Abstract
Susceptibility to parasite infection was examined in a field experiment for four populations of 0+ juvenile European bitterling (Rhodeus amarus): one sympatric to local parasite fauna, one allopatric, and two hybrid populations. Significantly higher parasite abundance was recorded in the allopatric bitterling population, suggesting a maladaptation of parasites to their sympatric host. Type of parasite life cycle played an important role in host–parasite interactions. While the abundance of allogenic species between populations was comparable, a significant difference was found in abundance of autogenic parasite species between fish populations, with the allopatric population more infected. These results correspond with a prediction of higher dispersion probability and higher gene flow among geographically distant populations of allogenic species as compared to autogenic species. Increased susceptibility to parasites that do not occur within the natural host's geographical distribution was found in the allopatric host, but only for autogenic species. A difference in infection susceptibility was detected among populations of early-hatched bitterling exposed to infection during a period of high parasite abundance and richness in the environment. Differences in parasite abundance and species diversity among populations diminished, however, with increasing time of exposure. No difference was found within late-hatched populations, probably due to a lower probability of infection in late-hatched cohorts.


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Ballabeni P (1994) Experimental differences in mortality patterns between European minnows, Phoxinus phoxinus, infected with sympatric and allopatric trematodes, Diplostomum phoxini. J Fish Biol 45:257–267
Ballabeni P, Ward PI (1993) Local adaptation of the trematode Diplostomum phoxini to the European minnow Phoxinus phoxinus, its 2nd intermediate host. Funct Ecol 7:84–90
Bryja J, Smith C, Konecny A, Reichard M (2010) Range-wide population genetic structure of the European bitterling (Rhodeus amarus) based on microsatellite and mitochondrial DNA analysis. Mol Ecol 19:4708–4722
Bush AO, Lafferty KD, Lotz JM, Shostak AW (1997) Parasitology meets ecology on its own terms: Margolis et al. Revisited. J Parasitol 83:575–583
Chubb JC (1977) Seasonal occurrence of helminths in freshwater fishes, Part 1. Monogenea. Adv Parasitol 15:133–199
Chubb JC (1979) Seasonal occurrence of helminths in freshwater fishes, Part 2. Trematoda. Adv Parasitol 17:142–313
Crawley MJ (2007) The R book. Wiley, Hoboken
Criscione CD, Blouin MS (2004) Life cycles shape parasite evolution: comparative population genetics of salmon trematodes. Evolution 58:198–202
Davidova M, Ondrackova M, Jurajda P, Gelnar M (2008) Parasite assemblages of European bitterling (Rhodeus amarus), composition and effects of habitat type and host body size. Parasitol Res 102:1001–1011
Davies CM, Webster JP, Kruger O, Munatsi A, Ndamba J, Woolhouse MEJ (1999) Host-parasite population genetics: a cross-sectional comparison of Bulinus globosus and Schistosoma haematobium. Parasitology 119:295–302
Divino JN, Tonn WM (2007) Effects of reproductive timing and hatch date on fathead minnow recruitment. Ecol Freshwat Fish 16:165–176
Ergens R, Lom J (1970) Causative agents of parasitic fish diseases. Academia, Praha (in Czech)
Fellis KJ, Esch GW (2005) Autogenic-allogenic status affects interpond community similarity and species area relationship of macroparasites in the bluegill sunfish, Lepomis macrochirus, from a series of freshwater ponds in the Piedmont area of North Carolina. J Parasitol 91:764–767
Gandon S, Michalakis Y (2002) Local adaptation, evolutionary potential and host-parasite coevolution: interactions between migration, mutation, population size and generation time. J Evol Biol 15:451–462
Gasnier N, Rondelaud D, Abrous M, Carreras F, Boulard C, Diez-Banos P, Cabaret J (2000) Allopatric combination of Fasciola hepatica and Lymnaea truncatula is more efficient than sympatric ones. Int J Parasitol 30:573–578
Hammer R, Harper DAT, Ryan PD (2001) PAST: paleontological statistics software package for education and data analysis. Palaeontol Electronica 4:9
Ibarz A, Padros F, Gallardo MA, Fernandez-Borras J, Blasco J, Tort L (2010) Low-temperature challenges to gilthead sea bream culture: review of cold-induced alterations and ‘Winter Syndrome’. Rev Fish Biol Fish 20:539–556
Kaltz O, Shykoff JA (1998) Local adaptation in host-parasite systems. Heredity 81:361–370
Magurran AE (2004) Measuring biological diversity. Blackwell Publishing, Oxford
Moravec F (2001) Checklist of the metazoan parasites of fishes of the Czech Republic and the Slovak Republic (1873–2000). Academia, Praha
Osnas EE, Lively CM (2005) Immune response to sympatric and allopatric parasites in a snail-trematode interaction. Front Zool 2:8
Poulin R (1998) Evolutionary ecology of parasites: from individuals to communities. Chapman and Hall, London
Poulin R (2003) The decay of similarity with geographical distance in parasite communities of vertebrate hosts. J Biogeogr 30:1609–1615
Reichard M, Ondrackova M, Bryjova A, Smith C, Bryja J (2009) Breeding resource distribution affects selection gradients on male phenotypic traits: experimental study on lifetime reproductive success in the bitterling fish (Rhodeus amarus). Evolution 63:377–390
Simkova A, Morand S, Matejusova I, Jurajda P, Gelnar M (2001) Local and regional influences on patterns of parasite species richness of central European fishes. Biodivers Conserv 10:511–525
Smith C, Reichard M, Jurajda P, Przybylski M (2004) The reproductive ecology of the European bitterling (Rhodeus sericeus). J Zool 262:107–124
Voutilainen A, Valdez H, Karvonen A, Kortet R, Kuukka H, Peuhkuri N, Piironen J, Taskinen J (2009) Infectivity of trematode eye flukes in farmed salmonid fish—effects of parasite and host origins. Aquaculture 293:108–112
Acknowledgements
We would like to thank the Týnec and Pardubice angling clubs for fish sampling permission and the Židlochovice Forest Enterprise, Lanžhot forest district, for field work permission. We are also very grateful to our colleagues from the Department of Fish Ecology, Institute of Vertebrate Biology, Academy of Sciences of the Czech Republic, for their help in the field and also to colleagues from the Parasitology Research Group, Department of Botany and Zoology, Masaryk University, for the help with parasitological dissection of the fish. We would also like to thank Kevin Roche for English correction. This study was supported by the Grant Agency of the Czech Republic, Grant No. GD526/09/H025, the Grant Agency of the Academy of Sciences of the Czech Republic, Grant No. KJB600930802, and the Ministry of Education, Youth and Sports of the Czech Republic (Ichthyoparasitology Research Centre), Project No. LC522.
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Francová, K., Ondračková, M. Host–parasite interactions in sympatric and allopatric populations of European bitterling. Parasitol Res 109, 801–808 (2011). https://doi.org/10.1007/s00436-011-2326-3
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DOI: https://doi.org/10.1007/s00436-011-2326-3

