OMIA:000944-30532 : Spongiform encephalopathy, susceptibility/resistance to in Dama dama (fallow deer)

In other species: Mallard , chicken , Ring-necked pheasant , white-tufted-ear marmoset , macaques , crab-eating macaque , Rhesus monkey , dog , domestic ferret , domestic cat , puma , horse , pig , Arabian camel , deer , Eurasian elk , Western roe deer , red deer , Eastern wapiti , sika deer , Manchurian Wapiti , reindeer , black-tailed deer , white-tailed deer , American bison , taurine cattle , goat , mouflon , sheep , eland , greater kudu , gemsbok , rabbit , golden hamster , domestic guinea pig , domestic yak , chital , cheetah , raccoon dog , bighorn sheep , blue antelope , Arabian oryx , scimitar-horned oryx , nyala , Spanish ibex , water buffalo , Japanese quail , Pyrenean chamois , Iberian red deer , Bank vole , American mink

Categories: Nervous system phene

Links to possible relevant human trait(s) and/or gene(s) in OMIM: 176640 (gene) , 245300 (trait)

Links to relevant human diseases in MONDO:

Mendelian trait/disorder: unknown

Disease-related: unknown

Cross-species summary: Spongiform encephalopathies are a class of fatal neurological diseases. Clinical signs are characteristic of a progressive degeneration of the central nervous system; they include pruritis, abnormalities of gait and recumbency. Death is inevitable. On post-mortem, brain histopathology shows a characteristic spongy appearance. The infectious agent is a modified form of a protein encoded by a gene in the host. The name given to this infectious particle is prion. The host gene is called the prion protein (PrP) gene, which is a normal part of the genome of mammals and chickens. Its polypeptide product, called cellular PrP(superscript C), is a naturally-occurring protein attached to the outer surface of neurones and some other cells. PrP(superscript C) appears to play a role in maintaining the Purkinje cells of the cerebellum, which are essential for balance and muscular function. The infectious agent, called scrapie PrP(superscript Sc), is a modifed form of PrP(superscript C), where the modifications involve glycosylation and the creation of intra-strand di-sulphide bonds. It is important to realise that these modifications involve no change in amino acid sequence. When PrP(superscript Sc) molecules enter a previously uninfected host, they convert the naturally occurring PrP(superscript C) molecules, produced by the host gene, into infectious PrP(superscript Sc) particles, which ultimately cause clinical signs in that animal, and which can spread to other animals, both horizontally (by infection) and vertically (by maternal transmission). In ruminants the disease has been called bovine spongiform encephalopathy (BSE) in cattle, scrapie in sheep and goats and chronic wasting disease (CWD) in cervids.

Cite this entry

Nicholas, F. W., Tammen, I., & Sydney Informatics Hub. (2020). OMIA:000944-30532: Online Mendelian Inheritance in Animals (OMIA) [dataset]. https://omia.org/. https://doi.org/10.25910/2AMR-PV70

References

Note: the references are listed in reverse chronological order (from the most recent year to the earliest year), and alphabetically by first author within a year.

2024 Ernst, S., Piestrzyńska-Kajtoch, A., Gethmann, J., Natonek-Wiśniewska, M., Sadeghi, B., Polak, M.P., Keller, M., Gavier-Widén, D., Moazami-Goudarzi, K., Houston, F., Groschup, M.H., Fast, C. :
Prion protein gene (PRNP) variation in German and Danish cervids. Vet Res 55:98, 2024. Pubmed reference: 39095901. DOI: 10.1186/s13567-024-01340-8.
2023 Arifin, M.I., Kaczmarczyk, L., Zeng, D., Hannaoui, S., Lee, C., Chang, S.C., Mitchell, G., McKenzie, D., Beekes, M., Jackson, W., Gilch, S. :
Heterozygosity for cervid S138N polymorphism results in subclinical CWD in gene-targeted mice and progressive inhibition of prion conversion. Proc Natl Acad Sci U S A 120:e2221060120, 2023. Pubmed reference: 37014866. DOI: 10.1073/pnas.2221060120.
Pereira, J.C., Gonçalves-Anjo, N., Orge, L., Pires, M.A., Rocha, S., Figueira, L., Matos, A.C., Silva, J., Mendonça, P., Carvalho, P., Tavares, P., Lima, C., Alves, A., Esteves, A., Pinto, M.L., Pires, I., Gama, A., Sargo, R., Silva, F., Seixas, F., Vieira-Pinto, M., Bastos, E. :
Estimating sequence diversity of prion protein gene (PRNP) in Portuguese populations of two cervid species: red deer and fallow deer. Prion 17:75-81, 2023. Pubmed reference: 36945178. DOI: 10.1080/19336896.2023.2191540.
2021 Orge, L., Lima, C., Machado, C., Tavares, P., Mendonça, P., Carvalho, P., Silva, J., Pinto, M.L., Bastos, E., Pereira, J.C., Gonçalves-Anjo, N., Gama, A., Esteves, A., Alves, A., Matos, A.C., Seixas, F., Silva, F., Pires, I., Figueira, L., Vieira-Pinto, M., Sargo, R., Pires, M.D.A. :
Neuropathology of animal prion diseases. Biomolecules 11:466, 2021. Pubmed reference: 33801117. DOI: 10.3390/biom11030466.
2019 Robinson, A.L., Williamson, H., Güere, M.E., Tharaldsen, H., Baker, K., Smith, S.L., Pérez-Espona, S., Krojerová-Prokešová, J., Pemberton, J.M., Goldmann, W., Houston, F. :
Variation in the prion protein gene (PRNP) sequence of wild deer in Great Britain and mainland Europe. Vet Res 50:59, 2019. Pubmed reference: 31366372. DOI: 10.1186/s13567-019-0675-6.
2018 Pitarch, J.L., Raksa, H.C., Arnal, M.C., Revilla, M., Martínez, D., Fernández de Luco, D., Badiola, J.J., Goldmann, W., Acín, C. :
Low sequence diversity of the prion protein gene (PRNP) in wild deer and goat species from Spain. Vet Res 49:33, 2018. Pubmed reference: 29631620. DOI: 10.1186/s13567-018-0528-8.

Edit History


  • Created by Frank Nicholas on 18 Apr 2018
  • Changed by Frank Nicholas on 15 May 2020