Clams and potential foodborne Toxoplasma gondii in Nunavut, Canada

Abstract The prevalence of Toxoplasma gondii exposure in Inuit living in Nunavut (20%) is twice that of the US (11%); however, routes of exposure for Inuit communities in North America are unclear. Exposure to T. gondii in humans has been linked with consumption of raw or undercooked shellfish that...

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Bibliographic Details
Published in:Zoonoses and Public Health
Main Authors: Fung, Rebecca, Manore, Anna J. W., Harper, Sherilee L., Sargeant, Jan M., Shirley, Jamal, Caughey, Amy, Shapiro, Karen
Other Authors: Natural Sciences and Engineering Research Council of Canada, ArcticNet
Format: Article in Journal/Newspaper
Language:English
Published: Wiley 2021
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Online Access:http://dx.doi.org/10.1111/zph.12822
https://onlinelibrary.wiley.com/doi/pdf/10.1111/zph.12822
https://onlinelibrary.wiley.com/doi/full-xml/10.1111/zph.12822
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Summary:Abstract The prevalence of Toxoplasma gondii exposure in Inuit living in Nunavut (20%) is twice that of the US (11%); however, routes of exposure for Inuit communities in North America are unclear. Exposure to T. gondii in humans has been linked with consumption of raw or undercooked shellfish that can accumulate environmentally resistant oocysts. Bivalve shellfish, such as clams, are an important, nutritious, affordable and accessible source of food in many Northern Communities. To date, presence of T. gondii in clams in Northern Canada has not been reported. In this study, we tested for T. gondii presence in clams ( Mya truncata ) that were harvested in Iqaluit, Nunavut over a 1‐week period in September 2016. Of 390 clams, eight (2.1%) were confirmed to contain T. gondii DNA (≥99.7% identity), as determined using polymerase chain reaction (PCR) and sequence confirmation. Additionally, three clams (0.8%) were confirmed to contain Neospora caninum ‐like DNA (≥99.2% identity). While N. caninum is not known to be a zoonotic pathogen, its presence in shellfish indicates contamination of the nearshore with canid faeces, and the potential for marine mammal exposure through marine food webs. Notably, the PCR assay employed in this study does not discriminate between viable and non‐viable parasites. These findings suggest a possible route for parasite exposure through shellfish in Iqaluit, Nunavut. Future research employing viability testing will further inform public health messaging on the infectious potential of T. gondii in shellfish.