Evidence map›Paper›PMID 34620247›Full record

ReviewVeterinary research2021

Review on PRNP genetics and susceptibility to chronic wasting disease of Cervidae.

Katayoun Moazami-Goudarzi, Olivier Andréoletti, Jean-Luc Vilotte, Vincent Béringue

Open access · goldAbstract readReview
In one paragraph

Review in Veterinary research, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
3.1field-weighted citation impact, top 7% 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

22 citing papers in PubMed, 48 citations in OpenAlex.

  1. A Practical Framework for GT-Seq Panel Optimization.Molecular ecology resources · 2026
    Article
  2. Article
  3. Novel Prion Protein Gene (bioRxiv : the preprint server for biology · 2026
    Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Identification of the Highly Polymorphic Prion Protein Gene (Animals : an open access journal from MDPI · 2025
    Article
  10. Review
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Propagation of PrPCommunications biology · 2023
    Article
  17. Article
  18. Article
  19. Article
  20. Review
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

4 authors at 3 institutions in 1 country.

Katayoun Moazami-GoudarziUniversity Paris-Saclay, INRAE, AgroParisTech, GABI, 78350, Jouy-en-Josas, France. Katayoun.goudarzi@inrae.fr.ORCID http://orcid.org/0000-0003-2860-5418
Olivier AndréolettiUMR INRAE ENVT 1225 - IHAP, École Nationale Vétérinaire de Toulouse, 31076, Toulouse, France.
Jean-Luc VilotteUniversity Paris-Saclay, INRAE, AgroParisTech, GABI, 78350, Jouy-en-Josas, France.
Vincent BéringueUniversity Paris-Saclay, INRAE, UVSQ, VIM, 78350, Jouy-en-Josas, France.
AgroParisTech · FRÉcole Nationale Vétérinaire de Toulouse · FRUniversité de Versailles Saint-Quentin-en-Yvelines · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

To date, chronic wasting disease (CWD) is the most infectious form of prion disease affecting several captive, free ranging and wild cervid species. Responsible for marked population declines in North America, its geographical spread is now becoming a major concern in Europe. Polymorphisms in the prion protein gene (PRNP) are an important factor influencing the susceptibility to prions and their rate of propagation. All reported cervid PRNP genotypes are affected by CWD. However, in each species, some polymorphisms are associated with lower attack rates and slower progression of the disease. This has potential consequences in terms of genetic selection, CWD diffusion and strain evolution. CWD also presents a zoonotic risk due to prions capacity to cross species barriers. This review summarizes our current understanding of CWD control, focusing on PRNP genetic, strain diversity and capacity to infect other animal species, including humans.

Indexed as

DeerAnimalsGenotypePolymorphism, GeneticPrion ProteinsSelection, GeneticWasting Disease, ChronicPrion ProteinsCervidaeCWDhost pathogen interactionpolymorphismsprionsstrainstransgenic micezoonosis

Identifiers

PMID34620247
PMCPMC8499490
OpenAlexW3201796792

What Socratic holds

Textmetadata
LicenceCC BY
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 Socratic graph.