1887

Abstract

Chronic wasting disease (CWD) of deer and elk is a highly communicable neurodegenerative disorder caused by prions. Investigations of CWD are hampered by slow bioassays in transgenic (Tg) mice. Towards the development of Tg mice that will be more susceptible to CWD prions, we created a series of chimeric elk/mouse transgenes that encode the N terminus of elk PrP (ElkPrP) up to residue Y168 and the C terminus of mouse PrP (MoPrP) beyond residue 169 (mouse numbering), designated Elk3M(SNIVVK). Between codons 169 and 219, six residues distinguish ElkPrP from MoPrP: N169S, T173N, V183I, I202V, I214V and R219K. Using chimeric elk/mouse PrP constructs, we generated 12 Tg mouse lines and determined incubation times after intracerebral inoculation with the mouse-passaged RML scrapie or Elk1P CWD prions. Unexpectedly, one Tg mouse line expressing Elk3M(SNIVVK) exhibited incubation times of <70 days when inoculated with RML prions; a second line had incubation times of <90 days. In contrast, mice expressing full-length ElkPrP had incubation periods of >250 days for RML prions. Tg(Elk3M,SNIVVK) mice were less susceptible to CWD prions than Tg(ElkPrP) mice. Changing three C-terminal mouse residues (202, 214 and 219) to those of elk doubled the incubation time for mouse RML prions and rendered the mice resistant to Elk1P CWD prions. Mutating an additional two residues from mouse to elk at codons 169 and 173 increased the incubation times for mouse prions to >300 days, but made the mice susceptible to CWD prions. Our findings highlight the role of C-terminal residues in PrP that control the susceptibility and replication of prions.

Loading

Article metrics loading...

/content/journal/jgv/10.1099/vir.0.045989-0
2013-02-01
2024-04-16
Loading full text...

Full text loading...

/deliver/fulltext/jgv/94/2/443.html?itemId=/content/journal/jgv/10.1099/vir.0.045989-0&mimeType=html&fmt=ahah

