Skip to main content
Log in

Agent-specific Shadoo Responses in Transmissible Encephalopathies

  • Published:
Journal of Neuroimmune Pharmacology Aims and scope Submit manuscript

Abstract

Transmissible spongiform encephalopathies (TSE) are neurodegenerative diseases caused by an infectious agent with viral properties. Host prion protein (PrP), a marker of late stage TSE pathology, is linked to a similar protein called Shadoo (Sho). Sho is reduced in mice infected with the RML scrapie agent, but has not been investigated in other TSEs. Although PrP is required for infection by TSE agents, it is not known if Sho is similarly required. Presumably Sho protects cells from toxic effects of misfolded PrP. We compared Sho and PrP changes after infection by very distinct TSE agents including sporadic CJD, Asiatic CJD, New Guinea kuru, vCJD (the UK epidemic bovine agent) and 22L sheep scrapie, all passaged in standard mice. We found that Sho reductions were agent-specific. Variable Sho reductions in standard mice could be partly explained by agent-specific differences in regional neuropathology. However, Sho did not follow PrP misfolding in any quantitative or consistent way. Tga20 mice with high murine PrP levels revealed additional agent-specific differences. Sho was unaffected by Asiatic CJD yet was markedly reduced by the kuru agent in Tga20 mice; in standard mice both agents induced the same Sho reductions. Analyses of neural GT1 cells demonstrated that Sho was not essential for TSE infections. Furthermore, because all infected GT1 cells appeared as healthy as uninfected controls, Sho was not needed to protect infected cells from their “toxic” burden of abundant abnormal PrP and intracellular amyloid.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Fig. 1
Fig. 2
Fig. 3
Fig. 4

Similar content being viewed by others

References

  • Akowitz A, Sklaviadis T, Manuelidis L (1994) Endogenous viral complexes with long RNA cosediment with the agent of Creutzfeldt-Jakob disease. Nucleic Acids Res 22:1101–1107

    Article  CAS  PubMed  Google Scholar 

  • Arjona A, Simarro L, Islinger F, Nishida N, Manuelidis L (2004) Two Creutzfeldt-Jakob disease agents reproduce prion protein-independent identities in cell cultures. Proc Natl Acad Sci U S A 101:8768–8773

    Article  CAS  PubMed  Google Scholar 

  • Baker CA, Manuelidis L (2003) Unique inflammatory RNA profiles of microglia in Creutzfeldt-Jakob disease. Proc Natl Acad Sci U S A 100:675–679

    Article  CAS  PubMed  Google Scholar 

  • Baker CA, Martin D, Manuelidis L (2002) Microglia from Creutzfeldt-Jakob disease-infected brains are infectious and show specific mRNA activation profiles. J Virol 76:10905–10913

    Article  CAS  PubMed  Google Scholar 

  • Baker CA, Lu ZY, Manuelidis L (2004) Early induction of interferon-responsive mRNAs in Creutzfeldt-Jakob disease. J Neurovirol 10:29–40

    Article  CAS  PubMed  Google Scholar 

  • Barron RM, Campbell SL, King D, Bellon A, Chapman KE, Williamson RA, Manson JC (2007) High titers of transmissible spongiform encephalopathy infectivity associated with extremely low levels of PrPSc in vivo. J Biol Chem 282:35878–35886

    Article  CAS  PubMed  Google Scholar 

  • Comoy EE, Casalone C, Lescoutra-Etchegaray N, Zanusso G, Freire S, Marce D, Auvre F, Ruchoux MM, Ferrari S, Monaco S, Sales N, Caramelli M, Leboulch P, Brown P, Lasmezas CI, Deslys JP (2008) Atypical BSE (BASE) transmitted from asymptomatic aging cattle to a primate. PLoS ONE 3:e3017

    Article  PubMed  Google Scholar 

  • Fischer M, Rulicke T, Raeber A, Sailer A, Moser M, Oesch B, Brandner S, Aguzzi A, Weissmann C (1996) Prion protein (PrP) with amino-proximal deletions restoring susceptibility of PrP knockout mice to scrapie. EMBO J 15:1255–1264

    CAS  PubMed  Google Scholar 

  • Forloni G, Angeretti N, Chiesa R, Monzani E, Salmona M, Bugiani O, Tagliavini F (1993) Neurotoxicity of a prion protein fragment. Nature 362:543–546

