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Synergistic Lethal Mutagenesis of Hepatitis C Virus
Author(s) -
Isabel Gallego,
María Eugenia Soria,
Josep Gregori,
Ana Isabel de Ávila,
Carlos GarcíaCrespo,
Elena Moreno,
Ignacio Gadea,
Jaime Esteban,
R. FernándezRoblas,
Juan Ignacio Esteban,
Jordi Gómez,
Josep Quer,
Esteban Domingo,
Celia Perales
Publication year - 2019
Publication title -
antimicrobial agents and chemotherapy
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.07
H-Index - 259
eISSN - 1070-6283
pISSN - 0066-4804
DOI - 10.1128/aac.01653-19
Subject(s) - favipiravir , mutagenesis , virology , ribavirin , virus , biology , mutation , viral replication , mutant , hepatitis c virus , genetics , medicine , covid-19 , gene , disease , pathology , infectious disease (medical specialty)
Lethal mutagenesis is an antiviral approach that consists of extinguishing a virus by an excess of mutations acquired during replication in the presence of a mutagenic agent, often a nucleotide analogue. One of its advantages is its broad-spectrum nature, which renders the strategy potentially effective against emergent RNA viral infections. Here we describe the synergistic lethal mutagenesis of hepatitis C virus (HCV) by a combination of favipiravir (T-705) and ribavirin.

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