References

  1. Agrimi U., Nonno R., Dell’Omo G., Di Bari M. A., Conte M., Chiappini B., Esposito E., Di Guardo G., Windl O.other authors 2008; Prion protein amino acid determinants of differential susceptibility and molecular feature of prion strains in mice and voles. PLoS Pathog 4:e1000113 [View Article][PubMed]
    [Google Scholar]
  2. Angers R. C., Browning S. R., Seward T. S., Sigurdson C. J., Miller M. W., Hoover E. A., Telling G. C. 2006; Prions in skeletal muscles of deer with chronic wasting disease. Science 311:1117 [View Article][PubMed]
    [Google Scholar]
  3. Bahmanyar S., Williams E. S., Johnson F. B., Young S., Gajdusek D. C. 1985; Amyloid plaques in spongiform encephalopathy of mule deer. J Comp Pathol 95:1–5 [View Article][PubMed]
    [Google Scholar]
  4. Barron R. M., Thomson V., Jamieson E., Melton D. W., Ironside J., Will R., Manson J. C. 2001; Changing a single amino acid in the N-terminus of murine PrP alters TSE incubation time across three species barriers. EMBO J 20:5070–5078 [View Article][PubMed]
    [Google Scholar]
  5. Brookmeyer R., Crowley J. 1982; A confidence interval for the median survival time. Biometrics 38:29–41 [View Article]
    [Google Scholar]
  6. Browning S. R., Mason G. L., Seward T., Green M., Eliason G. A., Mathiason C., Miller M. W., Williams E. S., Hoover E., Telling G. C. 2004; Transmission of prions from mule deer and elk with chronic wasting disease to transgenic mice expressing cervid PrP. J Virol 78:13345–13350 [View Article][PubMed]
    [Google Scholar]
  7. Büeler H., Fischer M., Lang Y., Bluethmann H., Lipp H.-P., DeArmond S. J., Prusiner S. B., Aguet M., Weissmann C. 1992; Normal development and behaviour of mice lacking the neuronal cell-surface PrP protein. Nature 356:577–582 [View Article][PubMed]
    [Google Scholar]
  8. Carlson G. A., Goodman P. A., Lovett M., Taylor B. A., Marshall S. T., Peterson-Torchia M., Westaway D., Prusiner S. B. 1988; Genetics and polymorphism of the mouse prion gene complex: control of scrapie incubation time. Mol Cell Biol 8:5528–5540[PubMed]
    [Google Scholar]
  9. Carlson G. A., Westaway D., DeArmond S. J., Peterson-Torchia M., Prusiner S. B. 1989; Primary structure of prion protein may modify scrapie isolate properties. Proc Natl Acad Sci U S A 86:7475–7479 [View Article][PubMed]
    [Google Scholar]
  10. Carlson G. A., Ebeling C., Yang S.-L., Telling G., Torchia M., Groth D., Westaway D., DeArmond S. J., Prusiner S. B. 1994; Prion isolate specified allotypic interactions between the cellular and scrapie prion proteins in congenic and transgenic mice. Proc Natl Acad Sci U S A 91:5690–5694 [View Article][PubMed]
    [Google Scholar]
  11. Chandler R. L. 1961; Encephalopathy in mice produced by inoculation with scrapie brain material. Lancet 277:1378–1379 [View Article][PubMed]
    [Google Scholar]
  12. Colby D. W., Wain R., Baskakov I. V., Legname G., Palmer C. G., Nguyen H. O., Lemus A., Cohen F. E., DeArmond S. J., Prusiner S. B. 2010; Protease-sensitive synthetic prions. PLoS Pathog 6:e1000736 [View Article][PubMed]
    [Google Scholar]
  13. Fox K. A., Jewell J. E., Williams E. S., Miller M. W. 2006; Patterns of PrPCWD accumulation during the course of chronic wasting disease infection in orally inoculated mule deer (Odocoileus hemionus). J Gen Virol 87:3451–3461 [View Article][PubMed]
    [Google Scholar]
  14. Giles K., Glidden D. V., Patel S., Korth C., Groth D., Lemus A., DeArmond S. J., Prusiner S. B. 2010; Human prion strain selection in transgenic mice. Ann Neurol 68:151–161 [View Article][PubMed]
    [Google Scholar]
  15. Giles K., De Nicola G. F., Patel S., Glidden D. V., Korth C., Oehler A., DeArmond S. J., Prusiner S. B. 2012; Identification of I137M and other mutations that modulate incubation periods for two human prion strains. J Virol 86:6033–6041 [View Article][PubMed]
    [Google Scholar]
  16. Gossert A. D., Bonjour S., Lysek D. A., Fiorito F., Wüthrich K. 2005; Prion protein NMR structures of elk and of mouse/elk hybrids. Proc Natl Acad Sci U S A 102:646–650 [View Article][PubMed]
    [Google Scholar]
  17. Green K. M., Browning S. R., Seward T. S., Jewell J. E., Ross D. L., Green M. A., Williams E. S., Hoover E. A., Telling G. C. 2008; The elk PRNP codon 132 polymorphism controls cervid and scrapie prion propagation. J Gen Virol 89:598–608 [View Article][PubMed]
    [Google Scholar]
  18. Hamir A. N., Miller J. M., Cutlip R. C., Kunkle R. A., Jenny A. L., Stack M. J., Chaplin M. J., Richt J. A. 2004; Transmission of sheep scrapie to elk (Cervus elaphus nelsoni) by intracerebral inoculation: final outcome of the experiment. J Vet Diagn Invest 16:316–321 [View Article][PubMed]
