Evidence map›Paper›PMID 25879730›Full record

ArticleBMC veterinary research2015

Decreased expression of endogenous feline leukemia virus in cat lymphomas: a case control study.

Milica Krunic, Reinhard Ertl, Benedikt Hagen, Fritz J Sedlazeck, Regina Hofmann-Lehmann, Arndt von Haeseler, Dieter Klein

Open access · goldAbstract read
In one paragraph

Article in BMC veterinary research, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.7field-weighted citation impact, top 23% 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

4 citing papers in PubMed, 14 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

7 authors at 4 institutions in 2 countries.

Milica KrunicCenter for Integrative Bioinformatics Vienna, Max F. Perutz Laboratories, University of Vienna, Medical University of Vienna, A-1030, Vienna, Austria. milica.krunic@univie.ac.at.
Reinhard ErtlVetCore Facility for Research, University of Veterinary Medicine Vienna, A-1210, Vienna, Austria. reinhard.ertl@vetmeduni.ac.at.
Benedikt HagenVetCore Facility for Research, University of Veterinary Medicine Vienna, A-1210, Vienna, Austria. benedikt.hagen@gmx.de.
Fritz J SedlazeckCenter for Integrative Bioinformatics Vienna, Max F. Perutz Laboratories, University of Vienna, Medical University of Vienna, A-1030, Vienna, Austria. fritz.sedlazeck@univie.ac.at.
Regina Hofmann-LehmannClinical Laboratory, and Center for Clinical Studies, Vetsuisse Faculty, University of Zurich, CH-8057, Zurich, Switzerland. rhofmann@vetclinics.uzh.ch.
Arndt von HaeselerCenter for Integrative Bioinformatics Vienna, Max F. Perutz Laboratories, University of Vienna, Medical University of Vienna, A-1030, Vienna, Austria. arndt.von.haeseler@univie.ac.at.
Dieter KleinVetCore Facility for Research, University of Veterinary Medicine Vienna, A-1210, Vienna, Austria. dieter.klein@vetmeduni.ac.at.
University of Veterinary Medicine Vienna · ATMax Perutz Labs · ATTU Wien · ATUniversity of Zurich · CH

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundCats infected with exogenous feline leukemia virus (exFeLV) have a higher chance of lymphoma development than uninfected cats. Furthermore, an increased exFeLV transcription has been detected in lymphomas compared to non-malignant tissues. The possible mechanisms of lymphoma development by exFeLV are insertional mutagenesis or persistent stimulation of host immune cells by viral antigens, bringing them at risk for malignant transformation. Vaccination of cats against exFeLV has in recent years decreased the overall infection rate in most countries. Nevertheless, an increasing number of lymphomas have been diagnosed among exFeLV-negative cats. Endogenous feline leukemia virus (enFeLV) is another retrovirus for which transcription has been observed in cat lymphomas. EnFeLV provirus elements are present in the germline of various cat species and share a high sequence similarity with exFeLV but, due to mutations, are incapable of producing infectious viral particles. However, recombination between exFeLV and enFeLV could produce infectious particles.

resultsWe examined the FeLV expression in cats that have developed malignant lymphomas and discussed the possible mechanisms that could have induced malignant transformation. For expression analysis we used next-generation RNA-sequencing (RNA-Seq) and for validation reverse transcription quantitative PCR (RT-qPCR). First, we showed that there was no expression of exFeLV in all samples, which eliminates the possibility of recombination between exFeLV and enFeLV. Next, we analyzed the difference in expression of three enFeLV genes between control and lymphoma samples. Our analysis showed an average of 3.40-fold decreased viral expression for the three genes in lymphoma compared to control samples. The results were confirmed by RT-qPCR.

conclusionsThere is a decreased expression of enFeLV genes in lymphomas versus control samples, which contradicts previous observations for the exFeLV. Our results suggest that a persistent stimulation of host immune cells is not an appropriate mechanism responsible for malignant transformation caused by feline endogenous retroviruses.

Indexed as

AnimalsBase SequenceCase-Control StudiesCat DiseasesCatsFemaleGene Expression Regulation, ViralLeukemia Virus, FelineLymphomaMaleRetroviridae InfectionsReverse Transcriptase Polymerase Chain ReactionRNA, ViralTumor Virus InfectionsRNA, Viral

Identifiers

PMID25879730
PMCPMC4424575
OpenAlexW2095880516

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.