Evidence map›Paper›PMID 33371254›Full record

ArticleViruses2020

Identification of an Intermediate Step in Foamy Virus Fusion.

Aurélie Dupont, Ivo M Glück, Dorothee Ponti, Kristin Stirnnagel, Sylvia Hütter, Florian Perrotton, Nicole Stanke, Stefanie Richter, Dirk Lindemann, Don C Lamb

Abstract read
In one paragraph

Article in Viruses, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Article
  2. Article
  3. Exosomal transmission of viruses, a two-edged biological sword.Cell communication and signaling : CCS · 2023
    Review
  4. 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

10 authors.

Aurélie DupontDepartment of Chemistry, Ludwig Maximilians-Universität München, Butenandtstraße 5-13, 81377 München, Germany.
Ivo M GlückDepartment of Chemistry, Ludwig Maximilians-Universität München, Butenandtstraße 5-13, 81377 München, Germany.
Dorothee PontiDepartment of Chemistry, Ludwig Maximilians-Universität München, Butenandtstraße 5-13, 81377 München, Germany.
Kristin StirnnagelMedical Faculty "Carl Gustav Carus", Institute of Virology, Technische Universität Dresden, Fetscherstr. 74, 01307 Dresden, Germany.
Sylvia HütterMedical Faculty "Carl Gustav Carus", Institute of Virology, Technische Universität Dresden, Fetscherstr. 74, 01307 Dresden, Germany.
Florian PerrottonDepartment of Chemistry, Ludwig Maximilians-Universität München, Butenandtstraße 5-13, 81377 München, Germany.
Nicole StankeMedical Faculty "Carl Gustav Carus", Institute of Virology, Technische Universität Dresden, Fetscherstr. 74, 01307 Dresden, Germany.
Stefanie RichterMedical Faculty "Carl Gustav Carus", Institute of Virology, Technische Universität Dresden, Fetscherstr. 74, 01307 Dresden, Germany.
Dirk LindemannMedical Faculty "Carl Gustav Carus", Institute of Virology, Technische Universität Dresden, Fetscherstr. 74, 01307 Dresden, Germany.ORCID 0000-0002-0320-4223
Don C LambDepartment of Chemistry, Ludwig Maximilians-Universität München, Butenandtstraße 5-13, 81377 München, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Viral glycoprotein-mediated membrane fusion is an essential step for productive infection of host cells by enveloped viruses; however, due to its rarity and challenges in detection, little is known about the details of fusion events at the single particle level. Here, we have developed dual-color foamy viruses (FVs) composed of eGFP-tagged prototype FV (PFV) Gag and mCherry-tagged Env of either PFV or macaque simian FV (SFVmac) origin that have been optimized for detection of the fusion process. Using our recently developed tracking imaging correlation (TrIC) analysis, we were able to detect the fusion process for both PFV and SFVmac Env containing virions. PFV Env-mediated fusion was observed both at the plasma membrane as well as from endosomes, whereas SFVmac Env-mediated fusion was only observed from endosomes. PFV Env-mediated fusion was observed to happen more often and more rapidly than as for SFVmac Env. Strikingly, using the TrIC method, we detected a novel intermediate state where the envelope and capsids are still tethered but separated by up to 400 nm before final separation of Env and Gag occurred.

Indexed as

Membrane FusionVirus InternalizationVirus ReplicationHumansLife Cycle StagesModels, BiologicalRetroviridae InfectionsSpumavirusVirioncapsidenvelope glycoproteinfluorescence live cell imagingfoamy virusretrovirussingle virus trackingspinning disk confocal microscopyviral fusion

Identifiers

PMID33371254
PMCPMC7766700

What OpenQuestion holds

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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.