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The evolutionary ecology of complex lifecycle parasites: linking phenomena with mechanisms

机译:复杂生命周期寄生虫的进化生态学:现象与机制的联系

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摘要

Many parasitic infections, including those of humans, are caused by complex lifecycle parasites (CLPs): parasites that sequentially infect different hosts over the course of their lifecycle. CLPs come from a wide range of taxonomic groups—from single-celled bacteria to multicellular flatworms—yet share many common features in their life histories. Theory tells us when CLPs should be favoured by selection, but more empirical studies are required in order to quantify the costs and benefits of having a complex lifecycle, especially in parasites that facultatively vary their lifecycle complexity. In this article, we identify ecological conditions that favour CLPs over their simple lifecycle counterparts and highlight how a complex lifecycle can alter transmission rate and trade-offs between growth and reproduction. We show that CLPs participate in dynamic host–parasite coevolution, as more mobile hosts can fuel CLP adaptation to less mobile hosts. Then, we argue that a more general understanding of the evolutionary ecology of CLPs is essential for the development of effective frameworks to manage the many diseases they cause. More research is needed identifying the genetics of infection mechanisms used by CLPs, particularly into the role of gene duplication and neofunctionalisation in lifecycle evolution. We propose that testing for signatures of selection in infection genes will reveal much about how and when complex lifecycles evolved, and will help quantify complex patterns of coevolution between CLPs and their various hosts. Finally, we emphasise four key areas where new research approaches will provide fertile opportunities to advance this field.
机译:许多寄生虫感染,包括人的寄生虫感染,都是由复杂的生命周期寄生虫(CLP)引起的:在整个生命周期中,这些寄生虫会依次感染不同的宿主。 CLP来自各种各样的分类组,从单细胞细菌到多细胞扁虫,但在其生活史上却具有许多共同的特征。理论告诉我们何时应该选择CLP,但是需要进行更多的经验研究才能量化拥有复杂生命周期的成本和收益,尤其是在寄生虫会随意改变其生命周期复杂性的情况下。在本文中,我们确定了比CLP生命周期更简单的生态条件,并强调了复杂的生命周期如何改变传播速率以及生长与繁殖之间的权衡。我们显示,随着更多的移动主机可以推动CLP适应更少的移动主机,CLP会参与动态的主机-寄生虫协同进化。然后,我们认为,对CLP进化生态学的更一般的了解对于开发有效的框架来管理它们引起的许多疾病至关重要。需要更多的研究来确定CLP使用的感染机制的遗传学,尤其是基因复制和新功能化在生命周期进化中的作用。我们建议测试感染基因中选择标记的特征将揭示有关复杂生命周期如何以及何时进化的更多信息,并将有助于量化CLP及其各种宿主之间协同进化的复杂模式。最后,我们强调了四个关键领域,其中新的研究方法将为推动该领域的发展提供丰富的机会。

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