Hostname: page-component-78c5997874-dh8gc Total loading time: 0 Render date: 2024-11-19T11:42:20.388Z Has data issue: false hasContentIssue false

Vicariance in a generalist fish parasite driven by climate and salinity tolerance of hosts

Published online by Cambridge University Press:  10 September 2020

D. Andreou*
Affiliation:
Department of Life and Environmental Sciences, Faculty of Science and Technology, Bournemouth University, Poole, Dorset, BH12 5BB, UK
C.M. Antognazza
Affiliation:
Department of Life and Environmental Sciences, Faculty of Science and Technology, Bournemouth University, Poole, Dorset, BH12 5BB, UK
C.F. Williams
Affiliation:
National Fisheries Services, Environment Agency, PE28 4NE, Brampton, Cambridgeshire, UK
H. Bradley
Affiliation:
National Fisheries Services, Environment Agency, PE28 4NE, Brampton, Cambridgeshire, UK
A.J. Reading
Affiliation:
National Fisheries Services, Environment Agency, PE28 4NE, Brampton, Cambridgeshire, UK
E.A. Hardouin
Affiliation:
Department of Life and Environmental Sciences, Faculty of Science and Technology, Bournemouth University, Poole, Dorset, BH12 5BB, UK
J.R. Stewart
Affiliation:
Department of Life and Environmental Sciences, Faculty of Science and Technology, Bournemouth University, Poole, Dorset, BH12 5BB, UK
D. Sheath
Affiliation:
Department of Life and Environmental Sciences, Faculty of Science and Technology, Bournemouth University, Poole, Dorset, BH12 5BB, UK
A. Galligar
Affiliation:
Department of Life and Environmental Sciences, Faculty of Science and Technology, Bournemouth University, Poole, Dorset, BH12 5BB, UK
E. Johnson
Affiliation:
Department of Life and Environmental Sciences, Faculty of Science and Technology, Bournemouth University, Poole, Dorset, BH12 5BB, UK
J.R. Britton
Affiliation:
Department of Life and Environmental Sciences, Faculty of Science and Technology, Bournemouth University, Poole, Dorset, BH12 5BB, UK
*
Author for correspondence: D. Andreou, E-mail: dandreou@bournemouth.ac.uk

Abstract

Acanthocephalans are parasites with complex lifecycles that are important components of aquatic systems and are often model species for parasite-mediated host manipulation. Genetic characterization has recently resurrected Pomphorhynchus tereticollis as a distinct species from Pomphorhynchus laevis, with potential implications for fisheries management and host manipulation research. Morphological and molecular examinations of parasites from 7 English rivers across 9 fish species revealed that P. tereticollis was the only Pomphorhynchus parasite present in Britain, rather than P. laevis as previously recorded. Molecular analyses included two non-overlapping regions of the mitochondrial gene – cytochrome oxidase and generated 62 sequences for the shorter fragment (295 bp) and 74 for the larger fragment (583 bp). These were combined with 61 and 13 sequences respectively, from Genbank. A phylogenetic analysis using the two genetic regions and all the DNA sequences available for P. tereticollis identified two distinct genetic lineages in Britain. One lineage, possibly associated with cold water tolerant fish, potentially spread to the northern parts of Britain from the Baltic region via a northern route across the estuarine area of what is now the North Sea during the last Glaciation. The other lineage, associated with temperate freshwater fish, may have arrived later via the Rhine/Thames fluvial connection during the last glaciation or early Holocene when sea levels were low. These results raise important questions on this generalist parasite and its variously environmentally adapted hosts, and especially in relation to the consequences for parasite vicariance.

