Parallel and costly changes to cellular immunity underlie the evolution of parasitoid resistance in three Drosophila species

PLoS Pathog. 2017 Oct 19;13(10):e1006683. doi: 10.1371/journal.ppat.1006683. eCollection 2017 Oct.

Abstract

A priority for biomedical research is to understand the causes of variation in susceptibility to infection. To investigate genetic variation in a model system, we used flies collected from single populations of three different species of Drosophila and artificially selected them for resistance to the parasitoid wasp Leptopilina boulardi, and found that survival rates increased 3 to 30 fold within 6 generations. Resistance in all three species involves a large increase in the number of the circulating hemocytes that kill parasitoids. However, the different species achieve this in different ways, with D. melanogaster moving sessile hemocytes into circulation while the other species simply produce more cells. Therefore, the convergent evolution of the immune phenotype has different developmental bases. These changes are costly, as resistant populations of all three species had greatly reduced larval survival. In all three species resistance is only costly when food is in short supply, and resistance was rapidly lost from D. melanogaster populations when food is restricted. Furthermore, evolving resistance to L. boulardi resulted in cross-resistance against other parasitoids. Therefore, whether a population evolves resistance will depend on ecological conditions including food availability and the presence of different parasite species.

MeSH terms

  • Animals
  • Biological Evolution*
  • Disease Resistance / genetics*
  • Disease Resistance / immunology
  • Drosophila / genetics
  • Drosophila / immunology*
  • Drosophila / parasitology*
  • Immunity, Cellular / genetics
  • Immunity, Cellular / immunology
  • Species Specificity
  • Wasps / immunology
  • Wasps / pathogenicity*

Grants and funding

This work was funded by an European Research Council grant to FMJ (281668, DrosophilaInfection) and a Natural Environment Research Council Grant (NE/P00184X/1) to FMJ. JEM was supported by a Biotechnology and Biological Sciences Research Council studentship. ABL was supported by an European Molecular Biology Organisation fellowship ALTF 1556-2015. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.