Gowler Camden D, Essington Haley, O'Brien Bruce, Shaw Clara L, Bilich Rebecca W, Clay Patrick A, Duffy Meghan A
Department of Ecology and Evolutionary Biology, University of Michigan, 48104 Ann Arbor, MI USA.
Department of Biology, The Pennsylvania State University, University Park, 16802 Pennsylvania, PA USA.
Evol Ecol. 2023;37(1):113-129. doi: 10.1007/s10682-022-10169-6. Epub 2022 Apr 12.
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 - model system to look for evidence of virulence evolution in nature. We monitored a large, naturally occurring outbreak of in , 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.
The online version contains supplementary material available at 10.1007/s10682-022-10169-6.
毒力是病原体对宿主造成伤害的程度,是宿主-病原体相互作用中一个重要但了解甚少的方面。毒力并非一成不变,而是取决于生态环境,并且可能迅速演变。例如,在疫情开始时,当易感宿主充足时,如果这能最大化病原体的内在生长速率,病原体可能会进化出更高的毒力。然而,如果在疫情期间宿主密度下降,理论预测毒力会进化降低。尽管在理论上有充分研究,但在疫情中毒力进化仍缺乏实证证据,尤其是在有本地宿主和病原体物种的自然环境中。在这里,我们在该模型系统中结合实地观察和实验室测定,寻找自然界中毒力进化的证据。我们监测了2016年一次大规模的自然爆发,感染率在约40%的种群被感染时达到峰值,且在爆发期间宿主密度急剧下降。在实验室的受控感染中,受感染宿主的寿命和繁殖能力低于未暴露的对照宿主以及暴露但未感染的宿主。我们未检测到宿主抗性或寄生虫感染力有任何显著变化,也未找到寄生虫毒力发生变化的证据(通过宿主寿命和宿主产生的卵块数量来量化)。然而,在疫情期间,寄生虫进化为在受感染宿主中产生显著更少的孢子。虽然这一发现出乎意料,但它可能反映了先前量化的权衡:在高死亡率(如高捕食率)环境中的寄生虫在感染时更快地从营养生长转变为孢子产生,从而降低孢子产量。未来跟踪更多种群中寄生虫孢子产量进化,并将这些变化与基因变化和捕食率联系起来的研究,将能更好地洞察野生环境中寄生虫进化的驱动因素。
在线版本包含可在10.1007/s10682-022-10169-6获取的补充材料。