Abstract

Chronic wasting disease (CWD) is a fatal prion disease of wild and captive cervids in North America. Prions are infectious agents composed of a misfolded version of a host-encoded protein, termed PrPSc. Infected cervids excrete and secrete prions, contributing to lateral transmission. Geographical distribution is expanding and case numbers in wild cervids are increasing. Recently, the first European cases of CWD have been reported in a wild reindeer and two moose from Norway. Therefore, methods to detect the infection early in the incubation time using easily available samples are desirable to facilitate effective disease management. We have adapted the real-time quaking induced conversion (RT-QuIC) assay, a sensitive in vitro prion amplification method, for pre-clinical detection of prion seeding activity in elk feces. Testing fecal samples from orally inoculated elk taken at various time points post infection revealed early shedding and detectable prion seeding activity throughout the disease course. Early shedding was also found in two elk encoding a PrP genotype associated with reduced susceptibility for CWD. In summary, we suggest that detection of CWD prions in feces by RT-QuIC may become a useful tool to support CWD surveillance in wild and captive cervids. The finding of early shedding independent of the elk’s prion protein genotype raises the question whether prolonged survival is beneficial, considering accumulation of environmental prions and its contribution to CWD transmission upon extended duration of shedding.

Highlights

  • Chronic wasting disease (CWD) is a prion disease which affects wild and farmed cervids such as white-tailed deer (WTD; Odocoileus virgianus), mule deer (MD; Odocoileus hemionus), elk (Cervus canadensis) and moose (Alces alces) mainly in North America and is found in 24 states of the United States as well as in 2 Canadian provinces [1; 2]

  • We demonstrate that fecal components inhibit real-time quaking induced conversion (RT-QuIC) amplification, which can be overcome by sodium phosphotungstic acid (NaPTA) precipitation [33] of PrPSc prior to RT-QuIC

  • Pre-mortem detection of PrPSc is mainly restricted to using biopsies of lymphoid tissues, which requires the stressful procedure of capturing wild cervids to obtain samples

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Summary

Introduction

Chronic wasting disease (CWD) is a prion disease which affects wild and farmed cervids such as white-tailed deer (WTD; Odocoileus virgianus), mule deer (MD; Odocoileus hemionus), elk (Cervus canadensis) and moose (Alces alces) mainly in North America and is found in 24 states of the United States as well as in 2 Canadian provinces [1; 2]. The disease was reported for the first time in Europe in a wild reindeer (Rangifer tarandus) and two moose in Norway [3]. Prions are infectious particles which consist only of protein, namely a beta-sheet. Detection of CWD Prions in Cervid Feces

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