Detection of prions in matching post-mortem skin and cerebrospinal fluid samples using second-generation real-time quaking-induced conversion assay
Jazyk angličtina Země Anglie, Velká Británie Médium electronic
Typ dokumentu časopisecké články
Grantová podpora
R01 NS074317
NINDS NIH HHS - United States
R01 NS103848
NINDS NIH HHS - United States
PubMed
38491063
PubMed Central
PMC10943125
DOI
10.1038/s41598-024-56789-6
PII: 10.1038/s41598-024-56789-6
Knihovny.cz E-zdroje
- MeSH
- biotest MeSH
- Creutzfeldtova-Jakobova nemoc * diagnóza mozkomíšní mok MeSH
- kůže metabolismus MeSH
- lidé MeSH
- prionová bílkovina MeSH
- prionové nemoci * diagnóza MeSH
- priony * metabolismus MeSH
- Check Tag
- lidé MeSH
- Publikační typ
- časopisecké články MeSH
- Názvy látek
- prionová bílkovina MeSH
- priony * MeSH
Real-time quaking-induced conversion assay (RT-QuIC) exploits templating activity of pathogenic prion protein for ultrasensitive detection of prions. We have utilized second generation RT-QuIC assay to analyze matching post-mortem cerebrospinal fluid and skin samples of 38 prion disease patients and of 30 deceased neurological controls. The analysis of cerebrospinal fluid samples led to 100% sensitivity and 100% specificity, but some samples had to be diluted before the analysis to alleviate the effect of present RT-QuIC inhibitors. The analysis of the corresponding skin samples provided 89.5% sensitivity and 100% specificity. The median seeding dose present in the skin was one order of magnitude higher than in the cerebrospinal fluid, despite the overall fluorescent signal of the skin samples was comparatively lower. Our data support the use of post-mortem cerebrospinal fluid for confirmation of prion disease diagnosis and encourage further studies of the potential of skin biopsy samples for intra-vitam prion diseases´ diagnostics.
Department Neurology Case Western Reserve University School of Medicine Cleveland OH 44106 USA
Department of Pathology Case Western Reserve University School of Medicine Cleveland OH 44106 USA
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Collinge J. Mammalian prions and their wider relevance in neurodegenerative diseases. Nature. 2016;539:217–226. doi: 10.1038/nature20415. PubMed DOI
Kang HE, Mo Y, Abd Rahim R, Lee HM, Ryou C. Prion diagnosis: Application of real-time quaking-induced conversion. Biomed. Res. Int. 2017;2017:5413936. doi: 10.1155/2017/5413936. PubMed DOI PMC
Collins SJ, et al. Determinants of diagnostic investigation sensitivities across the clinical spectrum of sporadic Creutzfeldt-Jakob disease. Brain. 2006;129:2278–2287. doi: 10.1093/brain/awl159. PubMed DOI
Cramm M, et al. Stability and reproducibility underscore utility of RT-QuIC for diagnosis of Creutzfeldt-Jakob disease. Mol. Neurobiol. 2016;53:1896–1904. doi: 10.1007/s12035-015-9133-2. PubMed DOI PMC
Wang F, Pritzkow S, Soto C. PMCA for ultrasensitive detection of prions and to study disease biology. Cell Tissue Res. 2023;392:307–321. doi: 10.1007/s00441-022-03727-5. PubMed DOI PMC
Takatsuki H, et al. Rapid and quantitative assay of amyloid-seeding activity in human brains affected with prion diseases. PLoS ONE. 2015;10:e0126930. doi: 10.1371/journal.pone.0126930. PubMed DOI PMC