Type
Research Article
Copyright
Copyright © The Author(s), 2020. Published by Cambridge University Press

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

Bernatchez, L (2001) The evolutionary history of brown trout (Salmo Trutta L.) inferred from phylogeographic, nested clade, and mismatch analyses of mitochondrial DNA variation. Evolution 55, 351379.CrossRefGoogle ScholarPubMed
Bombarova, M, Marec, F, Nguyen, P and Spakulova, M (2007) Divergent location of ribosomal genes in chromosomes of fish thorny-headed worms, Pomphorhynchus laevis And Pomphorhynchus Tereticollis (Acanthocephala). Genetica 131, 141149.CrossRefGoogle Scholar
Brace, S, Ruddy, M, Miller, R, Schreve, DC, Stewart, JR and Barnes, I (2016) The colonization history of British water vole (Arvicola amphibius (Linnaeus, 1758)): origins and development of the Celtic fringe. Proceedings of the Royal Society B-Biological Sciences 283, 20160130.CrossRefGoogle ScholarPubMed
Darriba, D, Taboada, GL, Doallo, R and Posada, D (2012) Jmodeltest 2: more models, new heuristics and parallel computing. Nature Methods 9, 772772.CrossRefGoogle ScholarPubMed
Ersmark, E, Baryshnikov, G, Higham, T, Argant, A, Castanos, P, Doppes, D, Gasparik, M, Germonpre, M, Liden, K, Lipecki, G, Marciszak, A, Miller, R, Moreno-Garcia, M, Pacher, M, Robu, M, Rodriguez-Varela, R, Guerra, MR, Sabol, M, Spassov, N, Stora, J, Valdiosera, C, Villaluenga, A, Stewart, JR and Dalen, L (2019) Genetic turnovers and northern survival during the last glacial maximum in European brown bears. Ecology and Evolution 9, 58915905.CrossRefGoogle ScholarPubMed
Evans, DW, Matthews, MA and McClintock, CA (2001) First record of Pomphorhynchus laevis (Acanthocephala) in fishes from Northern Ireland. Journal of Fish Biology 59, 166168.CrossRefGoogle Scholar
Excoffier, L and Lischer, HE (2010) Arlequin suite ver 3.5: a new series of programs to perform population genetics analyses under Linux and Windows. Molecular Ecology Resources 10, 564567.CrossRefGoogle ScholarPubMed
Fayard, M, Francois-Xavier, DM, Wattier, R and Perrot-Minnot, MJ (2020) Magnitude and direction of the parasite-induced phenotypic alterations: a meta-analysis in acanthocephalans. Biological Reviews 95, 12331251.Google ScholarPubMed
Graham, RW and Lundelius, EL (1984) Coevolutionary disequilibrium and pleistocene extinctions. In Martin, PS and Klein, RG (eds), Quaternary Extinctions: A Prehistoric Revolution. Tuscon: University of Arizona Press 223-249.Google Scholar
Hall, TA (1999) Bioedit: a user-friendly biological sequence alignment editor and analysis program for Windows 95/98/NT. Nucleic Acids Symposium 41, 9598.Google Scholar
Hanfling, B, Hellemans, B, Volckaert, FAM and Carvalho, GR (2002) Late glacial history of the cold-adapted freshwater fish Cottus Gobio, revealed by microsatellites. Molecular Ecology 11, 17171729.CrossRefGoogle ScholarPubMed
Kennedy, CR (2006) Ecology of the Acanthocephala. UK: Cambridge University Press.CrossRefGoogle Scholar
Kennedy, CR and Rumpus, A (1977) Long-term changes in size of Pomphorhynchus laevis (Acanthocephala) populations in river Avon. Journal of Fish Biology 10, 3542.CrossRefGoogle Scholar
Kennedy, CR, Bates, RM and Brown, AF (1989) Discontinuous distributions of the fish Acanthocephalans Pomphorhynchus laevis And Acanthocephalus Anguilae In Britain and Ireland- An hypothesis. Journal of Fish Biology 34, 607619.CrossRefGoogle Scholar
Kral'ova-Hromadova, I, Tietz, DF, Shinn, AP and Spakulova, M (2003) ITS rDNA sequences of Pomphorhynchus laevis (Zoega in Muller, 1776) and P-lucyi Williams & Rogers, 1984 (Acanthocephala: Palaeacanthocephala). Systematic Parasitology 56, 141145.CrossRefGoogle Scholar
