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Host-mediated selection impacts the diversity of Plasmodium falciparum antigens within infections

机译:宿主介导的选择影响感染中恶性疟原虫抗原的多样性

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Host immunity exerts strong selective pressure on pathogens. Population-level genetic analysis can identify signatures of this selection, but these signatures reflect the net selective effect of all hosts and vectors in a population. In contrast, analysis of pathogen diversity within hosts provides information on individual, host-specific selection pressures. Here, we combine these complementary approaches in an analysis of the malaria parasite Plasmodium falciparum using haplotype sequences from thousands of natural infections in sub-Saharan Africa. We find that parasite genotypes show preferential clustering within multi-strain infections in young children, and identify individual amino acid positions that may contribute to strain-specific immunity. Our results demonstrate that natural host defenses to P. falciparum act in an allele-specific manner to block specific parasite haplotypes from establishing blood-stage infections. This selection partially explains the extreme amino acid diversity of many parasite antigens and suggests that vaccines targeting such proteins should account for allele-specific immunity.
机译:宿主免疫力对病原体施加强大的选择压力。群体水平的遗传分析可以识别这种选择的特征,但是这些特征反映了群体中所有宿主和载体的净选择效应。相反,宿主内病原体多样性的分析提供了有关个体特定宿主选择压力的信息。在这里,我们使用来自撒哈拉以南非洲成千上万自然感染的单倍型序列,在疟疾寄生虫恶性疟原虫的分析中结合了这些互补方法。我们发现寄生虫基因型显示幼儿多菌株感染内的优先群集,并确定可能有助于菌株特异性免疫的单个氨基酸位置。我们的结果表明,对恶性疟原虫的天然宿主防御以等位基因特异性方式起作用,以阻止特定的寄生虫单倍型建立血液阶段感染。这种选择部分地解释了许多寄生虫抗原的极端氨基酸多样性,并表明靶向此类蛋白的疫苗应说明等位基因特异性免疫。

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