Fitness-Dependent, Mild Mutagenic Activity of Sofosbuvir for Hepatitis C Virus

The concept of a mild mutagen was coined to describe a minor mutagenic activity exhibited by some nucleoside analogues that potentiated their efficacy as antiretroviral agents. In the present study, we report the mild mutagen activity of sofosbuvir (SOF) for hepatitis C virus (HCV). Serial passages of HCV in human hepatoma cells, in the presence of SOF at a concentration well below its cytotoxic concentration 50 (CC50) led to pre-extinction populations whose mutant spectra exhibited a significant increase of C→U transitions, relative to populations passaged in the absence of SOF. This was reflected in an increase in several diversity indices that were used to characterize viral quasispecies. The mild mutagenic activity of SOF was largely absent when it was tested with isogenic HCV populations that displayed high replicative fitness. Thus, SOF can act as a mild mutagen for HCV, depending on HCV fitness. Possible mechanisms by which the SOF mutagenic activity may contribute to its antiviral efficacy are discussed.

Medienart:

E-Artikel

Erscheinungsjahr:

2023

Erschienen:

2023

Enthalten in:

Zur Gesamtaufnahme - volume:67

Enthalten in:

Antimicrobial agents and chemotherapy - 67(2023), 7 vom: 18. Juli, Seite e0039423

Sprache:

Englisch

Beteiligte Personen:

Martínez-González, Brenda [VerfasserIn]
Gallego, Isabel [VerfasserIn]
Gregori, Josep [VerfasserIn]
Soria, María Eugenia [VerfasserIn]
Somovilla, Pilar [VerfasserIn]
de Ávila, Ana Isabel [VerfasserIn]
García-Crespo, Carlos [VerfasserIn]
Durán-Pastor, Antoni [VerfasserIn]
Briones, Carlos [VerfasserIn]
Gómez, Jordi [VerfasserIn]
Quer, Josep [VerfasserIn]
Domingo, Esteban [VerfasserIn]
Perales, Celia [VerfasserIn]

Links:

Volltext

Themen:

49717AWG6K
Antiviral Agents
Antiviral agent
Journal Article
Lethal defection
Mutagens
Research Support, Non-U.S. Gov't
Ribavirin
Sofosbuvir
Ultradeep sequencing
Viral fitness
Viral quasispecies
WJ6CA3ZU8B

Anmerkungen:

Date Completed 17.07.2023

Date Revised 28.12.2023

published: Print-Electronic

Citation Status MEDLINE

doi:

10.1128/aac.00394-23

funding:

Förderinstitution / Projekttitel:

PPN (Katalog-ID):

NLM358688345