Your browser doesn't support javascript.
loading
"Luck Be a Lady": Retrospective Study of Disease-Associated Prion (PrPSc) Distribution and Lesions in Captive, Environmentally Exposed Female Rocky Mountain Elk (Cervus canadensis nelsoni) with 132LL Genotype.
Allen, Samantha E; O'Toole, Donal; Wood, Mary; Van Wick, Peach; Parrie, Lindsay E; Malmberg, Jennifer L; Edwards, William H.
Afiliação
  • Allen SE; Veterinary Services, Wyoming Game and Fish Department, 1212 S. Adams St., Laramie, Wyoming 82070, USA.
  • O'Toole D; Wyoming State Veterinary Laboratory, 1174 Snowy Range Rd., Laramie, Wyoming 82070, USA.
  • Wood M; Wyoming State Veterinary Laboratory, 1174 Snowy Range Rd., Laramie, Wyoming 82070, USA.
  • Van Wick P; Wildlife Health Program, Colorado Parks and Wildlife, 4330 Laporte Ave., Fort Collins, Colorado 80521, USA.
  • Parrie LE; Veterinary Services, Thorne/Williams Wildlife Research Facility, Wyoming Game and Fish Department, 2362 WY-34, Wheatland, Wyoming 82201, USA.
  • Malmberg JL; Wildlife Services, National Wildlife Research Center, Animal and Plant Health Inspection Service, US Department of Agriculture, 4101 LaPorte Ave., Fort Collins, Colorado 80521, USA.
  • Edwards WH; Wildlife Services, National Wildlife Research Center, Animal and Plant Health Inspection Service, US Department of Agriculture, 4101 LaPorte Ave., Fort Collins, Colorado 80521, USA.
J Wildl Dis ; 2024 Sep 17.
Article em En | MEDLINE | ID: mdl-39287595
ABSTRACT
Chronic wasting disease (CWD) is a fatal neurodegenerative disease of cervids caused by an infectious misfolded protein (prion). Several members of the Cervidae, including Rocky Mountain elk (Cervus canadensis nelsoni), are susceptible to CWD. There is no evidence of complete genetic resistance to CWD; the M132L polymorphism in the elk prion protein gene influences the incubation period longest in 132LL, intermediate in 132ML, and shortest in 132MM elk. We retrospectively analyzed six female 132LL elk housed in an environment heavily contaminated with prions to 1) document clinical outcomes and incubation periods, 2) describe PrPSc distribution and extent in tissues, and 3) characterize their histologic lesions. In five of six elk, PrPSc was detected postmortem, with a distribution pattern distinct from that of 132MM and 132ML elk; time to clinical CWD onset CWD ranged from 73 to 117 mo (6.1-9.8 yr). Although the remaining animal was observed for 220 mo (18.3 yr), PrPSc was not detected in its tissues postmortem. This study suggests that 132LL elk infected via natural exposure may live even longer with CWD than previously thought, but ultimately remain susceptible. We also report a distinct distribution of PrPSc in 132LL genotypes and highlight unusual histologic findings. Understanding the relationship between cervid genetics and CWD is of increasing importance, especially given the growing interest in leveraging genetics that delay disease onset despite not preventing infection.
Palavras-chave

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article