Evidence map›Paper›PMID 31852789›Full record

ArticleJournal of virology2020

Flow Cytometry Analysis of HIV-1 Env Conformations at the Surface of Infected Cells and Virions: Role of Nef, CD4, and SERINC5.

Isabelle Staropoli, Jérémy Dufloo, Anaïs Ducher, Pierre-Henri Commere, Anna Sartori-Rupp, Sophie Novault, Timothée Bruel, Valérie Lorin, Hugo Mouquet, Olivier Schwartz and 1 more

Open access · greenAbstract read
In one paragraph

Article in Journal of virology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
1.3field-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

17 citing papers in PubMed, 26 citations in OpenAlex.

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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

11 authors at 3 institutions in 1 country.

Isabelle Staropoli *Institut Pasteur, Virus and Immunity Unit, CNRS-UMR3569, Paris, France.
Jérémy Dufloo *Institut Pasteur, Virus and Immunity Unit, CNRS-UMR3569, Paris, France.
Anaïs DucherInstitut Pasteur, Virus and Immunity Unit, CNRS-UMR3569, Paris, France.
Pierre-Henri CommereInstitut Pasteur, Flow Cytometry Platform, Paris, France.
Anna Sartori-RuppInstitut Pasteur, Unit of Technology and Service Ultra-Structural Bio-Imaging, Paris, France.
Sophie NovaultInstitut Pasteur, Flow Cytometry Platform, Paris, France.
Timothée BruelInstitut Pasteur, Virus and Immunity Unit, CNRS-UMR3569, Paris, France.
Valérie LorinInstitut Pasteur, Laboratory of Humoral Immunology, Inserm U1222, Paris, France.
Hugo MouquetInstitut Pasteur, Laboratory of Humoral Immunology, Inserm U1222, Paris, France.
Olivier Schwartz *Institut Pasteur, Virus and Immunity Unit, CNRS-UMR3569, Paris, France schwartz@pasteur.fr nicoletta.casartelli@pasteur.fr.ORCID 0000-0002-0729-1475
Nicoletta Casartelli *Institut Pasteur, Virus and Immunity Unit, CNRS-UMR3569, Paris, France schwartz@pasteur.fr nicoletta.casartelli@pasteur.fr.
Centre National de la Recherche Scientifique · FRInstitut Pasteur · FRInserm · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The HIV-1 Env protein is exposed at the surface of virions and infected cells. Env fluctuates between different closed and open structural states and these conformations influence both viral infectivity and sensitivity to antibody binding and neutralization. We established a flow virometry assay to visualize Env proteins at the surface of human immunodeficiency virus type 1 (HIV-1) virions. The assay is performed on ultracentrifuged fluorescent viral particles that are stained with a panel of broadly neutralizing antibodies (bNAbs) and nonneutralizing antibodies (nnAbs) that probe different epitopes of Env. We used this assay to compare Env at the surface of producer cells and viral particles and to analyze the effect of Nef, CD4, and SERINC5 on Env accessibility to antibodies. We studied the laboratory-adapted strain NL4-3 and two transmitted/founder viruses, THRO and CH058. We confirm that antibody accessibility varies between viral strains and show that Nef, CD4, and SERINC5 additively impact Env conformations. We further demonstrate that the Env accessibility profile on virions is globally similar to that observed on HIV-1-infected cells, with some noticeable differences. For instance, nnAbs bind to virions more efficiently than to producer cells, likely reflecting changes in Env conformational states on mature viral particles. This test complements other techniques and provides a convenient and simple tool for quantifying and probing the structure of Env at the virion surface and to analyze the impact of viral and cellular proteins on these parameters.

Indexed as

Flow CytometryCD4 AntigensCell Lineenv Gene Products, Human Immunodeficiency VirusEpitopesHIV-1HIV AntibodiesHIV InfectionsHumansMembrane Proteinsnef Gene Products, Human Immunodeficiency VirusProtein ConformationVirionCD4 Antigensenv Gene Products, Human Immunodeficiency VirusEpitopesHIV AntibodiesMembrane Proteinsnef Gene Products, Human Immunodeficiency Virusnef protein, Human immunodeficiency virus 1SERINC5 protein, humanbroadly neutralizing antibodiesEnvflow virometryHIV-1nonneutralizing antibodies

Identifiers

PMID31852789
PMCPMC7158727
OpenAlexW2996730181

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.