Evidence map›Paper›PMID 41528641›Full record

ArticleActa parasitologica2026

Development of a Specific Primer-Based Method for Detecting Bithynia siamensis siamensis, an Intermediate Host of the Liver Fluke Opisthorchis viverrini.

Sattrachai Prasopdee, Panthong Kulsantiwong, Prapaporn Kumpay, Pannipha Kongkaew, Suchada Sumruayphol, Jutharat Kulsantiwong

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Article in Acta parasitologica, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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5 · Who and what money

Authors and funding

6 authors.

Sattrachai PrasopdeeChulabhorn International College of Medicine, Thammasat University, Klong-Luang, Pathum Thani, 12120, Thailand.
Panthong KulsantiwongDepartment of Biology, Faculty of Science, Udon Thani Rajabhat University, Udon Thani, 41000, Thailand.
Prapaporn KumpayDepartment of Biology, Faculty of Science, Udon Thani Rajabhat University, Udon Thani, 41000, Thailand.
Pannipha KongkaewDepartment of Biology, Faculty of Science, Udon Thani Rajabhat University, Udon Thani, 41000, Thailand.
Suchada SumruaypholDepartment of Medical Entomology, Faculty of Tropical Medicine, Mahidol University, Bangkok, 10400, Thailand.
Jutharat KulsantiwongDepartment of Biology, Faculty of Science, Udon Thani Rajabhat University, Udon Thani, 41000, Thailand. jutharat_kulsantiwong@yahoo.com.

Funding

Thailand Science, Research and Innovation Fund (TSRI) and the Fundamental Fund 64A162000010
6 · The paper itself

Abstract

backgroundThe liver fluke Opisthorchis viverrini is a major public health concern in Southeast Asia and a leading cause of cholangiocarcinoma. Its transmission relies on freshwater snails of the genus Bithynia as the first intermediate hosts. However, accurately identifying these morphologically similar snails remains challenging.

objectivesThis study aimed to develop species-specific primers for the accurate molecular identification of Bithynia siamensis siamensis, which serves as an important first intermediate host of O. viverrini.

methodsRandom amplified polymorphic DNA polymerase chain reaction (RAPD-PCR) was employed to isolate a unique DNA fragment specific to B. siamensis siamensis. A distinct 820 bp RAPD-derived fragment was obtained, sequenced, and analyzed. From this fragment, a conserved internal region was selected and used to design a species-specific primer pair (BSS2F/BSS2R), which produces a 280 bp diagnostic amplicon. The specificity and sensitivity of the newly developed assay were subsequently evaluated against other freshwater snail species.

resultsThe designed primers consistently amplified a 280 bp fragment exclusive to B. siamensis siamensis, with no cross-reactivity to B. siamensis goniomphalos, B. funiculata, or other cohabiting snail species. The assay detected as little as 5 ng of genomic DNA and achieved 90% amplification success across samples from four provinces.

conclusionThe RAPD-derived primer pair provides a rapid, reliable, and cost-effective molecular tool for the specific detection of B. siamensis siamensis. This approach enhances epidemiological surveillance of O. viverrini transmission and supports integrated One Health strategies for controlling opisthorchiasis in endemic regions.

Indexed as

DNA PrimersOpisthorchisSnailsAnimalsOpisthorchiasisRandom Amplified Polymorphic DNA TechniqueSensitivity and SpecificitySpecies SpecificityDNA PrimersBithynia siamensis siamensisCholangicarcinomaFreshwater snailsOpisthorchis viverriniSpecific primer

Identifiers

PMID41528641

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