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利用下一代测序技术揭示隐孢子虫中广泛的宿主内遗传多样性。

Extensive intra-host genetic diversity uncovered in Cryptosporidium parvum using Next Generation Sequencing.

机构信息

Massey University, Institute of Veterinary, Animal and Biomedical Sciences, Private Bag 11 222, Palmerston North 4442, New Zealand.

出版信息

Infect Genet Evol. 2013 Apr;15:18-24. doi: 10.1016/j.meegid.2012.08.017. Epub 2012 Sep 6.

DOI:10.1016/j.meegid.2012.08.017
PMID:22981926
Abstract

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 60kDa 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.

摘要

关于隐孢子虫生命周期的理论预测了宿主体内裂殖子的遗传多样性。然而,由于传统的桑格测序或扩增子电泳分辨率方法无法解决模板混合物的问题,隐孢子虫宿内遗传多样性难以研究。我们通过结合使用下一代测序和 PCR 扩增子的克隆以及数据库搜索,分析了两个具有共同亲缘关系的微小隐孢子虫分离株的株内遗传多样性。分析集中在单拷贝 70 kDa 热休克蛋白 (HSP70) 和 60 kDa 表面糖蛋白 (gp60) 基因上,这允许将任何多样性归因于裂殖子异质群体的存在。尽管最初使用桑格测序对每个基因座的一个等位基因进行了初步解析,但结果表明这些分离株存在前所未有的株内遗传多样性,有两个 HSP70 和 10 个 gp60 等位基因。在两个基因座上,主要等位基因是最初通过桑格测序鉴定的等位基因。先前在新西兰报道的 gp60 等位基因显著(p<0.01)过表达。这些结果进一步加深了我们对微小隐孢子虫种群遗传结构的理解,并揭示了使用非共生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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