Evidence map›Paper›PMID 25565633›Full record

ArticlePloS one2015

A bovine cell line that can be infected by natural sheep scrapie prions.

Anja M Oelschlegel, Markus Geissen, Matthias Lenk, Roland Riebe, Marlies Angermann, Herman Schatzl, Hermann Schaetzl, Martin H Groschup

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in PloS one, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing 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

10 citing papers in PubMed, 14 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. Review
  5. Article
  6. The use of PrP transgenicF1000Research · 2018
    Article
  7. Article
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors at 3 institutions in 2 countries.

Anja M OelschlegelInstitute of Novel and Emerging Infectious Diseases at the Friedrich-Loeffler-Institut, Greifswald-Isle of Riems, Germany; Project Group Neuropharmacology, Leibniz Institute for Neurobiology, Magdeburg, Germany.
Markus GeissenInstitute of Novel and Emerging Infectious Diseases at the Friedrich-Loeffler-Institut, Greifswald-Isle of Riems, Germany; Department of Vascular Medicine, University Heart Centre Hamburg, UKE, Hamburg, Germany.
Matthias LenkDepartment of Experimental Animal Facilities and Biorisk Management at the Friedrich-Loeffler-Institut, Greifswald-Isle of Riems, Germany.
Roland RiebeDepartment of Experimental Animal Facilities and Biorisk Management at the Friedrich-Loeffler-Institut, Greifswald-Isle of Riems, Germany.
Marlies AngermannInstitute of Novel and Emerging Infectious Diseases at the Friedrich-Loeffler-Institut, Greifswald-Isle of Riems, Germany; Administrative District Office Goerlitz, Goerlitz, Germany.
Herman Schatzl
Hermann SchaetzlDepartment of Comparative Biology and Experimental Medicine, Faculty of Veterinary Medicine, University of Calgary, Calgary, Canada.
Martin H GroschupInstitute of Novel and Emerging Infectious Diseases at the Friedrich-Loeffler-Institut, Greifswald-Isle of Riems, Germany.
Friedrich-Loeffler-Institut · DEUniversität Hamburg · DEUniversity of Calgary · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cell culture systems represent a crucial part in basic prion research; yet, cell lines that are susceptible to prions, especially to field isolated prions that were not adapted to rodents, are very rare. The purpose of this study was to identify and characterize a cell line that was susceptible to ruminant-derived prions and to establish a stable prion infection within it. Based on species and tissue of origin as well as PrP expression rate, we pre-selected a total of 33 cell lines that were then challenged with natural and with mouse propagated BSE or scrapie inocula. Here, we report the successful infection of a non-transgenic bovine cell line, a sub-line of the bovine kidney cell line MDBK, with natural sheep scrapie prions. This cell line retained the scrapie infection for more than 200 passages. Selective cloning resulted in cell populations with increased accumulation of PrPres, although this treatment was not mandatory for retaining the infection. The infection remained stable, even under suboptimal culture conditions. The resulting infectivity of the cells was confirmed by mouse bioassay (Tgbov mice, Tgshp mice). We believe that PES cells used together with other prion permissive cell lines will prove a valuable tool for ongoing efforts to understand and defeat prions and prion diseases.

Indexed as

AnimalsBiological AssayBlotting, WesternBrainCattleCell LineEncephalopathy, Bovine SpongiformEndopeptidase KEnzyme-Linked Immunosorbent AssayMiceMice, Inbred C57BLPrionsPrPSc ProteinsScrapieSheepEndopeptidase KPrionsPrPSc Proteins

Identifiers

PMID25565633
PMCPMC4286239
OpenAlexW1994626237

What OpenQuestion holds

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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.