Evidence map›Paper›PMID 30148080›Full record

ReviewOpen veterinary journal2018

Evolutionary biology and the risk of scrapie disease in sheep.

David Bruce Adams

Open access · goldAbstract readReview
In one paragraph

Review in Open veterinary journal, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
0.1field-weighted citation impact, top 52% 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

0 citing papers in PubMed, 2 citations in OpenAlex.

No citing paper in PubMed yet.

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

1 author at 1 institution in 2 countries.

David Bruce Adams24 Noala Street, Aranda, ACT 2614, Australia.
Reef Ecologic · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Scrapie in sheep occurs in two forms. Classical scrapie, along with chronic wasting disease in deer, differs from all other prion diseases in being contagious and occurring as propagating epidemics. By contrast, atypical scrapie occurs sporadically and like most other prion diseases, such as Creutzfeldt-Jakob disease in humans, is regarded as non-contagious under natural conditions. This difference motivates the present study, which uses the perspective of evolutionary biology to explore whether atypical or non-contagious scrapie can transform to classical or contagious scrapie when appropriate evolutionary forces are in play. The study begins with an explanation of relevant evolutionary concepts such as evolvability and object of selection and proposes some explicit definitions of key terms such as variation, replication, heritability and strain. Observations of the behaviour of scrapie strains during serial passage in sheep, goats and mice assign the functions of variation, replication and heritability to the scrapie agent and establish it as an object of selection with a capacity for evolvability. Similar observations of strain behaviour in other prion diseases establish prions in general as objects of selection that are able to evolve. Accordingly, it is tenable that non-contagious atypical scrapie can provide progenitors for the prions causing contagious classical scrapie and can be a latent epidemiological threat. A comparison of atypical and classical scrapie identifies an affinity of the scrapie agent for lymphoreticular tissue and predilections for portals of exit and entry as key gain-of-function mutations that endow prion populations in atypical scrapie with the function of communicability or contagiousness. The present study can be seen as the hazard identification step within a process of risk analysis that systematises knowledge in aid of animal health and welfare and biosecurity. It justifies completion of the remaining steps in risk assessment. This task can be assisted by further comparisons of atypical and classical scrapie enlightened by historical records of scrapie disease, the epidemiology of atypical scrapie, the general behaviour of prions and evolutionary biology.

Indexed as

EvolutionPrionRiskScrapieSheep

Identifiers

PMID30148080
PMCPMC6102421
OpenAlexW2888526376

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.