Methods for diagnosis of prion diseases
- Issue: Vol 54, No 5 (2009)
- Pages: 4-9
- Section: Articles
- Submitted: 09.06.2023
- Published: 15.10.2009
- URL: https://virusjour.crie.ru/jour/article/view/11933
- ID: 11933
Cite item
Full Text
Abstract
The epidemic of bovine spongiform encephalopathy (BSE) in the United Kingdom, its related occurrence of a new type of Creutzfeld-Jacob disease and proven cases of this type of the disease transmitted by blood transfusion initiated intensive studies to develop a inexpensive, prompt, and sensitive method for the early lifetime diagnosis of prion diseases. This would permit initiation of the timely treatment of the patients and prevention of contamination of foodstuffs. However, despite significant progress made in this direction, this objective has not yet been achieved. The present review highlights the currently available methods for the diagnosis of transmissible spongiform encephalopathies, as well as the latest developments in the ultrasensitive detection of these diseases, which is based on the misfolded prion protein complex.
References
- Григорьев В. Б. Прионные болезни человека и животных // Вопр. вирусол. - 2004. - Т. 6. - С. 4-12.
- Григорьев В. Б. Прионные инфекции // Медицинская вирусология. Руководство / Под ред. Д. К. Львова. - М., 2008. - С. 240-245.
- Aksamit А. J., Preissner С. M., Homburger H. A. Quantitation of 14-3-3 and neuron - specific enolase proteins in CFS in Creutzfeldt-Jacob disease // Neurology. - 2001. - Vol. 57, № 4. - P. 728-730.
- Andreoletti O., Berthon P., Marc D. el al . Early accumulation of PrPsc in gut-associated lymphoid and nervous tissues of susceptible sheep from a Romanov flock with natural scrapie // J. Gen .Virol. - 2000. - Vol. 81.- P. 3115-3126.
- Angelo M., Bari D., Chianini F. et al. The bank vole (Myodes glareolus) as a sensitive bioassay for sheep scrapie // J. Gen. Virol. - 2008. - Vol. 89. - P. 2975-2985.
- Atarashi R., Moore R. A., Sim V. L. et al. Ultrasensitive detection of scrapie prion protein using seeded conversion of recombinant prion protein. // Nat. Met. - 2007. - Vol. 4, № 8. - P. 645-650.
- Barletta J. M., Edelman D. C., Highsmith W. E., Conslatine N. T. Detection of ultra-low level of pathologic prion protein in scrapie infected hamster brain homogenates using real-time immuno-PCR // J. Virol. Meth. - 2005. - Vol. 127, № 2. - P. 154-164.
- Baron T. Mouse models of prion disease transmission // Trends Mol. Med. - 2002. -Vol. 8, № 10. - P. 495-500.
- Benestad S. L., Sarradin P., Thu B. et al. Cases of scrapie with unusual features in Norway and designation of new type. Nor98 // Vet. Res. - 2003. - Vol. 153, № 7. - P. 202-208.
- Birkmann E., Schafer O., Weinmann N. et al. Detection of prion particles in samples of BSE and scrapie by fluorescence correlation spectroscopy without proteinase К digestion // Biol. Chem. - 2006. - Vol. 387. - P. 95-102.
- Brown P., Will R. G., Bradley R. et al. Bovine spongiform encephalopathy and variant Creutzfeldt-Jacob disease: background, evolution, and current concerns. // Emerging Infect. Dis. - 2001. - Vol. 7, № 1. - P. 6-16.
- Brown P. Blood infectivity. processing and screening test in transmissible spongiform encephalopathy // Vox Sang. - 2005. - Vol. 89, № 2. - P. 63-70.
- Carmona P., Monleon E., Monzon M. el al. In vivo detection of scrapie cases from blood by infrared spectroscopyf // J. Gen. Virol. - 2005. - Vol. 86. - P. 3425-3431.
- Casalone C., Zanusso G., Acutis P. et al. Identification of second bovine amyloidotic spongiform encephalopathies: molecular similarities with sporadic Creutzfeldt-Jacob disease // Proc. Natl. Acad. Sci. USA. - 2004. - Vol. 101, № 9. - P. 3065- 3070.
- Castilla J., Saa P., Hetz C., Solo C. In vitro generation of infectious scrapie prions // Cell. - 2005. - Vol. 121. - P. 195- 206.
- Castilla J., Saa P., Soto C. Detection of prion in blood // Nat. Med. - 2005. - Vol. 11, № 9. - P. 982-985.
