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PCR-RFLP analysis of the oocyst wall protein (COWP) gene discriminates between and , and between isolates of human and animal origin

FEMS Microbiology Letters · 1997 · Vol. 150(2) · pp. 209–217
Furio SpanoLorenza PutignaniJ. McLauchlinDavid P. CasemoreAndrea Crisanti

Abstract

Cryptosporidium wrairi was isolated from guinea pigs during a spontaneous outbreak of cryptosporidiosis. Despite the morphological and antigenic similarities to C. parvum, C. wrairi displayed a different host range and site of infection and may represent a separate species or sub-species. We used the polymerase chain reaction to clone two distinct 550 bp-long DNA fragments, Wc-I and Wc-II, of the gene encoding the Cryptosporidium oocyst wall protein (COWP) of C. wrairi, which showed 98% identity to the C. parvum homologue. Within Wc-I, polymorphic Rsal restriction sites were used to develop a polymerase chain reaction-restriction fragment length polymorphism method able to distinguish C. wrairi from C. parvum and to identify two groups of C. parvum isolates differentially associated with animal and human infections.

Parasitic Infections and DiagnosticsAmoebic Infections and TreatmentsClostridium difficile and Clostridium perfringens researchCryptosporidium parvumRestriction fragment length polymorphismBiologyPolymerase chain reactionCryptosporidiumclone (Java method)GeneRestriction fragmentDNAMolecular biology

MeSH terms

Amino Acid SequenceAnimalsBase SequenceCryptosporidiosisCryptosporidiumGuinea PigsHumansMolecular Sequence DataPolymorphism, Restriction Fragment LengthRuminantsSpecies SpecificityGenetic VariationProtozoan ProteinsDNA, ProtozoanPolymerase Chain Reaction
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References
Rapid and simple method for purification of nucleic acids
Journal of Clinical Microbiology · 1990 · 5,277 citations
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PCR-RFLP analysis of the oocyst wall protein (COWP) gene discriminates between and , and between isolates of human and animal origin · Scinovex