International Livestock Research Institute, Nairobi 00100, Kenya.
BMC Genomics. 2012 Sep 23;13:503. doi: 10.1186/1471-2164-13-503.
Theileria parva is a tick-borne protozoan parasite, which causes East Coast Fever, a disease of cattle in sub-Saharan Africa. Like Plasmodium falciparum, the parasite undergoes a transient diploid life-cycle stage in the gut of the arthropod vector, which involves an obligate sexual cycle. As assessed using low-resolution VNTR markers, the crossover (CO) rate in T. parva is relatively high and has been reported to vary across different regions of the genome; non-crossovers (NCOs) and CO-associated gene conversions have not yet been characterised due to the lack of informative markers. To examine all recombination events at high marker resolution, we sequenced the haploid genomes of two parental strains, and two recombinant clones derived from ticks fed on cattle that had been simultaneously co-infected with two different parasite isolates.
By comparing the genome sequences, we were able to genotype over 64 thousand SNP markers with an average spacing of 127 bp in the two progeny clones. Previously unrecognized COs in sub-telomeric regions were detected. About 50% of CO breakpoints were accompanied by gene conversion events. Such a high fraction of COs accompanied by gene conversions demonstrated the contributions of meiotic recombination to the diversity and evolutionary success of T. parva, as the process not only redistributed existing genetic variations, but also altered allelic frequencies. Compared to COs, NCOs were more frequently observed and more uniformly distributed across the genome. In both progeny clones, genomic regions with more SNP markers had a reduced frequency of COs or NCOs, suggesting that the sequence divergence between the parental strains was high enough to adversely affect recombination frequencies. Intra-species polymorphism analysis identified 81 loci as likely to be under selection in the sequenced genomes.
Using whole genome sequencing of two recombinant clones and their parents, we generated maps of COs, NCOs, and CO-associated gene conversion events for T. parva. The data comprises one of the highest-resolution genome-wide analyses of the multiple outcomes of meiotic recombination for this pathogen. The study also demonstrates the usefulness of high throughput sequencing typing for detailed analysis of recombination in organisms in which conventional genetic analysis is technically difficult.
绵羊泰勒虫是一种蜱传原生动物寄生虫,可引起东非牛热,这是撒哈拉以南非洲牛的一种疾病。与恶性疟原虫一样,寄生虫在节肢动物载体的肠道中经历短暂的二倍体生命周期阶段,其中涉及强制性的性循环。使用低分辨率 VNTR 标记评估,泰勒虫的交叉(CO)率相对较高,并且据报道在基因组的不同区域有所不同; 由于缺乏信息标记,尚未对非交叉(NCO)和 CO 相关基因转换进行特征描述。为了在高标记分辨率下检查所有重组事件,我们对来自同时感染两种不同寄生虫分离株的牛蜱上进食的两个亲本株系和两个重组克隆的单倍体基因组进行了测序。
通过比较基因组序列,我们能够在两个后代克隆中对超过 64000 个 SNP 标记进行基因分型,平均间隔为 127bp。在亚端粒区域检测到以前未被识别的 CO。大约 50%的 CO 断点伴随着基因转换事件。如此高比例的 CO 伴随着基因转换表明减数分裂重组对泰勒虫的多样性和进化成功做出了贡献,因为该过程不仅重新分配了现有遗传变异,而且改变了等位基因频率。与 CO 相比,NCO 更频繁地观察到,并且在基因组中更均匀地分布。在两个后代克隆中,具有更多 SNP 标记的基因组区域 CO 或 NCO 的频率降低,这表明亲本株系之间的序列差异足够大,从而对重组频率产生不利影响。种内多态性分析确定了 81 个可能在测序基因组中受到选择的基因座。
使用两个重组克隆及其亲本的全基因组测序,我们为泰勒虫产生了 CO、NCO 和 CO 相关基因转换事件的图谱。该数据是对这种病原体减数分裂重组的多种结果进行的最高分辨率全基因组分析之一。该研究还证明了高通量测序分型在技术上难以进行常规遗传分析的生物体中详细分析重组的有用性。