    [Google Scholar]
  19. Kaneko K., Zulianello L., Scott M., Cooper C. M., Wallace A. C., James T. L., Cohen F. E., Prusiner S. B. 1997; Evidence for protein X binding to a discontinuous epitope on the cellular prion protein during scrapie prion propagation. Proc Natl Acad Sci U S A 94:10069–10074 [View Article][PubMed]
    [Google Scholar]
  20. Kaplan E. L., Meier P. 1958; Nonparametric estimation from incomplete observations. J Am Stat Assoc 53:457–481 [View Article]
    [Google Scholar]
  21. Kong Q., Huang S., Zou W., Vanegas D., Wang M., Wu D., Yuan J., Zheng M., Bai H.other authors 2005; Chronic wasting disease of elk: transmissibility to humans examined by transgenic mouse models. J Neurosci 25:7944–7949 [View Article][PubMed]
    [Google Scholar]
  22. Korth C., Kaneko K., Groth D., Heye N., Telling G., Mastrianni J., Parchi P., Gambetti P., Will R.other authors 2003; Abbreviated incubation times for human prions in mice expressing a chimeric mouse–human prion protein transgene. Proc Natl Acad Sci U S A 100:4784–4789 [View Article][PubMed]
    [Google Scholar]
  23. Kurt T. D., Telling G. C., Zabel M. D., Hoover E. A. 2009; Trans-species amplification of PrP(CWD) and correlation with rigid loop 170N. Virology 387:235–243 [View Article][PubMed]
    [Google Scholar]
  24. LaFauci G., Carp R. I., Meeker H. C., Ye X., Kim J. I., Natelli M., Cedeno M., Petersen R. B., Kascsak R., Rubenstein R. 2006; Passage of chronic wasting disease prion into transgenic mice expressing Rocky Mountain elk (Cervus elaphus nelsoni) PrPC.. J Gen Virol 87:3773–3780 [View Article][PubMed]
    [Google Scholar]
  25. Manson J. C., Jamieson E., Baybutt H., Tuzi N. L., Barron R., McConnell I., Somerville R., Ironside J., Will R.other authors 1999; A single amino acid alteration (101L) introduced into murine PrP dramatically alters incubation time of transmissible spongiform encephalopathy. EMBO J 18:6855–6864 [View Article][PubMed]
    [Google Scholar]
  26. Martin S., Jeffrey M., González L., Sisó S., Reid H. W., Steele P., Dagleish M. P., Stack M. J., Chaplin M. J., Balachandran A. 2009; Immunohistochemical and biochemical characteristics of BSE and CWD in experimentally infected European red deer (Cervus elaphus elaphus). BMC Vet Res 5:26 [View Article][PubMed]
    [Google Scholar]
  27. Mathiason C. K., Powers J. G., Dahmes S. J., Osborn D. A., Miller K. V., Warren R. J., Mason G. L., Hays S. A., Hayes-Klug J.other authors 2006; Infectious prions in the saliva and blood of deer with chronic wasting disease. Science 314:133–136 [View Article][PubMed]
    [Google Scholar]
  28. Miller M. W., Williams E. S., Hobbs N. T., Wolfe L. L. 2004; Environmental sources of prion transmission in mule deer. Emerg Infect Dis 10:1003–1006 [View Article][PubMed]
    [Google Scholar]
  29. Muramoto T., DeArmond S. J., Scott M., Telling G. C., Cohen F. E., Prusiner S. B. 1997; Heritable disorder resembling neuronal storage disease in mice expressing prion protein with deletion of an α-helix. Nat Med 3:750–755 [View Article][PubMed]
    [Google Scholar]
  30. Nichols T. A., Pulford B., Wyckoff A. C., Meyerett C., Michel B., Gertig K., Hoover E. A., Jewell J. E., Telling G. C., Zabel M. D. 2009; Detection of protease-resistant cervid prion protein in water from a CWD-endemic area. Prion 3:171–183 [View Article][PubMed]
    [Google Scholar]
  31. Perrier V., Wallace A. C., Kaneko K., Safar J., Prusiner S. B., Cohen F. E. 2000; Mimicking dominant negative inhibition of prion replication through structure-based drug design. Proc Natl Acad Sci U S A 97:6073–6078 [View Article][PubMed]
    [Google Scholar]
  32. Perrier V., Kaneko K., Safar J., Vergara J., Tremblay P., DeArmond S. J., Cohen F. E., Prusiner S. B., Wallace A. C. 2002; Dominant-negative inhibition of prion replication in transgenic mice. Proc Natl Acad Sci U S A 99:13079–13084 [View Article][PubMed]
    [Google Scholar]
  33. Prusiner S. B., Scott M., Foster D., Pan K.-M., Groth D., Mirenda C., Torchia M., Yang S.-L., Serban D.other authors 1990; Transgenetic studies implicate interactions between homologous PrP isoforms in scrapie prion replication. Cell 63:673–686 [View Article][PubMed]
    [Google Scholar]
  34. Safar J. G., Scott M., Monaghan J., Deering C., Didorenko S., Vergara J., Ball H., Legname G., Leclerc E.other authors 2002; Measuring prions causing bovine spongiform encephalopathy or chronic wasting disease by immunoassays and transgenic mice. Nat Biotechnol 20:1147–1150 [View Article][PubMed]
    [Google Scholar]
