Knapp J, Bart J M, Glowatzki M L, Ito A, Gerard S, Maillard S, Piarroux R, Gottstein B
Institute of Parasitology, Vetsuisse Faculty, University of Bern, Bern, Switzerland.
J Clin Microbiol. 2007 Sep;45(9):2943-50. doi: 10.1128/JCM.02107-06. Epub 2007 Jul 18.
Alveolar echinococcosis (AE)--caused by the cestode Echinococcus multilocularis--is a severe zoonotic disease found in temperate and arctic regions of the northern hemisphere. Even though the transmission patterns observed in different geographical areas are heterogeneous, the nuclear and mitochondrial targets usually used for the genotyping of E. multilocularis have shown only a marked genetic homogeneity in this species. We used microsatellite sequences, because of their high typing resolution, to explore the genetic diversity of E. multilocularis. Four microsatellite targets (EmsJ, EmsK, and EmsB, which were designed in our laboratory, and NAK1, selected from the literature) were tested on a panel of 76 E. multilocularis samples (larval and adult stages) obtained from Alaska, Canada, Europe, and Asia. Genetic diversity for each target was assessed by size polymorphism analysis. With the EmsJ and EmsK targets, two alleles were found for each locus, yielding two and three genotypes, respectively, discriminating European isolates from the other groups. With NAK1, five alleles were found, yielding seven genotypes, including those specific to Tibetan and Alaskan isolates. The EmsB target, a tandem repeated multilocus microsatellite, found 17 alleles showing a complex pattern. Hierarchical clustering analyses were performed with the EmsB findings, and 29 genotypes were identified. Due to its higher genetic polymorphism, EmsB exhibited a higher discriminatory power than the other targets. The complex EmsB pattern was able to discriminate isolates on a regional and sectoral level, while avoiding overdistinction. EmsB will be used to assess the putative emergence of E. multilocularis in Europe.
肺泡型包虫病(AE)——由多房棘球绦虫引起——是一种在北半球温带和北极地区发现的严重人畜共患病。尽管在不同地理区域观察到的传播模式各不相同,但通常用于多房棘球绦虫基因分型的核基因和线粒体靶点在该物种中仅显示出明显的遗传同质性。我们使用微卫星序列,因其具有高分型分辨率,来探索多房棘球绦虫的遗传多样性。在从阿拉斯加、加拿大、欧洲和亚洲获得的76个多房棘球绦虫样本(幼虫和成虫阶段)的样本组上测试了四个微卫星靶点(我们实验室设计的EmsJ、EmsK和EmsB,以及从文献中选择的NAK1)。通过大小多态性分析评估每个靶点的遗传多样性。对于EmsJ和EmsK靶点,每个位点发现了两个等位基因,分别产生了两种和三种基因型,将欧洲分离株与其他组区分开来。对于NAK1,发现了五个等位基因,产生了七种基因型,包括特定于西藏和阿拉斯加分离株的基因型。EmsB靶点是一个串联重复的多位点微卫星,发现了17个等位基因,呈现出复杂的模式。使用EmsB的结果进行层次聚类分析,鉴定出29种基因型。由于其更高的遗传多态性,EmsB比其他靶点表现出更高的鉴别力。复杂的EmsB模式能够在区域和部门层面区分分离株,同时避免过度区分。EmsB将用于评估欧洲多房棘球绦虫的假定出现情况。