[HTML][HTML] Seeded fibrillation as molecular basis of the species barrier in human prion diseases

L Luers, O Bannach, J Stöhr, MM Wördehoff, M Wolff… - PLoS …, 2013 - journals.plos.org
L Luers, O Bannach, J Stöhr, MM Wördehoff, M Wolff, L Nagel-Steger, D Riesner, D Willbold
PLoS One, 2013journals.plos.org
Prion diseases are transmissible spongiform encephalopathies in humans and animals,
including scrapie in sheep, bovine spongiform encephalopathy (BSE) in cattle, chronic
wasting disease (CWD) in deer, and Creutzfeldt-Jakob disease (CJD) in humans. The
hallmark of prion diseases is the conversion of the host-encoded prion protein (PrPC) to its
pathological isoform PrPSc, which is accompanied by PrP fibrillation. Transmission is not
restricted within one species, but can also occur between species. In some cases a species …
Prion diseases are transmissible spongiform encephalopathies in humans and animals, including scrapie in sheep, bovine spongiform encephalopathy (BSE) in cattle, chronic wasting disease (CWD) in deer, and Creutzfeldt-Jakob disease (CJD) in humans. The hallmark of prion diseases is the conversion of the host-encoded prion protein (PrPC) to its pathological isoform PrPSc, which is accompanied by PrP fibrillation. Transmission is not restricted within one species, but can also occur between species. In some cases a species barrier can be observed that results in limited or unsuccessful transmission. The mechanism behind interspecies transmissibility or species barriers is not completely understood. To analyse this process at a molecular level, we previously established an in vitro fibrillation assay, in which recombinant PrP (recPrP) as substrate can be specifically seeded by PrPSc as seed. Seeding with purified components, with no additional cellular components, is a direct consequence of the “prion-protein-only” hypothesis. We therefore hypothesise, that the species barrier is based on the interaction of PrPC and PrPSc. Whereas in our earlier studies, the interspecies transmission in animal systems was analysed, the focus of this study lies on the transmission from animals to humans. We therefore combined seeds from species cattle, sheep and deer (BSE, scrapie, CWD) with human recPrP. Homologous seeding served as a control. Our results are consistent with epidemiology, other in vitro aggregation studies, and bioassays investigating the transmission between humans, cattle, sheep, and deer. In contrast to CJD and BSE seeds, which show a seeding activity we can demonstrate a species barrier for seeds from scrapie and CWD in vitro. We could show that the seeding activity and therewith the molecular interaction of PrP as substrate and PrPSc as seed is sufficient to explain the phenomenon of species barriers. Therefore our data supports the hypothesis that CWD is not transmissible to humans.
PLOS