Yasukochi Yoshiki, Naka Izumi, Patarapotikul Jintana, Hananantachai Hathairad, Ohashi Jun
Department of Human Functional Genomics, Advanced Science Research Promotion Center, Mie University, 1577 Kurima-machiya, Tsu, Mie 514-8507, Japan.
Department of Biological Sciences, Graduate School of Science, The University of Tokyo, Tokyo 113-0033, Japan.
Infect Genet Evol. 2017 Apr;49:251-255. doi: 10.1016/j.meegid.2017.01.026. Epub 2017 Jan 27.
The 175-kDa erythrocyte binding antigen (EBA-175) of the malaria parasite Plasmodium falciparum is important for its invasion into human erythrocytes. The primary structure of eba-175 is divided into seven regions, namely I to VII. Region III contains highly divergent dimorphic segments, termed Fseg and Cseg. The allele frequencies of segmental dimorphism within a P. falciparum population have been extensively examined; however, the molecular evolution of segmental dimorphism is not well understood. A comprehensive comparison of nucleotide sequences among 32 P. falciparum eba-175 alleles identified in our previous study, two Plasmodium reichenowi, and one P. gaboni orthologous alleles obtained from the GenBank database was conducted to uncover the origin and evolutionary processes of segmental dimorphism in P. falciparum eba-175. In the eba-175 nucleotide sequence derived from a P. reichenowi CDC strain, both Fseg and Cseg were found in region III, which implies that the original eba-175 gene had both segments, and deletions of F- and C-segments generated Cseg and Fseg alleles, respectively. We also confirmed the presence of allele with Fseg and Cseg in another P. reichenowi strain (SY57), by re-mapping short reads obtained from the GenBank database. On the other hand, the segmental sequence of eba-175 ortholog in P. gaboni was quite diverged from those of the other species, suggesting that the original eba-175 dimorphism of P. falciparum can be traced back to the stem linage of P. falciparum and P. reichenowi. Our findings suggest that Fseg and Cseg alleles are derived from a single eba-175 allele containing both segments in the ancestral population of P. falciparum and P. reichenowi, and that the allelic dimorphism of eba-175 was shaped by the independent emergence of similar dimorphic lineage in different species that has never been observed in any evolutionary mode of allelic dimorphism at other loci in malaria genomes.
恶性疟原虫的175-kDa红细胞结合抗原(EBA-175)对其侵入人类红细胞至关重要。eba-175的一级结构分为七个区域,即I至VII。区域III包含高度不同的二态性片段,称为Fseg和Cseg。恶性疟原虫群体内片段二态性的等位基因频率已得到广泛研究;然而,片段二态性的分子进化尚未得到很好的理解。对我们之前研究中鉴定的32个恶性疟原虫eba-175等位基因、两个赖氏疟原虫以及从GenBank数据库获得的一个加蓬疟原虫直系同源等位基因的核苷酸序列进行了全面比较,以揭示恶性疟原虫eba-175中片段二态性的起源和进化过程。在源自赖氏疟原虫CDC菌株的eba-175核苷酸序列中,区域III中同时发现了Fseg和Cseg,这意味着原始的eba-175基因同时具有这两个片段,F片段和C片段的缺失分别产生了Cseg和Fseg等位基因。我们还通过重新映射从GenBank数据库获得的短读长,证实了另一个赖氏疟原虫菌株(SY57)中存在具有Fseg和Cseg的等位基因。另一方面,加蓬疟原虫eba-175直系同源物的片段序列与其他物种的片段序列差异很大,这表明恶性疟原虫原始的eba-175二态性可追溯到恶性疟原虫和赖氏疟原虫的主干谱系。我们的研究结果表明,Fseg和Cseg等位基因源自恶性疟原虫和赖氏疟原虫祖先群体中一个同时包含这两个片段的单一eba-175等位基因,并且eba-175的等位基因二态性是由不同物种中相似二态性谱系的独立出现所塑造的,这在疟疾基因组中其他位点的等位基因二态性的任何进化模式中都从未观察到。