网状细胞结合蛋白同源物 5 是巴布亚新几内亚恶性疟原虫种群平衡选择的一个目标

M. Naung, Elijah Martin, Wilson Wong, Z. Razook, Digjaya Utama, Andrew J. Guy, Shannon Takala Harrison, A. Cowman, E. Lin, Benson Kiniboro, M. Laman, Ivo Mueller, Alyssa E. Barry
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摘要

恶性疟原虫网状细胞结合蛋白同源物(RH5)是一种主要的候选疟疾疫苗,它对寄生虫侵入红细胞至关重要,能与人类宿主受体--basigin--相互作用。与其他血期抗原相比,RH5具有少量的多态性,体外研究表明,疫苗诱导的针对RH5的抗体具有株间传递性,但大多数调查RH5多样性的研究都是在非洲进行的。了解其他地区疟疾抗原的遗传多样性和进化情况对于验证它们是否可作为候选疫苗非常重要。本研究对巴布亚新几内亚(PNG)1-3 岁儿童纵向队列中 677 份样本的 rh5 基因进行了测序。在成功测序的 677 份样本中,有 566 份被确定为独立感染(即去除宿主内每对相同序列中的一个)。共鉴定出 14 个非同义多态性,其中 8 个在人群中 "常见"(小等位基因频率大于 1%),44 个单倍型的频率从 1%到 21%不等。根据 RH5/CyRPA/RIPR 复合物的低温电子显微镜结构对常见 SNP 进行建模,发现它们位于 Basigin 结合位点和 CyRPA 接触点附近。对相应核苷酸序列进行的田岛 D 分析产生了正值,表明存在潜在的平衡选择热点。我们试图通过测量同一宿主内独立感染之间的多态性率以及与临床症状的关联来确认这些信号是否是免疫选择所致,但没有发现这种关联。这些结果共同表明,虽然有证据表明巴新恶性疟原虫种群中的 RH5 多样性是由平衡选择驱动的,但在幼儿队列中并未观察到免疫逃逸。有限的免疫力和较低的选择压力可能解释了这一结果,另外,其他进化力量也可能有助于巴新 RH5 与BSG 结合界面的平衡选择。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Reticulocyte Binding Protein Homologue 5 is a target of balancing selection in the Plasmodium falciparum population of Papua New Guinea
Plasmodium falciparum Reticulocyte Binding Protein Homologue (RH5), a leading malaria vaccine candidate, is essential for erythrocyte invasion by the parasite, interacting with the human host receptor, basigin. RH5 has a small number of polymorphisms relative to other blood-stage antigens, and in vitro studies have shown that vaccine-induced antibodies raised against RH5 are strain-transcending, however most studies investigating RH5 diversity have been done in Africa. Understanding the genetic diversity and evolution of malaria antigens in other regions is important for their validation as vaccine candidates. In this study the rh5 gene was sequenced in 677 samples from a longitudinal cohort of Papua New Guinean (PNG) children aged 1-3 years. Of 677 samples successfully sequenced, 566 were identified as independent infections (i.e. one of each pair of identical sequences within hosts were removed). A total of 14 non-synonymous polymorphisms were identified, eight that are ‘common’ in the population (minor allele frequency > 1%), with 44 haplotypes ranging in frequency from 1% to 21%. Modeling of common SNPs to the cryo-EM structure of the RH5/CyRPA/RIPR complex mapped them to the Basigin binding site and near the contact point of CyRPA. Tajima’s D analyses of the corresponding nucleotide sequences produced positive values indicating potential hotspots of balancing selection. We attempted to confirm whether these signals were due to immune selection by measuring the rate of polymorphism between independent infections within the same host, and the association with clinical symptoms, however, no such associations were identified. Together these results suggest that while there is evidence of balancing selection driving RH5 diversity in the PNG P. falciparum population, immune escape was not observed within the cohort of young children. Limited immunity and therefore low selective pressure may explain this result, alternatively other evolutionary forces may contribute to balancing selection at the RH5-BSG binding interface in PNG.
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