A fixed brain seeded amplification assay to complement neuropathological prion disease diagnosis

Prion diseases are rare neurodegenerative disorders that share misfolding of the normal cellular prion protein into disease-causing isoforms known as "prions" as the critical pathophysiological event. Definite diagnosis can only be achieved through neuropathological confirmation. The neuropathological features of prion disease are well described; however, some molecular subtypes are typified by characteristic neuropathological features that are subtle or absent. Prion seeding assays have excellent specificity and have considerably improved premortem diagnostic accuracy but they have reduced sensitivity for some uncommon prion disease molecular subtypes. We developed a formalin-fixed, paraffin-embedded tissue-based prion seeding assay to serve as a complementary diagnostic tool for prion diseases. Fixed brain tissue was prepared through an optimized process involving careful defacing of tissue blocks prior to sampling and then stepwise deparaffinization and homogenization. Fixed tissue homogenates are then tested in an adapted version of a diagnostic cerebrospinal fluid (CSF) prion seeding assay, which utilizes full-length recombinant hamster prion protein as substrate. Two examples illustrate the utility of the assay by confirming prion seeding in fixed brain tissue from previously neuropathologically misdiagnosed obligate carriers of 2 different prion protein gene mutations. The importance of careful tissue sampling to rigorously maintain the diagnostic specificity of this assay is also highlighted.

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Publication Details

Journal
Journal of Neuropathology & Experimental Neurology
Published
2025-08-13
DOI
https://doi.org/10.1093/jnen/nlaf105
Primary Topic
Prion Diseases and Protein Misfolding
Type
article
Field-Weighted Citation Impact
0.00

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article

A fixed brain seeded amplification assay to complement neuropathological prion disease diagnosis

Laura J. Ellett, Christiane Stehmann, Steven John Collins, Victoria Lewis et al.
Journal of Neuropathology & Experimental Neurology
Prion Diseases and Protein Misfolding
article

A fixed brain seeded amplification assay to complement neuropathological prion disease diagnosis

Laura J. Ellett, Christiane Stehmann, Steven John Collins, Victoria Lewis, Catriona McLean, Matteo Senesi, Ian E. Birchall, Enie Lei
article en

Abstract

Prion diseases are rare neurodegenerative disorders that share misfolding of the normal cellular prion protein into disease-causing isoforms known as "prions" as the critical pathophysiological event. Definite diagnosis can only be achieved through neuropathological confirmation. The neuropathological features of prion disease are well described; however, some molecular subtypes are typified by characteristic neuropathological features that are subtle or absent. Prion seeding assays have excellent specificity and have considerably improved premortem diagnostic accuracy but they have reduced sensitivity for some uncommon prion disease molecular subtypes. We developed a formalin-fixed, paraffin-embedded tissue-based prion seeding assay to serve as a complementary diagnostic tool for prion diseases. Fixed brain tissue was prepared through an optimized process involving careful defacing of tissue blocks prior to sampling and then stepwise deparaffinization and homogenization. Fixed tissue homogenates are then tested in an adapted version of a diagnostic cerebrospinal fluid (CSF) prion seeding assay, which utilizes full-length recombinant hamster prion protein as substrate. Two examples illustrate the utility of the assay by confirming prion seeding in fixed brain tissue from previously neuropathologically misdiagnosed obligate carriers of 2 different prion protein gene mutations. The importance of careful tissue sampling to rigorously maintain the diagnostic specificity of this assay is also highlighted.

Journal of Neuropathology & Experimental NeurologyVol. 85(1)
The University of Melbourne (AU), Florey Institute of Neuroscience and Mental Health (AU), Alfred Health (AU)
Australian Government, Department of Health and Aged Care, Australian Government
Openalex Percentile: Top 79%
Prion Diseases and Protein Misfolding
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