Evidence map›Paper›PMID 40490555›Full record

ArticleThe EMBO journal2025

Morphology-dependent entry kinetics and spread of influenza A virus.

Sarah Peterl, Carmen M Lahr, Carl N Schneider, Janis Meyer, Xenia Podlipensky, Vera Lechner, Maria Villiou, Larissa Eis, Steffen Klein, Charlotta Funaya and 5 more

Abstract read
In one paragraph

Article in The EMBO journal, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
–field-weighted citation impact
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

7 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Implications of morphological variation in influenza viruses.Microbiology and molecular biology reviews : MMBR · 2025
    Review
  6. Article
  7. Article
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

15 authors.

Sarah PeterlSchaller Research Groups, Department of Infectious Diseases, Virology, Medical Faculty, Heidelberg University, Heidelberg, Germany.ORCID http://orcid.org/0000-0002-8082-3546
Carmen M LahrSchaller Research Groups, Department of Infectious Diseases, Virology, Medical Faculty, Heidelberg University, Heidelberg, Germany.ORCID http://orcid.org/0000-0001-9689-6232
Carl N SchneiderSchaller Research Groups, Department of Infectious Diseases, Virology, Medical Faculty, Heidelberg University, Heidelberg, Germany.
Janis MeyerBiomedical Computer Vision Group, BioQuant, IPMB, Heidelberg University, Heidelberg, Germany.
Xenia PodlipenskySchaller Research Groups, Department of Infectious Diseases, Virology, Medical Faculty, Heidelberg University, Heidelberg, Germany.
Vera LechnerSchaller Research Groups, Department of Infectious Diseases, Virology, Medical Faculty, Heidelberg University, Heidelberg, Germany.ORCID http://orcid.org/0009-0006-4528-3157
Maria VilliouInstitute for Molecular Systems Engineering and Advanced Materials (IMSEAM), Heidelberg University, Heidelberg, Germany.
Larissa EisElectron Microscopy Core Facility, Heidelberg University, Heidelberg, Germany.
Steffen KleinSchaller Research Groups, Department of Infectious Diseases, Virology, Medical Faculty, Heidelberg University, Heidelberg, Germany.
Charlotta FunayaElectron Microscopy Core Facility, Heidelberg University, Heidelberg, Germany.ORCID http://orcid.org/0000-0003-1375-1287
Elisabetta Ada Cavalcanti-AdamDepartment of Cellular Biophysics, Max Planck Institute for Medical Research, Heidelberg, Germany.
Frederik GrawDepartment of Internal Medicine 5, Hematology and Oncology, Friedrich-Alexander-Universität Erlangen-Nürnberg and Universitätsklinikum Erlangen, Erlangen, Germany.
Christine Selhuber-UnkelInstitute for Molecular Systems Engineering and Advanced Materials (IMSEAM), Heidelberg University, Heidelberg, Germany.ORCID http://orcid.org/0000-0002-5051-4822
Karl RohrBiomedical Computer Vision Group, BioQuant, IPMB, Heidelberg University, Heidelberg, Germany.
Petr ChlandaSchaller Research Groups, Department of Infectious Diseases, Virology, Medical Faculty, Heidelberg University, Heidelberg, Germany. petr.chlanda@bioquant.uni-heidelberg.de.ORCID http://orcid.org/0000-0002-7782-2139

Funding

Bundesministerium für Bildung und Forschung (BMBF) Flagship Initiative "Engineering Molecular Systems"Daimler und Benz Stiftung (Daimler and Benz Foundation) 32-09/24Deutsche Forschungsgemeinschaft (DFG) 240245660-SFB1129Deutsche Forschungsgemeinschaft (DFG) 390761711Deutsche Forschungsgemeinschaft (DFG) 437060729Deutsche Forschungsgemeinschaft (DFG) Excellence Strategy 2082/1-390761711EC | European Research Council (ERC) 101001797
6 · The paper itself

Abstract

Influenza A viruses (IAV) display a broad variety of morphologies ranging from spherical to long filamentous virus particles. These diverse phenotypes are believed to allow the virus to overcome various immunological and pulmonary barriers during entry into the airway epithelium, and to influence the viral entry pathway. Notably, laboratory-adapted IAV strains predominantly adopt a spherical form, yet the factors driving this preference as well as the factors favoring filamentous morphology in physiological settings remain unclear. To address this, we generated fluorescent reporter viruses with identical surface glycoproteins but distinct morphologies and developed a correlative light and scanning electron microscopy workflow. This enabled us to investigate the impact of viral morphology on spread, and to identify conditions favoring either form. Our findings demonstrate that filamentous IAV spread significantly slower in various cell lines, consistent with delayed entry kinetics and in-cell cryo-electron tomography, explaining the predominance of spherical forms in laboratory-adapted strains. Cellular junction integrity, neuraminidase activity, and mucin do not inhibit IAV spread in a morphology-dependent manner. However, filamentous virions confer a selective advantage under neutralizing-antibody pressure against hemagglutinin.

Indexed as

Influenza A virusInfluenza, HumanVirus InternalizationAnimalsCell LineCryoelectron MicroscopyDogsHumansKineticsMadin Darby Canine Kidney CellsVirionCLEMFilamentous influenza A virusIn situ cryo-ETMucinNeutralizing antibodies

Identifiers

PMID40490555
PMCPMC12264294

What OpenQuestion holds

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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.