Evidence map›Paper›PMID 27011352›Full record

ArticleeLife2016

Comparative analysis of viral RNA signatures on different RIG-I-like receptors.

Raul Y Sanchez David, Chantal Combredet, Odile Sismeiro, Marie-Agnès Dillies, Bernd Jagla, Jean-Yves Coppée, Marie Mura, Mathilde Guerbois Galla, Philippe Despres, Frédéric Tangy and 1 more

Open access · goldAbstract read
In one paragraph

Article in eLife, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 73 papers.

0numbers the graph read from it
0cells of the map it votes in
73citing papers in PubMed
6.1field-weighted citation impact, top 3% 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

73 citing papers in PubMed, 98 citations in OpenAlex.

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  9. The emerging role of oncolytic virotherapy in genitourinary malignancies.Frontiers in cell and developmental biology · 2026
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13 more citing papers are in PubMed but not listed here.

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 2 institutions in 1 country.

Raul Y Sanchez DavidUnité de Génomique Virale et Vaccination, Institut Pasteur, CNRS UMR-3569, Paris, France.
Chantal CombredetUnité de Génomique Virale et Vaccination, Institut Pasteur, CNRS UMR-3569, Paris, France.
Odile SismeiroTranscriptome and Epigenome, BioMics Pole, Center for Innovation and Technological Research, Institut Pasteur, Paris, France.
Marie-Agnès DilliesTranscriptome and Epigenome, BioMics Pole, Center for Innovation and Technological Research, Institut Pasteur, Paris, France.
Bernd JaglaTranscriptome and Epigenome, BioMics Pole, Center for Innovation and Technological Research, Institut Pasteur, Paris, France.
Jean-Yves CoppéeTranscriptome and Epigenome, BioMics Pole, Center for Innovation and Technological Research, Institut Pasteur, Paris, France.
Marie MuraUnité de Génomique Virale et Vaccination, Institut Pasteur, CNRS UMR-3569, Paris, France.
Mathilde Guerbois GallaUnité de Génomique Virale et Vaccination, Institut Pasteur, CNRS UMR-3569, Paris, France.
Philippe DespresTechnology Platform CYROI, University of Reunion Island, Saint-Clotilde, France.
Frédéric TangyUnité de Génomique Virale et Vaccination, Institut Pasteur, CNRS UMR-3569, Paris, France.
Anastassia V KomarovaUnité de Génomique Virale et Vaccination, Institut Pasteur, CNRS UMR-3569, Paris, France.ORCID http://orcid.org/0000-0002-9998-8447
Centre National de la Recherche Scientifique · FRInstitut Pasteur · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The RIG-I-like receptors (RLRs) play a major role in sensing RNA virus infection to initiate and modulate antiviral immunity. They interact with particular viral RNAs, most of them being still unknown. To decipher the viral RNA signature on RLRs during viral infection, we tagged RLRs (RIG-I, MDA5, LGP2) and applied tagged protein affinity purification followed by next-generation sequencing (NGS) of associated RNA molecules. Two viruses with negative- and positive-sense RNA genome were used: measles (MV) and chikungunya (CHIKV). NGS analysis revealed that distinct regions of MV genome were specifically recognized by distinct RLRs: RIG-I recognized defective interfering genomes, whereas MDA5 and LGP2 specifically bound MV nucleoprotein-coding region. During CHIKV infection, RIG-I associated specifically to the 3' untranslated region of viral genome. This study provides the first comparative view of the viral RNA ligands for RIG-I, MDA5 and LGP2 in the presence of infection.

Indexed as

Cell LineChikungunya virusDEAD Box Protein 58High-Throughput Nucleotide SequencingHumansInterferon-Induced Helicase, IFIH1Measles virusReceptors, ImmunologicRNA HelicasesRNA, ViralDEAD Box Protein 58DHX58 protein, humanIFIH1 protein, humanInterferon-Induced Helicase, IFIH1Receptors, ImmunologicRIGI protein, humanRNA HelicasesRNA, Viralhumanimmunologyinfectious diseaseinnate immunitymicrobiologyPAMPPRRribonucleoproteinsRIG-I-like receptorsvirus-host interactions

Identifiers

PMID27011352
PMCPMC4841775
OpenAlexW2324048849

What OpenQuestion 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 OpenQuestion graph.