Malaria Programme, Wellcome Sanger Institute, Wellcome Genome Campus, Hinxton, Cambridge, United Kingdom.
Faculty of Infectious and Tropical Diseases, London School of Hygiene and Tropical Medicine, London, United Kingdom.
PLoS Pathog. 2018 Nov 29;14(11):e1007436. doi: 10.1371/journal.ppat.1007436. eCollection 2018 Nov.
Invasion of human erythrocytes is essential for Plasmodium falciparum parasite survival and pathogenesis, and is also a complex phenotype. While some later steps in invasion appear to be invariant and essential, the earlier steps of recognition are controlled by a series of redundant, and only partially understood, receptor-ligand interactions. Reverse genetic analysis of laboratory adapted strains has identified multiple genes that when deleted can alter invasion, but how the relative contributions of each gene translate to the phenotypes of clinical isolates is far from clear. We used a forward genetic approach to identify genes responsible for variable erythrocyte invasion by phenotyping the parents and progeny of previously generated experimental genetic crosses. Linkage analysis using whole genome sequencing data revealed a single major locus was responsible for the majority of phenotypic variation in two invasion pathways. This locus contained the PfRh2a and PfRh2b genes, members of one of the major invasion ligand gene families, but not widely thought to play such a prominent role in specifying invasion phenotypes. Variation in invasion pathways was linked to significant differences in PfRh2a and PfRh2b expression between parasite lines, and their role in specifying alternative invasion was confirmed by CRISPR-Cas9-mediated genome editing. Expansion of the analysis to a large set of clinical P. falciparum isolates revealed common deletions, suggesting that variation at this locus is a major cause of invasion phenotypic variation in the endemic setting. This work has implications for blood-stage vaccine development and will help inform the design and location of future large-scale studies of invasion in clinical isolates.
人类红细胞的入侵对于疟原虫寄生虫的生存和发病机制至关重要,也是一个复杂的表型。虽然入侵的一些后期步骤似乎是不变的和必要的,但早期的识别步骤是由一系列冗余的、部分理解的受体-配体相互作用控制的。对实验室适应株的反向遗传学分析已经确定了多个可以改变入侵的基因,但每个基因的相对贡献如何转化为临床分离株的表型还远不清楚。我们使用正向遗传学方法来鉴定负责红细胞入侵的基因,方法是表型分析先前产生的实验遗传杂交的父母本和后代。使用全基因组测序数据的连锁分析显示,一个主要位点负责两种入侵途径的大多数表型变异。这个位点包含 PfRh2a 和 PfRh2b 基因,它们是主要入侵配体基因家族之一的成员,但通常不认为它们在指定入侵表型方面发挥如此突出的作用。入侵途径的变异与寄生虫系之间 PfRh2a 和 PfRh2b 表达的显著差异有关,通过 CRISPR-Cas9 介导的基因组编辑证实了它们在指定替代入侵中的作用。将分析扩展到一组大型临床疟原虫分离株中,发现了常见的缺失,表明该位点的变异是地方性环境中入侵表型变异的主要原因。这项工作对血阶段疫苗的开发具有重要意义,并将有助于指导未来在临床分离株中进行大规模入侵研究的设计和定位。