Evidence map›Paper›PMID 22973037›Full record

ArticleJournal of virology2012

Incorporation of host complement regulatory proteins into Newcastle disease virus enhances complement evasion.

Moanaro Biswas, John B Johnson, Sandeep R P Kumar, Griffith D Parks, Subbiah Elankumarana, Elankumaran Subbiah

Erratum issuedOpen 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. An erratum has been issued. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
2.7field-weighted citation impact, top 10% 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

32 citing papers in PubMed, 38 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. Cells · 2021
    Article
  8. Review
  9. Review
  10. Host-virus interaction and viral evasion.Cell biology international · 2021
    Review
  11. Article
  12. Article
  13. Interactions of viruses and the humoral innate immune response.Clinical immunology (Orlando, Fla.) · 2020
    Review
  14. In the Crosshairs: RNA Viruses OR Complement?Frontiers in immunology · 2020
    Review
  15. Review
  16. Article
  17. Article
  18. Article
  19. Article
  20. Article
4 · The record

Corrections and comments

  • Erratum issued
    Subbiah, Elankumaran [corrected to Elankumarana, Subbiah]
5 · Who and what money

Authors and funding

6 authors at 3 institutions in 1 country.

Moanaro BiswasDepartment of Biomedical Sciences and Pathobiology, Virginia-Maryland Regional College of Veterinary Medicine, Virginia Polytechnic Institute and State University, Blacksburg, Virginia, USA.
John B Johnson
Sandeep R P Kumar
Griffith D Parks
Subbiah Elankumarana
Elankumaran Subbiah
Virginia Tech · USWake Forest University · USVirginia–Maryland College of Veterinary Medicine · US

Funding

Paramyxovirus Activation and Inhibition of Complement PathwaysR01AI083253 · NIAID · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI PARKS, GRIFFITH D. · 2011 to 2015
$1.8M
Protease Activation of Newcastle Disease Virus for Oncolytic viral therapyR21AI070528 · NIAID · VIRGINIA POLYTECHNIC INST AND ST UNIV · PI SUBBIAH, ELANKUMARAN · 2007 to 2008
$429k
NIAID NIH HHS AI070528NIAID NIH HHS AI083253NIAID NIH HHS R01 AI083253NIAID NIH HHS R21 AI070528
6 · The paper itself

Abstract

Newcastle disease virus (NDV), an avian paramyxovirus, is inherently tumor selective and is currently being considered as a clinical oncolytic virus and vaccine vector. In this study, we analyzed the effect of complement on the neutralization of NDV purified from embryonated chicken eggs, a common source for virus production. Fresh normal human serum (NHS) neutralized NDV by multiple pathways of complement activation, independent of neutralizing antibodies. Neutralization was associated with C3 deposition and the activation of C2, C3, C4, and C5 components. Interestingly, NDV grown in mammalian cell lines was resistant to complement neutralization by NHS. To confirm whether the incorporation of regulators of complement activity (RCA) into the viral envelope afforded complement resistance, we grew NDV in CHO cells stably transfected with CD46 or HeLa cells, which strongly express CD46 and CD55. NDV grown in RCA-expressing cells was resistant to complement by incorporating CD46 and CD55 on virions. Mammalian CD46 and CD55 molecules on virions exhibited homologous restriction, since chicken sera devoid of neutralizing antibodies to NDV were able to effectively neutralize these virions. The incorporation of chicken RCA into NDV produced in embryonated eggs similarly provided species specificity toward chicken sera.

Indexed as

AnimalsCD55 AntigensChick EmbryoChlorocebus aethiopsCHO CellsComplement System ProteinsCricetinaeCricetulusEnzyme-Linked Immunosorbent AssayGreen Fluorescent ProteinsHeLa CellsHumansImmunoblottingMembrane Cofactor ProteinMicroscopy, Electron, TransmissionNeutralization TestsCD55 AntigensComplement System Proteinsenhanced green fluorescent proteinGreen Fluorescent ProteinsMembrane Cofactor Protein

Identifiers

PMID22973037
PMCPMC3497656
OpenAlexW2056825877

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.