- Cervenakova L, Brown P., Soukharev S. et al. Failture of immunocompetitive capillary electrophoresis assay to detect disease-specific prion protein in buffy coat from humans and chimpanzees with Creutzfeldt-Jacob disease // Electrophoresis. - 2003. - Vol. 24, № 5. - P. 853-859.
- Cervenakova L., Brown P. Advances in sreening test development for transmissible spongiform encephalopathies // Expert Rev. Anti. Infect. Ther. - 2004. - Vol. 2, № 6. - P. 873-880.
- Chang В., Cheng В., Yin S. et al. Test for detection of disease-associated prion aggregate in the blood infected but asymptomatic animals // Clin. Vaccine Immunol. - 2007. - Vol. 14, № 1. - P. 36-43.
- Colby D. W., Zhang Q., Wang S. et al. Prion detection by an amyloid seeding assay // Proc. Natl. Acad. Sci. USA. - 2007. - Vol. 104, № 52. - P. 20914-20919.
- Come J. H., Fraser P. E., Landsbury P. T. A kinetic model for amyloid formation in the prion diseases: importance of seeding // Proc. Natl. Acad. Sci. USA. - 1993. - Vol. 90, № 13. P. 5959-5963.
- Creminon C., Grassi J. Characterisation of anti-PrP antybodies and measurement of PrP using ELISA techniques // Methods and Tools in Biosciences and Medicine-Techniques in Prion Research / Eds. S. Lehmann, J. Grassi. Berlin. - 2004. - P. 117-131.
- Curin S. V., Bresjanac M., Popovic M. et al. Monoclonal antybody against a peptide of human prion protein discriminated between Creutzfeldt-Jacob disease and normal brain tissue // J. Biol. Chem. - 2004. - Vol. 279. - P. 3694-3698.
- DeArmond S. J., Prusiner S. B. Etiology and pathogenesis of prion diseases // Am. J. Pathol. - 1995. - Vol. 146, № 4. - P. 785-811.
- Deleault N. R., Harris В. Т., Rees J. R., Supattapone S. Formation of native prions from minimal components in vitro // Proc. Natl. Acad. Sci. USA. - 2007. - Vol. 104, № 23. - P. 9741- 9746.
- Clock В., Winter M., Rennhofer S. O. et al. Transcript level of eritroid differentiation-related factor, a candidate surrogate marker for transmissible spongiform encephalopathies diseases in blood, show a broad range of variation in healthy individuals // Trunsfusion. - 2003. - Vol. 43, № 12. - P. 1706-1710.
- Gonzaless- Romero D., Barria M. A., Leon P. et al Detection of infectious prion in urine // FEBS Lett. - 2008. - Vol. 582. - P. 3161-3166.
- Grassi J., Maillet S., Simon S., Morel N. Progress and limits of TSE diagnostic tools // Vet. Res. - 2008. - Vol. 39. - P. 1- 39.
- Green A. J., Jackman R., Marshal T. A., Thompson E. J. Increased S-100b in the cerebrospinal fluid of some cattle with bovine spongiform encephalopathy // Vet. Rec. - 1999. - Vol. 145, № 4. - P. 107-109.
- Grigoriev V. B., Escaig-Haye F., Streichenberger. N. et al. Submicroscopic immunodetection of PrP in the brain of a patient with of new-variant of Creutzfeld-Jakob disease // Neurosci. Lett. - 1999. - Vol. 263. - P. 59-63.
- Grosset A., Moskovotz K., Nelsen C. et al. Rapid presymptomatic detection of PrPsc via conformationally responsive palindromic PrP peptides // Peptides. - 2005. - Vol. 26, № 11. - P. 2193-2200.
- Hilton D. A., Ghani A. C., Conyers L. et al Accomulation of prion protein in tonsil and appendix: review of tissue samples // Brit. Med. J. - 2002. - Vol. 325, № 7365. - P. 633-634.
- Hilton D. A., Ghani A. C., Conyers L . et al. Prevalence of lymphoreticular prion protein accumulation in UK tissue samples // J. Pathol. - 2004. - Vol. 203, № 3. - P. 733-739.
- Hilton D. A. Pathogenesis and prevalence of variant Creutzfeldt-Jacob disease // J. Pathol. - 2006. - Vol. 208, № 2. - P. 134-141.
- Holada K., Vostal L. G. Different levels of prion protein (PrPc) expression on hamster, mouse and human blood cells // Br. J. Hematol. - 2000. - Vol. 110, № 2. - P. 472-480.
- Houston F., Foster J., Chong A. et al. Transmission of BSE by blood transfusion in sheep // Lancet. - 2000. - Vol. 356, № 9234. - P. 999-1000.
