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Comparative phylogeography of two monogenean species (Mazocraeidae) on the host of chub mackerel, Scomber japonicus, along the coast of China

Published online by Cambridge University Press:  18 February 2016

SHUAI YAN
Affiliation:
State Key Laboratory of Biocontrol and Center for Parasitic Organisms and Guangdong Provincial Key Laboratory for Improved Variety Reproduction of Aquatic Economic Animals, School of Life Sciences, Sun Yat-sen University, Guangzhou 510275, People's Republic of China
MING WANG
Affiliation:
State Key Laboratory of Biocontrol and Center for Parasitic Organisms and Guangdong Provincial Key Laboratory for Improved Variety Reproduction of Aquatic Economic Animals, School of Life Sciences, Sun Yat-sen University, Guangzhou 510275, People's Republic of China
CHAO-PIN YANG
Affiliation:
State Key Laboratory of Biocontrol and Center for Parasitic Organisms and Guangdong Provincial Key Laboratory for Improved Variety Reproduction of Aquatic Economic Animals, School of Life Sciences, Sun Yat-sen University, Guangzhou 510275, People's Republic of China
TING-TING ZHI
Affiliation:
State Key Laboratory of Biocontrol and Center for Parasitic Organisms and Guangdong Provincial Key Laboratory for Improved Variety Reproduction of Aquatic Economic Animals, School of Life Sciences, Sun Yat-sen University, Guangzhou 510275, People's Republic of China
CHRISTOPHER L. BROWN
Affiliation:
WorldFish, Bangladesh and South Asia, Benani, Dhaka, Bangladesh
TING-BAO YANG*
Affiliation:
State Key Laboratory of Biocontrol and Center for Parasitic Organisms and Guangdong Provincial Key Laboratory for Improved Variety Reproduction of Aquatic Economic Animals, School of Life Sciences, Sun Yat-sen University, Guangzhou 510275, People's Republic of China
*
*Corresponding author: State Key Laboratory of Biocontrol and Center for Parasitic Organisms and Guangdong Provincial Key Laboratory for Improved Variety Reproduction of Aquatic Economic Animals, School of Life Sciences, Sun Yat-sen University, Guangzhou 510275, People's Republic of China. E-mail: lssytb@mail.sysu.edu.cn

Summary

In the present paper, the phylogeographies of two monogenean species, Pseudokuhnia minor and Kuhnia scombri, on the same species of host, Scomber japonicus, were studied. Fragments of the mitochondrial cytochrome c oxidase subunit 1 gene were sequenced for 264 individuals of P. minor and 224 individuals of K. scombri collected from 10 localities along the coast of China. Genetic diversity of K. scombri was higher than that of P. minor, which may imply that P. minor has a lower evolution rate and/or is a younger species. The neighbour-joining (NJ) trees of both parasites were comprised of two clades without association to sample sites, which is the signature of remixing populations following past division. Analyses of molecular variance and pairwise fixation index revealed different genetic structures for the populations of these two closely related species along the coast of China: P. minor without significant genetic structure, while K. scombri has some genetic differentiation. Both neutrality tests and mismatch distribution suggested that the populations of these two species of parasites experienced population expansion in the late Pleistocene era due to the glacial–interglacial cycles induced by climatic oscillations.

