Evidence map›Paper›PMID 34601723›Full record

ArticleThe EMBO journal2021

SARS-CoV-2 Alpha, Beta, and Delta variants display enhanced Spike-mediated syncytia formation.

Maaran Michael Rajah, Mathieu Hubert, Elodie Bishop, Nell Saunders, Remy Robinot, Ludivine Grzelak, Delphine Planas, Jérémy Dufloo, Stacy Gellenoncourt, Alice Bongers and 8 more

Open access · bronzeAbstract read
In one paragraph

Article in The EMBO journal, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 125 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
125citing papers in PubMed, 1 pooled it
10.9field-weighted citation impact, top 1% 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

125 citing papers in PubMed, 1 synthesis or guideline pooled it, 194 citations in OpenAlex.

  1. JAK inhibitors and COVID-19.Journal for immunotherapy of cancer · 2022
    Pooled it
  2. Article
  3. Article
  4. Viral syncytia evolve to resist interferon.Nature communications · 2026
    Article
  5. Article
  6. Review
  7. Article
  8. Article
  9. Review
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Review
  18. Nonlytic Egress and Transmission in the Virus World.Annual review of biochemistry · 2025
    Review
  19. Article
  20. Review

65 more citing papers are in PubMed but not listed here.

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

18 authors at 2 institutions in 1 country.

Maaran Michael RajahVirus & Immunity Unit, Department of Virology, Institut Pasteur, CNRS UMR 3569, Paris, France.ORCID 0000-0002-6674-8850
Mathieu HubertVirus & Immunity Unit, Department of Virology, Institut Pasteur, CNRS UMR 3569, Paris, France.
Elodie BishopVirus & Immunity Unit, Department of Virology, Institut Pasteur, CNRS UMR 3569, Paris, France.
Nell SaundersVirus & Immunity Unit, Department of Virology, Institut Pasteur, CNRS UMR 3569, Paris, France.ORCID 0000-0002-0872-1529
Remy RobinotVirus & Immunity Unit, Department of Virology, Institut Pasteur, CNRS UMR 3569, Paris, France.
Ludivine GrzelakVirus & Immunity Unit, Department of Virology, Institut Pasteur, CNRS UMR 3569, Paris, France.
Delphine PlanasVirus & Immunity Unit, Department of Virology, Institut Pasteur, CNRS UMR 3569, Paris, France.
Jérémy DuflooVirus & Immunity Unit, Department of Virology, Institut Pasteur, CNRS UMR 3569, Paris, France.ORCID 0000-0002-4963-1378
Stacy GellenoncourtVirus & Immunity Unit, Department of Virology, Institut Pasteur, CNRS UMR 3569, Paris, France.ORCID 0000-0003-1896-7212
Alice BongersVirus & Immunity Unit, Department of Virology, Institut Pasteur, CNRS UMR 3569, Paris, France.
Marija ZivaljicIntegrative Neurobiology of Cholinergic Systems, Department of Neuroscience, Institut Pasteur, CNRS UMR 3571, Paris, France.
Cyril PlanchaisLaboratory of Humoral Immunology, Department of Immunology, Institut Pasteur, INSERM U1222, Paris, France.
Florence Guivel-BenhassineVirus & Immunity Unit, Department of Virology, Institut Pasteur, CNRS UMR 3569, Paris, France.
Françoise PorrotVirus & Immunity Unit, Department of Virology, Institut Pasteur, CNRS UMR 3569, Paris, France.
Hugo MouquetLaboratory of Humoral Immunology, Department of Immunology, Institut Pasteur, INSERM U1222, Paris, France.ORCID 0000-0002-4230-610X
Lisa A ChakrabartiVirus & Immunity Unit, Department of Virology, Institut Pasteur, CNRS UMR 3569, Paris, France.ORCID 0000-0002-1895-3630
Julian BuchrieserVirus & Immunity Unit, Department of Virology, Institut Pasteur, CNRS UMR 3569, Paris, France.ORCID 0000-0003-4790-7577
Olivier SchwartzVirus & Immunity Unit, Department of Virology, Institut Pasteur, CNRS UMR 3569, Paris, France.ORCID 0000-0002-0729-1475
Centre National de la Recherche Scientifique · FRInserm · FR

Funding

Agence Nationale de Recherches sur le Sida et les Hépatites Virales (ANRS)ANR CoronaMito AAP RA-COVID-19 V14ANR/FRM Flash Covid PROTEO-SARS-CoV-2EU (RECOVER)Fondation de France 00106077Fondation Pour la Recherche Médicale (FRM)French Ministry of Higher Education, Research and InnovationIDISCOVRINSERMInstitut PasteurInstitut Pasteur Department of Virology "Bourse de Soudure" fellowshipLabex IBEID ANR-10-LABX62-IBEIDMedecine-Sciences ENS-PSL ProgramMilieu Intérieur Program ANR-10-LABX-69- 01Pasteur-Paris University (PPU) International Doctoral ProgramREACTingRegion Ile-de-France program DIM1-HealthThe Vaccine Research InstituteThe Vaccine Research Institute ANR-10-LABX-77UPBI ANR-10-INSB-04-01Urgence COVID-19 Fundraising Campaign of Institut Pasteur
6 · The paper itself

Abstract

Severe COVID-19 is characterized by lung abnormalities, including the presence of syncytial pneumocytes. Syncytia form when SARS-CoV-2 spike protein expressed on the surface of infected cells interacts with the ACE2 receptor on neighboring cells. The syncytia forming potential of spike variant proteins remain poorly characterized. Here, we first assessed Alpha (B.1.1.7) and Beta (B.1.351) spread and fusion in cell cultures, compared with the ancestral D614G strain. Alpha and Beta replicated similarly to D614G strain in Vero, Caco-2, Calu-3, and primary airway cells. However, Alpha and Beta formed larger and more numerous syncytia. Variant spike proteins displayed higher ACE2 affinity compared with D614G. Alpha, Beta, and D614G fusion was similarly inhibited by interferon-induced transmembrane proteins (IFITMs). Individual mutations present in Alpha and Beta spikes modified fusogenicity, binding to ACE2 or recognition by monoclonal antibodies. We further show that Delta spike also triggers faster fusion relative to D614G. Thus, SARS-CoV-2 emerging variants display enhanced syncytia formation.

Indexed as

MutationAngiotensin-Converting Enzyme 2AnimalsAntibodies, MonoclonalCaco-2 CellsCell LineChlorocebus aethiopsGiant CellsHEK293 CellsHumansSARS-CoV-2Spike Glycoprotein, CoronavirusVero CellsVirus ReplicationACE2 protein, humanAngiotensin-Converting Enzyme 2Antibodies, MonoclonalSpike Glycoprotein, Coronavirusspike protein, SARS-CoV-2coronavirusfusionSARS-CoV-2spikesyncytia

Identifiers

PMID34601723
PMCPMC8646911
OpenAlexW3202714244

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.