Non-native gobies facilitate the transmission of Bucephalus polymorphus (Trematoda)
Jazyk angličtina Země Velká Británie, Anglie Médium electronic
Typ dokumentu časopisecké články, práce podpořená grantem
PubMed
26187653
PubMed Central
PMC4506608
DOI
10.1186/s13071-015-0999-7
PII: 10.1186/s13071-015-0999-7
Knihovny.cz E-zdroje
- MeSH
- nemoci ryb parazitologie přenos MeSH
- Perciformes parazitologie MeSH
- řeky MeSH
- stadia vývoje MeSH
- Trematoda růst a vývoj fyziologie MeSH
- zavlečené druhy MeSH
- zvířata MeSH
- Check Tag
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
BACKGROUND: Introduced species can modify local host-parasite dynamics by amplifying parasite infection which can 'spill-back' to the native fauna, whether they are competent hosts for local parasites, or by acting as parasite sinks with 'dilution' of infection decreasing the parasite burden of native hosts. Recently infection by the trematode Bucephalus polymorphus has increased in several European rivers, being attributed to the introduction of intermediate host species from the Ponto-Caspian region. Using a combination of field and experimental data, we evaluated the competence of non-native and native fish as intermediate hosts for B. polymorphus and its role for parasite development in a definitive host. METHODS: The density of 0+ juvenile fish (the second intermediate hosts for B. polymorphus) was measured in the River Morava, Czech Republic and fish were screened for natural metacercariae infection. The stomach contents of predatory fish that are definitive hosts of B. polymorphus were examined to assess the importance of non-native gobies for parasite transmission. In semi-natural conditions, parasite establishment, initial survival, and maturity rates in experimentally infected definitive hosts pikeperch Sander lucioperca were measured in flukes recovered from native white bream Abramis bjoerkna and non-native tubenose goby Proterorhinus semilunaris and round goby Neogobius melanostomus. Adult fluke size and egg production was also measured to evaluate the potential effect of intermediate host species on parasite fitness. RESULTS: We detected high natural infection parameters of B. polymorphus in native cyprinids and non-native gobies compared to data from the period prior to goby establishment. Both fish groups are consumed by predatory fish and represent a major component of the littoral fish community. Parasite establishment and adult size in definitive hosts was equivalent among the second intermediate host species, despite a lower size of metacercariae recovered from round gobies. However, development in the definitive host of flukes recovered from gobies was reduced, showing higher mortality, delayed maturity and lower egg production, in comparison with parasites from native hosts. CONCLUSIONS: Substantial 'spill-back' of B. polymorphus due to higher transmission rates after establishment of non-native gobies was partially buffered by decreased fitness of B. polymorphus that underwent development in gobies.
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Prenter J, MacNeil C, Dick JTA, Dunn AM. Roles of parasites in animal invasions. Trends Ecol Evol. 2004;19:385–90. doi: 10.1016/j.tree.2004.05.002. PubMed DOI
Dunn AM. Parasites and biological invasions. Adv Parasitol. 2009;68:161–84. doi: 10.1016/S0065-308X(08)00607-6. PubMed DOI
Poulin R, Mouillot D. Host introductions and the geography of parasite taxonomic diversity. J Biogeogr. 2003;30:837–45. doi: 10.1046/j.1365-2699.2003.00868.x. DOI
Gendron AD, Marcogliese DJ, Thomas M. Invasive species are less parasitized than native competitors, but for how long? The case of round goby in the Great Lakes-St, Lawrence Basin. Biol Inv. 2012;14:367–84. doi: 10.1007/s10530-011-0083-y. DOI
