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Molecular epidemiology of cryptosporidiosis outbreaks and transmission in British Columbia, Canada.

C S OngDepartment of Pathology and Laboratory Medicine, University of British Columbia, Vancouver, Canada.

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D L EislerDepartment of Pathology and Laboratory Medicine, University of British Columbia, Vancouver, Canada.

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S H GohDepartment of Pathology and Laboratory Medicine, University of British Columbia, Vancouver, Canada.

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J TomblinDepartment of Pathology and Laboratory Medicine, University of British Columbia, Vancouver, Canada.

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F M Awad-El-KariemDepartment of Pathology and Laboratory Medicine, University of British Columbia, Vancouver, Canada.

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C B BeardDepartment of Pathology and Laboratory Medicine, University of British Columbia, Vancouver, Canada.

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L XiaoDepartment of Pathology and Laboratory Medicine, University of British Columbia, Vancouver, Canada.

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I SulaimanDepartment of Pathology and Laboratory Medicine, University of British Columbia, Vancouver, Canada.

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A LalDepartment of Pathology and Laboratory Medicine, University of British Columbia, Vancouver, Canada.

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M FyfeDepartment of Pathology and Laboratory Medicine, University of British Columbia, Vancouver, Canada.

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A KingDepartment of Pathology and Laboratory Medicine, University of British Columbia, Vancouver, Canada.

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W R BowieDepartment of Pathology and Laboratory Medicine, University of British Columbia, Vancouver, Canada.

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J L Isaac-RentonDepartment of Pathology and Laboratory Medicine, University of British Columbia, Vancouver, Canada.

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Isolates from 25 (13 sporadic and 12 outbreak) cryptosporidiosis cases, 24 of which were from British Columbia, Canada, were characterized using nested polymerase chain reaction amplification of the polymorphic internal transcribed spacer 1 locus. Two predominant Cryptosporidium parvum genotypes were found. Twelve (8 sporadic and 4 outbreak) isolates amplified with the cry7/cry21 primer pair and 12 (5 sporadic and 7 outbreak) isolates amplified with the cry7/cryITS1 primer pair. Multi-locus gene analysis using sequence polymorphisms on 3 other loci, i.e., the thrombospondin-related adhesion protein gene, the dihydrofolate reductase gene, and the 18S rRNA gene on 8 (4 outbreak and 4 sporadic) isolates showed non-random association among the human and animal alleles of the 4 different C. parvum gene loci. Associations between these 2 parasite genotypes and different routes of cryptosporidiosis transmission such as zoonotic, anthroponotic, and waterborne transmission were studied using municipal population and agricultural information, as well as detection of C. parvum oocysts in municipal drinking water specimens of the residential communities of sporadic and outbreak cases.

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