Type
Research Article
Copyright
Copyright © Cambridge University Press 2016 

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References

REFERENCES

Avise, J. C. (2000). Phylogeography. The History and Formation of Species. Harvard University Press, Cambridge, MA.Google Scholar
Avise, J. C. (2004). Molecular Markers, Natural History, and Evolution, 2nd Edn. Sinauer Associates, Sunderland, Massachusetts.Google Scholar
Bandelt, H. J., Forster, P. and Röhl, A. (1999). Median-joining networks for inferring intraspecific phylogenies. Molecular Biology and Evolution 16, 3748.Google Scholar
Beebee, T. J. C. and Rowe, G. (2008). An Introduction to Molecular Ecology. Oxford University Press, USA.Google Scholar
Bond, G., Showers, W., Cheseby, M., Lotti, R., Almasi, P., DeMenocal, P., Priore, P., Cullen, H., Hajdas, I. and Bonani, G. (1997). A pervasive Millennial-Scale cycle in north Atlantic holocene and glacial climates. Science 278, 12571266.Google Scholar
Chen, L., Caballero, S., Zhou, K. and Yang, G. (2010). Molecular phylogenetics and population structure of Sousa chinensis in Chinese waters inferred from mitochondrial control region sequences. Biochemical Systematics and Ecology 38, 897905.Google Scholar
Collette, B. B. and Nauen, C. E. (1983). FAO Species Catalogue, vol. 2. Scombrids of the world. An annotated and illustrated catalogue of tunas, mackerels, bonitos and related species known to date. FAO Fisher Synop 125, 137.Google Scholar
Cribb, T. H., Pichelin, S., Dufour, V., Bray, R. A., Chauvet, C., Faliex, E., Galzin, R., Lo, C. M., Lo-Yat, A., Morand, S., Rigby, M. C. and Sasal, P. (2000). Parasites of recruiting coral reef fish larvae in New Caledonia. International Journal for Parasitology 30, 14451451.Google Scholar
Excoffier, L. and Lishcer, H. E. L. (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.Google Scholar
Fu, Y. (1997). Statistical tests of neutrality of mutations against population growth, hitchhiking and background selection. Genetics 147, 915925.Google Scholar
Gannicott, A. M. and Tinsley, R. C. (1998). Larval survival characteristics and behaviour of the gill monogenean Discocotyle sagittata . Parasitology 117, 491498.Google Scholar
Glennon, V., Perkins, E. M., Chisholm, L. A. and Whittington, I. D. (2008). Comparative phylogeography reveals host generalists, specialists and cryptic diversity: hexabothriid, microbothriid and monocotylid monogeneans from rhinobatid rays in southern Australia. International Journal for Parasitology 38, 1599–612.CrossRefGoogle ScholarPubMed
Grant, W. and Bowen, B. W. (1998). Shallow population histories in deep evolutionary lineages of marine fishes: insights from sardines and anchovies and lessons for conservation. Journal of Heredity 89, 415426.Google Scholar
Han, Z., Yanagimoto, T., Zhang, Y. and Gao, T. (2012). Phylogeography study of Ammodytes personatus in Northwestern Pacific: pleistocene isolation, temperature and current conducted secondary contact. PLoS ONE 7, 112.Google Scholar
Harpending, H. C. (1994). Signature of ancient population growth in a low-resolution mitochondrial DNA mismatch distribution. Human Biology 66, 591600.Google Scholar
Hewitt, G. (2000). The genetic legacy of the Quaternary ice ages. Nature 405, 907913.Google Scholar
Huyse, T., Poulin, R. and Théron, A. (2005). Speciation in parasites: a population genetics approach. Trends in Parasitology 21, 469475.Google Scholar
Lambeck, K., Esat, T. M. and Potter, E. (2002). Links between climate and sea levels for the past three million years. Nature 419, 199206.Google Scholar
Li, M., Shi, S. F., Brown, C. L. and Yang, T. B. (2011). Phylogeographical pattern of Mazocraeoides gonialosae (Monogenea, Mazocraeidae) on the dotted gizzard shad, Konosirus punctatus, along the coast of China. International Journal for Parasitology 41, 12631272.Google Scholar
Li, W. H. (1997). Molecular Evolution. Sinauer Associates, Inc., Publishers, Sunderland, Massachusetts, USA.Google Scholar
Liu, J. X., Gao, T. X., Yokogawa, K. and Zhang, Y. P. (2006). Differential population structuring and demographic history of two closely related fish species, Japanese sea bass (Lateolabrax japonicus) and spotted sea bass (Lateolabrax maculatus) in Northwestern Pacific. Molecular Phylogenetics and Evolution 39, 799811.Google Scholar
Lockwood, S. J. (1988). The Mackerel: Its Biology, Assessment and the Management of a Fishery. Fishing News Books, Farnham.Google Scholar
Miura, O., Torchin, M. E., Kuris, A. M., Hechinger, R. F. and Chiba, S. (2006). Introduced cryptic species of parasites exhibit different invasion pathways. Proceedings of the National Academy of Sciences of the United States of America 103, 1981819823.Google Scholar
Nei, M. (1987). Molecular Evolutionary Genetics. Columbia University Press, New York.Google Scholar
Nei, M. and Li, W. H. (1979). Mathematical model for studying genetic variation in terms of restriction endonucleases. Proceedings of the National Academy of Sciences of the United States of America 76, 52695273.CrossRefGoogle ScholarPubMed
