Evidence map›Paper›PMID 25889156›Full record

ArticleRetrovirology2015

Jaagsiekte sheep retrovirus infection of lung slice cultures.

Chris Cousens, Charline Alleaume, Esther Bijsmans, Henny M Martineau, Jeanie Finlayson, Mark P Dagleish, David J Griffiths

Open access · goldAbstract read
In one paragraph

Article in Retrovirology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.8field-weighted citation impact, top 16% 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

14 citing papers in PubMed, 19 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Review
  7. Review
  8. Article
  9. Article
  10. Article
  11. Article
  12. Review
  13. Use of Precision-Cut Lung Slices as anMolecular therapy. Methods & clinical development · 2018
    Article
  14. Article
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

7 authors at 2 institutions in 1 country.

Chris CousensMoredun Research Institute, Pentlands Science Park, Bush Loan, Penicuik, Edinburgh, UK. chris.cousens@moredun.ac.uk.
Charline AlleaumeMoredun Research Institute, Pentlands Science Park, Bush Loan, Penicuik, Edinburgh, UK. char.all@hotmail.fr.
Esther BijsmansMoredun Research Institute, Pentlands Science Park, Bush Loan, Penicuik, Edinburgh, UK. ebijsmans@rvc.ac.uk.
Henny M MartineauDepartment of Pathology and Infectious Diseases, Royal Veterinary College, Hawkshead Lane, North Mymms, Hatfield, Hertfordshire, UK. hmartineau@rvc.ac.uk.
Jeanie FinlaysonMoredun Research Institute, Pentlands Science Park, Bush Loan, Penicuik, Edinburgh, UK. jeanie.finlayson@moredun.ac.uk.
Mark P DagleishMoredun Research Institute, Pentlands Science Park, Bush Loan, Penicuik, Edinburgh, UK. mark.dagleish@moredun.ac.uk.
David J GriffithsMoredun Research Institute, Pentlands Science Park, Bush Loan, Penicuik, Edinburgh, UK. david.griffiths@moredun.ac.uk1.
Moredun Research Institute · GBRoyal Veterinary College · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundJaagsiekte sheep retrovirus (JSRV) is the causative agent of ovine pulmonary adenocarcinoma (OPA), a transmissible neoplastic disease of sheep. OPA is an economically important veterinary disease and is also a valuable naturally occurring animal model of human lung cancer, with which it shares a similar histological appearance and the activation of common cell signaling pathways. Interestingly, the JSRV Env protein is directly oncogenic and capable of driving cellular transformation in vivo and in vitro. Previous studies of JSRV infection in cell culture have been hindered by the lack of a permissive cell line for the virus. Here, we investigated the ability of JSRV to infect slices of ovine lung tissue cultured ex vivo.

resultsWe describe the use of precision cut lung slices from healthy sheep to study JSRV infection and transformation ex vivo. Following optimization of the culture system we characterized JSRV infection of lung slices and compared the phenotype of infected cells to natural field cases and to experimentally-induced OPA tumors from sheep. JSRV was able to infect cells within lung slices, to produce new infectious virions and induce cell proliferation. Immunohistochemical labeling revealed that infected lung slice cells express markers of type II pneumocytes and phosphorylated Akt and ERK1/2. These features closely resemble the phenotype of natural and experimentally-derived OPA in sheep, indicating that lung slice culture provides an authentic ex vivo model of OPA.

conclusionsWe conclude that we have established an ex vivo model of JSRV infection. This model will be valuable for future studies of JSRV replication and early events in oncogenesis and provides a novel platform for studies of JSRV-induced lung cancer.

Indexed as

AnimalsCell ProliferationJaagsiekte sheep retrovirusLungModels, TheoreticalOrgan Culture TechniquesSheep, Domestic

Identifiers

PMID25889156
PMCPMC4419405
OpenAlexW2012560104

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.