Effects of pathogen exposure on life-history variation in the gypsy moth (Lymantria dispar)

J Evol Biol. 2015 Oct;28(10):1828-39. doi: 10.1111/jeb.12699. Epub 2015 Aug 8.

Abstract

Investment in host defences against pathogens may lead to trade-offs with host fecundity. When such trade-offs arise from genetic correlations, rates of phenotypic change by natural selection may be affected. However, genetic correlations between host survival and fecundity are rarely quantified. To understand trade-offs between immune responses to baculovirus exposure and fecundity in the gypsy moth (Lymantria dispar), we estimated genetic correlations between survival probability and traits related to fecundity, such as pupal weight. In addition, we tested whether different virus isolates have different effects on male and female pupal weight. To estimate genetic correlations, we exposed individuals of known relatedness to a single baculovirus isolate. To then evaluate the effect of virus isolate on pupal weight, we exposed a single gypsy moth strain to 16 baculovirus isolates. We found a negative genetic correlation between survival and pupal weight. In addition, virus exposure caused late-pupating females to be identical in weight to males, whereas unexposed females were 2-3 times as large as unexposed males. Finally, we found that female pupal weight is a quadratic function of host mortality across virus isolates, which is likely due to trade-offs and compensatory growth processes acting at high and low mortality levels, respectively. Overall, our results suggest that fecundity costs may strongly affect the response to selection for disease resistance. In nature, baculoviruses contribute to the regulation of gypsy moth outbreaks, as pathogens often do in forest-defoliating insects. We therefore argue that trade-offs between host life-history traits may help explain outbreak dynamics.

Keywords: Lepidoptera; baculovirus; genetic correlations; heritability; host-pathogen interactions; sexual size dimorphism; trade-offs.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Animals
  • Baculoviridae / pathogenicity*
  • Female
  • Male
  • Moths / physiology*
  • Moths / virology