PLoS Pathogens (Jul 2008)

Prion protein amino acid determinants of differential susceptibility and molecular feature of prion strains in mice and voles.

  • Umberto Agrimi,
  • Romolo Nonno,
  • Giacomo Dell'Omo,
  • Michele Angelo Di Bari,
  • Michela Conte,
  • Barbara Chiappini,
  • Elena Esposito,
  • Giovanni Di Guardo,
  • Otto Windl,
  • Gabriele Vaccari,
  • Hans-Peter Lipp

DOI
https://doi.org/10.1371/journal.ppat.1000113
Journal volume & issue
Vol. 4, no. 7
p. e1000113

Abstract

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The bank vole is a rodent susceptible to different prion strains from humans and various animal species. We analyzed the transmission features of different prions in a panel of seven rodent species which showed various degrees of phylogenetic affinity and specific prion protein (PrP) sequence divergences in order to investigate the basis of vole susceptibility in comparison to other rodent models. At first, we found a differential susceptibility of bank and field voles compared to C57Bl/6 and wood mice. Voles showed high susceptibility to sheep scrapie but were resistant to bovine spongiform encephalopathy, whereas C57Bl/6 and wood mice displayed opposite features. Infection with mouse-adapted scrapie 139A was faster in voles than in C57Bl/6 and wood mice. Moreover, a glycoprofile change was observed in voles, which was reverted upon back passage to mice. All strains replicated much faster in voles than in mice after adapting to the new species. PrP sequence comparison indicated a correlation between the transmission patterns and amino acids at positions 154 and 169 (Y and S in mice, N and N in voles). This correlation was confirmed when inoculating three additional rodent species: gerbils, spiny mice and oldfield mice with sheep scrapie and 139A. These rodents were chosen because oldfield mice do have the 154N and 169N substitutions, whereas gerbil and spiny mice do not have them. Our results suggest that PrP residues 154 and 169 drive the susceptibility, molecular phenotype and replication rate of prion strains in rodents. This might have implications for the assessment of host range and molecular traceability of prion strains, as well as for the development of improved animal models for prion diseases.