Evidence map›Paper›PMID 22278252›Full record

ArticleJournal of virology2012

Canine distemper virus epithelial cell infection is required for clinical disease but not for immunosuppression.

Bevan Sawatsky, Xiao-Xiang Wong, Sarah Hinkelmann, Roberto Cattaneo, Veronika von Messling

Open access · bronzeAbstract read
In one paragraph

Article in Journal of virology, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 52 papers.

0numbers the graph read from it
0cells of the map it votes in
52citing papers in PubMed
4.7field-weighted citation impact, top 5% 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

52 citing papers in PubMed, 71 citations in OpenAlex.

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  10. Genetic Characterization ofTransboundary and emerging diseases · 2024
    Article
  11. Canine Distemper Virus Pathogenesis in the Ferret Model.Methods in molecular biology (Clifton, N.J.) · 2024
    Article
  12. Article
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  14. Review
  15. 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

5 authors at 4 institutions in 4 countries.

Bevan SawatskyINRS-Institut Armand-Frappier, University of Quebec, Laval, Canada. veronika.vonmessling@duke-nus.edu.sg
Xiao-Xiang Wong
Sarah Hinkelmann
Roberto Cattaneo
Veronika von Messling
Institut National de la Recherche Scientifique · CAArmand Frappier Museum · CAMayo Clinic · USUniversity of Veterinary Medicine Hannover, Foundation · DE

Funding

Immunosuppression and Innate Immunity Control by MorbillivirusesR01AI063476 · NIAID · MAYO CLINIC ROCHESTER · PI CATTANEO, ROBERTO B. · 2005 to 2014
$3.2M
CIHR MOP-66989NIAID NIH HHS R01 AI063476
6 · The paper itself

Abstract

To characterize the importance of infection of epithelial cells for morbillivirus pathogenesis, we took advantage of the severe disease caused by canine distemper virus (CDV) in ferrets. To obtain a CDV that was unable to enter epithelial cells but retained the ability to enter immune cells, we transferred to its attachment (H) protein two mutations shown to interfere with the interaction of measles virus H with its epithelial receptor, human nectin-4. As expected for an epithelial receptor (EpR)-blind CDV, this virus infected dog and ferret epithelial cells inefficiently and did not cause cell fusion or syncytium formation. On the other hand, the EpR-blind CDV replicated in cells expressing canine signaling lymphocyte activation molecule (SLAM), the morbillivirus immune cell receptor, with similar kinetics to those of wild-type CDV. While ferrets infected with wild-type CDV died within 12 days after infection, after developing severe rash and fever, animals infected with the EpR-blind virus showed no clinical signs of disease. Nevertheless, both viruses spread rapidly and efficiently in immune cells, causing similar levels of leukopenia and inhibition of lymphocyte proliferation activity, two indicators of morbillivirus immunosuppression. Infection was documented for airway epithelia of ferrets infected with wild-type CDV but not for those of animals infected with the EpR-blind virus, and only animals infected with wild-type CDV shed virus. Thus, epithelial cell infection is necessary for clinical disease and efficient virus shedding but not for immunosuppression.

Indexed as

AnimalsCell LineDistemperDistemper Virus, CanineDogsEpithelial CellsFerretsImmunosuppression TherapyReceptors, VirusVirus SheddingReceptors, Virus

Identifiers

PMID22278252
PMCPMC3302517
OpenAlexW2030892945

What OpenQuestion holds

Textmetadata
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.