Author(s):
Pereira, Jorge C. ; Machado, Ana ; Gonçalves-Anjo, Nuno ; Bastos, Estela ; Orge, Leonor ; Rocha, Sara ; Figueira, Luís ; Matos, Ana Cristina ; Silva, João ; Mendonça, Paula ; Carvalho, Paulo ; Tavares, Paula ; Lima, Carla ; Alves, Anabela ; Esteves, Alexandra ; Pinto, Maria de Lurdes ; Pires, Isabel ; Gama, Adelina ; Sargo, Roberto ; Silva, Filipe ; Seixas, Fernanda ; Pinto, Madalena Vieira ; Pires, Maria dos Anjos
Date: 2022
Persistent ID: http://hdl.handle.net/10400.11/8767
Origin: Repositório Científico do Instituto Politécnico de Castelo Branco
Subject(s): Prion protein gene; Red deer; Fallow deer; Roe deer
Description
Transmissible Spongiform Encephalopathy (TSE) or prion diseases are a family of neurodegenerative diseases caused by lethal infectious pathogens called Prions. Among the transmissible spongiform encephalopathies (TSEs), chronic wasting disease (CWD) in cervids is now the rising concern in wildlife within Europe, after the first case was detected in Norway in 2016, in a wild reindeer and until October 2021, a total of 40 cases were described in Norway, Sweden and Finland. The study of the genetics of the prion protein gene, PRNP, has been proved to be a valuable tool for determining the relative susceptibility to TSEs.