Department of Molecular Genetics and Microbiology, Duke University Medical Center, Durham, NC, USA.
Moi University School of Medicine, College of Health Sciences, Nandi Rd, Eldoret, Kenya.
Sci Rep. 2017 Jan 24;7:41108. doi: 10.1038/srep41108.
Large-scale molecular epidemiologic studies of Plasmodium falciparum parasites have provided insights into parasite biology and transmission, can identify the spread of drug resistance, and are useful in assessing vaccine targets. The polyclonal nature infections in high transmission settings is problematic for traditional genotyping approaches. Next-generation sequencing (NGS) approaches to parasite genotyping allow sensitive detection of minority variants, disaggregation of complex parasite mixtures, and scalable processing of large samples sets. Therefore, we designed, validated, and applied to field parasites an approach that leverages sequencing of individually barcoded samples in a multiplex manner. We utilize variant barcodes, invariant linker sequences and modular template-specific primers to allow for the simultaneous generation of high-dimensional sequencing data of multiple gene targets. This modularity permits a cost-effective and reproducible way to query many genes at once. In mixtures of reference parasite genomes, we quantitatively detected unique haplotypes comprising as little as 2% of a polyclonal infection. We applied this genotyping approach to field-collected parasites collected in Western Kenya in order to simultaneously obtain parasites genotypes at three unlinked loci. In summary, we present a rapid, scalable, and flexible method for genotyping individual parasites that enables molecular epidemiologic studies of parasite evolution, population structure and transmission.
大规模的疟原虫寄生虫分子流行病学研究为寄生虫生物学和传播提供了深入的了解,可以识别耐药性的传播,并且有助于评估疫苗靶标。在高传播环境中,寄生虫的多克隆感染对传统的基因分型方法提出了挑战。寄生虫基因分型的下一代测序 (NGS) 方法可以敏感地检测少数变体,分解复杂的寄生虫混合物,并对大量样本进行可扩展的处理。因此,我们设计、验证并将一种利用多重方式对个体条码化样本进行测序的方法应用于现场寄生虫。我们利用变异条码、不变的连接序列和模块化模板特异性引物,实现了多个基因靶标的高维测序数据的同时生成。这种模块化允许以具有成本效益和可重复的方式一次查询多个基因。在参考寄生虫基因组的混合物中,我们定量检测到仅占多克隆感染 2%的独特单倍型。我们将这种基因分型方法应用于在肯尼亚西部采集的现场寄生虫,以同时获得三个非连锁基因座的寄生虫基因型。总之,我们提出了一种快速、可扩展和灵活的个体寄生虫基因分型方法,可用于研究寄生虫进化、种群结构和传播的分子流行病学。