Prion Replication Environment Defines the Fate of Prion Strain Adaptation
- Description
- The research associated with this dataset explored cross-species prion transmission and the impact of cofactor environment on strain adaptation. Utilizing Protein Misfolding Cyclic Amplification with beads (PMCAb), hamster strain 263K was propagated under normal or RNA-depleted conditions first in mouse and then hamster substrates. A variety of readaptation experiments were conducted including brain analysis of hamsters inoculated with different PMCAb-derived material. Dataset includes Western blot and comparative histopathological brain images.
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S1 Figure
Analysis of RNA content in RNA-depleted NBH (PDF)
S2 FigureHistopathological analysis of spongiform in the brains from the 2nd passage of 263KMH, 263K(M)H or 263K(MH) (PDF)
S3 FigureLesion profile and PrP immunopositivity score in hamsters from the 2nd passage of 263KMH, 263K(M)H or 263K(MH) (PDF)
S4 FigureHistopathological Analysis of Spongiform Changes Using Staining with Hematoxylin and Eosin or PrP Immunoreactivity Using SAF-84 Antibody of Aged-Matched Control Group (PDF)
S5 FigureAnalysis of GdnHCl-Induced Denaturation Profiles of PrPSc (PDF)
S6 FigureHistopathological Analysis of Spongiform in the Brains From the 2nd and 3rd Passages of 263K MH and Animals Inoculated with 263K (PDF)
S7 FigureImmunostaining for PrP displayed the following types of PrP deposits: Diffuse/Synaptic fine deposits, intra- and perineuronal deposits, plaques and mini-plaques in the subependymal area, small granular accumulations on the ependyma, and amorphous plaque-like deposits in the subpial and subependymal regions (PDF)
S8 FigureLesion profile and PrP immunopositivity score in hamsters from the 2nd and 3rd passages of 263KMH and 263K groups (PDF)
S9 FigureHistopathological analysis of spongiform in the brains from the 3rd passage of 263K(M)H and 263K(MH) (PDF)