Evidence map›Paper›PMID 30872764›Full record

ArticleScientific reports2019

Super-resolution microscopy reveals significant impact of M2e-specific monoclonal antibodies on influenza A virus filament formation at the host cell surface.

Annasaheb Kolpe, Maria Arista-Romero, Bert Schepens, Silvia Pujals, Xavier Saelens, Lorenzo Albertazzi

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.9field-weighted citation impact, top 15% 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

13 citing papers in PubMed, 25 citations in OpenAlex.

  1. Implications of morphological variation in influenza viruses.Microbiology and molecular biology reviews : MMBR · 2025
    Review
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  7. Virus morphology: Insights from super-resolution fluorescence microscopy.Biochimica et biophysica acta. Molecular basis of disease · 2022
    Review
  8. 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

6 authors at 2 institutions in 3 countries.

Annasaheb KolpeVIB-UGent Center for Medical Biotechnology, Technologiepark-Zwijnaarde 71, Ghent, B-9052, Belgium.
Maria Arista-RomeroNanoscopy for Nanomedicine Group, Institute for Bioengineering of Catalonia (IBEC), C\Baldiri Reixac 15-21, Helix Building, 08028, Barcelona, Spain.
Bert SchepensVIB-UGent Center for Medical Biotechnology, Technologiepark-Zwijnaarde 71, Ghent, B-9052, Belgium.
Silvia PujalsNanoscopy for Nanomedicine Group, Institute for Bioengineering of Catalonia (IBEC), C\Baldiri Reixac 15-21, Helix Building, 08028, Barcelona, Spain.
Xavier SaelensVIB-UGent Center for Medical Biotechnology, Technologiepark-Zwijnaarde 71, Ghent, B-9052, Belgium. xavier.saelens@vib-ugent.be.
Lorenzo AlbertazziNanoscopy for Nanomedicine Group, Institute for Bioengineering of Catalonia (IBEC), C\Baldiri Reixac 15-21, Helix Building, 08028, Barcelona, Spain. lalbertazzi@ibecbarcelona.eu.ORCID 0000-0002-6837-0812
Ghent University · BEInstitute for Bioengineering of Catalonia · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Influenza A virions are highly pleomorphic, exhibiting either spherical or filamentous morphology. The influenza A virus strain A/Udorn/72 (H3N2) produces copious amounts of long filaments on the surface of infected cells where matrix protein 1 (M1) and 2 (M2) play a key role in virus filament formation. Previously, it was shown that an anti-M2 ectodomain (M2e) antibody could inhibit A/Udorn/72 virus filament formation. However, the study of these structures is limited by their small size and complex structure. Here, we show that M2e-specific IgG1 and IgG2a mouse monoclonal antibodies can reduce influenza A/Udorn/72 virus plaque growth and infectivity in vitro. Using Immuno-staining combined with super-resolution microscopy that allows us to study structures beyond the diffraction limit, we report that M2 is localized at the base of viral filaments that emerge from the membrane of infected cells. Filament formation was inhibited by treatment of A/Udorn/72 infected cells with M2e-specific IgG2a and IgG1 monoclonal antibodies and resulted in fragmentation of pre-existing filaments. We conclude that M2e-specific IgGs can reduce filamentous influenza A virus replication in vitro and suggest that in vitro inhibition of A/Udorn/72 virus replication by M2e-specific antibodies correlates with the inhibition of filament formation on the surface of infected cells.

Indexed as

AnimalsAntibodies, MonoclonalDogsFemaleHost-Pathogen InteractionsImmunoglobulin GInfluenza A Virus, H3N2 SubtypeMadin Darby Canine Kidney CellsMice, Inbred BALB CMicroscopy, ConfocalOrthomyxoviridae InfectionsViral Matrix ProteinsViroporin ProteinsAntibodies, MonoclonalImmunoglobulin GM2 protein, Influenza A virusViral Matrix ProteinsViroporin Proteins

Identifiers

PMID30872764
PMCPMC6418112
OpenAlexW2922336235

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.