Genetic diversity and relatedness of Fasciola spp. isolates from different hosts and geographic regions revealed by analysis of mitochondrial DNA sequences

Veterinary Parasitology

Volumn 181, Issue 2-4, 2011, Pages 329-334

  Ai, L ^a,b,c,d   Weng, Y B ^c   Elsheikha, H M ^e   Zhao, G H ^f   Alasaad, S ^g   Chen, J X ^d   Li, J ^c   Li, H L ^c   Wang, C R ^a   Chen, M X ^d   Lin, R Q ^b,c   Zhu, X Q ^a,b  

^a HEILONGJIANG BAYI AGRICULTURAL UNIVERSITY   (China)

^b INSTITUTE OF PLANT PROTECTION   (China)

^c SOUTH CHINA AGRICULTURAL UNIVERSITY   (China)

^d CHINESE CENTER FOR DISEASE CONTROL AND PREVENTION   (China)

^e UNIVERSITY OF NOTTINGHAM   (United Kingdom)

^f NORTHWEST A F UNIVERSITY   (China)

^g DEPARTMENT OF CONSERVATION BIOLOGY   (Spain)

Author keywords

Cytochrome c oxidase subunit 1 (cox1); Fasciola gigantica; Fasciola hepatica; Mitochondrial DNA (mtDNA); NADH dehydrogenase subunits 4 (nad4); NADH dehydrogenase subunits 5 (nad5); Phylogenetic analysis; The intermediate Fasciola

Indexed keywords

CYTOCHROME C OXIDASE; MITOCHONDRIAL DNA; PCOX1 PROTEIN; PNAD4 PROTEIN; PNAD5 PROTEIN; REDUCED NICOTINAMIDE ADENINE DINUCLEOTIDE DEHYDROGENASE; UNCLASSIFIED DRUG;

ARTICLE; CHINA; CONTROLLED STUDY; DNA DETERMINATION; DNA SEQUENCE; ENZYME SUBUNIT; FASCIOLA; FASCIOLA GIGANTICA; FASCIOLA HEPATICA; FRANCE; GENETIC VARIABILITY; GEOGRAPHY; HOST; MOLECULAR PHYLOGENY; NIGER; NONHUMAN; NUCLEOTIDE SEQUENCE; SEQUENCE HOMOLOGY; SPAIN; SPECIES DIFFERENCE; UNITED STATES;

ANIMALS; DNA, MITOCHONDRIAL; ELECTRON TRANSPORT COMPLEX IV; FASCIOLA; FASCIOLIASIS; GENETIC VARIATION; HOST-PARASITE INTERACTIONS; MAMMALS; NADH DEHYDROGENASE; PHYLOGENY; PROTEIN SUBUNITS; WORLD HEALTH;

FASCIOLA; FASCIOLA GIGANTICA; FASCIOLA HEPATICA;

EID: 80052539618     PISSN: 03044017     EISSN: 18732550     Source Type: Journal    
DOI: 10.1016/j.vetpar.2011.03.057     Document Type: Article

References (31)

