Literature DB >> 17499102

The biology of gyrodactylid monogeneans: the "Russian-doll killers".

T A Bakke1, J Cable, P D Harris.   

Abstract

This article reviews the history of gyrodactylid research focussing on the unique anatomy, behaviour, ecology and evolution of the viviparous forms while identifying gaps in our knowledge and directions for future research. We provide the first summary of research on the oviparous gyrodactylids from South American catfish, and highlight the plesiomorphic characters shared by gyrodactylids and other primitive monogeneans. Of these, the most important are the crawling, unciliated larva and the spike sensilla of the cephalic lobes. These characters allow gyrodactylids to transfer between hosts at any stage of the life cycle, without a specific transmission stage. We emphasise the importance of progenesis in shaping the evolution of the viviparous genera and discuss the relative extent of progenesis in the different genera. The validity of the familial classification is discussed and we conclude that the most significant division within the family is between the oviparous and the viviparous genera. The older divisions into Isancistrinae and Polyclithrinae should be allowed to lapse. We discuss approaches to the taxonomy of gyrodactylids, and we emphasise the importance of adequate morphological and molecular data in new descriptions. Host specificity patterns in gyrodactylids are discussed extensively and we note the importance of host shifts, revealed by molecular data, in the evolution of gyrodactylids. To date, the most closely related gyrodactylids have not been found on closely related hosts, demonstrating the importance of host shifts in their evolution. The most closely related species pair is that of G. salaris and G. thymalli, and we provide an account of the patterns of evolution taking place in different mitochondrial clades of this species complex. The host specificity of these clades is reviewed, demonstrating that, although each clade has its preferred host, there is a range of specificity to different salmonids, providing opportunities for complex patterns of survival and interbreeding in Scandinavia. At the same time, we identify trends in systematics and phylogeny relevant to the G. salaris epidemics on Atlantic salmon in Norway, which can be applied more generally to parasite epidemiology and evolution. Although much of gyrodactylid research in the last 30 years has been directed towards salmonid parasites, there is great potential in using other experimental systems, such as the gyrodactylids of poeciliids and sticklebacks. We also highlight the role of glacial lakes and modified river systems during the ice ages in gyrodactylid speciation, and suggest that salmon infecting clades of G. salaris first arose from G. thymalli in such lakes, but failed to spread fully across Scandinavia before further dispersal was ended by rising sea levels. This dispersal has been continued by human activity, leading to the appearance of G. salaris as a pathogen in Norway. We review the history and current status of the epidemic, and current strategies for elimination of the parasite from Norway. Finally, we consider opportunities for further spread of the parasite within and beyond Europe.

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Year:  2007        PMID: 17499102     DOI: 10.1016/S0065-308X(06)64003-7

Source DB:  PubMed          Journal:  Adv Parasitol        ISSN: 0065-308X            Impact factor:   3.870


  64 in total

1.  Morphologic and molecular characterization of Gyrodactylus cyclopteri Scyborskaja, 1948, from Cyclopterus lumpus L., 1758.

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Review 2.  Matrotrophy and placentation in invertebrates: a new paradigm.

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Journal:  Biol Rev Camb Philos Soc       Date:  2015-04-29

3.  Experimental evidence that parasites drive eco-evolutionary feedbacks.

Authors:  Franziska S Brunner; Jaime M Anaya-Rojas; Blake Matthews; Christophe Eizaguirre
Journal:  Proc Natl Acad Sci U S A       Date:  2017-03-20       Impact factor: 11.205

4.  Microparasite dispersal in metapopulations: a boon or bane to the host population?

Authors:  Christina P Tadiri; Marilyn E Scott; Gregor F Fussmann
Journal:  Proc Biol Sci       Date:  2018-08-29       Impact factor: 5.349

5.  Species delimitation of Gyrodactylus (Monogenea: Gyrodactylidae) infecting the southernmost cyprinids (Actinopterygii: Cyprinidae) in the New World.

Authors:  Carlos Daniel Pinacho-Pinacho; Miguel Calixto-Rojas; Adriana García-Vásquez; Ismael Guzmán-Valdivieso; Juan J Barrios-Gutiérrez; Miguel Rubio-Godoy
Journal:  Parasitol Res       Date:  2021-01-06       Impact factor: 2.289

6.  A scanning electron microscope technique for studying the sclerites of Cichlidogyrus.

Authors:  Wouter Fannes; Maarten P M Vanhove; Tine Huyse; Giuseppe Paladini
Journal:  Parasitol Res       Date:  2015-04-02       Impact factor: 2.289

7.  Supplemental diagnosis of Gyrodactylus nebulosus Kritsky and Mizelle, 1968 (Monogenea) on 0+ age Ameiurus nebulosus (Siluriformes) considered for commercial grow-out in Southwestern Nova Scotia, Canada.

Authors:  Eric Leis; Roland Leblanc; Russell Easy; Hillary Dort; David Cone
Journal:  Parasitol Res       Date:  2020-02-04       Impact factor: 2.289

8.  Does moving up a food chain increase aggregation in parasites?

Authors:  R J G Lester; R McVinish
Journal:  J R Soc Interface       Date:  2016-05       Impact factor: 4.118

9.  The Gyrodactylus (Monogenea, Gyrodactylidae) parasite fauna of freshwater sand gobies (Teleostei, Gobioidei) in their centre of endemism, with description of seven new species.

Authors:  Maarten P M Vanhove; Alcibiades N Economou; Stamatis Zogaris; Sofia Giakoumi; Davor Zanella; Filip A M Volckaert; Tine Huyse
Journal:  Parasitol Res       Date:  2013-11-28       Impact factor: 2.289

10.  Species of Gyrodactylus von Nordmann, 1832 (Platyhelminthes: Monogenea) from cichlids from Zambezi and Limpopo river basins in Zimbabwe and South Africa: evidence for unexplored species richness.

Authors:  Petra Zahradníčková; Maxwell Barson; Wilmien J Luus-Powell; Iva Přikrylová
Journal:  Syst Parasitol       Date:  2016-08-13       Impact factor: 1.431

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