» Articles » PMID: 8442326

Neuropathology of Chronic Wasting Disease of Mule Deer (Odocoileus Hemionus) and Elk (Cervus Elaphus Nelsoni)

Overview
Journal Vet Pathol
Date 1993 Jan 1
PMID 8442326
Citations 49
Authors
Affiliations
Soon will be listed here.
Abstract

The pathology of the central nervous system of nine mule deer (Odocoileus hemionus) and six elk (Cervus elaphus nelsoni) with chronic wasting disease, a spongiform encephalopathy of mule deer and elk, was studied by light microscopy. Lesions were similar in both species and were characterized by spongiform transformation of gray matter, intracytoplasmic vacuolation of neurons, neuronal degeneration and loss, astrocytic hypertrophy and hyperplasia, occurrence of amyloid plaques, and absence of significant inflammatory response. Distribution and severity of lesions were evaluated at 57 locations; there were only minor differences between deer and elk. Consistent, severe lesions occurred in olfactory tubercle and cortex, hypothalamus, and the parasympathetic vagal nucleus of deer, and sections examined from these regions would be sufficient to establish a diagnosis of chronic wasting disease. Lesions were milder in these locations in elk but were sufficiently apparent to be of diagnostic value. Other differences included increased severity of lesions in some thalamic nuclei in elk in contrast to deer, the occurrence of amyloid plaques demonstrable by hematoxylin and eosin and histochemical stains in deer in contrast to elk, and the presence of mild white matter lesions in elk but not in deer. Lesions of chronic wasting disease were qualitatively comparable to those of scrapie, bovine spongiform encephalopathy, transmissible mink encephalopathy, and the human spongiform encephalopathies. Topographic distribution and lesion severity of chronic wasting disease were most similar to those of scrapie and bovine spongiform encephalopathy. Duration of clinical disease did not significantly influence lesion distribution or severity in either species.

Citing Articles

Direct prion neuroinvasion following inhalation into the nasal cavity.

Kincaid A, Clouse M, Magrum S, Bartz J mSphere. 2024; 9(12):e0086324.

PMID: 39611853 PMC: 11656732. DOI: 10.1128/msphere.00863-24.


Comparative study of immunoassays, a microelectromechanical systems-based biosensor, and RT-QuIC for the diagnosis of chronic wasting disease in white-tailed deer.

Kobashigawa E, Muhsin S, Abdullah A, Allen K, Sinnott E, Zhang M BMC Vet Res. 2024; 20(1):518.

PMID: 39551756 PMC: 11571681. DOI: 10.1186/s12917-024-04351-x.


Chronic wasting disease alters the movement behavior and habitat use of mule deer during clinical stages of infection.

Barrile G, Cross P, Stewart C, Malmberg J, Jakopak R, Binfet J Ecol Evol. 2024; 14(5):e11418.

PMID: 38779534 PMC: 11108800. DOI: 10.1002/ece3.11418.


RT-QuIC detection of chronic wasting disease prion in platelet samples of white-tailed deer.

Kobashigawa E, Russell S, Zhang M, Sinnott E, Connolly M, Zhang S BMC Vet Res. 2024; 20(1):152.

PMID: 38654224 PMC: 11041042. DOI: 10.1186/s12917-024-04005-y.


Dynamics of CWD prion detection in feces and blood from naturally infected white-tailed deer.

Bravo-Risi F, Soto P, Benavente R, Nichols T, Morales R Sci Rep. 2023; 13(1):20170.

PMID: 37978207 PMC: 10656452. DOI: 10.1038/s41598-023-46929-9.