Lefevre, T, Lebarbenchon, C, Gauthier-Clerc, M, Misse, D, Poulin, R and Thomas, F (2009) The ecological significance of manipulative parasites. Trends in Ecology & Evolution 24, 4148.CrossRefGoogle ScholarPubMed
Leigh, JW and Bryant, D (2015) POPART: full-feature software for haplotype network construction. Methods in Ecology and Evolution 6, 11101116.CrossRefGoogle Scholar
Librado, P and Rozas, J (2009) DnaSP v5: a software for comprehensive analysis of DNA polymorphism data. Bioinformatics (Oxford, England) 25, 14511452.CrossRefGoogle ScholarPubMed
O'mahony, EM, Bradley, DG, Kennedy, CR and Holland, CV (2004) Evidence for the hypothesis of strain formation in Pomphorhynchus laevis (Acanthocephala): an investigation using mitochondrial DNA sequences. Parasitology 129, 341347.CrossRefGoogle ScholarPubMed
Pedreschi, D, Garcia-Rodriguez, O, Yannic, G, Cantarello, E, Diaz, A, Golicher, D, Korstjens, AH, Heckel, G, Searle, JB, Gillingham, P, Hardouin, EA and Stewart, JR (2019) Challenging the European southern refugium hypothesis: species-specific structures versus general patterns of genetic diversity and differentiation among small mammals. Global Ecology and Biogeography 28, 262274.CrossRefGoogle Scholar
Perrot-Minnot, MJ (2004) Larval morphology, genetic divergence, and contrasting levels of host manipulation between forms of Pomphorhynchus laevis (Acanthocephala). International Journal for Parasitology 34, 4554.CrossRefGoogle Scholar
Perrot-Minnot, MJ, Spakulova, M, Wattier, R, Kotlik, P, Dusen, S, Aydogdu, A and Tougard, C (2018) Contrasting phylogeography of two Western Palaearctic fish parasites despite similar life cycles. Journal of Biogeography 45, 101115.CrossRefGoogle Scholar
Reier, S, Sattmann, H, Schwaha, T, Harl, J, Konecny, R and Haring, E (2019) An integrative taxonomic approach to reveal the status of the genus Pomphorhynchus Monticelli, 1905 (Acanthocephala: Pomphorhynchidae) in Austria. International Journal for Parasitology: Parasites and Wildlife 8, 145155.Google Scholar
Ronquist, F, Teslenko, M, Van Der Mark, P, Ayres, DL, Darling, A, Hohna, S, Larget, B, Liu, L, Suchard, MA and Huelsenbeck, JP (2012) Mrbayes 3.2: efficient Bayesian phylogenetic inference and model choice across a large model space. Systematic Biology 61, 539542.CrossRefGoogle ScholarPubMed
Schlutter, D (2000) The Ecology of Adaptive Radiation. Oxford: OUP.Google Scholar
Schneider, CA, Rasband, WS and Eliceiri, KW (2012) NIH Image to ImageJ: 25 years of image analysis. Nature Methods 9, 671675.CrossRefGoogle ScholarPubMed
Sheath, DJ, Dick, JTA, Dickey, JWE, Guo, ZQ, Andreou, D and Britton, JR (2018) Winning the arms race: host – parasite shared evolutionary history reduces infection risks in fish final hosts. Biology Letters 14, 20180363.CrossRefGoogle ScholarPubMed
Spakulova, M, Perrot-Minnot, MJ and Neuhaus, B (2011) Resurrection of Pomphorhynchus Tereticollis (Rudolphi, 1809) (Acanthocephala: Pomphorhynchidae) based on new morphological and molecular data. Helminthologia 48, 268277.CrossRefGoogle Scholar
Sturt, F, Garrow, D and Bradley, S (2013) New models of North West European Holocene palaeogeography and inundation. Journal of Archaeological Science 40, 39633976.CrossRefGoogle Scholar
Supplementary material: File

Andreou et al. supplementary material

Andreou et al. supplementary material 1

Download Andreou et al. supplementary material(File)
File 20.1 KB
Supplementary material: PDF

Andreou et al. supplementary material

Andreou et al. supplementary material 2

Download Andreou et al. supplementary material(PDF)
PDF 9.1 MB