The uniquely facile transmission of chronic wasting disease (CWD) among cervids must underpin its uncontrolled expanding prevalence in North America, Asia and now Europe. The goal of this research is to elucidate how and why CWD is transmitted so efficiently in nature and what factors facilitate this process or influence the zoonotic risk CWD may pose. The central hypothesis for this work is that peripheral CWD prions possess characteristics that favor enhanced bioavailability, infectivity and perhaps altered zoonotic risk. CWD transmission must occur via exposure of nasal or oral mucosae to the very low concentrations of prions shed in secreta and excreta of infected cervids (6-7 log10 lower than in brain). It is likewise likely that in nature cervids are naturally exposed to excreted prions that are bound to particulates. The factors and mechanisms by which this low-level mucosal exposure initiates infection and facilitates CWD transmission remain largely mysterious and are the subject of this proposal. Amazingly, like viruses, prions can (unpredictably) evolve to cross species barriers. Humans and animals share environments and food sources contaminated with prions shed by CWD-infected cervids. The practical impact of peripheral tissue and shed prions and the role they may play in horizontal prion transmission, epidemiology, and risk posed to humans and animals remains relatively under-studied, and is the second subject of this proposal. We will address the above questions by harnessing our established robust and sensitive in vivo and in vitro prion detection methods using both native cervid and transgenic murine hosts to assess the infectivity and biochemical traits of peripheral and shed prions. These studies will be under-pinned by our unique CWD experience, facilities, and repository of tissues and excreted prions from longitudinal infection studies in deer. The study Aims are:
Aim 1 : To determine features of natural exposure that lead to the uniquely efficient transmission of CWD.
This aim will determine if multiple low dose and/or particle binding of excreted prions enhances transmission efficiency vs. the same total encountered in a single exposure.
Aim 2 : To determine whether peripheral vs. brain CWD prions differ biochemically or in infectivity. We will analyze the biophysical and biochemical properties as well as cross-species infectivity and zoonotic potential of peripheral vs. CNS prions.
This aim will determine whether shed CWD prions possess unique traits or broadened species barriers. The impact of this research will elucidate how and why CWD is transmitted so efficiently in nature and what factors facilitate this process or influence the zoonotic risk CWD may pose.

Public Health Relevance

Chronic wasting disease (CWD) of deer and elk is the most readily transmitted prion disease known. It continues to spread uncontrolled in North America, Asia and now Europe. Its facile transmission remains mysterious, yet important. The goal of this research is to determine how and why CWD is transmitted so efficiently in nature and what risk this rapid spread may pose for humans and other animal species.

Agency
National Institute of Health (NIH)
Institute
National Institute of Neurological Disorders and Stroke (NINDS)
Type
Research Project (R01)
Project #
2R01NS061902-09
Application #
9444907
Study Section
Cellular and Molecular Biology of Neurodegeneration Study Section (CMND)
Program Officer
Wong, May
Project Start
2009-09-30
Project End
2023-02-28
Budget Start
2018-03-01
Budget End
2019-02-28
Support Year
9
Fiscal Year
2018
Total Cost
Indirect Cost
Name
Colorado State University-Fort Collins
Department
Microbiology/Immun/Virology
Type
Schools of Veterinary Medicine
DUNS #
785979618
City
Fort Collins
State
CO
Country
United States
Zip Code
80523
Davenport, Kristen A; Mosher, Brittany A; Brost, Brian M et al. (2018) Assessment of Chronic Wasting Disease Prion Shedding in Deer Saliva with Occupancy Modeling. J Clin Microbiol 56:
Davenport, Kristen A; Hoover, Clare E; Bian, Jifeng et al. (2017) PrPC expression and prion seeding activity in the alimentary tract and lymphoid tissue of deer. PLoS One 12:e0183927
Hoover, Clare E; Davenport, Kristen A; Henderson, Davin M et al. (2017) Endogenous Brain Lipids Inhibit Prion Amyloid Formation In Vitro. J Virol 91:
Hoover, Clare E; Davenport, Kristen A; Henderson, Davin M et al. (2017) Pathways of Prion Spread during Early Chronic Wasting Disease in Deer. J Virol 91:
Bian, Jifeng; Khaychuk, Vadim; Angers, Rachel C et al. (2017) Prion replication without host adaptation during interspecies transmissions. Proc Natl Acad Sci U S A 114:1141-1146
Henderson, Davin M; Tennant, Joanne M; Haley, Nicholas J et al. (2017) Detection of chronic wasting disease prion seeding activity in deer and elk feces by real-time quaking-induced conversion. J Gen Virol 98:1953-1962
Haley, Nicholas J; Siepker, Chris; Hoon-Hanks, Laura L et al. (2016) Seeded Amplification of Chronic Wasting Disease Prions in Nasal Brushings and Recto-anal Mucosa-Associated Lymphoid Tissues from Elk by Real-Time Quaking-Induced Conversion. J Clin Microbiol 54:1117-26
Denkers, Nathaniel D; Henderson, Davin M; Mathiason, Candace K et al. (2016) Enhanced prion detection in biological samples by magnetic particle extraction and real-time quaking-induced conversion. J Gen Virol 97:2023-9
McNulty, Erin; Selariu, Anca I; Anderson, Kelly et al. (2016) Aspects of the husbandry and management of captive cervids. Lab Anim (NY) 45:140-2
Hoover, Clare E; Davenport, Kristen A; Henderson, Davin M et al. (2016) Detection and Quantification of CWD Prions in Fixed Paraffin Embedded Tissues by Real-Time Quaking-Induced Conversion. Sci Rep 6:25098

Showing the most recent 10 out of 29 publications