Evidence map›Paper›PMID 36996243›Full record

ArticlePLoS pathogens2023

Characterisation of the antiviral RNA interference response to Toscana virus in sand fly cells.

Akira J T Alexander, Marco Salvemini, Vattipally B Sreenu, Joseph Hughes, Erich L Telleria, Maxime Ratinier, Frédérick Arnaud, Petr Volf, Benjamin Brennan, Margus Varjak and 1 more

Open access · goldAbstract read
In one paragraph

Article in PLoS pathogens, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
1.2field-weighted citation impact, top 24% 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

4 citing papers in PubMed, 6 citations in OpenAlex.

  1. Article
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  3. The PAZ domain ofRNA (New York, N.Y.) · 2025
    Article
  4. Proteomics analysis of soluble secreted proteins ofFrontiers in cellular and infection microbiology · 2025
    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

11 authors at 5 institutions in 5 countries.

Akira J T AlexanderMRC-University of Glasgow Centre for Virus Research, Glasgow, United Kingdom.
Marco SalveminiDepartment of Biology, University of Naples Federico II, Italy.
Vattipally B SreenuMRC-University of Glasgow Centre for Virus Research, Glasgow, United Kingdom.
Joseph HughesMRC-University of Glasgow Centre for Virus Research, Glasgow, United Kingdom.
Erich L TelleriaDepartment of Parasitology, Faculty of Science, Charles University, Prague, Czech Republic.
Maxime RatinierIVPC UMR754, INRAE, Univ Lyon, Université Claude Bernard Lyon1, EPHE, PSL Research University, Lyon, France.
Frédérick ArnaudIVPC UMR754, INRAE, Univ Lyon, Université Claude Bernard Lyon1, EPHE, PSL Research University, Lyon, France.
Petr VolfDepartment of Parasitology, Faculty of Science, Charles University, Prague, Czech Republic.
Benjamin BrennanMRC-University of Glasgow Centre for Virus Research, Glasgow, United Kingdom.
Margus VarjakInstitute of Technology, University of Tartu, Tartu, Estonia.
Alain KohlMRC-University of Glasgow Centre for Virus Research, Glasgow, United Kingdom.ORCID 0000-0002-1523-9458
MRC University of Glasgow Centre for Virus Research · GBCharles University · CZUniversité Claude Bernard Lyon 1 · FRFederico II University Hospital · ITUniversity of Tartu · EE

Funding

Medical Research Council MC_UU_12014/12Medical Research Council MC_UU_12014/8Wellcome Trust 210462/Z/18/Z
6 · The paper itself

Abstract

Toscana virus (TOSV) (Bunyavirales, Phenuiviridae, Phlebovirus, Toscana phlebovirus) and other related human pathogenic arboviruses are transmitted by phlebotomine sand flies. TOSV has been reported in nations bordering the Mediterranean Sea among other regions. Infection can result in febrile illness as well as meningitis and encephalitis. Understanding vector-arbovirus interactions is crucial to improving our knowledge of how arboviruses spread, and in this context, immune responses that control viral replication play a significant role. Extensive research has been conducted on mosquito vector immunity against arboviruses, with RNA interference (RNAi) and specifically the exogenous siRNA (exo-siRNA) pathway playing a critical role. However, the antiviral immunity of phlebotomine sand flies is less well understood. Here we were able to show that the exo-siRNA pathway is active in a Phlebotomus papatasi-derived cell line. Following TOSV infection, distinctive 21 nucleotide virus-derived small interfering RNAs (vsiRNAs) were detected. We also identified the exo-siRNA effector Ago2 in this cell line, and silencing its expression rendered the exo-siRNA pathway largely inactive. Thus, our data show that this pathway is active as an antiviral response against a sand fly transmitted bunyavirus, TOSV.

Indexed as

ArbovirusesPhlebotomusPhlebovirusPsychodidaeSandfly fever Naples virusAnimalsHumansRNA InterferenceRNA, Small InterferingRNA, Small Interfering

Identifiers

PMID36996243
PMCPMC10112792
OpenAlexW4361255804

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.