Kelly DW, Patterson RA, Townsend CR, Poulin R, Tompkins DM. Parasite spillback. A neglected concept in invasion ecology? Ecology. 2009;90:2047–56. doi: 10.1890/08-1085.1. PubMed DOI
Poulin R, Paterson RA, Townsend CR, Tompkins DM, Kelly DW. Biological invasions and the dynamics of endemic diseases in freshwater ecosystems. Freshw Biol. 2011;56:676–88. doi: 10.1111/j.1365-2427.2010.02425.x. DOI
Keesing F, Holt RD, Ostfeld RS. Effects of species diversity on disease risk. Ecol Let. 2006;9:485–98. doi: 10.1111/j.1461-0248.2006.00885.x. PubMed DOI
Cribb TH, Chisholm LA, Bray RA. Diversity in the Monogenea and Digenea: does lifestyle matter? Int J Parasitol. 2002;32:321–8. doi: 10.1016/S0020-7519(01)00333-2. PubMed DOI
Zander CD, Strohbach U, Groenewold S. The importance of gobies (Gobiidae, Teleostei) as hosts and transmitters of parasites in the SW Baltic. Helgol Meeresunters. 1993;47:81–111. doi: 10.1007/BF02366186. DOI
Dávidová M, Blažek R, Trichkova T, Koutrakis E, Gaygusuz Ö, Ercan E, et al. The role of the European bitterling (Rhodeus amarus, Cyprinidae) in parasite accumulation and transmission in riverine ecosystems. Aquat Ecol. 2011;45:377–87. doi: 10.1007/s10452-011-9361-0. DOI
Kvach Y, Skóra KE. Metazoa parasites of the invasive round goby Apollonia melanostoma (Neogobius melanostomus) (Pallas) (Gobiidae: Osteichthyes) in the Gulf of Gdansk, Baltic Sea, Poland: a comparison with the Black Sea. Parasitol Res. 2006;100:767–74. doi: 10.1007/s00436-006-0311-z. PubMed DOI
Kvach Y, Kornyychuk Y, Mierzejewska K, Rubtsova N, Yurakhno V, Grabowska J, et al. Parasitization of invasive gobiids in the eastern part of the Central trans-European corridor of invasion of Ponto-Caspian hydrobionts. Parasitol Res. 2014;113:1605–24. doi: 10.1007/s00436-014-3791-2. PubMed DOI
Ondračková M, Dávidová M, Blažek R, Gelnar M, Jurajda P. The interaction between an introduced fish host and local parasite fauna: Neogobius kessleri in the middle Danube River. Parasitol Res. 2009;105:201–8. doi: 10.1007/s00436-009-1384-2. PubMed DOI
Ondračková M, Valová Z, Hudcová I, Michálková V, Šimková A, Borcherding J, et al. Temporal effects on host-parasite associations in four naturalized goby species living in sympatry. Hydrobiologia. 2015;746:233–43. doi: 10.1007/s10750-014-1967-5. DOI
Krakau M, Thieltges DW, Reise K. Native parasites adopt introduced bivalves of the North Sea. Biol Inv. 2006;8:919–25. doi: 10.1007/s10530-005-4734-8. DOI
Roche KF, Janáč M, Jurajda P. A review of Gobiid expansion along the Danube-Rhine corridor – geopolitical change as a driver for invasion. Knowl Managt Aquatic Ecosyst. 2013;411:01. doi: 10.1051/kmae/2013066. DOI
Overstreet RM, Curran SS. Superfamily Bucephaloidae Pche, 1907. In: Gibson DI, Jones A, Bray RA, editors. Keys to the Trematoda. London: CABI; 2002. pp. 67–110.
Moravec F. Checklist of the metazoan parasites of fishes of the Czech Republic and the Slovak Republic (1873–2000) Praha: Academia; 2001.
Mühlegger JM, Jirsa F, Konecny R, Frank C. Parasites of Apollonia melanostoma (Pallas 1814) and Neogobius kessleri (Guenther 1861) (Osteichthyes, Gobiidae) from the Danube River in Austria. J Helminthol. 2010;84:87–92. doi: 10.1017/S0022149X09990095. PubMed DOI
Kvach Y, Mierziejewska K. Non-indigenous benthic species as new hosts for Bucephalus polymorphus Baer, 1827 (Digenea: Bucephalidae) in the Vistula River basin, Poland. Knowl Managt Aquatic Ecosyst. 2011;400:02. doi: 10.1051/kmae/2010034. DOI
Naidenova NN. Parasite fauna of gobiid fishes of the Black Sea and Sea of Azov. Kiev: Naukova Dumka; 1974.
