Institute of Tropical Medicine, University of Tuebingen, Wilhelmstr. 27, 72074, Tuebingen, Germany.
Malaria Programme, Wellcome Trust Sanger Institute, Hinxton, CB10 1SA, UK.
Malar J. 2018 Oct 22;17(1):376. doi: 10.1186/s12936-018-2503-2.
Plasmodium falciparum exhibits a high degree of inter-isolate genetic diversity in its variant surface antigen (VSA) families: P. falciparum erythrocyte membrane protein 1, repetitive interspersed family (RIFIN) and subtelomeric variable open reading frame (STEVOR). The role of recombination for the generation of this diversity is a subject of ongoing research. Here the genome of E5, a sibling of the 3D7 genome strain is presented. Short and long read whole genome sequencing (WGS) techniques (Ilumina, Pacific Bioscience) and a set of 84 microsatellites (MS) were employed to characterize the 3D7 and non-3D7 parts of the E5 genome. This is the first time that VSA genes in sibling parasites were analysed with long read sequencing technology.
Of the 5733 E5 genes only 278 genes, mostly var and rifin/stevor genes, had no orthologues in the 3D7 genome. WGS and MS analysis revealed that chromosomal crossovers occurred at a rate of 0-3 per chromosome. var, stevor and rifin genes were inherited within the respective non-3D7 or 3D7 chromosomal context. 54 of the 84 MS PCR fragments correctly identified the respective MS as 3D7- or non-3D7 and this correlated with var and rifin/stevor gene inheritance in the adjacent chromosomal regions. E5 had 61 var and 189 rifin/stevor genes. One large non-chromosomal recombination event resulted in a new var gene on chromosome 14. The remainder of the E5 3D7-type subtelomeric and central regions were identical to 3D7.
The data show that the rifin/stevor and var gene families represent the most diverse compartments of the P. falciparum genome but that the majority of var genes are inherited without alterations within their respective parental chromosomal context. Furthermore, MS genotyping with 54 MS can successfully distinguish between two sibling progeny of a natural P. falciparum cross and thus can be used to investigate identity by descent in field isolates.
恶性疟原虫在其变异表面抗原(VSA)家族中表现出高度的种间遗传多样性:恶性疟原虫红细胞膜蛋白 1、重复散在家族(RIFIN)和端粒可变开放阅读框(STEVOR)。重组在产生这种多样性中的作用是一个正在进行的研究课题。本文介绍了 E5 基因组,E5 是 3D7 基因组株系的一个同胞。采用短读长和长读长全基因组测序(WGS)技术(Illumina、Pacific Bioscience)和一套 84 个微卫星(MS)对 3D7 和非 3D7 部分的 E5 基因组进行了特征分析。这是首次使用长读长测序技术分析同胞寄生虫中的 VSA 基因。
在 5733 个 E5 基因中,只有 278 个基因(主要是 var 和 rifin/stevor 基因)在 3D7 基因组中没有同源基因。WGS 和 MS 分析表明,染色体交叉发生的频率为 0-3 个/染色体。var、stevor 和 rifin 基因在相应的非 3D7 或 3D7 染色体背景中遗传。84 个 MS-PCR 片段中有 54 个正确地将各自的 MS 鉴定为 3D7 或非 3D7,这与相邻染色体区域 var 和 rifin/stevor 基因的遗传相关。E5 有 61 个 var 和 189 个 rifin/stevor 基因。一次大的非染色体重组事件导致 14 号染色体上出现一个新的 var 基因。E5 的其余 3D7 型端粒和中心区域与 3D7 相同。
数据表明,rifin/stevor 和 var 基因家族代表恶性疟原虫基因组中最多样化的部分,但大多数 var 基因在其各自的亲本染色体背景中遗传而没有改变。此外,用 54 个 MS 进行 MS 基因分型可以成功地区分天然疟原虫杂交的两个同胞后代,因此可以用于研究田间分离株的血缘关系。