This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrowReprints and Permissions
Right arrow Copyright Information
Right arrow Books from ASM Press
Right arrow MicrobeWorld
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Bossers, A.
Right arrow Articles by Smits, M. A.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Bossers, A.
Right arrow Articles by Smits, M. A.

 Previous Article  |  Next Article 

Journal of Virology, February 2000, p. 1407-1414, Vol. 74, No. 3
0022-538X/00/$04.00+0
Copyright © 2000, American Society for Microbiology. All rights reserved.

Susceptibility of Sheep for Scrapie as Assessed by In Vitro Conversion of Nine Naturally Occurring Variants of PrP

Alex Bossers, Ruth de Vries, and Mari A. Smits*

Institute for Animal Science and Health, Lelystad, The Netherlands

Received 21 June 1999/Accepted 18 October 1999

Polymorphisms in the prion protein (PrP) gene are associated with phenotypic expression differences of transmissible spongiform encephalopathies in animals and humans. In sheep, at least 10 different mutually exclusive polymorphisms are present in PrP. In this study, we determined the efficiency of the in vitro formation of protease-resistant PrP of nine sheep PrP allelic variants in order to gauge the relative susceptibility of sheep for scrapie. No detectable spontaneous protease-resistant PrP formation occurred under the cell-free conditions used. All nine host-encoded cellular PrP (PrPC) variants had distinct conversion efficiencies induced by PrPSc isolated from sheep with three different homozygous PrP genotypes. In general, PrP allelic variants with polymorphisms at either codon 136 (Ala to Val) or codon 141 (Leu to Phe) and phylogenetic wild-type sheep PrPC converted with highest efficiency to protease-resistant forms, which indicates a linkage with a high susceptibility of sheep for scrapie. PrPC variants with polymorphisms at codons 171 (Gln to Arg), 154 (Arg to His), and to a minor extent 112 (Met to Thr) converted with low efficiency to protease-resistant isoforms. This finding indicates a linkage of these alleles with a reduced susceptibility or resistance for scrapie. In addition, PrPSc with the codon 171 (Gln-to-His) polymorphism is the first variant reported to induce higher conversion efficiencies with heterologous rather than homologous PrP variants. The results of this study strengthen our views on polymorphism barriers and have further implications for scrapie control programs by breeding strategies.


* Corresponding author. Mailing address: Institute for Animal Science and Health, Lelystad, The Netherlands. Phone: 31-320-238270. Fax: 31-320-238153. E-mail: m.a.smits{at}id.dlo.nl.


Journal of Virology, February 2000, p. 1407-1414, Vol. 74, No. 3
0022-538X/00/$04.00+0
Copyright © 2000, American Society for Microbiology. All rights reserved.



This article has been cited by other articles:

