Detection of Human Prion Seeding Activity in Formalin-Fixed Paraffin-Embedded Archival Tissues
Jazyk angličtina Země Velká Británie, Anglie Médium print
Typ dokumentu časopisecké články
Grantová podpora
Ministry of Health of the Czech Republic
00064165
Conceptual Development of Research Organization, General University Hospital
00064190
Conceptual Development of Research Organization, Thomayer University Hospital
NU23-04-00173
Czech Health Research Council
LX22NPO5107
National Institute for Neurological Research (European Union-Next Generation EU)
362521
Charles University
PubMed
40631394
PubMed Central
PMC12239053
DOI
10.1111/nan.70028
Knihovny.cz E-zdroje
- Klíčová slova
- FFPE, RT‐QuIC, SAA, formalin‐fixed paraffin‐embedded, prion, prion disease, real‐time quaking‐induced conversion assay, seeding amplification assay,
- MeSH
- fixace tkání metody MeSH
- formaldehyd MeSH
- lidé MeSH
- mozek * patologie metabolismus MeSH
- prionová bílkovina MeSH
- prionové nemoci * patologie diagnóza metabolismus MeSH
- priony * metabolismus MeSH
- zalévání tkání do parafínu metody MeSH
- zvířata MeSH
- Check Tag
- lidé MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- Názvy látek
- formaldehyd MeSH
- prionová bílkovina MeSH
- priony * MeSH
AIMS: Formalin-fixed paraffin-embedded (FFPE) samples, routinely used in neuropathology, represent an invaluable resource for studying rare diseases like transmissible spongiform encephalopathies (TSE). Despite fixation-induced protein cross-linking, prion seeding activity can be effectively detected using the seeding amplification assays. In this study, we employed the second-generation real-time quaking-induced conversion (RT-QuIC) assay to analyse and quantify human prion seeding activity in FFPE brain tissues. METHODS: FFPE frontal brain tissues were deparaffinised in xylene, followed by rehydration through descending concentrations of ethanol. The prion seeding activity in tissue homogenates was assessed by RT-QuIC assay utilising short recombinant hamster prion protein (rHaPrP90-231) as a substrate. RESULTS: A total of 60 samples, including 30 cases of confirmed TSE, comprising both sporadic and genetic forms, as well as 30 non-TSE controls, were analysed. Prion seeding activity has been detected in all TSE samples except one sCJD (VV2) and one GSS (P102L) case, corresponding to an assay sensitivity of 93.3%. Conversely, we did not detect any RT-QuIC positivity in the control group, resulting in 100% specificity. The mean 50% prion seeding dose of FFPE sporadic TSE samples was 107.8/g of brain tissue. CONCLUSION: Our study emphasises high sensitivity and specificity of RT-QuIC assay for prion detection in archival human FFPE brain tissues and demonstrates its diagnostic reliability comparable to other tissue types even after years of storage. The applicability of FFPE samples in RT-QuIC assays facilitates retrospective diagnostics and provides logistical advantages for sample preservation and transportation.
Department of Neurology Case Western Reserve University School of Medicine Cleveland Ohio USA
Department of Pathology Case Western Reserve University School of Medicine Cleveland Ohio USA
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Orrú C. D., Groveman B. R., Foutz A., et al., “Ring Trial of 2nd Generation RT‐QuIC Diagnostic Tests for Sporadic CJD,” Annals of Clinical and Translational Neurology 7, no. 11 (2020): 2262–2271. PubMed PMC
Safar J., Roller P. P., Ruben G. C., Gajdusek D. C., and C. J. Gibbs, Jr. , “Secondary Structure of Proteins Associated in Thin Films,” Biopolymers 33, no. 9 (1993): 1461–1476. PubMed
Safar J., Roller P. P., Gajdusek D. C., and C. J. Gibbs, Jr. , “Thermal Stability and Conformational Transitions of Scrapie Amyloid (Prion) Protein Correlate With Infectivity,” Protein Science 2, no. 12 (1993): 2206–2216. PubMed PMC
Hoover C. E., Davenport K. A., Henderson D. M., et al., “Detection and Quantification of CWD Prions in Fixed Paraffin Embedded Tissues by Real‐Time Quaking‐Induced Conversion,” Scientific Reports 6, no. 1 (2016): 25098. PubMed PMC
Manne S., Kondru N., Jin H., et al., “α‐Synuclein Real‐Time Quaking‐Induced Conversion in the Submandibular Glands of Parkinson's Disease Patients,” Movement Disorders 35, no. 2 (2020): 268–278. PubMed PMC
Manne S., Kondru N., Jin H., et al., “Blinded RT‐QuIC Analysis of α‐Synuclein Biomarker in Skin Tissue From Parkinson's Disease Patients,” Movement Disorders 35, no. 12 (2020): 2230–2239. PubMed PMC
Shin C., Han J. Y., Kim S. I., et al., “In Vivo and Autopsy Validation of Alpha‐Synuclein Seeding Activity Using RT‐QuIC Assay in the Gastrointestinal Tract of Patients With Parkinson's Disease,” Parkinsonism and Related Disorders 103 (2022): 23–28. PubMed
Baranová S., Moško T., Brůžová M., et al., “Detection of Prions in Matching Post‐Mortem Skin and Cerebrospinal Fluid Samples Using Second‐Generation Real‐Time Quaking‐Induced Conversion Assay,” Scientific Reports 14, no. 1 (2024): 6294. PubMed PMC
World Health Organization , “WHO Manual for Surveillance of Human Transmissible Spongiform Encephalopathies, Including Variant Creutzfeldt‐Jakob Disease,” World Health Organization; (2003), 90p, https://iris.who.int/handle/10665/42656.