1. Adlard R.D., Barker S.C., Blair D., Cribb T.H. Comparison of the second internal transcribed spacer (ribosomal DNA) from populations and species of Fasciolidae (Digenea). Int. J. Parasitol. 1993, 23:423-425.
2. Ai L., Dong S.J., Zhang W.Y., Elsheikha H.M., Mahmmod Y.S., Lin R.Q., Yuan Z.G., Shi Y.L., Huang W.Y., Zhu X.Q. Specific PCR-based assays for the identification of Fasciola species: their development, evaluation and potential usefulness in prevalence surveys. Ann. Trop. Med. Parasitol. 2010, 104:65-72.
3. Ai L., Li C., Elsheikha H.M., Hong S.J., Chen J.X., Chen S.H., Li X., Cai X.Q., Chen M.X., Zhu X.Q. Rapid identification and differentiation of Fasciola hepatica and Fasciola gigantica by a loop-mediated isothermal amplification (LAMP) assay. Vet. Parasitol. 2010, 174:228-233.
4. Ali H., Ai L., Song H.Q., Ali S., Lin R.Q., Seyni B., Issa G., Zhu X.Q. Genetic characterisation of Fasciola samples from different host species and geographical localities revealed the existence of F. hepatica and F. gigantica in Niger. Parasitol. Res. 2008, 102:1021-1024.
5. Ashrafi K., Valero M.A., Panova M., Periago M.V., Massoud J., Mas-Coma S. Phenotypic analysis of adults of Fasciola hepatica, Fasciola gigantica and intermediate forms from the endemic region of Gilan. Iran. Parasitol. Int. 2006, 55:249-260.
6. Bowles J., Blair D., McManus D.P. Genetic variants within the genus Echinococcus identified by mitochondrial DNA sequencing. Mol. Biochem. Parasitol. 1992, 54:165-173.
7. Chilton N.B., Gasser R.B., Beveridge I. Differences in a ribosomal DNA sequence of morphologically indistinguishable species within the Hypodontus macropi complex (Nematoda: Strongyloidea). Int. J. Parasitol. 1995, 25:647-651.
8. Gasser R.B. PCR-based technology in veterinary parasitology. Vet. Parasitol. 1999, 84:229-258.
9. Huang W.Y., He B., Wang C.R., Zhu X.Q. Characterisation of Fasciola species from Mainland China by ITS-2 ribosomal DNA sequence. Vet. Parasitol. 2004, 120:75-83.
10. Hurtrez-Bousses S., Durand P., Jabbour-Zahab R., Guegan J.F., Meunier C., Bargues M.D., Mas-Coma S., Renaud F. Isolation and characterisation of microsatellite markers in the liver fluke (Fasciola hepatica). Mol. Ecol. Notes 2004, 4:689-690.
11. Ichikawa M., Itagaki T. Discrimination of the ITS1 types of Fasciola spp. based on a PCR-RFLP method. Parasitol. Res. 2010, 106:757-761.
12. Itagaki T., Kikawa M., Terasaki K., Shibahara T., Fukuda K. Molecular characterization of parthenogenic Fasciola sp. in Korea on the basis of DNA sequences of ribosomal ITS1 and mitochondrial NDI gene. J. Vet. Med. Sci. 2005, 67:1115-1118.
13. Itagaki T., Kikawa M., Sakaguchi K., Shimo J., Terasaki K., Shibahara T., Fukuda K. Genetic characterization of parthenogenic Fasciola sp. in Japan on the basis of the sequences of ribosomal and mitochondrial DNA. Parasitology 2005, 131:679-685.
14. Itagaki T., Sakaguchi K., Terasaki K., Sasaki O., Yoshihara S., Van Dung T. Occurrence of spermic diploid and aspermic triploid forms of Fasciola in Vietnam and their molecular characterization based on nuclear and mitochondrial DNA. Parasitol. Int. 2009, 58:81-85.
15. Kendall S.B. Relationships between the species of Fasciola and their molluscan hosts. Adv. Parasitol. 1965, 3:59-98.
16. Le T.H., De N.V., Agatsuma T., Thi Nguyen T.G., Nguyen Q.D., McManus D.P., Blair D. Human fascioliasis and the presence of hybrid/introgressed forms of Fasciola hepatica and Fasciola gigantica in Vietnam. Int. J. Parasitol. 2008, 38:725-730.
17. Mas-Coma S., Funatsu I.R., Bargues M.D. Fasciola hepatica and lymnaeid snails occurring at a very high altitude in South America. Parasitology 2001, 123:S115-S127.
18. Mas-Coma S., Bargues M.D., Valero M.A. Fascioliasis and other plant-borne trematode zoonoses. Int. J. Parasitol. 2005, 35:1255-1278.
19. Mera y Sierra R., Artigas P., Cuervo P., Deis E., Sidoti L., Mas-Coma S., Bargues M.D. Fascioliasis transmission by Lymnaea neotropica confirmed by nuclear rDNA and mtDNA sequencing in Argentina. Vet. Parasitol. 2009, 166:73-79.
20. Nguyen T.G., Van De N., Vercruysse J., Dorny P., Le T.H. Genotypic characterization and species identification of Fasciola spp. with implications regarding the isolates infecting goats in Vietnam. Exp. Parasitol. 2009, 123:354-361.
21. Page R.D. TREEVIEW: an application to display phylogenetic trees on personal computers. Comput. Appl. Biosci. 1996, 12:357-358.
22. Semyenova S.K., Morozova E.V., Chrisanfova G.C., Asatrian A.M., Movsessian S.O., Ryskov A.P. RAPD variability and genetic diversity in two populations of the liver fluke, Fasciola hepatica. Acta Parasitol. 2003, 48:125-130.
23. Semyenova S.K., Morozova E.V., Chrisanfova G.G., Gorokhov V.V., Arkhipov I.A., Moskvin A.S., Movsessyan S.O., Ryskov A.P. Genetic differentiation in eastern European and western Asian populations of the liver fluke. Fasciola hepatica, as revealed by mitochondrial nad1 and cox1 genes. J. Parasitol. 2006, 92:525-530.
24. Spithill T.W., Dalton J.P. Progress in development of liver fluke vaccines. Parasitol. Today 1998, 14:224-228.
25. Strimmer K., von Haeseler A. Quartet puzzling: a quartet maximum likelihood method for reconstructing tree topologies. Mol. Biol. Evol. 1996, 13:964-969.
26. Swofford D.L. PAUP*: Phylogenetic Analysis Using Parsimony (and other Methods) 2002, Sinauer Associates, Sunderland, MA.
27. Thompson J.D., Gibson T.J., Plewniak F., Jeanmougin F., Higgins D.G. The Clustal X windows interface: flexible strategies for multiple sequence alignment aided by quality analysis tools. Nucl. Acids Res. 1997, 24:4876-4882.
28. Walker S.M., Prodöhl P.A., Fletcher H.L., Hanna R.E., Kantzoura V., Hoey E.M., Trudgett A. Evidence for multiple mitochondrial lineages of Fasciola hepatica (liver fluke) within infrapopulations from cattle and sheep. Parasitol. Res. 2007, 101:117-125.
29. Yamaguti S. Systema Helminthum, Vol. I. The Digenetic Trematodes of Vertebrates 1958, Interscience Publishers, Inc., New York.
30. Zarowiecki M.Z., Huyse T., Littlewood D.T. Making the most of mitochondrial genomes-markers for phylogeny, molecular ecology and barcodes in Schistosoma (Platyhelminthes: Digenea). Int. J. Parasitol. 2007, 37:1401-1418.
31. Zhao G.H., Mo X.H., Zou F.C., Li J., Weng Y.B., Lin R.Q., Xia C.M., Zhu X.Q. Genetic variability among Schistosoma japonicum isolates from different endemic regions in China revealed by sequences of three mitochondrial DNA genes. Vet. Parasitol. 2009, 162:67-74.