Literature DB >> 24140031

No detection of the NS5B S282T mutation in treatment-naïve genotype 1 HCV/HIV-1 coinfected patients using deep sequencing.

Sandra Franco1, Maria Casadellà, Marc Noguera-Julian, Bonaventura Clotet, Cristina Tural, Roger Paredes, Miguel Angel Martinez.   

Abstract

BACKGROUND: The S282T mutation is the main variant described associated with resistance to nucleos(t)ide analogues hepatitis C virus (HCV) NS5B polymerase inhibitors.
OBJECTIVE: We aimed here to investigate whether this substitution pre-existed in treatment naive HCV/HIV-1 coinfected patients. STUDY
DESIGN: NS5B polymerase deep sequencing was performed at a median coverage per base of 4471 in 16 patient samples.
RESULTS: No S282T variant was detected in the 16 analyzed samples.
CONCLUSION: This finding is in agreement with the high genetic barrier of nucleoside analogues NS5B polymerase inhibitors and the clinical efficacy of these compounds.
Copyright © 2013 Elsevier B.V. All rights reserved.

Entities:  

Keywords:  Deep sequencing; HCV; NS5B; Resistance; S282T

Mesh:

Substances:

Year:  2013        PMID: 24140031     DOI: 10.1016/j.jcv.2013.09.022

Source DB:  PubMed          Journal:  J Clin Virol        ISSN: 1386-6532            Impact factor:   3.168


  6 in total

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