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Assessment of Use of Microsatellite Polymorphism Analysis for Improving Spatial Distribution Tracking of Echinococcus multilocularis

机译:利用微卫星多态性分析改善多球棘球chin虫的空间分布追踪的评估

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摘要

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.
机译:肺est棘球co虫病(AE)是由多头E虫(Echinococcus multilocularis)引起的,是在北半球温带和北极地区发现的一种严重的人畜共患病。即使在不同地理区域观察到的传播模式是异质的,但通常用于多眼大肠杆菌的基因分型的核和线粒体靶标在该物种中仅显示出显着的遗传同质性。由于它们的高分型分辨率,我们使用微卫星序列来探索多眼大肠杆菌的遗传多样性。在从美国阿拉斯加,加拿大,欧洲获得的76种多眼大肠杆菌样品(幼虫和成年阶段)的面板上测试了四个微卫星靶标(在我们实验室中设计的EmsJ,EmsK和EmsB,以及从文献中选择的NAK1)。和亚洲。通过大小多态性分析评估每个靶标的遗传多样性。对于EmsJ和EmsK靶标,每个基因座均发现两个等位基因,分别产生两个和三个基因型,从而将欧洲分离株与其他群体区分开。使用NAK1,发现了5个等位基因,产生了7个基因型,包括特异于藏族和阿拉斯加分离株的基因型。 EmsB靶标是串联重复的多基因座微卫星,发现了17个等位基因,显示出复杂的模式。根据EmsB的发现进行分层聚类分析,并鉴定出29个基因型。由于其更高的遗传多态性,EmsB表现出比其他靶标更高的歧视能力。复杂的EmsB模式能够在区域和部门级别上区分分离株,同时避免了过度区分。 EmsB将用于评估欧洲多眼大肠杆菌的假定出现。

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