  • Saunders, G. C., Lantier, I., Cawthraw, S., Berthon, P., Moore, S. J., Arnold, M. E., Windl, O., Simmons, M. M., Andreoletti, O., Bellworthy, S., Lantier, F. (2009). Protective effect of the T112 PrP variant in sheep challenged with bovine spongiform encephalopathy. J. Gen. Virol. 90: 2569-2574 [Abstract] [Full Text]  
  • Laegreid, W. W., Clawson, M. L., Heaton, M. P., Green, B. T., O'Rourke, K. I., Knowles, D. P. (2008). Scrapie Resistance in ARQ Sheep. J. Virol. 82: 10318-10320 [Abstract] [Full Text]  
  • Vaccari, G., D'Agostino, C., Nonno, R., Rosone, F., Conte, M., Di Bari, M. A., Chiappini, B., Esposito, E., De Grossi, L., Giordani, F., Marcon, S., Morelli, L., Borroni, R., Agrimi, U. (2007). Prion Protein Alleles Showing a Protective Effect on the Susceptibility of Sheep to Scrapie and Bovine Spongiform Encephalopathy. J. Virol. 81: 7306-7309 [Abstract] [Full Text]  
  • Kirby, L., Goldmann, W., Houston, F., Gill, A. C., Manson, J. C. (2006). A novel, resistance-linked ovine PrP variant and its equivalent mouse variant modulate the in vitro cell-free conversion of rPrP to PrPres. J. Gen. Virol. 87: 3747-3751 [Abstract] [Full Text]  
  • Eiden, M., Palm, G. J., Hinrichs, W., Matthey, U., Zahn, R., Groschup, M. H. (2006). Synergistic and strain-specific effects of bovine spongiform encephalopathy and scrapie prions in the cell-free conversion of recombinant prion protein. J. Gen. Virol. 87: 3753-3761 [Abstract] [Full Text]  
  • Acutis, P. L., Bossers, A., Priem, J., Riina, M. V., Peletto, S., Mazza, M., Casalone, C., Forloni, G., Ru, G., Caramelli, M. (2006). Identification of prion protein gene polymorphisms in goats from Italian scrapie outbreaks.. J. Gen. Virol. 87: 1029-1033 [Abstract] [Full Text]  
  • Slate, J. (2005). Molecular evolution of the sheep prion protein gene. Proc R Soc B 272: 2371-2377 [Abstract] [Full Text]  
  • Sander, P., Hamann, H., Drogemuller, C., Kashkevich, K., Schiebel, K., Leeb, T. (2005). Bovine Prion Protein Gene (PRNP) Promoter Polymorphisms Modulate PRNP Expression and May Be Responsible for Differences in Bovine Spongiform Encephalopathy Susceptibility. J. Biol. Chem. 280: 37408-37414 [Abstract] [Full Text]  
  • Rigter, A., Bossers, A. (2005). Sheep scrapie susceptibility-linked polymorphisms do not modulate the initial binding of cellular to disease-associated prion protein prior to conversion. J. Gen. Virol. 86: 2627-2634 [Abstract] [Full Text]  
  • Williams, E. S. (2005). Chronic Wasting Disease. Vet Pathol 42: 530-549 [Abstract] [Full Text]  
  • Jewell, J. E., Conner, M. M., Wolfe, L. L., Miller, M. W., Williams, E. S. (2005). Low frequency of PrP genotype 225SF among free-ranging mule deer (Odocoileus hemionus) with chronic wasting disease. J. Gen. Virol. 86: 2127-2134 [Abstract] [Full Text]  
  • Gonzalez, L., Martin, S., Houston, F. E., Hunter, N., Reid, H. W., Bellworthy, S. J., Jeffrey, M. (2005). Phenotype of disease-associated PrP accumulation in the brain of bovine spongiform encephalopathy experimentally infected sheep. J. Gen. Virol. 86: 827-838 [Abstract] [Full Text]  
  • Lysek, D. A., Schorn, C., Nivon, L. G., Esteve-Moya, V., Christen, B., Calzolai, L., von Schroetter, C., Fiorito, F., Herrmann, T., Guntert, P., Wuthrich, K. (2005). Prion protein NMR structures of cats, dogs, pigs, and sheep. Proc. Natl. Acad. Sci. USA 102: 640-645 [Abstract] [Full Text]  
  • Seabury, C. M., Honeycutt, R. L., Rooney, A. P., Halbert, N. D., Derr, J. N. (2004). Prion protein gene (PRNP) variants and evidence for strong purifying selection in functionally important regions of bovine exon 3. Proc. Natl. Acad. Sci. USA 101: 15142-15147 [Abstract] [Full Text]  
