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Favipiravir Inhibits Mayaro Virus Infection in Mice
Michèle Bengue1, Ai-Rada Pintong1, Florian Liegeois1
1MIVEGEC, Univ. Montpellier, IRD, CNRS, 34394 Montpellier, France.
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.
Insights
Favipiravir effectively reduced Mayaro virus (MAYV) replication when given before or during infection in mice. Early administration of this antiviral is crucial for inhibiting MAYV disease progression and associated liver damage.
Area of Science:
- Virology
- Infectious Diseases
- Pharmacology
Background:
- Mayaro virus (MAYV) causes debilitating fever, arthralgia, and myalgia.
- Emergent alphavirus infections pose significant public health challenges.
- There is a lack of specific antiviral treatments for MAYV infections.
Purpose of the Study:
- To evaluate the in vivo efficacy of Favipiravir against Mayaro virus (MAYV).
- To determine the impact of Favipiravir administration timing on MAYV replication.
- To assess Favipiravir's effect on MAYV-induced liver damage markers.
Main Methods:
- Immunocompetent mice were infected with MAYV.
- Favipiravir (300 mg/kg/dose) was administered orally at pre-, concurrent-, or post-infection timepoints.
- Viral load (infectious particles and RNA) and liver enzyme levels were measured.
Main Results:
- Pre- and concurrent Favipiravir administration significantly reduced viral RNA and infectious particles in blood and tissues.
- Post-infection Favipiravir treatment did not inhibit viral replication.
- Favipiravir significantly decreased aspartate and alanine aminotransferase levels in concurrently and pre-treated mice.
Conclusions:
- Favipiravir demonstrates potent antiviral activity against MAYV in vivo.
- Timely administration of Favipiravir, particularly before or during infection, is critical for efficacy.
- Favipiravir may serve as a potential therapeutic option for Mayaro virus infections.
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