Evidence map›Paper›PMID 38875296›Full record

ArticlePLoS pathogens2024

Antiviral activity of intracellular nanobodies targeting the influenza virus RNA-polymerase core.

Mélissa Bessonne, Jessica Morel, Quentin Nevers, Bruno Da Costa, Allison Ballandras-Colas, Florian Chenavier, Magali Grange, Alain Roussel, Thibaut Crépin, Bernard Delmas

Abstract read
In one paragraph

Article in PLoS pathogens, 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
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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

10 authors.

Mélissa BessonneUnité de Virologie et Immunologie moléculaires, INRAE, Université Paris-Saclay, Jouy-en-Josas, France.
Jessica MorelUnité de Virologie et Immunologie moléculaires, INRAE, Université Paris-Saclay, Jouy-en-Josas, France.
Quentin NeversUnité de Virologie et Immunologie moléculaires, INRAE, Université Paris-Saclay, Jouy-en-Josas, France.
Bruno Da CostaUnité de Virologie et Immunologie moléculaires, INRAE, Université Paris-Saclay, Jouy-en-Josas, France.
Allison Ballandras-ColasInstitut de biologie structurale, CNRS, Université de Grenoble, Grenoble, France.
Florian ChenavierInstitut de biologie structurale, CNRS, Université de Grenoble, Grenoble, France.
Magali GrangeLaboratoire d'Ingénierie des Systèmes Macromoléculaires (LISM), CNRS, Université d'Aix-Marseille, Marseille, France.
Alain RousselLaboratoire d'Ingénierie des Systèmes Macromoléculaires (LISM), CNRS, Université d'Aix-Marseille, Marseille, France.
Thibaut CrépinInstitut de biologie structurale, CNRS, Université de Grenoble, Grenoble, France.
Bernard DelmasUnité de Virologie et Immunologie moléculaires, INRAE, Université Paris-Saclay, Jouy-en-Josas, France.ORCID 0000-0002-2713-4768

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Influenza viruses transcribe and replicate their genome in the nucleus of the infected cells, two functions that are supported by the viral RNA-dependent RNA-polymerase (FluPol). FluPol displays structural flexibility related to distinct functional states, from an inactive form to conformations competent for replication and transcription. FluPol machinery is constituted by a structurally-invariant core comprising the PB1 subunit stabilized with PA and PB2 domains, whereas the PA endonuclease and PB2 C-domains can pack in different configurations around the core. To get insights into the functioning of FluPol, we selected single-domain nanobodies (VHHs) specific of the influenza A FluPol core. When expressed intracellularly, some of them exhibited inhibitory activity on type A FluPol, but not on the type B one. The most potent VHH (VHH16) binds PA and the PA-PB1 dimer with an affinity below the nanomolar range. Ectopic intracellular expression of VHH16 in virus permissive cells blocks multiplication of different influenza A subtypes, even when induced at late times post-infection. VHH16 was found to interfere with the transport of the PA-PB1 dimer to the nucleus, without affecting its handling by the importin β RanBP5 and subsequent steps in FluPol assembly. Using FluPol mutants selected after passaging in VHH16-expressing cells, we identified the VHH16 binding site at the interface formed by PA residues with the N-terminus of PB1, overlapping or close to binding sites of two host proteins, ANP32A and RNA-polymerase II RPB1 subunit which are critical for virus replication and transcription, respectively. These data suggest that the VHH16 neutralization is likely due to several activities, altering the import of the PA-PB1 dimer into the nucleus as well as inhibiting specifically virus transcription and replication. Thus, the VHH16 binding site represents a new Achilles' heel for FluPol and as such, a potential target for antiviral development.

Indexed as

Antiviral AgentsInfluenza A virusRNA-Dependent RNA PolymeraseSingle-Domain AntibodiesVirus ReplicationAnimalsDogsHEK293 CellsHumansInfluenza, HumanMadin Darby Canine Kidney CellsViral ProteinsAntiviral AgentsRNA-Dependent RNA PolymeraseSingle-Domain AntibodiesViral Proteins

Identifiers

PMID38875296
PMCPMC11210859

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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.