    Article  CAS  PubMed  Google Scholar 

  • Gossner AG, Bennet N, Hunter N, Hopkins J (2009) Differential expression of Prnp and Sprn in scrapie infected sheep also reveals Prnp genotype specific differences. Biochem Biophys Res Commun 378:862–866

    Article  CAS  PubMed  Google Scholar 

  • Hunter N, Cairns D (1998) Scrapie-free Merino and Poll Dorset sheep from Australia and New Zealand have normal frequencies of scrapie-susceptible PrP genotypes. J Gen Virol 79(Pt 8):2079–2082

    CAS  PubMed  Google Scholar 

  • Lloyd SE, Grizenkova J, Pota H, Collinge J (2009) Shadoo (Sprn) and prion disease incubation time in mice. Mamm Genome 20:367–374

    Article  CAS  PubMed  Google Scholar 

  • Lu ZY, Baker CA, Manuelidis L (2004) New molecular markers of early and progressive CJD brain infection. J Cell Biochem 93:644–652

    Article  CAS  PubMed  Google Scholar 

  • Manuelidis L (1994) The dimensions of Creutzfeldt-Jakob disease. Transfusion 34:915–928

    Article  CAS  PubMed  Google Scholar 

  • Manuelidis L (1998) Vaccination with an attenuated Creutzfeldt-Jakob disease strain prevents expression of a virulent agent. Proc Natl Acad Sci U S A 95:2520–2525

    Article  CAS  PubMed  Google Scholar 

  • Manuelidis L (2006) A 25 nm virion is the likely cause of transmissible spongiform encephalopathies. J Cell Biochem 100:897–915

    Article  Google Scholar 

  • Manuelidis L (2010) Transmissible encephalopathy agents: virulence, geography and clockwork. Virulence 1:1–4

    Google Scholar 

  • Manuelidis L, Fritch W (1996) Infectivity and host responses in Creutzfeldt-Jakob disease. Virology 216:46–59

    Article  CAS  PubMed  Google Scholar 

  • Manuelidis L, Lu ZY (2000) Attenuated Creutzfeldt-Jakob disease agents can hide more virulent infections. Neurosci Lett 293:163–166

    Article  CAS  PubMed  Google Scholar 

  • Manuelidis EE, Kim J, Angelo JN, Manuelidis L (1976) Serial propagation of Creutzfeldt-Jakob disease in guinea pigs. Proc Natl Acad Sci U S A 73:223–227

    Article  CAS  PubMed  Google Scholar 

  • Manuelidis EE, Gorgacz EJ, Manuelidis L (1978) Transmission of Creutzfeldt-Jakob disease with scrapie-like syndromes to mice. Nature 271:778–779

    Article  CAS  PubMed  Google Scholar 

  • Manuelidis L, Sklaviadis T, Akowitz A, Fritch W (1995) Viral particles are required for infection in neurodegenerative Creutzfeldt-Jakob disease. Proc Natl Acad Sci U S A 92:5124–5128

    Article  CAS  PubMed  Google Scholar 

  • Manuelidis L, Fritch W, Xi YG (1997) Evolution of a strain of CJD that induces BSE-like plaques. Science 277:94–98

    Article  CAS  PubMed  Google Scholar 

  • Manuelidis L, Yu ZX, Banquero N, Mullins B (2007) Cells infected with scrapie and Creutzfeldt-Jakob disease agents produce intracellular 25-nm virus-like particles. Proc Natl Acad Sci U S A 104:1965–1970

    Article  CAS  PubMed  Google Scholar 

  • Manuelidis L, Chakrabarty T, Miyazawa K, Nduom NA, Emmerling K (2009a) The kuru infectious agent is a unique geographic isolate distinct from Creutzfeldt-Jakob disease and scrapie agents. Proc Natl Acad Sci U S A 106:13529–13534

    Article  CAS  PubMed  Google Scholar 

  • Manuelidis L, Liu Y, Mullins B (2009b) Strain-specific viral properties of variant Creutzfeldt-Jakob disease (vCJD) are encoded by the agent and not by host prion protein. J Cell Biochem 106:220–231

