Evidence map›Paper›PMID 39297643›Full record

ArticleJournal of virology2024

The Rac1-PAK1-Arp2/3 signaling axis regulates CHIKV nsP1-induced filopodia and optimal viral genome replication.

Olivier Aïqui-Reboul-Paviet, William Bakhache, Eric Bernard, Lise Holsteyn, Aymeric Neyret, Laurence Briant

Abstract read
In one paragraph

Article in Journal of virology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

  1. Review
  2. The SMARCA4-TMEM47 axis plays an essential role in chikungunya virus RNA replication.Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  3. Review
  4. Article
  5. Article
  6. 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

6 authors.

Olivier Aïqui-Reboul-Paviet *RNA Viruses and Metabolism Team, IRIM-CNRS UMR9004, Montpellier, France.
William Bakhache *RNA Viruses and Metabolism Team, IRIM-CNRS UMR9004, Montpellier, France.ORCID 0000-0002-2047-4866
Eric BernardRNA Viruses and Metabolism Team, IRIM-CNRS UMR9004, Montpellier, France.
Lise HolsteynRNA Viruses and Metabolism Team, IRIM-CNRS UMR9004, Montpellier, France.
Aymeric NeyretRNA Viruses and Metabolism Team, IRIM-CNRS UMR9004, Montpellier, France.
Laurence BriantRNA Viruses and Metabolism Team, IRIM-CNRS UMR9004, Montpellier, France.ORCID 0000-0002-1995-3501

Funding

Agence Nationale de la Recherche (ANR) ANR-18-CE11-0026-01Fondation pour la Recherche Médicale (FRM)Mediterranee Infection, Infectiopole Sud Foundation
6 · The paper itself

Abstract

Alphavirus infection induces dramatic remodeling of host cellular membranes, producing filopodia-like and intercellular extensions. The formation of filopodia-like extensions has been primarily assigned to the replication protein nsP1, which binds and reshapes the host plasma membrane when expressed alone. While reported decades ago, the molecular mechanisms behind nsP1 membrane deformation remain unknown. Using mammalian epithelial cells and Chikungunya virus (CHIKV) as models, we characterized nsP1-induced membrane deformations as highly dynamic actin-rich lamellipodia and filopodia-like extensions. Through pharmacological inhibition and genetic invalidation, we identified the critical contribution of the Rac1 GTPase and its downstream effectors PAK1 and the actin nucleator Arp2 in nsP1-induced membrane deformation. An intact Rac1-PAK1-Arp2 signaling axis was also required for optimal CHIKV genome replication. Therefore, our results designate the Rac1-PAK1-Arp2 pathway as an essential signaling node for CHIKV infection and establish a parallel requirement for host factors involved in nsP1-induced plasma membrane reshaping and assembly of a functional replication complex.IMPORTANCEThe alphavirus nsP1 protein dramatically remodels host cellular membranes, resulting in the formation of filopodia-like extensions. Although described decades ago, the molecular mechanisms controlling these membrane deformations and their functional importance remain elusive. Our study provides mechanistic insight, uncovering the critical role of the Rac1 GTPase, along with its downstream effectors PAK1 and the actin nucleator Arp2, in the nsP1-associated phenotype. Furthermore, we demonstrate that the Rac1-PAK1-Arp2 pathway is essential for optimal CHIKV genome replication. Our findings establish a parallel in the cellular mechanisms governing nsP1-induced plasma membrane reshaping and the production of a functional replication complex in infected cells.

Indexed as

Actin-Related Protein 2-3 ComplexChikungunya virusp21-Activated KinasesPseudopodiarac1 GTP-Binding ProteinSignal TransductionVirus ReplicationActin-Related Protein 2AnimalsCell LineCell MembraneChlorocebus aethiopsGenome, ViralHost-Pathogen InteractionsHumansViral Nonstructural ProteinsActin-Related Protein 2Actin-Related Protein 2-3 Complexp21-Activated KinasesPAK1 protein, humanrac1 GTP-Binding ProteinRAC1 protein, humanViral Nonstructural Proteinsalphaviruscell signalingChikungunya viruscytoskeletongenome replicationmembrane rearrangementnonstructural protein 1nsP1

Identifiers

PMID39297643
PMCPMC11495065

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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.