Characterization of prion strains and peripheral prion infectivity patterns in E200K genetic CJD patients.

Abstract

The mutation E200K in the prion protein gene (PRNP) is the most common variant in genetic Creutzfeldt-Jakob disease (gCJD). The clinical and pathological features observed in patients with E200K gCJD led to the hypothesis that the prion strains responsible for this form of the disease may be related to those involved in sporadic CJD (sCJD). In this study, we characterized the prion strains responsible for E200K gCJD cases from Slovakia (n = 12), Spain (n = 9), and France (n = 3) using transgenic mouse models expressing human prion protein (PrP). The cohort included patients with various PRNP genotypes: E200K-Met129/Met129, E200K-Met129/E200K-Met129, E200K-Met129/Val129, and E200K-Val129/Val129. Prion strain characterization revealed that the strains isolated from E200K gCJD cases corresponded to the two most common strains identified in sCJD cases: M1CJD and V2CJD. Depending on the individual, these strains were either present as pure M1CJD or V2CJD, or as a mixture of both (M1CJD + V2CJD). Additionally, peripheral tissues from E200K-Met129/Met129 patients (n = 4) and one E200K-Met129/Val129 case were analyzed for prion infectivity and seeding activity. Similar to sCJD patients, low but detectable levels of prions were found in various peripheral tissues of E200K gCJD cases. Overall, our findings suggest that the prion strains and their distribution in the body are highly similar between E200K gCJD and sCJD patients. These similarities indicate that individuals carrying the E200K mutation may serve as a valuable model for understanding CJD pathogenesis during the preclinical phase of the disease.