Prion diseases are fatal neurodegenerative diseases of humans and animals. The long-term goal of the proposed research is to define the pathway(s) and mechanism(s) involved in prion transmission. These events are central to understanding the pathogenesis of prion diseases, but the route(s) of horizontal transmission has not been adequately defined despite the importance of prion diseases to human, livestock, and free-ranging cervid health. Blocking the spread of the prion agent among hosts is one approach towards preventing these contagious diseases. Within an infected host, the dissemination of the prion agent to mucosal surfaces could result in prion agent shedding into bodily fluids. Since neurons replicate the prion agent to high levels, exposure of susceptible hosts to infectious sources derived from prion-infected neurons at the mucosa would likely contain the highest dose of infectivity and therefore, be the most effective at establishing a new prion infection. The specific hypothesis behind the proposed research is that the prion agent can be shed from olfactory neurons into nasal secretions and the amount of prion infectivity released will be enhanced under conditions that promote disruption of the olfactory epithelium. To test this concept the amount of prion infectivity shed into nasal lavages will be measured in the absence or presence of viral infection of the nasal cavity or after treatment with nasotoxic drugs. These studies can determine the role of olfactory neurons in prion shedding into nasal secretions and determine whether the ability of a common insult to the nasal epithelium to promote prion agent shedding could represent a novel mechanism to enhance prion transmission.

Public Health Relevance

Prion diseases are fatal neurodegenerative diseases of humans and animals that can be transmitted vertically as well as horizontally through environmental contamination, ingestion of contaminated food, or by accidental exposure during medical procedures. These studies will investigate the role of prion agent shedding from olfactory neurons and the influence of common viral infections of the upper respiratory tract on enhanced prion shedding into nasal secretions. Identification of the route(s) of prion agent transmission is important in the development of therapeutic interventions that can prevent disease dissemination.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Exploratory/Developmental Grants (R21)
Project #
5R21AI084094-02
Application #
7876795
Study Section
Cellular and Molecular Biology of Neurodegeneration Study Section (CMND)
Program Officer
Beisel, Christopher E
Project Start
2009-06-19
Project End
2011-05-31
Budget Start
2010-06-01
Budget End
2011-05-31
Support Year
2
Fiscal Year
2010
Total Cost
$178,125
Indirect Cost
Name
Montana State University - Bozeman
Department
Veterinary Sciences
Type
Schools of Earth Sciences/Natur
DUNS #
625447982
City
Bozeman
State
MT
Country
United States
Zip Code
59717
Bessen, Richard A; Wilham, Jason M; Lowe, Diana et al. (2012) Accelerated shedding of prions following damage to the olfactory epithelium. J Virol 86:1777-88
Bessen, Richard A; Shearin, Harold; Martinka, Scott et al. (2010) Prion shedding from olfactory neurons into nasal secretions. PLoS Pathog 6:e1000837