Publication: Multiplex PCR assay for discrimination of Centrocestus caninus and Stellantchasmus falcatus
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Issued Date
2017
Resource Type
File Type
application/pdf
ISSN
22211691
Other identifier(s)
2-s2.0-85008146960
Rights Holder(s)
Scopus
Bibliographic Citation
Asian Pacific Journal of Tropical Biomedicine. Vol 7, No.2 (2017), p.103-106
Suggested Citation
Chontananarth T. Multiplex PCR assay for discrimination of Centrocestus caninus and Stellantchasmus falcatus. Asian Pacific Journal of Tropical Biomedicine. Vol 7, No.2 (2017), p.103-106. doi:10.1016/j.apjtb.2016.11.018 Retrieved from: https://hdl.handle.net/20.500.14740/4256
Author(s)
Abstract
Objective To develop the multiplex PCR method based on the internal transcribed spacer 2 to discriminate the intestinal trematodes, Centrocestus caninus (C. caninus), and Stellantchasmus falcatus (S. falcatus). Methods Four species of heterophyid trematodes including C. caninus, S. falcatus, Haplorchis taichui and Haplorchoides sp. were amplified and the specific primer was designed based on the internal transcribed spacer 2 region. Two specific primers were used to validate the optimized PCR conditions: the specificity test and the sensitivity test. Results Both of these specific primers confirmed the specificity through multiplex PCR reaction which generated both PCR products (231 and 137 bp) in the mixed DNA template of C. caninus and S. falcatus with no cross-reaction with other heterophyid trematodes. The optimum annealing temperature of both primers was 54–59 °C. The sensitivity test used the two-fold serial dilution DNA template, which was concentrated between 10 and 0.312 5 ng/μL. The lowest concentration of the DNA template of this multiplex PCR was 2.5 ng/μL. Conclusions The technique described here proved to be a species-specific technique and was found to be a rapid method for the diagnosis of C. caninus and S. falcatus in terms of the larval and adult stages in intermediate and/or definitive hosts in the endemic area. © 2017 Hainan Medical University