Evidence map›Paper›PMID 34648608›Full record

ReviewPLoS pathogens2021

Deconstructing virus condensation.

Nora Lopez, Gabriela Camporeale, Mariano Salgueiro, Silvia Susana Borkosky, Araceli Visentín, Ramon Peralta-Martinez, María Eugenia Loureiro, Gonzalo de Prat-Gay

Open access · goldAbstract readReview
In one paragraph

Review in PLoS pathogens, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 43 papers.

0numbers the graph read from it
0cells of the map it votes in
43citing papers in PubMed
9.9field-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

43 citing papers in PubMed, 77 citations in OpenAlex.

  1. Review
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  11. Protein-RNA condensation kinetics via filamentous nanoclusters.Protein science : a publication of the Protein Society · 2025
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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

8 authors at 2 institutions in 1 country.

Nora LopezCentro de Virología Animal (CEVAN), Consejo Nacional de Investigaciones Científicas y Tecnológicas (CONICET)-Universidad Abierta Interamericana, Buenos Aires, Argentina.ORCID 0000-0003-1932-1843
Gabriela CamporealeFundación Instituto Leloir, IIB-BA Conicet, Buenos Aires, Argentina.ORCID 0000-0001-9159-1974
Mariano SalgueiroFundación Instituto Leloir, IIB-BA Conicet, Buenos Aires, Argentina.ORCID 0000-0002-1536-7222
Silvia Susana BorkoskyFundación Instituto Leloir, IIB-BA Conicet, Buenos Aires, Argentina.
Araceli VisentínFundación Instituto Leloir, IIB-BA Conicet, Buenos Aires, Argentina.
Ramon Peralta-MartinezFundación Instituto Leloir, IIB-BA Conicet, Buenos Aires, Argentina.
María Eugenia LoureiroCentro de Virología Animal (CEVAN), Consejo Nacional de Investigaciones Científicas y Tecnológicas (CONICET)-Universidad Abierta Interamericana, Buenos Aires, Argentina.ORCID 0000-0001-7965-0177
Gonzalo de Prat-GayFundación Instituto Leloir, IIB-BA Conicet, Buenos Aires, Argentina.ORCID 0000-0001-5748-6863
Fundación Instituto Leloir · ARConsejo Nacional de Investigaciones Científicas y Técnicas · AR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Viruses have evolved precise mechanisms for using the cellular physiological pathways for their perpetuation. These virus-driven biochemical events must be separated in space and time from those of the host cell. In recent years, granular structures, known for over a century for rabies virus, were shown to host viral gene function and were named using terms such as viroplasms, replication sites, inclusion bodies, or viral factories (VFs). More recently, these VFs were shown to be liquid-like, sharing properties with membrane-less organelles driven by liquid-liquid phase separation (LLPS) in a process widely referred to as biomolecular condensation. Some of the best described examples of these structures come from negative stranded RNA viruses, where micrometer size VFs are formed toward the end of the infectious cycle. We here discuss some basic principles of LLPS in connection with several examples of VFs and propose a view, which integrates viral replication mechanisms with the biochemistry underlying liquid-like organelles. In this view, viral protein and RNA components gradually accumulate up to a critical point during infection where phase separation is triggered. This yields an increase in transcription that leads in turn to increased translation and a consequent growth of initially formed condensates. According to chemical principles behind phase separation, an increase in the concentration of components increases the size of the condensate. A positive feedback cycle would thus generate in which crucial components, in particular nucleoproteins and viral polymerases, reach their highest levels required for genome replication. Progress in understanding viral biomolecular condensation leads to exploration of novel therapeutics. Furthermore, it provides insights into the fundamentals of phase separation in the regulation of cellular gene function given that virus replication and transcription, in particular those requiring host polymerases, are governed by the same biochemical principles.

Indexed as

Inclusion Bodies, ViralVirusesVirus Replication

Identifiers

PMID34648608
PMCPMC8516229
OpenAlexW3207206005

What Socratic holds

Textmetadata
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 Socratic graph.