Evidence map›Paper›PMID 26205536›Full record

ArticleBMC research notes2015

Further characterisation of transmissible spongiform encephalopathy phenotypes after inoculation of cattle with two temporally separated sources of sheep scrapie from Great Britain.

Timm Konold, Romolo Nonno, John Spiropoulos, Melanie J Chaplin, Michael J Stack, Steve A C Hawkins, Saira Cawthraw, John W Wilesmith, Gerald A H Wells, Umberto Agrimi and 5 more

Open access · goldAbstract read
In one paragraph

Article in BMC research notes, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.1field-weighted citation impact, top 24% 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

11 citing papers in PubMed, 17 citations in OpenAlex.

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  8. Bovine spongiform encephalopathy (BSE) cases born after the total feed ban.EFSA journal. European Food Safety Authority · 2017
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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

15 authors at 5 institutions in 3 countries.

Timm KonoldSpecialist Scientific Support Department, Animal and Plant Health Agency Weybridge, New Haw, Addlestone, Surrey, KT15 3NB, UK. Timm.Konold@apha.gsi.gov.uk.
Romolo NonnoDepartment of Veterinary Public Health and Food Safety, Istituto Superiore di Sanità (ISS), Viale Regina Elena 299, 00161, Rome, Italy. romolo.nonno@iss.it.
John SpiropoulosPathology Department, Animal and Plant Health Agency Weybridge, New Haw, Addlestone, Surrey, KT15 3NB, UK. John.Spiropoulos@apha.gsi.gov.uk.
Melanie J ChaplinPrion Unit, Virology Department, Animal and Plant Health Agency Weybridge, New Haw, Addlestone, Surrey, KT15 3NB, UK. Melanie.Chaplin@apha.gsi.gov.uk.
Michael J StackPrion Unit, Virology Department, Animal and Plant Health Agency Weybridge, New Haw, Addlestone, Surrey, KT15 3NB, UK. stackmichael@hotmail.co.uk.
Steve A C HawkinsPathology Department, Animal and Plant Health Agency Weybridge, New Haw, Addlestone, Surrey, KT15 3NB, UK. Steve.Hawkins@apha.gsi.gov.uk.
Saira CawthrawSpecialist Scientific Support Department, Animal and Plant Health Agency Weybridge, New Haw, Addlestone, Surrey, KT15 3NB, UK. Saira.Cawthraw@apha.gsi.gov.uk.
John W WilesmithFormerly Epidemiology Department, Veterinary Laboratories Agency Weybridge, New Haw, Addlestone, Surrey, KT15 3NB, UK. johnwilesmith@barrscourt.plus.com.
Gerald A H WellsFormerly Neuropathology, Veterinary Laboratories Agency Weybridge, New Haw, Addlestone, Surrey, KT15 3NB, UK. geraldwells5@btinternet.com.
Umberto AgrimiDepartment of Veterinary Public Health and Food Safety, Istituto Superiore di Sanità (ISS), Viale Regina Elena 299, 00161, Rome, Italy. umberto.agrimi@iss.it.
Michele A Di BariDepartment of Veterinary Public Health and Food Safety, Istituto Superiore di Sanità (ISS), Viale Regina Elena 299, 00161, Rome, Italy. michele.dibari@iss.it.
Olivier AndréolettiUMR INRA-ENVT 1225, Interactions Hôte Agent Pathogène, École Nationale Vétérinaire de Toulouse, 31076, Toulouse Cedex 3, France. o.andreoletti@envt.fr.
Juan C EspinosaCentro de Investigación en Sanidad Animal (CISA-INIA), Madrid, Spain. espinosa.juan@inia.es.
Patricia Aguilar-CalvoCentro de Investigación en Sanidad Animal (CISA-INIA), Madrid, Spain. patriciaaguilar@ucsd.edu.
Juan M TorresCentro de Investigación en Sanidad Animal (CISA-INIA), Madrid, Spain. jmtorres@inia.es.
Animal and Plant Health Agency · GBCentro de Investigación en Sanidad AnimalIstituto Superiore di Sanità · ITÉcole Nationale Vétérinaire de Toulouse · FRVeterinary Medicines Directorate · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe infectious agent responsible for the bovine spongiform encephalopathy (BSE) epidemic in Great Britain is a transmissible spongiform encephalopathy (TSE) strain with uniform properties but the origin of this strain remains unknown. Based on the hypothesis that classical BSE may have been caused by a TSE strain present in sheep, cattle were inoculated intracerebrally with two different pools of brains from scrapie-affected sheep sourced prior to and during the BSE epidemic to investigate resulting disease phenotypes and characterise their causal agents by transmission to rodents.

resultsAs reported in 2006, intracerebral inoculation of cattle with pre-1975 and post-1990 scrapie brain pools produced two distinct disease phenotypes, which were unlike classical BSE. Subsequent to that report none of the remaining cattle, culled at 10 years post inoculation, developed a TSE. Retrospective Western immunoblot examination of the brains from TSE cases inoculated with the pre-1975 scrapie pool revealed a molecular profile similar to L-type BSE. The inoculation of transgenic mice expressing the bovine, ovine, porcine, murine or human prion protein gene and bank voles with brains from scrapie-affected cattle did not detect classical or atypical BSE strains but identified two previously characterised scrapie strains of sheep.

conclusionsCharacterisation of the causal agents of disease resulting from exposure of cattle to naturally occurring scrapie agents sourced in Great Britain did not reveal evidence of classical or atypical BSE, but did identify two distinct previously recognised strains of scrapie. Although scrapie was still recognizable upon cattle passage there were irreconcilable discrepancies between the results of biological strain typing approaches and molecular profiling methods, suggesting that the latter may not be appropriate for the identification and differentiation of atypical, particularly L-type, BSE agents from cattle experimentally infected with a potential mixture of classical scrapie strains from sheep sources.

Indexed as

PhenotypeAnimalsArvicolinaeBlotting, WesternBrainCattleEncephalopathy, Bovine SpongiformGene ExpressionHumansInjections, IntraventricularMiceMice, TransgenicPrPSc ProteinsScrapieSheepSheep, DomesticPrPSc Proteins

Identifiers

PMID26205536
PMCPMC4618938
OpenAlexW1669710872

What OpenQuestion 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 OpenQuestion graph.