<?xml version="1.0" encoding="UTF-8"?>
<xml>
  <records>
    <record>
      <source-app name="Horizon">Horizon</source-app>
      <rec-number>1</rec-number>
      <foreign-keys>
        <key app="Horizon" db-id="fdi:010083796">1</key>
      </foreign-keys>
      <ref-type name="Journal Article">17</ref-type>
      <work-type>ACL : Articles dans des revues avec comité de lecture répertoriées par l'AERES</work-type>
      <contributors>
        <authors>
          <author>
            <style face="bold" font="default" size="100%">Bengue, Michèle</style>
          </author>
          <author>
            <style face="normal" font="default" size="100%">Pintong, A.</style>
          </author>
          <author>
            <style face="bold" font="default" size="100%">Liégeois, Florian</style>
          </author>
          <author>
            <style face="normal" font="default" size="100%">Nougairede, A.</style>
          </author>
          <author>
            <style face="bold" font="default" size="100%">Hamel, Rodolphe</style>
          </author>
          <author>
            <style face="bold" font="default" size="100%">Pompon, Julien</style>
          </author>
          <author>
            <style face="normal" font="default" size="100%">Lamballerie, X. de</style>
          </author>
          <author>
            <style face="normal" font="default" size="100%">Roques, P.</style>
          </author>
          <author>
            <style face="normal" font="default" size="100%">Choumet, V.</style>
          </author>
          <author>
            <style face="bold" font="default" size="100%">Missé, Dorothée</style>
          </author>
        </authors>
      </contributors>
      <titles>
        <title>Favipiravir inhibits Mayaro virus infection in mice</title>
        <secondary-title>Viruses</secondary-title>
      </titles>
      <pages>2213 [17 ]</pages>
      <keywords>
        <keyword>alphavirus</keyword>
        <keyword>arbovirus</keyword>
        <keyword>mayaro</keyword>
        <keyword>favipiravir</keyword>
        <keyword>antiviral drug</keyword>
      </keywords>
      <dates>
        <year>2021</year>
      </dates>
      <call-num>fdi:010083796</call-num>
      <language>ENG</language>
      <periodical>
        <full-title>Viruses</full-title>
      </periodical>
      <accession-num>ISI:000726022400001</accession-num>
      <number>11</number>
      <electronic-resource-num>10.3390/v13112213</electronic-resource-num>
      <urls>
        <related-urls>
          <url>https://www.documentation.ird.fr/hor/fdi:010083796</url>
        </related-urls>
        <pdf-urls>
          <url>https://horizon.documentation.ird.fr/exl-doc/pleins_textes/2022-01/010083796.pdf</url>
        </pdf-urls>
      </urls>
      <volume>13</volume>
      <remote-database-provider>Horizon (IRD)</remote-database-provider>
      <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>
      <custom6>052 ; 050 ; 080</custom6>
      <custom1>UR224 / UR190</custom1>
      <custom7>Guinée</custom7>
    </record>
  </records>
</xml>
