Population expansion and individual age affect endoparasite richness and diversity in a recolonising large carnivore population

Sci Rep. 2017 Jan 27:7:41730. doi: 10.1038/srep41730.

Abstract

The recent recolonisation of the Central European lowland (CEL) by the grey wolf (Canis lupus) provides an excellent opportunity to study the effect of founder events on endoparasite diversity. Which role do prey and predator populations play in the re-establishment of endoparasite life cycles? Which intrinsic and extrinsic factors control individual endoparasite diversity in an expanding host population? In 53 individually known CEL wolves sampled in Germany, we revealed a community of four cestode, eight nematode, one trematode and 12 potential Sarcocystis species through molecular genetic techniques. Infections with zoonotic Echinococcus multilocularis, Trichinella britovi and T. spiralis occurred as single cases. Per capita endoparasite species richness and diversity significantly increased with population size and changed with age, whereas sex, microsatellite heterozygosity, and geographic origin had no effect. Tapeworm abundance (Taenia spp.) was significantly higher in immigrants than natives. Metacestode prevalence was slightly higher in ungulates from wolf territories than from control areas elsewhere. Even though alternative canid definitive hosts might also play a role within the investigated parasite life cycles, our findings indicate that (1) immigrated wolves increase parasite diversity in German packs, and (2) prevalence of wolf-associated parasites had declined during wolf absence and has now risen during recolonisation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Biodiversity*
  • DNA, Mitochondrial
  • DNA, Satellite
  • Geography
  • Helminths / classification
  • Helminths / genetics
  • Host-Parasite Interactions
  • Parasites / classification*
  • Parasites / genetics
  • Population Density*
  • Wolves / classification*
  • Wolves / genetics
  • Wolves / parasitology*

Substances

  • DNA, Mitochondrial
  • DNA, Satellite