Evidence map›Paper›PMID 37747806›Full record

ArticleThe Biochemical journal2023

Genetic modulation of CWD prion propagation in cervid PrP Drosophila.

Alana M Thackray, Erin E McNulty, Amy V Nalls, Alzbeta Cardova, Linh Tran, Glenn Telling, Sylvie L Benestad, Sabine Gilch, Candace K Mathiason, Raymond Bujdoso

Open access · hybridAbstract read
In one paragraph

Article in The Biochemical journal, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
2.6field-weighted citation impact, top 10% 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

3 citing papers in PubMed, 17 citations in OpenAlex.

  1. Article
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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 3 institutions in 3 countries.

Alana M ThackrayDepartment of Veterinary Medicine, University of Cambridge, Madingley Road, Cambridge CB3 0ES, U.K.
Erin E McNultyPrion Research Center (PRC) and the Department of Microbiology, Immunology and Pathology, Colorado State University, Fort Collins, CO, U.S.A.
Amy V NallsPrion Research Center (PRC) and the Department of Microbiology, Immunology and Pathology, Colorado State University, Fort Collins, CO, U.S.A.
Alzbeta CardovaDepartment of Veterinary Medicine, University of Cambridge, Madingley Road, Cambridge CB3 0ES, U.K.
Linh TranDepartment of Biohazard and Pathology, WOAH Reference Laboratory for CWD (SLB), National Veterinary Institute, Postboks 64, 1431 Ås, Norway.
Glenn TellingPrion Research Center (PRC) and the Department of Microbiology, Immunology and Pathology, Colorado State University, Fort Collins, CO, U.S.A.
Sylvie L BenestadDepartment of Biohazard and Pathology, WOAH Reference Laboratory for CWD (SLB), National Veterinary Institute, Postboks 64, 1431 Ås, Norway.
Sabine GilchFaculty of Veterinary Medicine, University of Calgary, 3330 Hospital Drive NW, Calgary, AB T2N 4N1, Canada.
Candace K MathiasonPrion Research Center (PRC) and the Department of Microbiology, Immunology and Pathology, Colorado State University, Fort Collins, CO, U.S.A.
Raymond BujdosoDepartment of Veterinary Medicine, University of Cambridge, Madingley Road, Cambridge CB3 0ES, U.K.ORCID 0000-0002-5068-3247
Colorado State University · USUniversity of Cambridge · GBUniversity of Calgary · CA

Funding

Zoonotic potential of CWD and influence of environmental contamination on prion propagationP01AI077774 · NIAID · UNIVERSITY OF TEXAS MED BR GALVESTON · PI CLAUDIO SOTO · 2008 to 2026
$36.1M
Detection and Characterization of Blood-borne PrionsR01AI112956 · NIAID · COLORADO STATE UNIVERSITY · PI MATHIASON, CANDACE K. · 2014 to 2024
$4.6M
NIAID NIH HHS P01 AI077774NIAID NIH HHS R01 AI112956
6 · The paper itself

Abstract

Chronic wasting disease is a fatal prion condition of cervids such as deer, elk, moose and reindeer. Secretion and excretion of prion infectivity from North American cervids with this condition causes environmental contamination and subsequent efficient lateral transmission in free-ranging and farmed cervids. Variants of cervid PrP exist that affect host susceptibility to chronic wasting disease. Cervid breeding programmes aimed at increasing the frequency of PrP variants associated with resistance to chronic wasting disease may reduce the burden of this condition in animals and lower the risk of zoonotic disease. This strategy requires a relatively rapid and economically viable model system to characterise and support selection of prion disease-modifying cervid PrP variants. Here, we generated cervid PrP transgenic Drosophila to fulfil this purpose. We have generated Drosophila transgenic for S138 wild type cervid PrP, or the N138 variant associated with resistance to chronic wasting disease. We show that cervid PrP Drosophila accumulate bona fide prion infectivity after exposure to cervid prions. Furthermore, S138 and N138 PrP fly lines are susceptible to cervid prion isolates from either North America or Europe when assessed phenotypically by accelerated loss of locomotor ability or survival, or biochemically by accumulation of prion seeding activity. However, after exposure to European reindeer prions, N138 PrP Drosophila accumulated prion seeding activity with slower kinetics than the S138 fly line. These novel data show that prion susceptibility characteristics of cervid PrP variants are maintained when expressed in Drosophila, which highlights this novel invertebrate host in modelling chronic wasting disease.

Indexed as

PrionsWasting Disease, ChronicAnimalsAnimals, Genetically ModifiedDeerDrosophilaReindeerPrionscervidCWDDrosophila melanogasterinfectivityneurodegenerationprion

Identifiers

PMID37747806
PMCPMC10586768
OpenAlexW4387012617

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.