Departamento de Microbiología, Facultad de Medicina, Universidad de Buenos Aires, Paraguay 2155, piso 13, 1121 Buenos Aires, Argentina.
Int J Parasitol. 2011 Mar;41(3-4):439-48. doi: 10.1016/j.ijpara.2010.11.010. Epub 2011 Jan 8.
The aetiological agent of cystic hydatid disease, the platyhelminth parasite Echinococcus granulosus, undergoes a series of metamorphic events during its complex life cycle. One of its developmental stages, the protoscolex, shows a remarkable degree of heterogeneous morphogenesis, being able to develop either into the vesicular or strobilar direction. Another level of complexity is added by the existence of genotypes or strains that differ in the range of intermediate hosts where they can develop and form fertile cysts. These features make E. granulosus an interesting model for developmental studies. Hence, we focused on the study of the regulation of gene expression by microRNAs (miRNAs), one of the key mechanisms that control development in metazoans and plants and which has not been analysed in E. granulosus yet. In this study, we cloned 38 distinct miRNAs, including four candidate new miRNAs that seem to be specific to Echinococcus spp. Thirty-four cloned sequences were orthologous to miRNAs already described in other organisms and were grouped in 16 metazoan miRNA families, some of them known for their role in the development of other organisms. The expression of some of the cloned miRNAs differs according to the parasite life cycle stage analysed, showing differential developmental expression. We did not detect differences in the expression of the analysed miRNAs between protoscoleces of two parasite genotypes. This work sets the scene for the study of gene regulation mediated by miRNAs in E. granulosus and provides a new approach to study the molecules involved in its developmental plasticity and intermediate host specificity. Understanding the developmental processes of E. granulosus may help to find new strategies for the control of cystic hydatid disease, caused by the metacestode stage of the parasite.
包虫病的病原、扁形动物寄生虫细粒棘球绦虫,在其复杂的生活史中经历了一系列的变态事件。其发育阶段之一的原头蚴显示出显著的异质性形态发生程度,能够向囊泡或幼节方向发育。另一个复杂程度是存在基因型或菌株的差异,它们在能够发育和形成有活力的包囊的中间宿主范围内有所不同。这些特征使细粒棘球绦虫成为发育研究的有趣模型。因此,我们专注于研究微 RNA(miRNA)对基因表达的调控,miRNA 是控制后生动物和植物发育的关键机制之一,而在细粒棘球绦虫中尚未进行分析。在这项研究中,我们克隆了 38 种不同的 miRNA,包括似乎是棘球属特有的 4 种候选新 miRNA。34 个克隆序列与已在其他生物体中描述的 miRNA 是同源的,并被分为 16 个后生动物 miRNA 家族,其中一些家族因其在其他生物体发育中的作用而闻名。一些克隆 miRNA 的表达根据分析的寄生虫生命周期阶段而不同,表现出差异发育表达。我们没有检测到两种寄生虫基因型的原头蚴中分析的 miRNA 表达存在差异。这项工作为细粒棘球绦虫中 miRNA 介导的基因调控研究奠定了基础,并为研究参与其发育可塑性和中间宿主特异性的分子提供了新的方法。了解细粒棘球绦虫的发育过程可能有助于找到控制包虫病的新策略,包虫病是由寄生虫的囊蚴阶段引起的。