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PCR-based molecular discrimination between Maritrema eroliae and Probolocoryphe uca (Digenea: Microphallidae) in Kuwait Bay

Published online by Cambridge University Press:  07 January 2013

W.Y. Al-Kandari*
Affiliation:
Department of Biological Sciences, Faculty of Science, Kuwait University
S.A. Al-Bustan
Affiliation:
Department of Biological Sciences, Faculty of Science, Kuwait University
M. Alnaqeeb
Affiliation:
Department of Biological Sciences, Faculty of Science, Kuwait University
A.M. Isaac
Affiliation:
Department of Biological Sciences, Faculty of Science, Kuwait University
*
*Fax: (+965) 24847054 E-mail: [email protected]

Abstract

Microphallid trematodes are common parasites in marine snails and crustacean hosts at Kuwait Bay. The larval stages of two microphallids, Maritrema eroliae and Probolocoryphe uca, are difficult to differentiate morphologically. In this study, two PCR-based techniques were established for quick and accurate discrimination between the larval stages of the two microphallid species, employing restriction fragment length polymorphism (PCR-RFLP) and species-specific primers. Both techniques utilized nucleotide differences in the second internal transcribed region (ITS2) of the ribosomal DNA (rDNA) in the two species. For the PCR-RFLP technique, restriction enzyme AvaII was selected and it generated different restriction profiles among the two microphallids. In addition, species-specific primers were prepared for each microphallid species that amplified distinctive fragments. Both techniques showed that the larval stages of the two microphallid species can be identified accurately. However, direct PCR amplification using species-specific primers was more advantageous than the PCR-RFLP technique since it allowed rapid and specific discrimination between the two species. This technique provides a useful tool that can be used in future studies for the study of the distribution of microphallid species and their definitive hosts at different localities of Kuwait Bay.