  35. Scott M., Foster D., Mirenda C., Serban D., Coufal F., Wälchli M., Torchia M., Groth D., Carlson G.other authors 1989; Transgenic mice expressing hamster prion protein produce species-specific scrapie infectivity and amyloid plaques. Cell 59:847–857 [View Article][PubMed]
    [Google Scholar]
  36. Scott M. R., Köhler R., Foster D., Prusiner S. B. 1992; Chimeric prion protein expression in cultured cells and transgenic mice. Protein Sci 1:986–997 [View Article][PubMed]
    [Google Scholar]
  37. Scott M., Groth D., Foster D., Torchia M., Yang S.-L., DeArmond S. J., Prusiner S. B. 1993; Propagation of prions with artificial properties in transgenic mice expressing chimeric PrP genes. Cell 73:979–988 [View Article][PubMed]
    [Google Scholar]
  38. Scott M. R., Peretz D., Nguyen H.-O. B., DeArmond S. J., Prusiner S. B. 2005; Transmission barriers for bovine, ovine, and human prions in transgenic mice. J Virol 79:5259–5271 [View Article][PubMed]
    [Google Scholar]
  39. Sigurdson C. J. 2008; A prion disease of cervids: chronic wasting disease. Vet Res 39:41 [View Article][PubMed]
    [Google Scholar]
  40. Sigurdson C. J., Williams E. S., Miller M. W., Spraker T. R., O’Rourke K. I., Hoover E. A. 1999; Oral transmission and early lymphoid tropism of chronic wasting disease PrPres in mule deer fawns (Odocoileus hemionus). J Gen Virol 80:2757–2764[PubMed]
    [Google Scholar]
  41. Sigurdson C. J., Nilsson K. P., Hornemann S., Heikenwalder M., Manco G., Schwarz P., Ott D., Rülicke T., Liberski P. P.other authors 2009; De novo generation of a transmissible spongiform encephalopathy by mouse transgenesis. Proc Natl Acad Sci U S A 106:304–309 [View Article][PubMed]
    [Google Scholar]
  42. Tamgüney G., Giles K., Bouzamondo-Bernstein E., Bosque P. J., Miller M. W., Safar J., DeArmond S. J., Prusiner S. B. 2006; Transmission of elk and deer prions to transgenic mice. J Virol 80:9104–9114 [View Article][PubMed]
    [Google Scholar]
  43. Tamgüney G., Miller M. W., Giles K., Lemus A., Glidden D. V., DeArmond S. J., Prusiner S. B. 2009a; Transmission of scrapie and sheep-passaged bovine spongiform encephalopathy prions to transgenic mice expressing elk prion protein. J Gen Virol 90:1035–1047 [View Article][PubMed]
    [Google Scholar]
  44. Tamgüney G., Miller M. W., Wolfe L. L., Sirochman T. M., Glidden D. V., Palmer C., Lemus A., DeArmond S. J., Prusiner S. B. 2009b; Asymptomatic deer excrete infectious prions in faeces. Nature 461:529–532 [View Article][PubMed]
    [Google Scholar]
  45. Tamgüney G., Richt J. A., Hamir A. N., Greenlee J. J., Miller M. W., Wolfe L. L., Sirochman T. M., Young A. J., Glidden D. V.other authors 2012; Salivary prions in sheep and deer. Prion 6:52–61 [View Article][PubMed]
    [Google Scholar]
  46. Telling G. C., Scott M., Hsiao K. K., Foster D., Yang S.-L., Torchia M., Sidle K. C. L., Collinge J., DeArmond S. J., Prusiner S. B. 1994; Transmission of Creutzfeldt–Jakob disease from humans to transgenic mice expressing chimeric human–mouse prion protein. Proc Natl Acad Sci U S A 91:9936–9940 [View Article][PubMed]
    [Google Scholar]
  47. Telling G. C., Scott M., Mastrianni J., Gabizon R., Torchia M., Cohen F. E., DeArmond S. J., Prusiner S. B. 1995; Prion propagation in mice expressing human and chimeric PrP transgenes implicates the interaction of cellular PrP with another protein. Cell 83:79–90 [View Article][PubMed]
    [Google Scholar]
  48. Telling G. C., Haga T., Torchia M., Tremblay P., DeArmond S. J., Prusiner S. B. 1996; Interactions between wild-type and mutant prion proteins modulate neurodegeneration in transgenic mice. Genes Dev 10:1736–1750 [View Article][PubMed]
    [Google Scholar]
  49. Trifilo M. J., Ying G., Teng C., Oldstone M. B. 2007; Chronic wasting disease of deer and elk in transgenic mice: oral transmission and pathobiology. Virology 365:136–143 [View Article][PubMed]
    [Google Scholar]
  50. Williams E. S. 2005; Chronic wasting disease. Vet Pathol 42:530–549 [View Article][PubMed]
    [Google Scholar]
  51. Zulianello L., Kaneko K., Scott M., Erpel S., Han D., Cohen F. E., Prusiner S. B. 2000; Dominant-negative inhibition of prion formation diminished by deletion mutagenesis of the prion protein. J Virol 74:4351–4360 [View Article][PubMed]
    [Google Scholar]
http://instance.metastore.ingenta.com/content/journal/jgv/10.1099/vir.0.045989-0
Loading
/content/journal/jgv/10.1099/vir.0.045989-0
Loading

Data & Media loading...

This is a required field
Please enter a valid email address
Approval was a Success
Invalid data
An Error Occurred
Approval was partially successful, following selected items could not be processed due to error