    Article  CAS  PubMed  Google Scholar 

  • Massignan T, Stewart RS, Biasini E, Solomon IH, Bonetto V, Chiesa R, Harris DA (2009) A novel, drug-based, cellular assay for the activity of neurotoxic mutants of the prion protein. J Biol Chem. doi:10.1074/jbc.M109.064949

  • Nishida N, Katamine S, Manuelidis L (2005) Reciprocal interference between specific CJD and scrapie agents in neural cell cultures. Science 310:493–496

    Article  CAS  PubMed  Google Scholar 

  • Premzl M, Sangiorgio L, Strumbo B, Marshall Graves JA, Simonic T, Gready JE (2003) Shadoo, a new protein highly conserved from fish to mammals and with similarity to prion protein. Gene 314:89–102

    Article  CAS  PubMed  Google Scholar 

  • Prusiner SB (1998) Prions. Proc Natl Acad Sci U S A 95:13363–13383

    Article  CAS  PubMed  Google Scholar 

  • Sakaguchi S, Katamine S, Yamanouchi K, Kishikawa M, Moriuchi R, Yasukawa N, Doi T, Miyamoto T (1993) Kinetics of infectivity are dissociated from PrP accumulation in salivary glands of Creutzfeldt-Jakob disease agent-inoculated mice. J Gen Virol 74(Pt 10):2117–2123

    Article  CAS  PubMed  Google Scholar 

  • Silveira JR, Raymond GJ, Hughson AG, Race RE, Sim VL, Hayes SF, Caughey B (2005) The most infectious prion protein particles. Nature 437:257–261

    Article  CAS  PubMed  Google Scholar 

  • Sklaviadis T, Dreyer R, Manuelidis L (1992) Analysis of Creutzfeldt-Jakob disease infectious fractions by gel permeation chromatography and sedimentation field flow fractionation. Virus Res 26:241–254

    Article  CAS  PubMed  Google Scholar 

  • Sklaviadis T, Akowitz A, Manuelidis EE, Manuelidis L (1993) Nucleic acid binding proteins in highly purified Creutzfeldt-Jakob disease preparations. Proc Natl Acad Sci U S A 90:5713–5717

    Article  CAS  PubMed  Google Scholar 

  • Sun R, Liu Y, Zhang H, Manuelidis L (2008) Quantitative recovery of scrapie agent with minimal protein from highly infectious cultures. Viral Immunol 21:293–302

    Article  CAS  PubMed  Google Scholar 

  • Tateishi J, Ohta M, Koga M, Sato Y, Kuroiwa Y (1979) Transmission of chronic spongiform encephalopathy with kuru plaques from humans to small rodents. Ann Neurol 5:581–584

    Article  CAS  PubMed  Google Scholar 

  • Watts JC, Drisaldi B, Ng V, Yang J, Strome B, Horne P, Sy MS, Yoong L, Young R, Mastrangelo P, Bergeron C, Fraser PE, Carlson GA, Mount HT, Schmitt-Ulms G, Westaway D (2007) The CNS glycoprotein Shadoo has PrP(C)-like protective properties and displays reduced levels in prion infections. EMBO J 26:4038–4050

    Article  CAS  PubMed  Google Scholar 

  • Xi YG, Ingrosso L, Ladogana A, Masullo C, Pocchiari M (1992) Amphotericin B treatment dissociates in vivo replication of the scrapie agent from PrP accumulation. Nature 356:598–601

    Article  CAS  PubMed  Google Scholar 

Download references

Acknowledgements

We thank Kaitlin Emmerling and Carolyn Brokowski for manuscript improvements. This work was supported by Neurological Disorders and Stroke Grant RO1 012674 and National Institutes of Allergy and Infectious Diseases Grant R21 A1076645.

Conflict of Interest

None

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Laura Manuelidis.

Additional information

Grant support: NINDS RO1 012674; NIAID R21 A1076645

Rights and permissions

Reprints and permissions

About this article

Cite this article

Miyazawa, K., Manuelidis, L. Agent-specific Shadoo Responses in Transmissible Encephalopathies. J Neuroimmune Pharmacol 5, 155–163 (2010). https://doi.org/10.1007/s11481-010-9191-1

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s11481-010-9191-1

Keywords

Navigation