Type
Research Papers
Copyright
Copyright © Cambridge University Press 2013 

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References

Abdul-Salam, J. & Sreelatha, B.S. (1998) A list of larval digenetic trematodes parasitizing some marine invertebrates of Kuwait Bay. Kuwait Journal of Science and Engineering 25, 409434.Google Scholar
Abdul-Salam, J. & Sreelatha, B.S. (2000) Surface morphology of Probolocoryphe uca (Sarkisian 1957) (Digenea: Microphallidae) from Kuwait Bay. Systematic Parasitology 46, 209214.Google Scholar
Abdul-Salam, J., Sreelatha, B.S. & Ashkanani, H. (1994) Seasonal prevalence of trematode cercariae in Clypeomorus bifasciata (Gastropoda: Prosobranchia) in Kuwait Bay. Folia Parasitologica 41, 247252.Google Scholar
Abdul-Salam, J., Sreelatha, B.S. & Al-Kandari, W. (1997) Temporal variations in the infection of population of Clypeomorus bifasciata (Gastropoda: Prosobranchia) by a digenean microphallid larva in Kuwait Bay. Journal of Helminthology 71, 17.Google Scholar
Al-Kandari, M.A., Abdul-Salam, J., Moussa, M.A. & Sreelatha, B.S. (2007) Seasonal dynamics of the cercarial and metacercarial stages of the microphallid trematode Maritrema eroliae (Digenea: Microphallidae). Acta Zoologica Sinica 53, 463469.Google Scholar
Al-Kandari, W. & Al-Bustan, S. (2010) Molecular identification of Probolocoryphe uca (Sarkisian, 1957; Digenea: Microphallidae) from Kuwait Bay using ITS1 and ITS2 sequences. Parasitology Research 106, 11891195.Google Scholar
Al-Kandari, W.Y., Abdul-Salam, J. & Meakins, R. (2000) Temporal variations in the infection of a population of Cerithidea cingulata by larval trematodes in Kuwait Bay. Journal of Helminthology 74, 1722.Google Scholar
Al-Kandari, W., Al-Bustan, S. & Alnaqeeb, M. (2011) Ribosomal DNA sequence characterization of Maritrema cf. eroliae Yamaguti, 1939 (Digenea: Microphallidae) and its life cycle. Journal of Parasitology 97, 10671074.Google Scholar
Barber, K.E., Mkoji, G.M. & Loker, E.S. (2000) PCR-RFLP analysis of the ITS2 region to identify Schistosoma haematobium and S. bovis from Kenya. American Journal of Tropical Medicine and Hygiene 62, 434440.Google Scholar
Després, L., Imbert-Establet, D., Combes, C. & Bonhomme, F. (1992) Molecular evidence linking hominid evolution to recent radiation of schistosomes (Platyhelminthes: Trematoda). Molecular Phylogenetics and Evolution 1, 295304.Google Scholar
Francisco, C.J., Almeida, A., Castro, A.M. & Santos, M.J. (2010) Development of PCR-RFLP marker to genetically distinguish Prosorhynchus crucibulum and Prosorhynchus aculeatus. Parasitology International 59, 4043.Google Scholar
Fredensborg, B.L. & Poulin, R. (2006) Parasitism shaping host life-history evolution: adaptive responses in a marine gastropod to infection by trematodes. Journal of Animal Ecology 75, 4453.Google Scholar
Fredensborg, B.L., Mouritsen, K.N. & Poulin, R. (2005) Impact of trematodes on host survival and population density in the intertidal gastropod Zeacumantus subcarinatus. Marine Ecology Progress Series 290, 253265.Google Scholar
Hust, J., Frydenberg, J., Sauriau, P., Le Gall, P., Mouritsen, K. & Jensen, K. (2004) Use of ITS rDNA for discriminating of larval stages of two microphallid (Digenea) species using Hydrobia ulvae (Pennant, 1777) and Corophium volutator (Pallas, 1766) as intermediate hosts. Parasitology Research 93, 304310.Google Scholar
Ichikawa, M. & Itagaki, T. (2010) Discrimination of the ITS1 types of Fasciola spp. based on a PCR-RFLP method. Parasitology Research 106, 757761.CrossRefGoogle ScholarPubMed
Jokela, J. & Lively, C.M. (1995) Spatial variation in infection by digenetic trematodes in a population of freshwater snails (Potamopyrgus antipodarum). Oecologia 103, 509517.Google Scholar
Kang, S., Sultana, T., Loktev, V., Wongratanacheewin, S., Sohn, W., Eom, K. & Park, J. (2008) Molecular identification and phylogenetic analysis of nuclear rDNA sequences among three opisthorchid liver fluke species (Opisthorchiidae: Trematoda). Parasitology International 57, 191197.Google Scholar
Kralova-Hromadova, I., Spakulova, M., Horackova, E., Turcekova, L., Novobilsky, A., Beck, R., Koudela, B., Marinculic, A., Rajsky, D. & Pybus, M. (2008) Sequence analysis of ribosomal and mitochondrial genes of the giant liver fluke Fascioloides magna (Trematoda: Fasciolidae): intraspecific variation and differentiation from Fasciola hepatica. Journal of Parasitology 94, 5867.Google Scholar
Madhavi, R., Umadevi, K. & Swarnakumari, V.G. (1997) Community structure of larval trematode fauna of the snail Thiara tuberculata from a freshwater stream at Visakhapatnam Andhra Pradesh. Current Science 72, 582585.Google Scholar
Morgan, J.A. & Blair, D. (1995) Nuclear rDNA ITS sequence variation in the trematode genus Echinostoma: an aid to establishing relationships within the 37-collar spine group. Parasitology 111, 609615.CrossRefGoogle Scholar
Rice, P., Longden, I. & Bleasby, A. (2000) EMBOSS: The European molecular biology open software suite. Trends in Genetics 16, 276277.CrossRefGoogle ScholarPubMed
Rozen, S. & Skaletsky, H.J. (2000) Primer3 on the WWW for general users and for biologist programmers. pp. 365386in Krawetz, S. & Minsener, S. (Eds) Bioinformatics methods and protocols: Methods in molecular biology. Totowa, Humana Press.Google Scholar
Sugiyama, H., Morishima, Y., Kameoka, Y. & Kawanaka, M. (2002) Polymerase chain reaction (PCR)-based molecular discrimination between Paragonimus westermani and P. miyazakii at the metacercarial stage. Molecular and Cellular Probes 16, 231236.Google Scholar
Thompson, J., Higgins, D.G. & Gibson, T. (1994) CLUSTAL W: improving the sensitivity of progressive multiple sequence alignment through sequence weighting, positions-specific gap penalties and weight matrix choice. Nucleic Acids Research 22, 46734680.CrossRefGoogle ScholarPubMed
Vincze, T., Posfai, J. & Roberts, R.J. (2003) NEBcutter: a program to cleave DNA with restriction enzymes. Nucleic Acids Research 31, 36883691.Google Scholar