Molecular differentiation of Schistosoma japonicum and Schistosoma mekongi by real-time PCR with high resolution melting analysis

9Citations
Citations of this article
32Readers
Mendeley users who have this article in their library.

Abstract

Human schistosomiasis caused by Schistosoma japonicum and Schistosoma mekongi is a chronic and debilitating helminthic disease still prevalent in several countries of Asia. Due to morphological similarities of cercariae and eggs of these 2 species, microscopic differentiation is difficult. High resolution melting (HRM) real-time PCR is developed as an alternative tool for the detection and differentiation of these 2 species. A primer pair was designed for targeting the 18S ribosomal RNA gene to generate PCR products of 156 base pairs for both species. The melting points of S. japonicum and S. mekongi PCR products were 84.5±0.07 °C and 85.7±0.07 °C, respectively. The method permits amplification from a single cercaria or an egg. The HRM real-time PCR is a rapid and simple tool for differentiation of S. japonicum and S. mekongi in the intermediate and final hosts. © 2013, Korean Society for Parasitology and Tropical Medicine.

Cite

CITATION STYLE

APA

Kongklieng, A., Kaewkong, W., Intapan, P. M., Sanpool, O., Janwan, P., Thanchomnang, T., … Maleewong, W. (2013). Molecular differentiation of Schistosoma japonicum and Schistosoma mekongi by real-time PCR with high resolution melting analysis. Korean Journal of Parasitology, 51(6), 651–656. https://doi.org/10.3347/kjp.2013.51.6.651

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free