Niu, D., Chen, H., Wang, S., Lin, G. and Li, J. (2010). Population genetic structure of Sinonovacula constricta along the coast of China. Chinese Journal of Zoology 45, 1118. (In Chinese with English abstract)Google Scholar
Pariselle, A., Boeger, W. A., Snoeks, J., Bilong-Bilong, C. F., Morand, S. and Vanhove, M. P. (2011). The monogenean parasite fauna of cichlids: a potential tool for host biogeography. International Journal of Evolutionary Biology 2011, 115.Google Scholar
Plaisance, L., Rousset, V., Morand, S. and Littlewood, D. T. J. (2007). Colonization of Pacific islands by parasites of low dispersal ability: phylogeography of two monogenean species parasitizing butterflyfishes in the South Pacific Ocean. Journal of Biogeography 35, 7687.CrossRefGoogle Scholar
Polzin, T. and Daneshmand, S. V. (2003). On Steiner trees and minimum spanning trees in hypergraphs. Operations Research Letters 31, 1220.Google Scholar
Posada, D. and Crandall, K. A. (1998). MODELTEST: testing the model of DNA substitution. Bioinformatics 14, 817818.CrossRefGoogle ScholarPubMed
Ramos-Onsins, S. E. and Rozas, J. (2002). Statistical properties of new neutrality tests against population growth. Molecular Biology and Evolution 19, 20922100.Google Scholar
Raymond, M. and Rousset, F. (1995). An exact test for population differentiation. Evolution 49, 12801283.Google Scholar
Rogers, A. R. (1995). Genetic evidence for a pleistocene population explosion. Evolution 49, 608615.Google Scholar
Rogers, A. R. and Harpending, H. (1992). Population growth makes waves in the distribution of pairwise genetic differences. Molecular Biology and Evolution 9, 552569.Google Scholar
Rohde, K. and Watson, N. (1985). Morphology and geographical variation of Pseudokuhnia minor n.g., N.comb. (Monogenea: Polyopisthocotylea). International Journal for Parasitology 15, 557567.Google Scholar
Ronquist, F., Teslenko, M., van der, M. P., Ayres, D. L., Darling, A., Höhna, S., Larget, B., Liu, L., Suchard, M. A. and Huelsenbeck, J. P. (2012). MrBayes 3.2: efficient Bayesian phylogenetic inference and model choice across a large model space. Systematic Biology 61, 539542.Google Scholar
Saitou, N. and Nei, M. (1987). The neighbor-joining method: a new method for reconstructing phylogenetic trees. Molecular Biology and Evolution 4, 406425.Google Scholar
Shi, S., Li, M., Yan, S., Wang, M., Yang, C. P., Lun, Z. R., Brown, C. L. and Yang, T. B. (2014). Phylogeography and demographic history of Gotocotyla sawara (Monogenea: Gotocotylidae) on Japanese spanish mackerel (Scomberomorus niphonius) along the coast of China. Journal of Parasitology 100, 8592.CrossRefGoogle ScholarPubMed
Slatkin, M. (1993). Isolation by distance in equilibrium and Non-Equilibrium populations. Evolution 47, 264279.Google Scholar
Sproston, N. G. (1945). The genus Kuhnia n.g. (Trematoda: Monogenea) an examination of the value of some specific characters, including factors of relative growth. Parasitology 36, 176190.Google Scholar
Tajima, F. (1983). Evolutionary relationship of DNA sequences in finite populations. Genetics 105, 437460.Google Scholar
Tajima, F. (1989). Statistical method for testing the neutral mutation hypothesis by DNA polymorphism. Genetics 123, 585595.Google Scholar
Tamaki, K. and Honza, E. (1991). Global tectonics and formation of marginal basins: role of the western Pacific. Episodes 224230.Google Scholar
Tamura, K. and Nei, M. (1993). Estimation of the number of nucleotide substitutions in the control region of mitochondrial DNA in humans and chimpanzees. Molecular Biology and Evolution 10, 512526.Google Scholar
Tamura, K., Stecher, G., Peterson, D., Filipski, A. and Kumar, S. (2013). MEGA6: molecular evolutionary genetics analysis version 6.0. Molecular Biology and Evolution 30, 27252729.CrossRefGoogle ScholarPubMed
Wang, C., Li, C. and Li, S. (2008). Mitochondrial DNA-inferred population structure and demographic history of the mitten crab (Eriocheir sensu stricto) found along the coast of mainland China. Molecular Ecology 17, 35153527.Google Scholar
Wang, P. (1999). Response of Western Pacific marginal seas to glacial cycles: paleoceanographic and sedimentological features. Marine Geology 156, 539.Google Scholar
Wang, P. and Sun, X. (1994). Last glacial maximum in China: comparison between land and sea. Catena 23, 341353.Google Scholar
Yan, S., Catanese, G., Brown, C., Wang, M., Yang, C. P. and Yang, T. B. (2015). Phylogeographic study on the chub mackerel (Scomber japonicus) in the Northwestern Pacific indicates the late Pleistocene population isolation. Marine Ecology 36, 753765.CrossRefGoogle Scholar
Zardoya, R., Castilho, R., Grande, C., Favre-Krey, L., Caetano, S., Marcato, S., Krey, G. and Patarnello, T. (2004). Differential population structuring of two closely related fish species, the mackerel (Scomber scombrus) and the chub mackerel (Scomber japonicus), in the Mediterranean Sea. Molecular Ecology 13, 17851798.Google Scholar
Zhang, J., Yang, T. and Liu, L. (2001). Monogeneans of Chinese Marine Fishes. Agriculture Press, Beijing, China (In Chinese).Google Scholar