自然发生的寄生虫爆发期间的毒力进化。

IF 1.8 3区 环境科学与生态学 Q3 ECOLOGY
Camden D Gowler, Haley Essington, Bruce O'Brien, Clara L Shaw, Rebecca W Bilich, Patrick A Clay, Meghan A Duffy
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引用次数: 3

摘要

毒力,即病原体对宿主的伤害程度,是宿主-病原体相互作用的一个重要但鲜为人知的方面。毒力不是静态的,而是取决于生态环境,并可能迅速演变。例如,在流行病开始时,当易感宿主大量存在时,病原体可能会进化出更强的毒性,如果这使其内在生长速度最大化。然而,如果宿主密度在流行病期间下降,理论预测毒性降低的进化。尽管在理论上得到了充分的研究,但关于流行病中毒力进化的经验证据仍然很少,特别是在具有本地宿主和病原体物种的自然环境中。在这里,我们在水蚤-巴氏菌模型系统中使用现场观察和实验室分析相结合的方法来寻找自然界中毒力进化的证据。我们监测了一次大型的、自然发生的拉莫氏巴氏菌在齿水蚤中的暴发,在暴发期间,感染流行率达到峰值,约占受感染人群的40%,宿主密度急剧下降。在实验室的控制感染中,受感染宿主的寿命和繁殖低于未暴露的对照宿主和暴露但未感染的宿主。我们没有发现宿主抗性或寄生虫传染性的任何显著变化,也没有发现寄生虫毒力变化的证据(通过宿主寿命和宿主产生的幼虫数量来量化)。然而,在流行病期间,寄生虫进化到在受感染的宿主中产生的孢子明显减少。虽然这一发现出乎意料,但它可能反映了以前量化的权衡:在高死亡率(例如,高捕食)环境中的寄生虫在感染中更快地从营养生长转向产生孢子,从而减少了孢子的产量。未来的研究将追踪更多种群中寄生虫孢子产量的进化,并将这些变化与遗传变化和捕食率联系起来,这将更好地了解野生寄生虫进化的驱动因素。补充信息:在线版本包含补充资料,下载地址:10.1007/s10682-022-10169-6。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Virulence evolution during a naturally occurring parasite outbreak.

Virulence evolution during a naturally occurring parasite outbreak.

Virulence evolution during a naturally occurring parasite outbreak.

Virulence evolution during a naturally occurring parasite outbreak.

Virulence, the degree to which a pathogen harms its host, is an important but poorly understood aspect of host-pathogen interactions. Virulence is not static, instead depending on ecological context and potentially evolving rapidly. For instance, at the start of an epidemic, when susceptible hosts are plentiful, pathogens may evolve increased virulence if this maximizes their intrinsic growth rate. However, if host density declines during an epidemic, theory predicts evolution of reduced virulence. Although well-studied theoretically, there is still little empirical evidence for virulence evolution in epidemics, especially in natural settings with native host and pathogen species. Here, we used a combination of field observations and lab assays in the Daphnia-Pasteuria model system to look for evidence of virulence evolution in nature. We monitored a large, naturally occurring outbreak of Pasteuria ramosa in Daphnia dentifera, where infection prevalence peaked at ~ 40% of the population infected and host density declined precipitously during the outbreak. In controlled infections in the lab, lifespan and reproduction of infected hosts was lower than that of unexposed control hosts and of hosts that were exposed but not infected. We did not detect any significant changes in host resistance or parasite infectivity, nor did we find evidence for shifts in parasite virulence (quantified by host lifespan and number of clutches produced by hosts). However, over the epidemic, the parasite evolved to produce significantly fewer spores in infected hosts. While this finding was unexpected, it might reflect previously quantified tradeoffs: parasites in high mortality (e.g., high predation) environments shift from vegetative growth to spore production sooner in infections, reducing spore yield. Future studies that track evolution of parasite spore yield in more populations, and that link those changes with genetic changes and with predation rates, will yield better insight into the drivers of parasite evolution in the wild.

Supplementary information: The online version contains supplementary material available at 10.1007/s10682-022-10169-6.

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来源期刊
Evolutionary Ecology
Evolutionary Ecology 环境科学-进化生物学
CiteScore
3.00
自引率
5.30%
发文量
70
审稿时长
3 months
期刊介绍: Evolutionary Ecology is a concept-oriented journal of biological research at the interface of ecology and evolution. We publish papers that therefore integrate both fields of research: research that seeks to explain the ecology of organisms in the context of evolution, or patterns of evolution as explained by ecological processes. The journal publishes original research and discussion concerning the evolutionary ecology of organisms. These may include papers addressing evolutionary aspects of population ecology, organismal interactions and coevolution, behaviour, life histories, communication, morphology, host-parasite interactions and disease ecology, as well as ecological aspects of genetic processes. The objective is to promote the conceptual, theoretical and empirical development of ecology and evolutionary biology; the scope extends to any organism or system. In additional to Original Research articles, we publish Review articles that survey recent developments in the field of evolutionary ecology; Ideas & Perspectives articles which present new points of view and novel hypotheses; and Comments on articles recently published in Evolutionary Ecology or elsewhere. We also welcome New Tests of Existing Ideas - testing well-established hypotheses but with broader data or more methodologically rigorous approaches; - and shorter Natural History Notes, which aim to present new observations of organismal biology in the wild that may provide inspiration for future research. As of 2018, we now also invite Methods papers, to present or review new theoretical, practical or analytical methods used in evolutionary ecology. Students & Early Career Researchers: We particularly encourage, and offer incentives for, submission of Reviews, Ideas & Perspectives, and Methods papers by students and early-career researchers (defined as being within one year of award of a PhD degree) – see Students & Early Career Researchers
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