- Ingrosso L.,Vetugno V., Cardone F., Pocchiari M. Molecular diagnostics of transmissible spongiform encephalopathies // Trend Mol. Med. - 2002. - Vol. 8, № 6. - P. 273-280.
- Klohn P. C., Stoltze L., Flechsig E. et al. A quantitative, highly sensitive cell-based infectivity assay for mouse scrapie prions // Proc. Natl. Acad. Sci. USA. - 2003. - Vol. 100, № 20. - P. 11666-11671.
- Korth C., Stierli P., Streit P. et al. Prion (PrPsc)-specific epitope defined by a monoclonal antibody // Nature. - 1997. - Vol. 390, № 6655. - P. 74-77.
- Korth C., Kaneko K., Groth D. et al. Abbreviated incubation times for human prions in mice expressing a chimeric mouse-human prion protein transgen // Proc. Natl. Acad. Sci. USA - 2003. - Vol. 100, № 8. - P. 4784-4789.
- Lane A., Stanley C. J., Dealler S., Wilson S. M. Polymeric ligands with specificity for aggregated prion protein // Clin. Chem. - 2003. - Vol. 49, № 10. - P. 1774-1775.
- Lehto M., Peery H. E., Cashman N. R. Current and future molecular diagnostics for prion diseases // Expert Rev. Mol. Diagn. - 2006. - Vol. 6, № 4. - P. 597-611.
- Maissen M., Roeckl C., Glatzel M. et al. Plasminogen binds to disease-associated prion protein of multiple species // Lancet. - 2001. - Vol. 357, № 9273. - P. 2026-2028.
- MacGregor I., Drummond Q., Turner M. et al. Distribution normal prion protein in blood // Transfus. Sci. - 2000. - Vol. 22, № 1-2. - P. 51.
- Miele G., Manson J., Clinton M. A novel eritroid-specific marker of transmissible spongiform encephalopathies // Nat. Med. - 2001. - Vol. 19, № 3. - P. 361-364.
- Missler U., Wiesmann M., Wittmann G. et al. Measurment of glial fibrillary acidic protein in human blood: analytical method and preliminary clinical results // Clin. Chem. - 1999. - Vol. 45, № 1. - P. 138-141.
- Moronchini G., Mangierieri M., Моrbin M. et al. Pathologic prion protein is specifically recognized in situ by a novel PrP conformational antybody // Neurobiol. Dis. - 2006. - Vol. 23. - P. 717-724.
- Moussa A., Coleman A. W., Bencsik A. et al. Use of streptomycin for precipitation and detection of proteinase К resistant prion protein (PrPsc) in biological samples // Chem. Commun. (Camb.). - 2006. - Vol. 9. - P. 973-975.
- Murayama Y., Yoshioka M., Horii H. Specific detection of prion antigenic determinants retained in bovine meat and bone meal by flow microbead immunoassay // J. Appl. Microbiol. - Vol. 101, № 2. - P. 369-376.
- Oesch В., Westaway D., Walchli M. et al A cellular gene encodes scrapie PrP 27-30 protein // Cell. - 1985. - Vol. 40, № 4. - P. 735-746.
- Otto M., Wiltfang J., Сереc L. et al. Tau protein and 14-3-3 protein in differential diagnosis of Creutzfeldt-Jacob disease // Neurology. - 2002. - Vol. 58, № 2. - P. 192-197.
- Pan Т., Chang В., Wong P. et al. An aggregation-specific enzyme-linked immunosorbent assay: detection of conformational differences between recombinant PrP protein dimmers and PrPsc aggregates // J. Virol. - 2005. - Vol. 79. № 19. - P. 12355-12364.
- Pan Т., Sethi J., Nelsen C. et al. Detection of misfolded prion protein in blood with conformationally sensitive peptides // Transfusion. - 2007. - Vol. 47, № 8. - P. 1418-1425.
- Panza G., Stohr J., Dumpitak C. et al. Spontaneous and BSE - prion-seeded amyloid formation of full length recombinant bovine prion protein // Biochem. Biophys. Res. Commun. 2008. - Vol. 373, № 4. - P. 493-497.
- Paramithiotis E., Pinard M., Lawton T. et al. A prion protein epitope selective for the pathlogically misfolded conformation // Nat. Med. - 2003. - Vol. 9, № 7. - P. 893-899.
- Parveen I., Moorby J., Allison G., Jackman R. The use of non- prion biomarkers for the diagnosis of transmissible spongiform encephalopathies in the live animal // Vet. Res. - 2005. -- Vol. 36, № 5-6. - P. 665-683.
