Literature DB >> 28122251

Early life stress affects mortality rate more than social behavior, gene expression or oxidative damage in honey bee workers.

Olav Rueppell1, Babak Yousefi2, Juan Collazo2, Daniel Smith2.   

Abstract

Early life stressors can affect aging and life expectancy in positive or negative ways. Individuals can adjust their behavior and molecular physiology based on early life experiences but relatively few studies have connected such mechanisms to demographic patterns in social organisms. Sociality buffers individuals from environmental influences and it is unclear how much early life stress affects later life history. Workers of the honey bee (Apis mellifera L.) were exposed to two stressors, Varroa parasitism and Paraquat exposure, early in life. Consequences were measured at the molecular, behavioral, and demographic level. While treatments did not significantly affect levels of oxidative damage, expression of select genes, and titers of the common deformed wing virus, most of these measures were affected by age. Some of the age effects, such as declining levels of deformed wing virus and oxidative damage, were opposite to our predictions but may be explained by demographic selection. Further analyses suggested some influences of worker behavior on mortality and indicated weak treatment effects on behavior. The latter effects were inconsistent among the two experiments. However, mortality rate was consistently reduced by Varroa mite stress during development. Thus, mortality was more responsive to early life stress than our other response variables. The lack of treatment effects on these measures may be due to the social organization of honey bees that buffers the individual from the impact of stressful developmental conditions.
Copyright © 2017 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Developmental stress; Parasitism; Pesticide; Predictive behavioral demography; Social evolution

Mesh:

Substances:

Year:  2017        PMID: 28122251      PMCID: PMC5346452          DOI: 10.1016/j.exger.2017.01.015

Source DB:  PubMed          Journal:  Exp Gerontol        ISSN: 0531-5565            Impact factor:   4.032


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