Department of Parasitology, Biosciences Institute, Univ Estadual Paulista, Botucatu, São Paulo, Brazil.
Exp Parasitol. 2011 Feb;127(2):334-9. doi: 10.1016/j.exppara.2010.08.006. Epub 2010 Aug 27.
Strongyloides venezuelensis is a parasitic nematode that has been used as a model to study human and animal strongyloidiasis. In this study, we compared the sensitivity between traditional methodologies and PCR assay to characterize the dynamics of S. venezuelensis infection and its migration route in Lewis rats subcutaneously infected with 4000 L3. The dynamics of the infection was determined by counting the number of eggs and by detecting parasite deoxyribonucleic acid in faeces samples. Both techniques similarly detected the infection at day 6 after larvae inoculation. However, PCR performed with the genus primer showed higher sensitivity during the recovery phase. Histological analysis and PCR assay were then used to follow parasite tissue migration. S. venezuelensis migration route included the muscular fibers below the skin, the pulmonary alveoli and the small intestine vilosities. The sensitivity of these two techniques to detect parasite's presence in these tissues was statistically similar.
委内瑞拉钩虫是一种寄生线虫,已被用作研究人类和动物钩虫病的模型。在这项研究中,我们比较了传统方法和 PCR 检测方法的敏感性,以描述皮下感染 4000 条 L3 的刘易斯大鼠中 S. venezuelensis 感染的动态及其迁移途径。通过计数粪便样本中的卵数和检测寄生虫脱氧核糖核酸来确定感染的动态。两种技术在幼虫接种后第 6 天同样检测到了感染。然而,使用属引物进行的 PCR 检测在恢复期显示出更高的敏感性。然后进行组织学分析和 PCR 检测以跟踪寄生虫的组织迁移。S. venezuelensis 的迁移途径包括皮肤下的肌肉纤维、肺泡和小肠绒毛。这两种技术检测寄生虫在这些组织中存在的敏感性在统计学上是相似的。