Extinction of West Nile Virus by Favipiravir through Lethal Mutagenesis
Favipiravir is an antiviral agent effective against several RNA viruses. The drug has been shown to protect mice against experimental infection with a lethal dose of West Nile virus (WNV), a mosquito-borne flavivirus responsible for outbreaks of meningitis and encephalitis for which no antiviral the...
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creator | Escribano-Romero, Estela Jiménez de Oya, Nereida Domingo, Esteban Saiz, Juan Carlos |
description | Favipiravir is an antiviral agent effective against several RNA viruses. The drug has been shown to protect mice against experimental infection with a lethal dose of West Nile virus (WNV), a mosquito-borne flavivirus responsible for outbreaks of meningitis and encephalitis for which no antiviral therapy has been licensed; however, the mechanism of action of the drug is still not well understood. Here, we describe the potent
antiviral activity of favipiravir against WNV, showing that it decreases virus-specific infectivity and drives the virus to extinction. Two passages of WNV in the presence of 1 mM favipiravir-a concentration that is more than 10-fold lower than its 50% cytotoxic concentration (CC
)-resulted in a significant increase in mutation frequency in the mutant spectrum and in a bias toward A→G and G→A transitions relative to the population passaged in the absence of the drug. These data, together with the fact that the drug is already licensed in Japan against influenza virus and in a clinical trial against Ebola virus, point to favipiravir as a promising antiviral agent to fight medically relevant flaviviral infections, such as that caused by WNV. |
doi_str_mv | 10.1128/aac.01400-17 |
format | Article |
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antiviral activity of favipiravir against WNV, showing that it decreases virus-specific infectivity and drives the virus to extinction. Two passages of WNV in the presence of 1 mM favipiravir-a concentration that is more than 10-fold lower than its 50% cytotoxic concentration (CC
)-resulted in a significant increase in mutation frequency in the mutant spectrum and in a bias toward A→G and G→A transitions relative to the population passaged in the absence of the drug. These data, together with the fact that the drug is already licensed in Japan against influenza virus and in a clinical trial against Ebola virus, point to favipiravir as a promising antiviral agent to fight medically relevant flaviviral infections, such as that caused by WNV.</description><identifier>ISSN: 0066-4804</identifier><identifier>EISSN: 1098-6596</identifier><identifier>DOI: 10.1128/aac.01400-17</identifier><identifier>PMID: 28848019</identifier><language>eng</language><publisher>United States: American Society for Microbiology</publisher><subject>Amides ; Amides - pharmacology ; Animals ; Antiviral Agents ; Antiviral Agents - pharmacology ; Cercopithecus aethiops ; Dose-Response Relationship, Drug ; Mutagenesis ; Mutagenesis - drug effects ; Pyrazines ; Pyrazines - pharmacology ; Vero Cells ; West Nile virus ; West Nile virus - drug effects ; West Nile virus - genetics ; West Nile virus - pathogenicity</subject><ispartof>Antimicrobial agents and chemotherapy, 2017-11, Vol.61 (11)</ispartof><rights>Copyright © 2017 American Society for Microbiology.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-a472t-c9c5620ce29ecb1c42d3f2b7d0da442037f94d8bebe30e782685a1cea7fd6b233</citedby><cites>FETCH-LOGICAL-a472t-c9c5620ce29ecb1c42d3f2b7d0da442037f94d8bebe30e782685a1cea7fd6b233</cites><orcidid>0000-0002-5036-7607</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>315,781,785,27929,27930</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/28848019$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Escribano-Romero, Estela</creatorcontrib><creatorcontrib>Jiménez de Oya, Nereida</creatorcontrib><creatorcontrib>Domingo, Esteban</creatorcontrib><creatorcontrib>Saiz, Juan Carlos</creatorcontrib><title>Extinction of West Nile Virus by Favipiravir through Lethal Mutagenesis</title><title>Antimicrobial agents and chemotherapy</title><addtitle>Antimicrob Agents Chemother</addtitle><addtitle>Antimicrob Agents Chemother</addtitle><description>Favipiravir is an antiviral agent effective against several RNA viruses. The drug has been shown to protect mice against experimental infection with a lethal dose of West Nile virus (WNV), a mosquito-borne flavivirus responsible for outbreaks of meningitis and encephalitis for which no antiviral therapy has been licensed; however, the mechanism of action of the drug is still not well understood. Here, we describe the potent
antiviral activity of favipiravir against WNV, showing that it decreases virus-specific infectivity and drives the virus to extinction. Two passages of WNV in the presence of 1 mM favipiravir-a concentration that is more than 10-fold lower than its 50% cytotoxic concentration (CC
