Species-specific limits to lifespan (lifespan setpoint) determine the life expectancy of any given organism. Whether limiting lifespan provides an evolutionary benefit or is the result of an inevitable decline in fitness remains controversial. The identification of mutations extending lifespan suggests that aging is under genetic control, but the evolutionary driving forces limiting lifespan have not been defined. By examining the impact of lifespan on pathogen spread in a population, we propose that epidemics drive lifespan setpoints' evolution. Shorter lifespan limits infection spread and accelerates pathogen clearance when compared to populations with longer-lived individuals. Limiting longevity is particularly beneficial in the context of zoonotic transmissions, where pathogens must undergo adaptation to a new host. Strikingly, in populations exposed to pathogens, shorter-living variants outcompete individuals with longer lifespans. We submit that infection outbreaks can contribute to control the evolution of species' lifespan setpoints.

译文

物种特定的寿命限制 (寿命设定点) 决定了任何给定生物的预期寿命。限制寿命是否会带来进化上的好处,还是不可避免的适应性下降的结果,仍存在争议。对延长寿命的突变的鉴定表明,衰老处于遗传控制之下,但是尚未定义限制寿命的进化驱动力。通过研究寿命对人群中病原体传播的影响,我们建议流行病推动寿命设定点的演变。与寿命较长的个体相比,较短的寿命限制了感染的传播并加速了病原体的清除。在人畜共患病传播的情况下,限制寿命特别有益,在这种情况下,病原体必须适应新的宿主。令人惊讶的是,在暴露于病原体的人群中,寿命较短的变异体胜过寿命较长的个体。我们认为,感染暴发有助于控制物种寿命设定点的演变。

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