  • Acutis, P. L., Sbaiz, L., Verburg, F., Riina, M. V., Ru, G., Moda, G., Caramelli, M., Bossers, A. (2004). Low frequency of the scrapie resistance-associated allele and presence of lysine-171 allele of the prion protein gene in Italian Biellese ovine breed. J. Gen. Virol. 85: 3165-3172 [Abstract] [Full Text]  
  • Buschmann, A., Luhken, G., Schultz, J., Erhardt, G., Groschup, M. H. (2004). Neuronal accumulation of abnormal prion protein in sheep carrying a scrapie-resistant genotype (PrPARR/ARR). J. Gen. Virol. 85: 2727-2733 [Abstract] [Full Text]  
  • Thuring, C. M. A., Erkens, J. H. F., Jacobs, J. G., Bossers, A., Van Keulen, L. J. M., Garssen, G. J., Van Zijderveld, F. G., Ryder, S. J., Groschup, M. H., Sweeney, T., Langeveld, J. P. M. (2004). Discrimination between Scrapie and Bovine Spongiform Encephalopathy in Sheep by Molecular Size, Immunoreactivity, and Glycoprofile of Prion Protein. J. Clin. Microbiol. 42: 972-980 [Abstract] [Full Text]  
  • Billinis, C., Psychas, V., Leontides, L., Spyrou, V., Argyroudis, S., Vlemmas, I., Leontides, S., Sklaviadis, T., Papadopoulos, O. (2004). Prion protein gene polymorphisms in healthy and scrapie-affected sheep in Greece. J. Gen. Virol. 85: 547-554 [Abstract] [Full Text]  
  • Caughey, B. (2003). Prion protein conversions: insight into mechanisms, TSE transmission barriers and strains. Br Med Bull 66: 109-120 [Abstract] [Full Text]  
  • Kirby, L., Birkett, C. R., Rudyk, H., Gilbert, I. H., Hope, J. (2003). In vitro cell-free conversion of bacterial recombinant PrP to PrPres as a model for conversion. J. Gen. Virol. 84: 1013-1020 [Abstract] [Full Text]  
  • Vorberg, I., Groschup, M. H., Pfaff, E., Priola, S. A. (2003). Multiple Amino Acid Residues within the Rabbit Prion Protein Inhibit Formation of Its Abnormal Isoform. J. Virol. 77: 2003-2009 [Abstract] [Full Text]  
  • Billinis, C., Panagiotidis, C. H., Psychas, V., Argyroudis, S., Nicolaou, A., Leontides, S., Papadopoulos, O., Sklaviadis, T. (2002). Prion protein gene polymorphisms in natural goat scrapie. J. Gen. Virol. 83: 713-721 [Abstract] [Full Text]  
  • Crozet, C., Flamant, F., Bencsik, A., Aubert, D., Samarut, J., Baron, T. (2001). Efficient Transmission of Two Different Sheep Scrapie Isolates in Transgenic Mice Expressing the Ovine PrP Gene. J. Virol. 75: 5328-5334 [Abstract] [Full Text]  
  • Priola, S. A., Chabry, J., Chan, K. (2001). Efficient Conversion of Normal Prion Protein (PrP) by Abnormal Hamster PrP Is Determined by Homology at Amino Acid Residue 155. J. Virol. 75: 4673-4680 [Abstract] [Full Text]  
  • Vilette, D., Andreoletti, O., Archer, F., Madelaine, M. F., Vilotte, J. L., Lehmann, S., Laude, H. (2001). Ex vivo propagation of infectious sheep scrapie agent in heterologous epithelial cells expressing ovine prion protein. Proc. Natl. Acad. Sci. USA 10.1073/pnas.061337998v1 [Abstract] [Full Text]  
  • Lawson, V. A., Priola, S. A., Wehrly, K., Chesebro, B. (2001). N-terminal Truncation of Prion Protein Affects Both Formation and Conformation of Abnormal Protease-resistant Prion Protein Generated in Vitro. J. Biol. Chem. 276: 35265-35271 [Abstract] [Full Text]  
  • Vilette, D., Andreoletti, O., Archer, F., Madelaine, M. F., Vilotte, J. L., Lehmann, S., Laude, H. (2001). Ex vivo propagation of infectious sheep scrapie agent in heterologous epithelial cells expressing ovine prion protein. Proc. Natl. Acad. Sci. USA 98: 4055-4059 [Abstract] [Full Text]