- Pastrana M. A., Sajnani G., Onisko B. et al. Isolation and characterization of a proteinase K-sensitive PrPsc fraction // Biochemistry. - 2006. - Vol. 45. - P. 15710-15717.
- Peden A. H., Head M. W., Ritchie D. L. et al. Preclinical vCDJ after blood transfusion in PRNP codon 129 heterozygous patient // Lancet. - 2004. - Vol. 364, № 9433. - P. 527-529.
- Rhie A., Kirby L., Sayer N. et al. Characterisation of 2-fluoro-RNA aptamers that bind preferentially to disease-associated conformations of prion protein and inhibit conversion. // J. Biol. Chem. - 2003. - Vol. 278, № 41. - P. 39697-39705.
- Prusiner S. B. Novel proteinaceous infectiaous particles cause scrapie // Science. 1982. - Vol. 216, № 4542. - P. 136-144.
- Prusiner S. Prions // Proc. Natl. Acad. Sci. USA. - 1998. - Vol. 95. - P. 13363-13383.
- Rubenstein R., Gray P. C., Wehlburg C. M. et al. Detection and discrimination of PrPsc by multi-spectral ultraviolet fluorescence // Biochem. Biophys. Res. Commun. - 1998. - Vol. 246, № 1. - P. 100-106.
- Saborio G. P., Permanne В., Soto C. Sensitive detection of pathological prion protein by cyclic amplification of protein misfolding // Nature. - 2001. - Vol. 411, № 6839. - P. 810- 813.
- Safar J., Wille H., Itri V. et al. Eight prion strain have PrPsc molecules with different conformation // Nat. Med. - 1998. - Vol. 4, № 10. - P. 1157-1165.
- Sakudo A., Nakamura I., Ikuta K., Onodera T. Recent developments in prion disease research: Tools and in vitro cell culture models. // J. Vet. Med. Sci. - 2007. - Vol. 69, № 4. - P. 329-337.
- Sanchez-Valle R.. Saiz A., Graus F. Cerebrospinal fluid biomarkers in the diagnosis of Creutzfeldt-Jacob disease // Neurosci. Lett. - 2002. - Vol. 320. - P. 69-72.
- Sigurdson C. J., Nilsson K. P., Hornemann S. et al. Prion strain discrimination using luminescent conjugated polymers // Nature Meth. - 2007. - Vol. 4, № 12. - P. 1023-1030.
- Simдk J., Holada K., D'Agnillo F. et al Cellular prion protein is expressed on endothelial cells and is released during apoptosis on membrane microparticles found in human plasma // Trunsfusion. - 2002. - Vol. 42. - P. 334-342.
- Simon S., Nugier J., Morel N. et al. Rapid typing of transmissible spongiform encephalopathies strains with differential ELISA // Emerg. Infect. Dis. - 2008. - Vol. 14, № 4. - P. 608-616.
- Stack M. Western immunoblotting techniques for the study of transmissible spongiform encephalopathies // Methods and tools in Biosciences and Medicine-Techniques in prion research / Eds. S. Lehmann, J. Grassi. Berlin. - 2004. - P. 97-116.
- Tcherkasskaya O., Davidson E. A., Schmerr M. J., Orser C. S. Conformational biosensor for diagnosis of prion disease // Biotechn. Lett. - 2005. - Vol. 27. - P. 671-675.
- Trieschmann L., Navarrete S. A., Kaschig K. et al. Ultra-sensitive detection of prion protein fibrils by flow cytometry in blood from cattle affected with bovine spongiform encephalopathy // BMC Biotechnology. - 2005. - Vol. 5. - P. 26.
- Watts J. C., Westway D. The prion protein family: Diversity, rivalry, and dysfunction // Biochim. Biophys. Acta. - 2007. - Vol. 1772, № 6. - P. 654-672.
- Wroe S. J., Pal S., Siddique D. et al. Clinical presentation and pre-mortem diagnosis of variant Creutzfeldt-Jacob disease associated with blood transfusion; a case report, // Lancet. - 2006. - Vol. 368, № 9552. - P. 2061-2067.
- Yang W. C., Schmerr M. J., Jackman R. et al. Capillary electrophoresis-based noncompetitive immunoassay for the prion protein using fluorescin-labeled protein as a fluorescent probe // Anal. Chem. - 2005. - Vol. 77, № 14. - P. 4489-4494.
- Zou W. Q., Zheng J., Gry D. M. et al. Antybody to DNA detectes scrapie but not normal prion protein // Proc. Natl. Acad. Sci. USA. - 2004. - Vol. 101, № 5. - P. 1380-1385.