Abstract

Chronic wasting disease (CWD) is a transmissible spongiform encephalopathy (TSE) that causes a fatal neurodegenerative disease in cervids. Cases of CWD are rapidly increasing in North America among wild and farmed cervid populations, and potential for zoonotic transmission is not yet determined. Therefore, in order to manage the disease, it is imperative to devise a system that can detect CWD during its early phases to prevent spread to new captive herds through introduction of CWD-affected animals into otherwise CWD-free herds. Real-time quaking–induced conversion (RT-QuIC) assays have been applied to detect the presence of disease-associated prions from various samples in both animals and humans. In this study, we have tested the use of five Hofmeister anions that range from weakly hydrating to strongly hydrating: Na3citrate, Na2SO4, NaCl, NaI, and NaClO4 in RT-QuIC reactions for CWD seeding activity using different recombinant prion proteins as substrates. This work shows how the ionic environment of the RT-QuIC reaction can enhance or diminish the seeding activity. The use of Na2SO4 or NaI as the sodium salt for RT-QuIC using bank vole recombinant prion substrate for the detection of CWD using brain samples reduces the lag time to detect with reasonable specificity. For detection of the CWD in fecal samples, only NaI showed comparable reduction in lag time relative to NaCl but required reduced temperature to alleviate spontaneous fibril formation in negative control samples. Selection of the proper ion environment and recombinant prion protein substrate will make RT-QuIC a powerful diagnostic tool for early detection of CWD prions, further supporting CWD surveillance in wild and captive cervids.

Highlights

  • Prion diseases, called transmissible spongiform encephalopathies (TSEs), are a class of fatal neurodegenerative diseases affecting humans and animals, some of which are zoonotic

  • We investigated Hofmeister ion effects on Real-time quaking–induced conversion (RT-QuIC) reactions prepared with recombinant Bank Vole (BV) prion protein substrate and seeded with the brain material from CWDinfected white-tailed deer (WTD)

  • We analyzed the effects of five Hofmeister anions on the RT-QuIC seeding activity of chronic wasting disease (CWD) prions found in the brain material and feces of CWD-infected white-tailed deer

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Summary

Introduction

Called transmissible spongiform encephalopathies (TSEs), are a class of fatal neurodegenerative diseases affecting humans and animals, some of which are zoonotic. They include Creutzfeldt–Jakob disease (CJD) in humans, bovine spongiform encephalopathy (BSE) in cattle, scrapie in sheep and goats, and chronic wasting disease (CWD) in cervids (Prusiner, 1982; Prusiner, 1998; Collinge, 2001; Cheng et al, 2016). It has been shown that CWD-infected animals shed prions via saliva, urine, and feces Due to this shedding, CWD spreads in both captive and free-ranging cervids. There is a lack of effective CWD management strategies to stop the spread, which indicates that the management will rely on early detection of prions in CWD-infected animals

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