Atarashi R, et al. Ultrasensitive human prion detection in cerebrospinal fluid by real-time quaking-induced conversion. Nat. Med. 2011;17:175–178. doi: 10.1038/nm.2294. PubMed DOI
Orru CD, et al. Rapid and sensitive RT-QuIC detection of human Creutzfeldt-Jakob disease using cerebrospinal fluid. mBio. 2015 doi: 10.1128/mBio.02451-14. PubMed DOI PMC
Orrú CD, et al. Ring trial of 2nd generation RT-QuIC diagnostic tests for sporadic CJD. Ann. Clin. Transl. Neurol. 2020;7:2262–2271. doi: 10.1002/acn3.51219. PubMed DOI PMC
Orrú CD, et al. A test for Creutzfeldt-Jakob disease using nasal brushings. N. Engl. J. Med. 2014;371:519–529. doi: 10.1056/NEJMoa1315200. PubMed DOI PMC
Bongianni M, et al. Diagnosis of human prion disease using real-time quaking-induced conversion testing of olfactory mucosa and cerebrospinal fluid samples. JAMA Neurol. 2017;74:155–162. doi: 10.1001/jamaneurol.2016.4614. PubMed DOI
Orru CD, et al. Prion seeding activity and infectivity in skin samples from patients with sporadic Creutzfeldt-Jakob disease. Sci. Transl. Med. 2017 doi: 10.1126/scitranslmed.aam7785. PubMed DOI PMC
Wang Z, et al. Early preclinical detection of prions in the skin of prion-infected animals. Nat. Commun. 2019;10:247. doi: 10.1038/s41467-018-08130-9. PubMed DOI PMC
Mammana A, et al. Detection of prions in skin punch biopsies of Creutzfeldt-Jakob disease patients. Ann. Clin. Transl. Neurol. 2020;7:559–564. doi: 10.1002/acn3.51000. PubMed DOI PMC
Xiao K, et al. Validation and application of skin RT-QuIC to patients in China with probable CJD. Pathogens. 2021 doi: 10.3390/pathogens10121642. PubMed DOI PMC
Mosko T, Galuskova S, Matej R, Bruzova M, 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. 2021 doi: 10.3390/pathogens10060750. PubMed DOI PMC
Wilham JM, et al. Rapid end-point quantitation of prion seeding activity with sensitivity comparable to bioassays. PLoS Pathog. 2010;6:e1001217. doi: 10.1371/journal.ppat.1001217. PubMed DOI PMC
Arroyo A, Rosel P, Marron T. Cerebrospinal fluid: Postmortem biochemical study. J. Clin. Forensic Med. 2005;12:153–156. doi: 10.1016/j.jcfm.2004.11.001. PubMed DOI
Mok TH, et al. Bank vole prion protein extends the use of RT-QuIC assays to detect prions in a range of inherited prion diseases. Sci. Rep. 2021;11:5231. doi: 10.1038/s41598-021-84527-9. PubMed DOI PMC
Bellomo G, et al. Cerebrospinal fluid lipoproteins inhibit alpha-synuclein aggregation by interacting with oligomeric species in seed amplification assays. Mol. Neurodegener. 2023;18:20. doi: 10.1186/s13024-023-00613-8. PubMed DOI PMC
Hoover CE, Davenport KA, Henderson DM, Zabel MD, Hoover EA. Endogenous brain lipids inhibit prion amyloid formation in vitro. J. Virol. 2017 doi: 10.1128/JVI.02162-16. PubMed DOI PMC
Fiorini M, et al. High diagnostic accuracy of RT-QuIC assay in a prospective study of patients with suspected sCJD. Int. J. Mol. Sci. 2020 doi: 10.3390/ijms21030880. PubMed DOI PMC
Brouckova A, Holada K. Cellular prion protein in blood platelets associates with both lipid rafts and the cytoskeleton. Thromb. Haemost. 2009;102:966–974. doi: 10.1160/TH09-02-0074. PubMed DOI
Franceschini A, et al. High diagnostic value of second generation CSF RT-QuIC across the wide spectrum of CJD prions. Sci. Rep. 2017;7:10655. doi: 10.1038/s41598-017-10922-w. PubMed DOI PMC