一种致病寄生虫及其牡蛎宿主的共系地理结构。

IF 2.1 3区 医学 Q2 PARASITOLOGY Parasitology Pub Date : 2024-06-01 Epub Date: 2024-05-21 DOI:10.1017/S0031182024000611
Elizabeth Faye Weatherup, Ryan Carnegie, Allan E Strand, Erik E Sotka
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引用次数: 0

摘要

随着下一代测序技术越来越经济实惠,逐基因型测序已成为生态学家和保护生物学家描述物种进化史的一种经济有效的工具。对于宿主与寄生虫的相互作用,逐基因型测序可以同时检测宿主和寄生虫的基因组,从而深入了解共同进化的过程。东部牡蛎(Crassostrea virginica)是美国最重要的水产养殖物种之一。自然界和养殖的牡蛎种群会受到由一种腔肠原生动物 Perkinsus marinus 引起的 "Dermo "病的严重影响。在这里,我们使用限制性位点相关 DNA 测序(RADseq)同时研究宿主和寄生虫的空间种群遗传结构。我们从墨西哥湾(GOM)和大西洋中部海岸线的 36 个牡蛎个体中分析了 393 个 P. marinus 单核苷酸多态性(SNPs)和 52,100 个 C. virginica 单核苷酸多态性(SNPs)。所有分析均显示,在 GOM 和大西洋中部海岸种群之间,C. virginica 和 P. marinus 的遗传差异具有统计学意义,在切萨皮克湾和弗吉尼亚州外海岸之间,C. virginica 和 P. marinus 的遗传差异具有统计学意义,但 P. marinus 的遗传差异不明显。共系统进化分析证实了宿主和寄生虫之间在大空间尺度上的显著耦合进化变化。海洋盆地之间强烈的遗传差异可能会导致任何一个盆地的牡蛎都不能很好地适应另一个盆地的寄生虫基因型和表型,这就需要谨慎对待大西洋和大洋盆地之间牡蛎和寄生虫的转移。更广泛地说,我们的研究结果证明了 RADseq 在描述与耦合进化一致的遗传差异空间模式方面的潜力。
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Co-phylogeographic structure in a disease-causing parasite and its oyster host.

With the increasing affordability of next-generation sequencing technologies, genotype-by-sequencing has become a cost-effective tool for ecologists and conservation biologists to describe a species' evolutionary history. For host–parasite interactions, genotype-by-sequencing can allow the simultaneous examination of host and parasite genomes and can yield insight into co-evolutionary processes. The eastern oyster, Crassostrea virginica, is among the most important aquacultured species in the United States. Natural and farmed oyster populations can be heavily impacted by ‘dermo’ disease caused by an alveolate protist, Perkinsus marinus. Here, we used restricted site-associated DNA sequencing (RADseq) to simultaneously examine spatial population genetic structure of host and parasite. We analysed 393 single-nucleotide polymorphisms (SNPs) for P. marinus and 52,100 SNPs for C. virginica from 36 individual oysters from the Gulf of Mexico (GOM) and mid-Atlantic coastline. All analyses revealed statistically significant genetic differentiation between the GOM and mid-Atlantic coast populations for both C. virginica and P. marinus, and genetic divergence between Chesapeake Bay and the outer coast of Virginia for C. virginica, but not for P. marinus. A co-phylogenetic analysis confirmed significant coupled evolutionary change between host and parasite across large spatial scales. The strong genetic divergence between marine basins raises the possibility that oysters from either basin would not be well adapted to parasite genotypes and phenotypes from the other, which would argue for caution with regard to both oyster and parasite transfers between the Atlantic and GOM regions. More broadly, our results demonstrate the potential of RADseq to describe spatial patterns of genetic divergence consistent with coupled evolution.

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来源期刊
Parasitology
Parasitology 医学-寄生虫学
CiteScore
4.80
自引率
4.20%
发文量
280
审稿时长
3-8 weeks
期刊介绍: Parasitology is an important specialist journal covering the latest advances in the subject. It publishes original research and review papers on all aspects of parasitology and host-parasite relationships, including the latest discoveries in parasite biochemistry, molecular biology and genetics, ecology and epidemiology in the context of the biological, medical and veterinary sciences. Included in the subscription price are two special issues which contain reviews of current hot topics, one of which is the proceedings of the annual Symposia of the British Society for Parasitology, while the second, covering areas of significant topical interest, is commissioned by the editors and the editorial board.
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