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Diagnostic of Biomphalaria snails and Schistosoma mansoni: DNA obtained from traces of shell organic materials (2004)

Abstract
Freshwater snails belonging to the genus Biomphalaria act as intermediate hosts for the parasite trematode Schistosoma mansoni in Africa and in the neotropical region. Identification of such molluscs is carried out based on morphological characters and the presence of cercariae is verified through squeezing snails between two glass slides or by exposing them to artificial light. However, sometimes, the material collected includes molluscs with decomposed bodies or, yet, only empty shells, which precludes their identification and S. mansoni detection. Due to these difficulties, we have developed a methodology in which DNA may be extracted from traces of organic material from inside shells in order to identify molluscs through polymerase chain reaction and restriction fragment length polymorphism and to detect S. mansoni into these snails, by using low stringency polymerase chain reaction. Species-specific profiles obtained from B. glabrata, B. straminea, and B. tenagophila snails and their shells, maintained in laboratory for ten years, showed the same profiles. S. mansoni profiles showed to be present in shell specimens as far as the eighth week after being removed from aquarium.

Publication details
Download http://bioline.utsc.utoronto.ca/archive/00002413/
http://bioline.utsc.utoronto.ca/archive/00002413/01/oc04107.pdf
http://hdl.handle.net/1807/3560
Publisher Fundação Oswaldo Cruz, Fiocruz
Repository T-Space at The University of Toronto Libraries (Canada)
Keywords Tropical Diseases, Microbiology, Biomphalaria - Schistosoma mansoni - molluscs - shell - DNA - polymerase chain reaction oc04107, Tropical Diseases
Type Journal (Paginated)
Language English

Cited publications (2)
The Last Fifteen Years of Schistosomiasis in Venezuela: Features and Evolution (1999)
Characterization of Biomphalaria orbignyi, Biomphalaria peregrina and Biomphalaria oligoza by polymerase chain reaction and restriction enzyme digestion of the internal transcribed spacer region of the RNA ribosomal gene (2000)