Publications by authors named "Mick J Stack"

This communication reports final observations on experimental transmission of chronic wasting disease (CWD) from mule deer to cattle by the intracerebral route. Thirteen calves were inoculated intracerebrally with brain suspension from mule deer naturally affected with CWD. Three other calves were kept as uninoculated controls.

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This is a final report of an experimental transmission of sheep scrapie agent by intracerebral inoculation to Rocky Mountain elk (Cervus elaphus nelsoni). It documents results obtained in experimental (n = 6) and control (n = 2) elk. During the first 2 years postinoculation (PI), 3 animals died or were euthanized because of infection or injuries other than spongiform encephalopathy (SE).

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  • The study investigated the transmissibility of transmissible mink encephalopathy (TME) to raccoons, using 4 inoculated raccoon kits and one control.
  • All 4 raccoons showed neurological symptoms, were euthanized, and exhibited spongiform encephalopathy without gross lesions, confirming TME's transmissibility.
  • Current diagnostic techniques for detecting transmissible spongiform encephalopathies (TSEs) in livestock were effective in identifying prion proteins in raccoon tissues, indicating potential for further study on raccoon models for TSE differentiation.
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Detection of the scrapie-associated protease-resistant prion protein (PrPres) in sheep brains in the early phase after intracerebral inoculation of the scrapie agent has not been documented. Fourteen 4-mo-old, genetically susceptible lambs (QQ homozygous at codon 171 of the PrP gene) were obtained for this study. Twelve lambs were inoculated intracerebrally with a brain suspension from sheep naturally affected with scrapie, and 2 served as uninoculated controls.

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Background: Transmissible spongiform encephalopathies (TSEs) are neurodegenerative diseases affecting both humans and animals. They are associated with post-translational conversion of the normal cellular prion protein (PrPC) into a heat- and protease-resistant abnormal isoform (PrPSc). Detection of PrPSc in individuals is widely utilized for the diagnosis of prion diseases.

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Feline spongiform encephalopathy (FSE) is thought to have resulted from consumption of food contaminated with bovine spongiform encephalopathy and the latter is believed to result from the consumption of food contaminated with scrapie. However, no direct experimental documentation exists to indicate that the scrapie agent is capable of amplifying in cats, and, therefore, crossing the species barrier. During 1979, 6 cats ranging in age from 3.

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  • A study found that 47% of adult raccoons in Iowa showed signs of neuroaxonal dystrophy (NAD), with severe lesions more common in older animals and none found in young kits.
  • The condition affected specific areas in the medulla oblongata, leading to neuron degeneration and loss without the presence of inflammatory cells or prion proteins.
  • Given the low prevalence of NAD in raccoons from other regions, the study suggests that factors beyond age, like genetics or environment, may contribute to this high occurrence in Iowa.
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