, although third stage (filariform) larvae occurred in the intestinal contents of dogs when they were examined at necropsy. In 3 of the 5 dogs, the adult worm recovery exceeded the inoculated dose greatly and, in one of these, adults and rhabditiform larvae were found in distant, extraintestinal sites. In the remaining 2 of the 5 dogs, the adult worm population was less than the inoculated dose, but, in both, the infection was terminated by the host's death before hyperinfection could have developed. The observations demonstrate that autoinfection occurs in dogs infected with S. stercoralis and that, if it is allowed to continue for a sufficiently long time in immunosuppressed hosts, massive hyperinfection, and even disseminated infection, may occur. This spectrum of increasingly invasive parasitism closely resembles strongyloidiasis in humans. Therefore, the S. stercoralis/dog system has excellent potential as a model for human hyperinfective and disseminated strongyloidiasis.
由粪类圆线虫(Strongyloides stercoralis)引起的高度感染性粪类圆线虫病在人类和灵长类动物中广为人知。尽管这种线虫也经常寄生于犬类,但犬类高度感染性粪类圆线虫病尚未见报道。为了确定犬类是否会出现线虫发育的暴发性模式,并测试粪类圆线虫/犬系统是否适合作为人类高度感染性和播散性粪类圆线虫病的模型,通过定量回收粪便中的幼虫,对5只感染了源自犬类的粪类圆线虫菌株的犬进行了监测。即使是3个月大的幼犬也成功控制了最初的感染,90天内排出的幼虫数量降至接近零。用泼尼松龙、泼尼松龙和硫唑嘌呤或硝唑咪进行免疫抑制治疗后,根据幼虫排出量判断,感染强度迅速恢复到之前的水平或更高。粪便中仅排出第一期(杆状)幼虫,尽管在尸检时在犬的肠道内容物中发现了第三期(丝状)幼虫。在5只犬中的3只中,成虫回收率大大超过接种剂量,其中1只在远处非肠道部位发现了成虫和杆状幼虫。在5只犬中的另外2只中,成虫数量少于接种剂量,但在这两只犬中,感染均在宿主死亡前终止,此时尚未发展为高度感染。这些观察结果表明,感染粪类圆线虫的犬会发生自身感染,如果在免疫抑制宿主中持续足够长的时间,可能会发生大规模高度感染,甚至播散性感染。这种侵袭性逐渐增强的寄生虫病谱与人类粪类圆线虫病非常相似。因此,粪类圆线虫/犬系统作为人类高度感染性和播散性粪类圆线虫病的模型具有很大的潜力。