Bauer ON. Key to parasites of freshwater fishes of the fauna of the USSR. Part III. Leningrad: Nauka; 1987.
Kakacheva-Avramova D, Margaritov N, Grupcheva G. Limnology of Bulgarian Stretch of the Danube River, BAS. Sofia: Publishing House of the Bulgarian Academy of Sciences; 1978. Fish parasites in the Bulgarian stretch of the Danube River; pp. 250–71.
Francová K, Ondračková M, Polačik M, Jurajda P. Parasite fauna of native and non-native populations of Neogobius melanostomus (Pallas, 1814) (Gobiidae) in the longitudinal profile of the Danube River. J Appl Ichthyol. 2011;27:879–86. doi: 10.1111/j.1439-0426.2010.01582.x. DOI
Ondračková M, Trichkova T, Jurajda P. Present and historical occurrence of metazoan parasites in Neogobius kessleri (Pisces: Gobiidae) in the Bulgarian Section of the Danube River. Acta Zool Bulg. 2006;58:399–406.
Ondračková M, Francová K, Dávidová M, Polačik M, Jurajda P. Condition status and parasite infection of Neogobius kessleri and Neogobius melanostomus (Gobiidae) in their native and non-native area of distribution of the Danube River. Ecol Res. 2010;25:857–66. doi: 10.1007/s11284-010-0716-0. DOI
Ondračková M, Šimková A, Civáňová K, Vyskočilová M, Jurajda P. Parasite diversity and microsatellite variability in native and introduced populations of four Neogobius species (Gobiidae) Parasitology. 2012;139:1493–505. doi: 10.1017/S0031182012000844. PubMed DOI
Kelly DW, Paterson RA, Townsend CR, Poulin R, Tompkins DM. Has the introduction of brown trout altered disease patterns in native New Zealand fish? Freshw Biol. 2009;54:1805–18. doi: 10.1111/j.1365-2427.2009.02228.x. DOI
Yao H, Song J, Liu C, Luo K, Han J, Li Y, et al. Use of ITS2 region as the universal DNA barcode for plants and animals. PLoS One. 2010;5 doi: 10.1371/journal.pone.0013102. PubMed DOI PMC
Shostak AW, Dharampaul S, Belosevic M. Effects of source of metacercariae on experimental infection of Zygocotyle lunata (Digenea: Paramphistomidae) in CD-1 mice. J Parasitol. 1993;79:922–9. doi: 10.2307/3283731. PubMed DOI
Poulin R. Egg production in adult trematodes: adaptation or constraint? Parasitology. 1997;114:195–204. doi: 10.1017/S0031182096008372. PubMed DOI
Karvonen A, Cheng G-H, Seppälä O, Valtonen T. Intestinal distribution and fecundity of two species of Diplostomum parasites in definitive hosts. Parasitology. 2006;132:357–62. doi: 10.1017/S0031182005009091. PubMed DOI
Petkeviciute R, Stunzenas V, Staneviciute G. Differentiation of European freshwater bucephalids (Digenea: Bucephalidae) based on karyotypes and DNA sequences. Syst Parasitol. 2014;87:199–212. doi: 10.1007/s11230-013-9465-0. PubMed DOI
Hartigan A, Fiala I, Dyková I, Jirků M, Okimoto B, Rose K, et al. A suspected parasite spill-back of two novel Myxidium spp. (Myxosporea) causing disease in Australian endemic frogs found in the invasive Cane Toad. PLoS ONE. 2011;6 doi: 10.1371/journal.pone.0018871. PubMed DOI PMC
Mastitsky SE, Veres J. Field evidence for a parasite spillback caused by exotic mollusc Dreissena polymorpha in an invaded lake. Parasitol Res. 2010;106:667–75. doi: 10.1007/s00436-010-1730-4. PubMed DOI
Telfer S, Bown KJ, Sekules R, Begon M, Hayden T, Birtles R. Disruption of a host-parasite system following the introduction of an exotic host species. Parasitology. 2005;130:661–8. doi: 10.1017/S0031182005007250. PubMed DOI
Uvíra V. Slavicka mnohotvara (Dreissena polymorpha) v zatopenych piskovnach a lomech na Morave [Zebra mussel (Dreissena polymorpha) in flooded sandpits and stonepits in the Moravia region] Limnological News. 2009;2:1–5.
