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      <title>Favipiravir inhibits Mayaro virus infection in mice</title>
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    <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.</abstract>
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    <subject>
      <topic>alphavirus</topic>
      <topic>arbovirus</topic>
      <topic>mayaro</topic>
      <topic>favipiravir</topic>
      <topic>antiviral drug</topic>
    </subject>
    <classification authority="local">052</classification>
    <classification authority="local">050</classification>
    <classification authority="local">080</classification>
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      <titleInfo>
        <title>Viruses</title>
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      <part>
        <detail type="volume">
          <number>13</number>
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        <detail type="volume">
          <number>11</number>
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        <extent unit="pages">
          <list>2213 [17 ]</list>
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        <dateIssued>2021</dateIssued>
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    <identifier type="uri">https://www.documentation.ird.fr/hor/fdi:010083796</identifier>
    <identifier type="doi">10.3390/v13112213</identifier>
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