Evidence map›Paper›PMID 34835018›Full record

ArticleViruses2021

Favipiravir Inhibits Mayaro Virus Infection in Mice.

Michèle Bengue, Ai-Rada Pintong, Florian Liegeois, Antoine Nougairède, Rodolphe Hamel, Julien Pompon, Xavier de Lamballerie, Pierre Roques, Valérie Choumet, Dorothée Missé

Open access · goldAbstract read
In one paragraph

Article in Viruses, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.4field-weighted citation impact, top 36% 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

7 citing papers in PubMed, 8 citations in OpenAlex.

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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 at 4 institutions in 2 countries.

Michèle BengueMIVEGEC, Univ. Montpellier, IRD, CNRS, 34394 Montpellier, France.
Ai-Rada PintongMIVEGEC, Univ. Montpellier, IRD, CNRS, 34394 Montpellier, France.
Florian LiegeoisMIVEGEC, Univ. Montpellier, IRD, CNRS, 34394 Montpellier, France.ORCID 0000-0003-1048-0661
Antoine NougairèdeUnité des Virus Emergents (UVE), Institut de Recherche pour le Développement 190, IHU Méditerranée Infection, Institut National de la Santé et de la Recherche Médicale 1207, Aix Marseille Université, 13005 Marseille, France.
Rodolphe HamelMIVEGEC, Univ. Montpellier, IRD, CNRS, 34394 Montpellier, France.ORCID 0000-0001-8603-7039
Julien PomponMIVEGEC, Univ. Montpellier, IRD, CNRS, 34394 Montpellier, France.ORCID 0000-0003-1110-9039
Xavier de LamballerieUnité des Virus Emergents (UVE), Institut de Recherche pour le Développement 190, IHU Méditerranée Infection, Institut National de la Santé et de la Recherche Médicale 1207, Aix Marseille Université, 13005 Marseille, France.
Pierre RoquesUnité de Virologie, Institut Pasteur de Guinée, Conakry BP4416, Guinea.ORCID 0000-0003-1825-1054
Valérie ChoumetUnité Environnement et Risques Infectieux Groupe Arbovirus, Institut Pasteur, Université de Paris, 75724 Paris, France.ORCID 0000-0003-4714-1006
Dorothée MisséMIVEGEC, Univ. Montpellier, IRD, CNRS, 34394 Montpellier, France.ORCID 0000-0002-6485-3841
Centre National de la Recherche Scientifique · FRAix-Marseille Université · FRInserm · FRInstitut Pasteur · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Mayaro virus (MAYV) is an emergent alphavirus that causes MAYV fever. It is often associated with debilitating symptoms, particularly arthralgia and myalgia. MAYV infection is becoming a considerable health issue that, unfortunately, lacks a specific antiviral treatment. Favipiravir, a broad-spectrum antiviral drug, has recently been shown to exert anti-MAYV activity in vitro. In the present study, the potential of Favipiravir to inhibit MAYV replication in an in vivo model was evaluated. Immunocompetent mice were orally administrated 300 mg/kg/dose of Favipiravir at pre-, concurrent-, or post-MAYV infection. The results showed a significant reduction in infectious viral particles and viral RNA transcripts in the tissues and blood of the pre- and concurrently treated infected mice. A significant reduction in the presence of both viral RNA transcript and infectious viral particles in the tissue and blood of pre- and concurrently treated infected mice was observed. By contrast, Favipiravir treatment post-MAYV infection did not result in a reduction in viral replication. Interestingly, Favipiravir strongly decreased the blood levels of the liver disease markers aspartate- and alanine aminotransferase in the pre- and concurrently treated MAYV-infected mice. Taken together, these results suggest that Favipiravir is a potent antiviral drug when administered in a timely manner.

Indexed as

Alanine TransaminaseAlphavirusAlphavirus InfectionsAmidesAnimalsAntiviral AgentsAspartate AminotransferasesCell LineChlorocebus aethiopsDisease Models, AnimalFemaleLiverMiceMice, Inbred C57BLPyrazinesVero CellsAlanine TransaminaseAmidesAntiviral AgentsAspartate AminotransferasesfavipiravirPyrazinesalphavirusantiviral drugarbovirusfavipiravirmayaro

Identifiers

PMID34835018
PMCPMC8622800
OpenAlexW3209683956

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.