32Honey bee workers display remarkable flexibility in the aging process. 33This plasticity is closely tied to behavioral maturation. Workers who initiate 34 foraging behavior at earlier ages have shorter lifespans, and much of the 35 variation in total lifespan can be explained by differences in pre-foraging lifespan. 36Vitellogenin (Vg), a yolk precursor protein, influences worker lifespan both as a 37 regulator of behavioral maturation and through anti-oxidant and immune 38 functions. Experimental reduction of Vg mRNA, and thus Vg protein levels, in 39 wild-type bees results in precocious foraging behavior, decreased lifespan, and 40 increased susceptibility to oxidative damage. We sought to separate the effects 41 of Vg on lifespan due to behavioral maturation from those due to immune and 42 antioxidant function using two selected strains of honey bees that differ in their 43 phenotypic responsiveness to Vg gene knockdown. Surprisingly, we found that 44 lifespans lengthen in the strain described as behaviorally and hormonally 45 insensitive to Vg reduction. We then performed targeted gene expression 46 analyses on genes hypothesized to mediate aging and lifespan: the insulin-like 47 peptides (Ilp1 and 2) and manganese superoxide dismutase (mnSOD). The two 48 honey bee Ilps are the most upstream components in the insulin-signaling 49 pathway, which influences lifespan in Drosophila melanogaster and other 50 organisms., while manganese superoxide dismutase encodes an enzyme with 51 antioxidant functions in animals. We found expression differences in the llps in fat 52 body related to behavior (llp1 and 2) and genetic background (Ilp2), but did not 53 find strain by treatment effects. Expression of mnSOD was also affected by 54 behavior and genetic background. Additionally, we observed a differential 55 response to Vg knockdown in fat body expression of mnSOD, suggesting that 56 antioxidant pathways may partially explain the strain-specific lifespan responses 57 to Vg knockdown. 58 59