Evolution of increased early-life fecundity but faster reproductive senescence in Drosophila melanogaster females through adaptation to chronic live-yeast deprivation

Abstract

AbstractDietary restriction is a common ecological challenge that limits reproduction. Yet only a few studies have explored adaptation under chronic protein deprivation. We subjected four replicate laboratory-adapted populations (YLB) of Drosophila melanogaster to a complete deprivation of live-yeast to mimic diet restricted ecology. In this insect, live-yeast is a critical source of protein that strongly affect reproductive output, especially in females. Following 24 generations of experimental evolution, compared to their matched controls (BL), females from YLB populations showed increase in reproductive output early in life, both in presence and absence of live-yeast. The observed increase in reproductive output was not associated with any accommodating alteration in average egg size; and development time, pre-adult survivorship, and body mass at eclosion of the progeny. Interestingly, adult lifespan was also found to be unaffected. However, YLB females were found to have a significantly faster rate of reproductive senescence albeit without any change in a measure of lifetime reproductive output. Taken together, adaptation to LYD ecology shows that reproductive output can evolve without affecting lifespan, suggesting that widely observed reproduction-survival trade-off is not universal. Populations can optimize fitness by fine tuning the scheduling of reproduction even when lifetime reproductive output is constrained.