Evidence map›Paper›PMID 38862527›Full record

ArticleNature communications2024

Dynamic label-free analysis of SARS-CoV-2 infection reveals virus-induced subcellular remodeling.

Nell Saunders, Blandine Monel, Nadège Cayet, Lorenzo Archetti, Hugo Moreno, Alexandre Jeanne, Agathe Marguier, Julian Buchrieser, Timothy Wai, Olivier Schwartz and 1 more

Abstract read
In one paragraph

Article in Nature communications, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing 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

12 citing papers in PubMed.

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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.

Nell SaundersVirus & Immunity Unit, Institut Pasteur, Université Paris Cité, CNRS, UMR 3569, Paris, France.
Blandine MonelVirus & Immunity Unit, Institut Pasteur, Université Paris Cité, CNRS, UMR 3569, Paris, France.
Nadège CayetInstitut Pasteur, Université Paris Cité, Ultrastructural Bioimaging Unit, 75015, Paris, France.
Lorenzo Archetti *Deep Quantitative Biology Department, Nanolive SA, Tolochenaz, Switzerland.ORCID 0009-0007-2473-4980
Hugo Moreno *Deep Quantitative Biology Department, Nanolive SA, Tolochenaz, Switzerland.ORCID 0009-0007-3399-1145
Alexandre Jeanne *Deep Quantitative Biology Department, Nanolive SA, Tolochenaz, Switzerland.ORCID 0009-0002-8909-755X
Agathe MarguierDeep Quantitative Biology Department, Nanolive SA, Tolochenaz, Switzerland.ORCID 0009-0001-6384-3887
Julian BuchrieserVirus & Immunity Unit, Institut Pasteur, Université Paris Cité, CNRS, UMR 3569, Paris, France.ORCID 0000-0003-4790-7577
Timothy WaiMitochondrial Biology Group, Institut Pasteur, Université Paris Cité, CNRS, UMR 3691, Paris, France.ORCID 0000-0002-6770-6222
Olivier SchwartzVirus & Immunity Unit, Institut Pasteur, Université Paris Cité, CNRS, UMR 3569, Paris, France. Olivier.schwartz@pasteur.fr.ORCID 0000-0002-0729-1475
Mathieu FréchinDeep Quantitative Biology Department, Nanolive SA, Tolochenaz, Switzerland. Mathieu.frechin@nanolive.ch.ORCID 0000-0002-2310-5230

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Assessing the impact of SARS-CoV-2 on organelle dynamics allows a better understanding of the mechanisms of viral replication. We combine label-free holotomographic microscopy with Artificial Intelligence to visualize and quantify the subcellular changes triggered by SARS-CoV-2 infection. We study the dynamics of shape, position and dry mass of nucleoli, nuclei, lipid droplets and mitochondria within hundreds of single cells from early infection to syncytia formation and death. SARS-CoV-2 infection enlarges nucleoli, perturbs lipid droplets, changes mitochondrial shape and dry mass, and separates lipid droplets from mitochondria. We then used Bayesian network modeling on organelle dry mass states to define organelle cross-regulation networks and report modifications of organelle cross-regulation that are triggered by infection and syncytia formation. Our work highlights the subcellular remodeling induced by SARS-CoV-2 infection and provides an Artificial Intelligence-enhanced, label-free methodology to study in real-time the dynamics of cell populations and their content.

Indexed as

Bayes TheoremCOVID-19Lipid DropletsMitochondriaSARS-CoV-2AnimalsArtificial IntelligenceCell NucleolusCell NucleusChlorocebus aethiopsHumansVero CellsVirus Replication

Identifiers

PMID38862527
PMCPMC11166935

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.