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Low sequence diversity of the prion protein gene (PRNP) in wild deer and goat species from Spain

The first European cases of chronic wasting disease (CWD) in free-ranging reindeer and wild elk were confirmed in Norway in 2016 highlighting the urgent need to understand transmissible spongiform encephalopathies (TSEs) in the context of European deer species and the many individual populations thr...

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Autores principales: Pitarch, José Luis, Raksa, Helen Caroline, Arnal, María Cruz, Revilla, Miguel, Martínez, David, Fernández de Luco, Daniel, Badiola, Juan José, Goldmann, Wilfred, Acín, Cristina
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5892000/
https://www.ncbi.nlm.nih.gov/pubmed/29631620
http://dx.doi.org/10.1186/s13567-018-0528-8
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author Pitarch, José Luis
Raksa, Helen Caroline
Arnal, María Cruz
Revilla, Miguel
Martínez, David
Fernández de Luco, Daniel
Badiola, Juan José
Goldmann, Wilfred
Acín, Cristina
author_facet Pitarch, José Luis
Raksa, Helen Caroline
Arnal, María Cruz
Revilla, Miguel
Martínez, David
Fernández de Luco, Daniel
Badiola, Juan José
Goldmann, Wilfred
Acín, Cristina
author_sort Pitarch, José Luis
collection PubMed
description The first European cases of chronic wasting disease (CWD) in free-ranging reindeer and wild elk were confirmed in Norway in 2016 highlighting the urgent need to understand transmissible spongiform encephalopathies (TSEs) in the context of European deer species and the many individual populations throughout the European continent. The genetics of the prion protein gene (PRNP) are crucial in determining the relative susceptibility to TSEs. To establish PRNP gene sequence diversity for free-ranging ruminants in the Northeast of Spain, the open reading frame was sequenced in over 350 samples from five species: Iberian red deer (Cervus elaphus hispanicus), roe deer (Capreolus capreolus), fallow deer (Dama dama), Iberian wild goat (Capra pyrenaica hispanica) and Pyrenean chamois (Rupicapra p. pyrenaica). Three single nucleotide polymorphisms (SNPs) were found in red deer: a silent mutation at codon 136, and amino acid changes T98A and Q226E. Pyrenean chamois revealed a silent SNP at codon 38 and an allele with a single octapeptide-repeat deletion. No polymorphisms were found in roe deer, fallow deer and Iberian wild goat. This apparently low variability of the PRNP coding region sequences of four major species in Spain resembles previous findings for wild mammals, but implies that larger surveys will be necessary to find novel, low frequency PRNP gene alleles that may be utilized in CWD risk control.
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spelling pubmed-58920002018-04-11 Low sequence diversity of the prion protein gene (PRNP) in wild deer and goat species from Spain Pitarch, José Luis Raksa, Helen Caroline Arnal, María Cruz Revilla, Miguel Martínez, David Fernández de Luco, Daniel Badiola, Juan José Goldmann, Wilfred Acín, Cristina Vet Res Research Article The first European cases of chronic wasting disease (CWD) in free-ranging reindeer and wild elk were confirmed in Norway in 2016 highlighting the urgent need to understand transmissible spongiform encephalopathies (TSEs) in the context of European deer species and the many individual populations throughout the European continent. The genetics of the prion protein gene (PRNP) are crucial in determining the relative susceptibility to TSEs. To establish PRNP gene sequence diversity for free-ranging ruminants in the Northeast of Spain, the open reading frame was sequenced in over 350 samples from five species: Iberian red deer (Cervus elaphus hispanicus), roe deer (Capreolus capreolus), fallow deer (Dama dama), Iberian wild goat (Capra pyrenaica hispanica) and Pyrenean chamois (Rupicapra p. pyrenaica). Three single nucleotide polymorphisms (SNPs) were found in red deer: a silent mutation at codon 136, and amino acid changes T98A and Q226E. Pyrenean chamois revealed a silent SNP at codon 38 and an allele with a single octapeptide-repeat deletion. No polymorphisms were found in roe deer, fallow deer and Iberian wild goat. This apparently low variability of the PRNP coding region sequences of four major species in Spain resembles previous findings for wild mammals, but implies that larger surveys will be necessary to find novel, low frequency PRNP gene alleles that may be utilized in CWD risk control. BioMed Central 2018-04-10 2018 /pmc/articles/PMC5892000/ /pubmed/29631620 http://dx.doi.org/10.1186/s13567-018-0528-8 Text en © The Author(s) 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Pitarch, José Luis
Raksa, Helen Caroline
Arnal, María Cruz
Revilla, Miguel
Martínez, David
Fernández de Luco, Daniel
Badiola, Juan José
Goldmann, Wilfred
Acín, Cristina
Low sequence diversity of the prion protein gene (PRNP) in wild deer and goat species from Spain
title Low sequence diversity of the prion protein gene (PRNP) in wild deer and goat species from Spain
title_full Low sequence diversity of the prion protein gene (PRNP) in wild deer and goat species from Spain
title_fullStr Low sequence diversity of the prion protein gene (PRNP) in wild deer and goat species from Spain
title_full_unstemmed Low sequence diversity of the prion protein gene (PRNP) in wild deer and goat species from Spain
title_short Low sequence diversity of the prion protein gene (PRNP) in wild deer and goat species from Spain
title_sort low sequence diversity of the prion protein gene (prnp) in wild deer and goat species from spain
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5892000/
https://www.ncbi.nlm.nih.gov/pubmed/29631620
http://dx.doi.org/10.1186/s13567-018-0528-8
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