Discrimination of classical and atypical BSE by a distinct immunohistochemical PrPSc profile

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creativework.keywords - en
Immunohistochemistry
Transmissible spongiform encephalopathies
Bovine spongiform encephalopathy
BSE
Mad cow disease
TSE
Prion disease
Prions
creativework.keywords - fr
Immunocytochimie
Encéphalopathie spongiforme bovine
Encéphalopathies spongiformes transmissibles
ESB
Maladie de la vache folle
Maladies à prions
Prions
dc.contributor.author
Fast, Christine
Graham, Catherine
Kaatz, Martin
Santiago-Mateo, Kristina
Kaatz, Tammy
MacPherson, Kendra
Balkema-Buschmann, Anne
Ziegler, Ute
Groschup, Martin H.
Czub, Stefanie
dc.date.accepted
2023-02-15
dc.date.accessioned
2024-09-10T13:34:07Z
dc.date.available
2024-09-10T13:34:07Z
dc.date.issued
2023-02-20
dc.date.submitted
2023-01-14
dc.description.abstract - en
Bovine spongiform encephalopathy (BSE) belongs to the group of transmissible spongiform encephalopathies and is associated with the accumulation of a pathological isoform of the host-encoded glycoprotein, designated prion protein (PrPSc). Classical BSE (C-type) and two atypical BSE forms (L- and H-type) are known, and can be discriminated by biochemical characteristics. The goal of our study was to identify type-specific PrPSc profiles by using Immunohistochemistry. In our study, brain samples from 21 cattle, intracerebrally inoculated with C-, H-, and L-type BSE, were used. In addition, the corresponding samples from three orally C-type BSE infected animals were also included. From all animals, a lesion and PrPSc-profiles of six brain regions were determined. The lesion profile and the neuroanatomical distribution of PrPSc was highly consistent between the groups, but the immunohistochemical analysis revealed a distinct PrPSc profile for the different BSE-types, which included both the topographic and cellular pattern of PrPSc. This qualitative and quantitative analysis of PrPSc affected structures sheds new light into the pathogenesis of the different BSE types. Furthermore, immunohistochemical characterization is supported as an additional diagnostic tool in BSE surveillance programs, especially when only formalin-fixed tissue samples are available.
dc.identifier.citation
Fast, C., Graham, C., Kaatz, M., Santiago-Mateo, K., Kaatz, T., MacPherson, K., Balkema-Buschmann, A., Ziegler, U., Groschup, M. H., & Czub, S. (2023). Discrimination of classical and atypical BSE by a distinct immunohistochemical prpsc profile. Pathogens, 12(2), 353. https://doi.org/10.3390/pathogens12020353
dc.identifier.doi
https://doi.org/10.3390/pathogens12020353
dc.identifier.uri
https://open-science.canada.ca/handle/123456789/2926
dc.language.iso
en
dc.publisher
MDPI
dc.rights - en
Creative Commons Attribution 4.0 International (CC BY 4.0)
dc.rights - fr
Creative Commons Attribution 4.0 International (CC BY 4.0)
dc.rights.openaccesslevel - en
Gold
dc.rights.openaccesslevel - fr
Or
dc.rights.uri - en
https://creativecommons.org/licenses/by/4.0/
dc.rights.uri - fr
https://creativecommons.org/licenses/by/4.0/deed.fr
dc.subject - en
Agriculture
Health and safety
dc.subject - fr
Agriculture
Santé et sécurité
dc.subject.en - en
Agriculture
Health and safety
dc.subject.fr - fr
Agriculture
Santé et sécurité
dc.title - en
Discrimination of classical and atypical BSE by a distinct immunohistochemical PrPSc profile
dc.type - en
Article
dc.type - fr
Article
local.acceptedmanuscript.articlenum
353
local.article.journalissue
2
local.article.journaltitle
Pathogens
local.article.journalvolume
12
local.peerreview - en
Yes
local.peerreview - fr
Oui
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