)-resulted in a significant increase in mutation frequency in the mutant spectrum and in a bias toward A→G and G→A transitions relative to the population passaged in the absence of the drug. These data, together with the fact that the drug is already licensed in Japan against influenza virus and in a clinical trial against Ebola virus, point to favipiravir as a promising antiviral agent to fight medically relevant flaviviral infections, such as that caused by WNV.</description><subject>Amides</subject><subject>Amides - pharmacology</subject><subject>Animals</subject><subject>Antiviral Agents</subject><subject>Antiviral Agents - pharmacology</subject><subject>Cercopithecus aethiops</subject><subject>Dose-Response Relationship, Drug</subject><subject>Mutagenesis</subject><subject>Mutagenesis - drug effects</subject><subject>Pyrazines</subject><subject>Pyrazines - pharmacology</subject><subject>Vero Cells</subject><subject>West Nile virus</subject><subject>West Nile virus - drug effects</subject><subject>West Nile virus - genetics</subject><subject>West Nile virus - pathogenicity</subject><issn>0066-4804</issn><issn>1098-6596</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kD1PwzAQhi0EoqWwMSOvSKScHcexx6pqC1KBhY8xcpxL66pNIjtB9N8TKLCx3OlePXp1egi5ZDBmjKtbY-wYmACIWHpEhgy0imSi5TEZAkgZCQViQM5C2EB_JxpOyYAr1cdMD8li9tG6yraurmhd0jcMLX10W6SvzneB5ns6N--ucb6fnrZrX3erNV1iuzZb-tC1ZoUVBhfOyUlptgEvfvaIvMxnz9O7aPm0uJ9OlpERKW8jq20iOVjkGm3OrOBFXPI8LaAwQnCI01KLQuWYYwyYKi5VYphFk5aFzHkcj8jNodf6OgSPZdZ4tzN-nzHIvnxkk8k0-_aRsbTHrw-4CTueberOV_13_7FXB7bp8h0Wf8W_suJP2K1oOg</recordid><startdate>20171101</startdate><enddate>20171101</enddate><creator>Escribano-Romero, Estela</creator><creator>Jiménez de Oya, Nereida</creator><creator>Domingo, Esteban</creator><creator>Saiz, Juan Carlos</creator><general>American Society for Microbiology</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><orcidid>https://orcid.org/0000-0002-5036-7607</orcidid></search><sort><creationdate>20171101</creationdate><title>Extinction of West Nile Virus by Favipiravir through Lethal Mutagenesis</title><author>Escribano-Romero, Estela ; Jiménez de Oya, Nereida ; Domingo, Esteban ; Saiz, Juan Carlos</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a472t-c9c5620ce29ecb1c42d3f2b7d0da442037f94d8bebe30e782685a1cea7fd6b233</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Amides</topic><topic>Amides - pharmacology</topic><topic>Animals</topic><topic>Antiviral Agents</topic><topic>Antiviral Agents - pharmacology</topic><topic>Cercopithecus aethiops</topic><topic>Dose-Response Relationship, Drug</topic><topic>Mutagenesis</topic><topic>Mutagenesis - drug effects</topic><topic>Pyrazines</topic><topic>Pyrazines - pharmacology</topic><topic>Vero Cells</topic><topic>West Nile virus</topic><topic>West Nile virus - drug effects</topic><topic>West Nile virus - genetics</topic><topic>West Nile virus - pathogenicity</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Escribano-Romero, Estela</creatorcontrib><creatorcontrib>Jiménez de Oya, Nereida</creatorcontrib><creatorcontrib>Domingo, Esteban</creatorcontrib><creatorcontrib>Saiz, Juan Carlos</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><jtitle>Antimicrobial agents and chemotherapy</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Escribano-Romero, Estela</au><au>Jiménez de Oya, Nereida</au><au>Domingo, Esteban</au><au>Saiz, Juan Carlos</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Extinction of West Nile Virus by Favipiravir through Lethal Mutagenesis</atitle><jtitle>Antimicrobial agents and chemotherapy</jtitle><stitle>Antimicrob Agents Chemother</stitle><addtitle>Antimicrob Agents Chemother</addtitle><date>2017-11-01</date><risdate>2017</risdate><volume>61</volume><issue>11</issue><issn>0066-4804</issn><eissn>1098-6596</eissn><abstract>Favipiravir is an antiviral agent effective against several RNA viruses. The drug has been shown to protect mice against experimental infection with a lethal dose of West Nile virus (WNV), a mosquito-borne flavivirus responsible for outbreaks of meningitis and encephalitis for which no antiviral therapy has been licensed; however, the mechanism of action of the drug is still not well understood. Here, we describe the potent
antiviral activity of favipiravir against WNV, showing that it decreases virus-specific infectivity and drives the virus to extinction. Two passages of WNV in the presence of 1 mM favipiravir-a concentration that is more than 10-fold lower than its 50% cytotoxic concentration (CC
)-resulted in a significant increase in mutation frequency in the mutant spectrum and in a bias toward A→G and G→A transitions relative to the population passaged in the absence of the drug. These data, together with the fact that the drug is already licensed in Japan against influenza virus and in a clinical trial against Ebola virus, point to favipiravir as a promising antiviral agent to fight medically relevant flaviviral infections, such as that caused by WNV.</abstract><cop>United States</cop><pub>American Society for Microbiology</pub><pmid>28848019</pmid><doi>10.1128/aac.01400-17</doi><tpages>9</tpages><orcidid>https://orcid.org/0000-0002-5036-7607</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Amides Amides - pharmacology Animals Antiviral Agents Antiviral Agents - pharmacology Cercopithecus aethiops Dose-Response Relationship, Drug Mutagenesis Mutagenesis - drug effects Pyrazines Pyrazines - pharmacology Vero Cells West Nile virus West Nile virus - drug effects West Nile virus - genetics West Nile virus - pathogenicity |
title | Extinction of West Nile Virus by Favipiravir through Lethal Mutagenesis |
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