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PNAS Plus: Evidence of strain structure in Plasmodium falciparum var gene repertoires in children from Gabon West Africa

机译:PNAS Plus:来自西非加蓬的儿童恶性疟原虫var基因库中菌株结构的证据

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摘要

Existing theory on competition for hosts between pathogen strains has proposed that immune selection can lead to the maintenance of strain structure consisting of discrete, weakly overlapping antigenic repertoires. This prediction of strain theory has conceptual overlap with fundamental ideas in ecology on niche partitioning and limiting similarity between coexisting species in an ecosystem, which oppose the hypothesis of neutral coexistence. For Plasmodium falciparum, strain theory has been specifically proposed in relation to the major surface antigen of the blood stage, known as PfEMP1 and encoded by the multicopy multigene family known as the var genes. Deep sampling of the DBLα domain of var genes in the local population of Bakoumba, West Africa, was completed to define whether patterns of repertoire overlap support a role of immune selection under the opposing force of high outcrossing, a characteristic of areas of intense malaria transmission. Using a 454 high-throughput sequencing protocol, we report extremely high diversity of the DBLα domain and a large parasite population with DBLα repertoires structured into nonrandom patterns of overlap. Such population structure, significant for the high diversity of var genes that compose it at a local level, supports the existence of “strains” characterized by distinct var gene repertoires. Nonneutral, frequency-dependent competition would be at play and could underlie these patterns. With a computational experiment that simulates an intervention similar to mass drug administration, we argue that the observed repertoire structure matters for the antigenic var diversity of the parasite population remaining after intervention.
机译:现有的关于病原体菌株之间的宿主竞争的理论已经提出,免疫选择可以导致维持由离散的,弱重叠的抗原组成组成的菌株结构。应变理论的这种预测与生态学中有关生态位分配和限制生态系统中共存物种之间相似性的基本思想在概念上重叠,这反对中立共存的假设。对于恶性疟原虫,已经针对血期的主要表面抗原(称为PfEMP1)特别提出了应变理论,并由称为var基因的多拷贝多基因家族编码。已完成对西非Bakoumba当地居民var基因的DBLα结构域的深度采样,以定义所有谱系重叠的模式是否在高异型交配(强烈疟疾传播地区的特征)的反向作用下是否支持免疫选择的作用。 。我们使用454高通量测序协议,报告了DBLα域的极高多样性和大量寄生虫种群,其中DBLα组成被构造为重叠的非随机模式。这种种群结构对于组成地方基因的var基因的高度多样性具有重要意义,它支持以不同的var基因组成为特征的“菌株”的存在。非中立的,依赖频率的竞争将发挥作用,并可能成为这些模式的基础。通过计算实验,模拟了类似于大规模药物管理的干预措施,我们认为所观察到的库结构对于干预后剩余的寄生虫种群的抗原变体多样性至关重要。

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