Foutz A., Appleby B. S., Hamlin C., et al., “Diagnostic and Prognostic Value of Human Prion Detection in Cerebrospinal Fluid,” Annals of Neurology 81, no. 1 (2017): 79–92. PubMed PMC
Moško T., Galušková S., Matěj R., Brůžová M., and Holada K., “Detection of Prions in Brain Homogenates and CSF Samples Using a Second‐Generation RT‐QuIC Assay: A Useful Tool for Retrospective Analysis of Archived Samples,” Pathogens 10, no. 6 (2021): 750. PubMed PMC
Orrú C. D., Groveman B. R., Hughson A. G., Zanusso G., Coulthart M. B., and Caughey B., “Rapid and Sensitive RT‐QuIC Detection of Human Creutzfeldt‐Jakob Disease Using Cerebrospinal Fluid,” MBio 6, no. 1 (2015): e02451‐14, 10.1128/mBio.02451-14. PubMed DOI PMC
Wilham J. M., Orrú C. D., Bessen R. A., et al., “Rapid End‐Point Quantitation of Prion Seeding Activity With Sensitivity Comparable to Bioassays,” PLOS Pathogens 6, no. 12 (2010): e1001217. PubMed PMC
Dong T., Akagi A., Nonaka T., et al., “Formalin RT‐QuIC Assay Detects Prion‐Seeding Activity in Formalin‐Fixed Brain Samples From Sporadic Creutzfeldt–Jakob Disease Patients,” Neurobiology of Disease 159 (2021): 105504. PubMed
Hepker M., Clabaugh G., Jin H., and Kanthasamy A. G., “New Protocol for Kinetic Assay Seeding Ability Recovery “KASAR” From Formalin‐Fixed Paraffin‐Embedded Tissues,” Frontiers in Molecular Biosciences 10 (2023): 1087982. PubMed PMC
Hoover C. E., Davenport K. A., Henderson D. M., Zabel M. D., and Hoover E. A., “Endogenous Brain Lipids Inhibit Prion Amyloid Formation In Vitro,” Journal of Virology 91, no. 9 (2017): e02162‐16, 10.1128/JVI.02162-16. PubMed DOI PMC
Watanabe M., Hashida S., Yamamoto H., et al., “Estimation of Age‐Related DNA Degradation From Formalin‐Fixed and Paraffin‐Embedded Tissue According to the Extraction Methods,” Experimental and Therapeutic Medicine 14, no. 3 (2017): 2683–2688. PubMed PMC
Nicholson E. M., Greenlee J. J., and Hwang S., “Aqueous Extraction of Formalin‐Fixed Paraffin‐Embedded Tissue and Detection of Prion Disease Using Real‐Time Quaking‐Induced Conversion,” BMC Research Notes 17, no. 1 (2024): 266. PubMed PMC
Mok T. H., Nihat A., Luk C., et al., “Bank Vole Prion Protein Extends the Use of RT‐QuIC Assays to Detect Prions in a Range of Inherited Prion Diseases,” Scientific Reports 11, no. 1 (2021): 5231. PubMed PMC
Poleggi A., Baiardi S., Ladogana A., and Parchi P., “The Use of Real‐Time Quaking‐Induced Conversion for the Diagnosis of Human Prion Diseases,” Frontiers in Aging Neuroscience 14 (2022): 874734. PubMed PMC
Sano K., Satoh K., Atarashi R., et al., “Early Detection of Abnormal Prion Protein in Genetic Human Prion Diseases Now Possible Using Real‐Time QUIC Assay,” PLoS ONE 8, no. 1 (2013): e54915. PubMed PMC