Oral transmission and early lymphoid tropism of chronic wasting disease PrPres in mule deer fawns (Odocoileus hemionus)

• Published in: Journal of general virology Vol. 80; no. 10; pp. 2757 - 2764
• Main Authors: Sigurdson, C.J, Williams, E.S, Miller, M.W, Spraker, T.R, O'Rourke, K.I, Hoover, E.A
• Format: Journal Article
• Language: English
• Published: England Soc General Microbiol 01-10-1999
• Subjects: Animals; Chronic Disease; Deer; disease transmission; Lymphoid Tissue - metabolism; prion diseases; Prion Diseases - etiology; Prion Diseases - pathology; Prion Diseases - veterinary; Prions - analysis; Staining and Labeling; Time Factors; Tissue Distribution; Wasting Syndrome - etiology; Wasting Syndrome - pathology; Wasting Syndrome - veterinary
• ISSN: 0022-1317; 1465-2099
• DOI: 10.1099/0022-1317-80-10-2757

Mule deer fawns (Odocoileus hemionus) were inoculated orally with a brain homogenate prepared from mule deer with naturally occurring chronic wasting disease (CWD), a prion-induced transmissible spongiform encephalopathy. Fawns were necropsied and examined for PrP(res), the abnormal prion protein isoform, at 10, 42, 53, 77, 78 and 80 days post-inoculation (p.i.) using an immunohistochemistry assay modified to enhance sensitivity. PrP(res) was detected in alimentary-tract-associated lymphoid tissues (one or more of the following: retropharyngeal lymph node, tonsil, Peyer's patch and ileocaecal lymph node) as early as 42 days p.i. and in all fawns examined thereafter (53 to 80 days p.i.). No PrP(res) staining was detected in lymphoid tissue of three control fawns receiving a control brain inoculum, nor was PrP(res) detectable in neural tissue of any fawn. PrP(res)-specific staining was markedly enhanced by sequential tissue treatment with formic acid, proteinase K and hydrated autoclaving prior to immunohistochemical staining with monoclonal antibody F89/160.1.5. These results indicate that CWD PrP(res) can be detected in lymphoid tissues draining the alimentary tract within a few weeks after oral exposure to infectious prions and may reflect the initial pathway of CWD infection in deer. The rapid infection of deer fawns following exposure by the most plausible natural route is consistent with the efficient horizontal transmission of CWD in nature and enables accelerated studies of transmission and pathogenesis in the native species.