确定非洲流行的恶性疟原虫复杂基因背景:多国基因组流行病学分析。

IF 20.9 1区 生物学 Q1 INFECTIOUS DISEASES Lancet Microbe Pub Date : 2024-11-07 DOI:10.1016/j.lanmic.2024.07.004
Olivo Miotto, Alfred Amambua-Ngwa, Lucas N Amenga-Etego, Muzamil M Abdel Hamid, Ishag Adam, Enoch Aninagyei, Tobias Apinjoh, Gordon A Awandare, Philip Bejon, Gwladys I Bertin, Marielle Bouyou-Akotet, Antoine Claessens, David J Conway, Umberto D'Alessandro, Mahamadou Diakite, Abdoulaye Djimdé, Arjen M Dondorp, Patrick Duffy, Rick M Fairhurst, Caterina I Fanello, Anita Ghansah, Deus S Ishengoma, Mara Lawniczak, Oumou Maïga-Ascofaré, Sarah Auburn, Anna Rosanas-Urgell, Varanya Wasakul, Nina F D White, Alexandria Harrott, Jacob Almagro-Garcia, Richard D Pearson, Sonia Goncalves, Cristina Ariani, Zbynek Bozdech, William L Hamilton, Victoria Simpson, Dominic P Kwiatkowski
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引用次数: 0

摘要

背景:恶性疟原虫的种群结构可以揭示其潜在的适应性进化过程。维持复杂遗传背景的选择性压力会鼓励近亲繁殖,从而产生可通过种群结构分析识别的独特寄生虫集群:我们分析了 MalariaGEN Pf7 数据集提供的非洲 21 个国家 3783 个恶性疟原虫基因组的种群结构。我们使用主坐标分析法对寄生虫进行聚类,使用世系认同(IBD)法确定聚类成员共有的基因组区域,并使用连锁分析法确定它们的共同遗传模式。通过从头组装重建了结构变异,并通过长线程测序进行了验证:我们发现了一个差异很大的寄生虫集群,命名为 AF1,在分析的 3783 个样本中占 47 个(1-2%),分布在非洲 13 个国家,相距 7000 多公里。该寄生虫群的成员具有复杂的遗传背景,由多达 23 个基因位点组成,其中有许多高度分化的变异体,在该寄生虫群之外很少能观察到这些变异体。IBD 分析显示,无论取样地点在哪里,这些基因位点都有共同的祖先。然而,在共同位点之外,AF1 成员似乎与同域寄生虫进行了近亲繁殖。AF1 分化变种包括结构变异,包括涉及 dblmsp 和 dblmsp2 基因的基因转换,以及大量单核苷酸多态性。携带这些变异的几个基因在功能上是相关的,通常涉及与红细胞的相互作用,包括侵入、排出和红细胞抗原输出:我们认为,AF1寄生虫已经适应了某种未知的进化生态位,可能涉及与宿主红细胞的相互作用。这种适应涉及一个复杂的相互作用变体汇编,在非洲很少观察到这种变体,尽管发生了重组事件,但大多数变体仍然保持完整。术语 "隐型"(cryptotype)被用来描述一种共同的背景,其中夹杂着源自当地的基因组区域:比尔及梅琳达-盖茨基金会
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Identification of complex Plasmodium falciparum genetic backgrounds circulating in Africa: a multicountry genomic epidemiology analysis.

Background: The population structure of the malaria parasite Plasmodium falciparum can reveal underlying adaptive evolutionary processes. Selective pressures to maintain complex genetic backgrounds can encourage inbreeding, producing distinct parasite clusters identifiable by population structure analyses.

Methods: We analysed population structure in 3783 P falciparum genomes from 21 countries across Africa, provided by the MalariaGEN Pf7 dataset. We used Principal Coordinate Analysis to cluster parasites, identity by descent (IBD) methods to identify genomic regions shared by cluster members, and linkage analyses to establish their co-inheritance patterns. Structural variants were reconstructed by de novo assembly and verified by long-read sequencing.

Findings: We identified a strongly differentiated cluster of parasites, named AF1, comprising 47 (1·2%) of 3783 samples analysed, distributed over 13 countries across Africa, at locations over 7000 km apart. Members of this cluster share a complex genetic background, consisting of up to 23 loci harbouring many highly differentiated variants, rarely observed outside the cluster. IBD analyses revealed common ancestry at these loci, irrespective of sampling location. Outside the shared loci, however, AF1 members appear to outbreed with sympatric parasites. The AF1 differentiated variants comprise structural variations, including a gene conversion involving the dblmsp and dblmsp2 genes, and numerous single nucleotide polymorphisms. Several of the genes harbouring these mutations are functionally related, often involved in interactions with red blood cells including invasion, egress, and erythrocyte antigen export.

Interpretation: We propose that AF1 parasites have adapted to some unidentified evolutionary niche, probably involving interactions with host erythrocytes. This adaptation involves a complex compendium of interacting variants that are rarely observed in Africa, which remains mostly intact despite recombination events. The term cryptotype was used to describe a common background interspersed with genomic regions of local origin.

Funding: Bill & Melinda Gates Foundation.

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来源期刊
Lancet Microbe
Lancet Microbe Multiple-
CiteScore
27.20
自引率
0.80%
发文量
278
审稿时长
6 weeks
期刊介绍: The Lancet Microbe is a gold open access journal committed to publishing content relevant to clinical microbiologists worldwide, with a focus on studies that advance clinical understanding, challenge the status quo, and advocate change in health policy.
期刊最新文献
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