Detection of a genetic footprint of the sofosbuvir resistance-associated substitution S282T after HCV treatment failure

Virology Journal

Dieter Häussinger¹  Sandra Filke¹  Hans H. Bock¹  Nadine Lübke²  Andreas Walker²  Jörg Timm²  Rolf Kaiser³  Martin Obermeier⁴ 

[1] Department of Gastroenterology, Hepatology and Infectious Diseases, Heinrich-Heine-University, University Hospital;Institute for Virology, Heinrich-Heine-University, University Hospital;Institute of Virology, University of Cologne;Medical Center for Infectious Diseases (MIB);

关键词: Sofosbuvir;    Daclatasvir;    Resistance;    Genotype 3a;    Breakthrough;    S282T;   

DOI  :  10.1186/s12985-017-0779-4

来源: DOAJ

【 摘 要 】

Abstract Background The major resistance-associated substitution for sofosbuvir (S282T) in HCV NS5B causes severe viral fitness costs and rapidly reverts back to prototype in the absence of selection pressure. Accordingly, resistance against sofosbuvir is rarely detected even in patients after treatment failure. Case presentation We report a case of a GT3a infected patient with viral breakthrough under SOF/DCV therapy. At the time of breakthrough the RAS S282T was predominant in NS5B and then rapidly disappeared during follow-up by week 12 after treatment. Interestingly, despite only serine was encoded in position 282 during follow-up, two distinct genetic pathways for reversion were detectable. In 31% of the quasispecies the original codon for serine was present whereas in the majority of the quasispecies an alternative codon was selected. This alternative codon usage was unique for all GT3a isolates from the HCV database and remained detectable as a genetic footprint for prior resistance selection at the RNA level for at least 6 months. Conclusions Comparative analyses of viral sequences at the codon level before and after DAA treatment may help to elucidate the patient’s history of resistance selection, which is particularly valuable for highly unfit substitutions that are detectable only for a short period of time. If such codon changes increase the risk of re-selection of resistance upon a second exposure to SOF remains to be addressed.

【 授权许可】

Unknown