Roy Scott W, Weedall Gareth D, da Silva Rogério L, Polley Spencer D, Ferreira Marcelo U
National Center for Biotechnology Information, National Library of Medicine, National Institutes of Health, Building 38A, Bethesda, MD 20894, USA.
Gene. 2009 Aug 15;443(1-2):12-21. doi: 10.1016/j.gene.2009.05.007. Epub 2009 May 20.
Immune evasion by Plasmodium falciparum is favored by extensive allelic diversity of surface antigens. Some of them, most notably the vaccine-candidate merozoite surface protein (MSP)-1, exhibit a poorly understood pattern of allelic dimorphism, in which all observed alleles group into two highly diverged allelic families with few or no inter-family recombinants. Here we describe contrasting levels and patterns of sequence diversity in genes encoding three MSP-1-associated surface antigens of P. falciparum, ranging from an ancient allelic dimorphism in the Msp-6 gene to a near lack of allelic divergence in Msp-9 to a more classical multi-allele polymorphism in Msp-7. Other members of the Msp-7 gene family exhibit very little polymorphism in non-repetitive regions. A comparison of P. falciparum Msp-6 sequences to an orthologous sequence from P. reichenowi provided evidence for distinct evolutionary histories of the 5' and 3' segments of the dimorphic region in PfMsp-6, consistent with one dimorphic lineage having arisen from recombination between now-extinct ancestral alleles. In addition, we uncovered two surprising patterns of evolution in repetitive sequence. First, in Msp-6, large deletions are associated with (nearly) identical sequence motifs at their borders. Second, a comparison of PfMsp-9 with the P. reichenowi ortholog indicated retention of a significant inter-unit diversity within an 18-base pair repeat within the coding region of P. falciparum, but homogenization in P. reichenowi.
恶性疟原虫的免疫逃避因表面抗原的广泛等位基因多样性而受到青睐。其中一些抗原,最显著的是作为疫苗候选物的裂殖子表面蛋白(MSP)-1,呈现出一种了解甚少的等位基因二态性模式,即所有观察到的等位基因都归为两个高度分化的等位基因家族,家族间几乎没有重组体。在此,我们描述了恶性疟原虫三种与MSP-1相关的表面抗原编码基因中序列多样性的不同水平和模式,从Msp-6基因中的古老等位基因二态性到Msp-9基因中几乎不存在等位基因差异,再到Msp-7基因中更典型的多等位基因多态性。Msp-7基因家族的其他成员在非重复区域表现出很少的多态性。将恶性疟原虫Msp-6序列与赖氏疟原虫的直系同源序列进行比较,为PfMsp-6中二态性区域5'和3'片段的不同进化历史提供了证据,这与一个二态性谱系源于现已灭绝的祖先等位基因之间的重组一致。此外,我们还发现了重复序列中两种令人惊讶的进化模式。第一,在Msp-6中,大的缺失与其边界处(几乎)相同的序列基序相关。第二,将PfMsp-9与赖氏疟原虫的直系同源物进行比较表明,恶性疟原虫编码区域内一个18碱基对重复序列中的单元间多样性在赖氏疟原虫中得以保留,但在赖氏疟原虫中发生了同质化。