Evidence map›Paper›PMID 22761385›Full record

ArticleJournal of virology2012

Virion-associated complement regulator CD55 is more potent than CD46 in mediating resistance of mumps virus and vesicular stomatitis virus to neutralization.

John B Johnson, Douglas S Lyles, Martha A Alexander-Miller, Griffith D Parks

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 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
1.0field-weighted citation impact, top 22% 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

22 citing papers in PubMed, 25 citations in OpenAlex.

  1. Article
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  8. Interactions of viruses and the humoral innate immune response.Clinical immunology (Orlando, Fla.) · 2020
    Review
  9. In the Crosshairs: RNA Viruses OR Complement?Frontiers in immunology · 2020
    Review
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  11. Article
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  16. 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

4 authors at 1 institution in 1 country.

John B JohnsonDepartment of Microbiology and Immunology, Wake Forest School of Medicine, Winston-Salem, North Carolina, USA.
Douglas S Lyles
Martha A Alexander-Miller
Griffith D Parks
Wake Forest University · US

Funding

FUSION OF VIRUS ENVELOPE WITH CELL MEMBRANESR01AI015892 · NIAID · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI LYLES, DOUGLAS S. · 1985 to 2013
$4.0M
Paramyxovirus Activation and Inhibition of Complement PathwaysR01AI083253 · NIAID · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI PARKS, GRIFFITH D. · 2011 to 2015
$1.8M
ASSEMBLY OF ENVELOPED VIRUSESR55AI015892 · NIAID · WAKE FOREST UNIVERSITY · PI LYLES, DOUGLAS S. · 1991 to 1991
–
NIAID NIH HHS AI015892NIAID NIH HHS AI083253NIAID NIH HHS R01 AI015892NIAID NIH HHS R01 AI083253
6 · The paper itself

Abstract

Enveloped viruses can incorporate host cell membrane proteins during the budding process. Here we demonstrate that mumps virus (MuV) and vesicular stomatitis virus (VSV) assemble to include CD46 and CD55, two host cell regulators which inhibit propagation of complement pathways through distinct mechanisms. Using viruses which incorporated CD46 alone, CD55 alone, or both CD46 and CD55, we have tested the relative contribution of these regulators in resistance to complement-mediated neutralization. Virion-associated CD46 and CD55 were biologically active, with VSV showing higher levels of activity of both cofactors, which promoted factor I-mediated cleavage of C3b into iC3b as well as decay-accelerating factor (DAF) activity against the C3 convertase, than MuV. Time courses of in vitro neutralization with normal human serum (NHS) showed that both regulators could delay neutralization, but viruses containing CD46 alone were neutralized faster and more completely than viruses containing CD55 alone. A dominant inhibitory role for CD55 was most evident for VSV, where virus containing CD55 alone was not substantially different in neutralization kinetics from virus harboring both regulators. Electron microscopy showed that VSV neutralization proceeded through virion aggregation followed by lysis, with virion-associated CD55 providing a delay in both aggregation and lysis more substantial than that conferred by CD46. Our results demonstrate the functional significance of incorporation of host cell factors during virion envelope assembly. They also define pathways of virus complement-mediated neutralization and suggest the design of more effective viral vectors.

Indexed as

AnimalsCD55 AntigensCHO CellsComplement ActivationCricetinaeCricetulusHost-Pathogen InteractionsHumansMembrane Cofactor ProteinMicroscopy, ImmunoelectronMumps virusNeutralization TestsVesiculovirusVirus AssemblyCD46 protein, humanCD55 AntigensMembrane Cofactor Protein

Identifiers

PMID22761385
PMCPMC3446622
OpenAlexW2158058519

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.