Limited amplification of chronic wasting disease prions in the peripheral tissues of intracerebrally inoculated cattle

• Published in: Journal of general virology 2016-07, Vol.97 (7), p.1720-1724
• Main Authors: Haley, Nicholas J, Siepker, Christopher, Greenlee, Justin J, Richt, Jürgen A
• Format: Article
• Language: English
• Subjects: Animals; Cattle - metabolism; Central Nervous System - pathology; Cervidae; Deer - metabolism; Encephalopathy, Bovine Spongiform - pathology; Prion Proteins - metabolism; Prions - metabolism; Protein Folding; Wasting Disease, Chronic - pathology; Wasting Disease, Chronic - transmission
• ISSN: 0022-1317; 1465-2099
• DOI: 10.1099/jgv.0.000438

Chronic wasting disease (CWD) is a fatal neurodegenerative disease, classified as a prion disease or transmissible spongiform encephalopathy (TSE) similar to bovine spongiform encephalopathy (BSE). Cervids affected by CWD accumulate an abnormal protease-resistant prion protein throughout the central nervous system (CNS), as well as in both lymphatic and excretory tissues - an aspect of prion disease pathogenesis not observed in cattle with BSE. Using seeded amplification through real-time quaking-induced conversion, we investigated whether the bovine host or prion agent was responsible for this aspect of TSE pathogenesis. We blindly examined numerous central and peripheral tissues from cattle inoculated with CWD for prion seeding activity. Seeded amplification was readily detected in the CNS, though rarely observed in peripheral tissues, with a limited distribution similar to that of BSE prions in cattle. This seems to indicate that prion peripheralization in cattle is a host-driven characteristic of TSE infection.