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作为适应性驱动力量的传染病决定寿命基准点。

Epidemics as an adaptive driving force determining lifespan setpoints.

机构信息

Department of Microbiology and Immunology, University of California, San Francisco, CA 94143-2280

出版信息

Proc Natl Acad Sci U S A. 2020 Jul 28;117(30):17937-17948. doi: 10.1073/pnas.1920988117. Epub 2020 Jul 10.

Abstract

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.

摘要

物种特有的寿命限制(寿命设定点)决定了任何给定生物体的预期寿命。寿命限制是否提供了进化优势,或者是适应度不可避免下降的结果,这仍然存在争议。延长寿命的突变的鉴定表明,衰老受遗传控制,但限制寿命的进化驱动力尚未确定。通过研究寿命对种群中病原体传播的影响,我们提出传染病推动了寿命设定点的进化。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,因为病原体必须适应新宿主。引人注目的是,在暴露于病原体的种群中,寿命较短的变体比寿命较长的个体更具竞争力。我们认为感染爆发有助于控制物种寿命设定点的进化。

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