Janáč M, Valová Z, Jurajda P. Range expansion and habitat preferences of non-native 0 + tubenose goby (Proterorhinus semilunaris) in two lowland rivers in the Danube basin. Fundam Appl Limnol. 2012;181:73–85. doi: 10.1127/1863-9135/2012/0321. DOI
Koval VP, Pashkevichute AS, Boshko OG, Kovalenko AA, Stavrovskij KB. The fish parasite fauna of the Kachowka Reservoir on the sixteen years of its existence. Visn Kyyivs Univ (Ser Biol). 1973;15:135–8.
Dobson AP. Models for multi-species parasite-host communities. In: Esch GW, Bush AO, Aho JM, editors. Parasite communities: patterns and processes. London: Chapman and Hall; 1990. pp. 261–88.
Thompson HE, Simon TP. Diet shift in round goby, Neogobius melanostomus, based on size, sex, depth, and habitat in the western basin of Lake Erie. J Appl Ichtyol. 2014;30:955–61. doi: 10.1111/jai.12441. DOI
Vašek M, Všetičková L, Roche KF, Jurajda P. Diet of two invading gobiid species (Proterorhinus semilunaris and Neogobius melanostomus) durig the breeding and hatching season: No field evidence of extensive predation on fish eggs and fry. Limnologica. 2014;46:31–6. doi: 10.1016/j.limno.2013.11.003. DOI
Všetičková L, Janáč M, Vašek M, Roche K, Jurajda P. Non-native western tubenose gobies Proterorhinus semilunaris show distinct site, sex and age-related differences in diet. Knowl Managt Aquatic Ecosyst. 2014;414:1–19.
Lambrignos JG. How interactions between ecology and evolution influence contemporary invasion dynamics. Ecology. 2004;85:2061–70. doi: 10.1890/03-8013. DOI
Facon BB, Genton BJ, Skyhoff J, Jarne P, Estoup A, David P. A general eco-evolutionary framework for understanding bioinvasions. Trends Ecol Evol. 2006;21:130–5. doi: 10.1016/j.tree.2005.10.012. PubMed DOI
Fredensborg BL, Poulin R. Larval helminths in intermediate hosts: Does competition early in life determine the fitness of adult parasites? Int J Parasitol. 2005;35:1061–70. doi: 10.1016/j.ijpara.2005.05.005. PubMed DOI
Benesh DP, Hafer N. Growth and ontogeny of the tameworm Schistocephalus solidus in its copepod first host affects performance in its stickleback second intermediate host. Parasit Vect. 2012;5:90. doi: 10.1186/1756-3305-5-90. PubMed DOI PMC
de Lima HL, Stefani LM, de Araújo Peron F, Baldissera MD, Schafer Da Silva A. Pro-inflammatory cytokines in the Serum of silver catfish (Rhamdia quelen) naturally infected by Clinostomum complanatum: a preliminary study. J Parasitol. 2014;100:142–3. doi: 10.1645/13-300.1. PubMed DOI
Poulin R. Evolutionary ecology of parasites. 2. Princeton and Oxford: Princeton University Press; 2007.