Prions from Sporadic Creutzfeldt-Jakob Disease Patients Propagate as Strain Mixtures
Hervé Cassard, Alvina Huor, Juan Carlos Espinosa, Jean‐Yves Douet, Séverine Lugan, Naïma Aron, Didier Vilette, Marie‐Bernadette Delisle, Alba Marín‐Moreno, Patrice Péran, Vincent Béringue, Juan María Torres, James W. Ironside, Olivier Andréoletti
Abstract
sCJD occurrence is currently assumed to result from spontaneous and stochastic formation of a misfolded PrP nucleus in the brains of affected patients. This original nucleus then recruits and converts nascent PrP C into PrP Sc , leading to the propagation of prions in the patient’s brain. Our study demonstrates the coexistence of two prion strains in the brains of a majority of the 23 sCJD patients investigated. The relative proportion of these sCJD strains varied both between patients and between brain areas in a single patient. These findings strongly support the view that the replication of an sCJD prion strain in the brain of a patient can result in the propagation of different prion strain subpopulations. Beyond its conceptual importance for our understanding of prion strain properties and evolution, the sCJD strain mixture phenomenon and its frequency among patients have important implications for the development of therapeutic strategies for prion diseases.