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
Affiliations
Michèle Bengue
MIVEGEC, Univ. Montpellier, IRD, CNRS, 34394 Montpellier, France
Ai-rada Pintong
MIVEGEC, Univ. Montpellier, IRD, CNRS, 34394 Montpellier, France
Florian Liegeois
MIVEGEC, Univ. Montpellier, IRD, CNRS, 34394 Montpellier, France
Antoine Nougairède
Unité 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 Hamel
MIVEGEC, Univ. Montpellier, IRD, CNRS, 34394 Montpellier, France
Julien Pompon
MIVEGEC, Univ. Montpellier, IRD, CNRS, 34394 Montpellier, France
Xavier de Lamballerie
Unité 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 Roques
Unité de Virologie, Institut Pasteur de Guinée, Conakry BP4416, Guinea
Valérie Choumet
Unité Environnement et Risques Infectieux Groupe Arbovirus, Institut Pasteur, Université de Paris, 75724 Paris, France
Dorothée Missé
MIVEGEC, Univ. Montpellier, IRD, CNRS, 34394 Montpellier, France
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.