Evidence map›Paper›PMID 24352451›Full record

ArticleJournal of virology2014

Role of the goat K222-PrP(C) polymorphic variant in prion infection resistance.

Patricia Aguilar-Calvo, Juan Carlos Espinosa, Belén Pintado, Alfonso Gutiérrez-Adán, Elia Alamillo, Alberto Miranda, Irene Prieto, Alex Bossers, Olivier Andreoletti, Juan María Torres

Open access · bronzeAbstract read
In one paragraph

Article in Journal of virology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed
2.2field-weighted citation impact, top 12% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

36 citing papers in PubMed, 63 citations in OpenAlex.

  1. Incomplete protection of the KVeterinary research · 2026
    Article
  2. Article
  3. Article
  4. Classical BSE emergence from Nor98/atypical scrapie: Unraveling the shift vs. selection dichotomy in the prion field.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  5. Article
  6. Article
  7. Article
  8. Polymorphisms of Codons 110, 146, 211 and 222 at the GoatAnimals : an open access journal from MDPI · 2021
    Article
  9. Canine DScientific reports · 2021
    Article
  10. MetNeuropathology and applied neurobiology · 2021
    Article
  11. Genetic Variation in the Prion Protein Gene (Animals : an open access journal from MDPI · 2021
    Article
  12. Article
  13. Article
  14. Review
  15. Animals : an open access journal from MDPI · 2021
    Article
  16. Article
  17. Article
  18. Goats naturally devoid of PrPVeterinary research · 2020
    Article
  19. Article
  20. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors at 5 institutions in 3 countries.

Patricia Aguilar-CalvoCentro de Investigación en Sanidad Animal (CISA-INIA), Valdeolmos, Madrid, Spain.
Juan Carlos Espinosa
Belén Pintado
Alfonso Gutiérrez-Adán
Elia Alamillo
Alberto Miranda
Irene Prieto
Alex Bossers
Olivier Andreoletti
Juan María Torres
Centro de Investigación en Sanidad AnimalCentro Regional de Selección y Reproducción Animal · ESCentro Nacional de Biotecnología · ESÉcole Nationale Vétérinaire de Toulouse · FRWageningen University & Research · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

unlabelledThe prion protein-encoding gene (prnp) strongly influences the susceptibility of small ruminants to transmissible spongiform encephalopathies (TSEs). Hence, selective breeding programs have been implemented to increase sheep resistance to scrapie. For goats, epidemiological and experimental studies have provided some association between certain polymorphisms of the cellular prion protein (PrP(C)) and resistance to TSEs. Among them, the Q/K polymorphism at PrP(C) codon 222 (Q/K222) yielded the most promising results. In this work, we investigated the individual effects of the K222-PrP(C) variant on the resistance/susceptibility of goats to TSEs. For that purpose, we generated two transgenic mouse lines, expressing either the Q222 (wild type) or K222 variant of goat PrP(C). Both mouse lines were challenged intracerebrally with a panel of TSE isolates. Transgenic mice expressing the wild-type (Q222) allele were fully susceptible to infection with all tested isolates, whereas transgenic mice expressing similar levels of the K222 allele were resistant to all goat scrapie and cattle BSE isolates but not to goat BSE isolates. Finally, heterozygous K/Q222 mice displayed a reduced susceptibility to the tested panel of scrapie isolates. These results demonstrate a highly protective effect of the K222 variant against a broad panel of different prion isolates and further reinforce the argument supporting the use of this variant in breeding programs to control TSEs in goat herds. IMPORTANCE: The objective of this study was to determine the role of the K222 variant of the prion protein (PrP) in the susceptibility/resistance of goats to transmissible spongiform encephalopathies (TSEs). Results showed that transgenic mice expressing the goat K222-PrP polymorphic variant are resistant to scrapie and bovine spongiform encephalopathy (BSE) agents. This protective effect was also observed in heterozygous Q/K222 animals. Therefore, the single amino acid exchange from Q to K at codon 222 of the cellular prion protein provides resistance against TSEs. All the results presented here support the view that the K222 polymorphic variant is a good candidate for selective breeding programs to control and eradicate scrapie in goat herds.

Indexed as

Polymorphism, GeneticAnimalsCattleCodonDisease ResistanceEncephalopathy, Bovine SpongiformFemaleGene ExpressionGenetic Predisposition to DiseaseGenotypeGoatsMaleMiceMice, TransgenicPrPC ProteinsScrapieCodonPrPC Proteins

Identifiers

PMID24352451
PMCPMC3958052
OpenAlexW2118608420

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.