首页> 外文期刊>Infection, Genetics and Evolution: Journal of Molecular Epidemiology and Evolutionary Genetics in Infectious Diseases >Extensive intra-host genetic diversity uncovered in Cryptosporidium parvum using next generation sequencing.
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Extensive intra-host genetic diversity uncovered in Cryptosporidium parvum using next generation sequencing.

机译:使用下一代测序技术,在小隐隐孢子虫中发现了广泛的宿主内部遗传多样性。

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The theory about the Cryptosporidium life cycle predicts genetic diversity of sporozoites within the host. Nevertheless, the Cryptosporidium intra-host genetic diversity is difficult to study using conventional Sanger sequencing or electrophoretic resolution of amplicons, due to the methods' inability to resolve mixtures of templates. We analysed the within-isolate genetic diversity of two Cryptosporidium parvum isolates sharing common descent, by combining the use of Next Generation Sequencing and cloning of PCR amplicons with database searches. The analysis focused on the single-copy 70 kDa heat shock protein (HSP70) and the 60 kDa surface glycoprotein (gp60) genes, which allowed any diversity to be ascribed to the presence of a heterogeneous population of sporozoites. The results indicated an unprecedented intra-host genetic diversity, with two HSP70 and 10 gp60 alleles in these isolates, in spite of the initial resolution of one allele per locus using Sanger sequencing. At both loci, the predominant alleles were those initially identified by Sanger sequencing. A significant (p<0.01) overrepresentation of gp60 alleles previously reported in New Zealand was observed. These results further our understanding of the genetic structure of C. parvum populations, and expose the limitations of the use of non-axenic isolates as operational taxonomic units of genetic studies of cryptosporidiosis.
机译:有关隐孢子虫生命周期的理论预测宿主内子孢子的遗传多样性。然而,由于方法无法解析模板混合物,因此难以使用常规的Sanger测序或扩增子的电泳解析来研究隐孢子虫宿主内部的遗传多样性。通过结合下一代测序和PCR扩增子克隆与数据库搜索的结合,我们分析了两个具有共同血统的隐孢子虫分离株的分离物内遗传多样性。分析集中在单拷贝70 kDa热激蛋白(HSP70)和60 kDa表面糖蛋白(gp60)基因上,这使得任何多样性都归因于子孢子异质种群的存在。结果表明,尽管使用Sanger测序每个位点最初解析了一个等位基因,但在这些分离物中仍存在前所未有的宿主内遗传多样性,其中有两个HSP70和10 gp60等位基因。在两个基因座上,主要的等位基因都是最初通过Sanger测序鉴定的。观察到以前在新西兰报道的gp60等位基因显着(p <0.01)过量表达。这些结果进一步加深了我们对细小隐孢子虫种群遗传结构的理解,并揭示了使用非树突分离株作为隐孢子虫病遗传研究的操作分类单位的局限性。

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