Abstract

Chronic wasting disease (CWD) is a transmissible prion disorder, primarily affecting free-ranging and captive cervids in North America (United States and Canada), South Korea, and Europe (Finland, Norway, and Sweden). Current diagnostic methods used in the United States for detection of CWD in hunter harvested deer involve demonstration of the causal misfolded prion protein (PrPCWD) in the obex or retropharyngeal lymph nodes (RLNs) using an antigen detection ELISA as a screening tool, followed by a confirmation by the gold standard method, immunohistochemistry (IHC). Real-time quaking-induced conversion (RT-QuIC) assay is a newer approach that amplifies misfolded CWD prions in vitro and has facilitated CWD prion detection in a variety of tissues, body fluids, and excreta. The current study was undertaken to compare ELISA, IHC, and RT-QuIC on RLNs (n = 1,300 animals) from white-tailed deer (WTD) in Michigan. In addition, prescapular, prefemoral and popliteal lymph nodes collected from a small subset (n = 7) of animals were tested. Lastly, the location of the positive samples within Michigan was documented and the percentage of CWD positive RLNs was calculated by sex and age. ELISA and RT-QuIC detected PrPCWD in 184 and 178 out of 1,300 RLNs, respectively. Of the 184 ELISA positive samples, 176 were also IHC positive for CWD. There were seven discordant results when comparing IHC and ELISA. RT-QuIC revealed that six of the seven samples matched the IHC outcomes. One RLN was negative by IHC, but positive by ELISA and RT-QuIC. RT-QuIC, IHC, and ELISA also detected PrPCWD in prescapular, prefemoral and popliteal lymph nodes. CWD infection heterogeneities were observed in different age and sex groups, with young males having higher CWD prevalence. All, except one, CWD positive RLNs analyzed were from ten Counties geographically located in the West Michigan region of the Lower Peninsula. Taken together, we show evidence that the RT-QuIC assay is comparable to ELISA and IHC and could be helpful for routine CWD detection in surveillance programs. RT-QuIC also demonstrated that CWD prions are distributed across lymph nodes in a variety of anatomic locations. A multi-laboratory validation on blinded sample panels is underway and is likely to help to provide insight into the variability (lab-to-lab), analytical sensitivity, and specificity of gold standard diagnostics vs. RT-QuIC assay.

Highlights

  • Chronic wasting disease (CWD) is the only known transmissible spongiform encephalopathy to occur in free-ranging wildlife populations, naturally infecting elk, moose, and various deer species

  • CWD was first identified more than 50 years ago in a captive mule deer at Colorado State University (Fort Collins, Colorado)

  • Since 2015, when the first free-ranging CWD-positive deer was identified in Michigan, the disease has been reported in Frontiers in Veterinary Science | www.frontiersin.org

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Summary

Introduction

Chronic wasting disease (CWD) is the only known transmissible spongiform encephalopathy to occur in free-ranging wildlife populations, naturally infecting elk, moose, and various deer species. The disease has been reported in 26 American states, four Canadian provinces, South Korea, Norway, Finland, and Sweden [1,2,3,4,5] It continues to spread across North America through new and ongoing outbreaks. Urine, feces, or aerosols from infected animals, as well as indirect (environmental) contact through the ingestion of infectious prions bound to soil or plants, and vertical transmission, likely contribute to disease spread [6,7,8]. The long incubation period contributes to CWD transmission as asymptomatic infected animals can substantially contaminate the environment through body secretions such as urine, saliva, and feces [12,13,14]. Animals in the first stages of the disease contain concentration of prions in their tissues that cannot be detected by standard methods such as ELISA or immunohistochemistry (IHC)

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