Author/Authors :
Bruzzone Bianca نويسنده Hygiene Unit, IRCCS AOU San Martino, IST, Genoa, 16132,
Italy , De Leo Pasqualina نويسنده Infectious Disease Unit, San Paolo Hospital, Savona,
17100, Italy , Sticchi Laura نويسنده Hygiene Unit, IRCCS AOU San Martino, IST, Genoa, 16132,
Italy , Canepa Paola نويسنده Department of Health Sciences, University of Genoa, 16132,
Italy , Rappazzo Emanuela نويسنده Department of Health Sciences, University of Genoa, 16132,
Italy , Anselmo Marco نويسنده Infectious Disease Unit, San Paolo Hospital, Savona,
17100, Italy , Icardi Giancarlo نويسنده Hygiene Unit, IRCCS AOU San Martino, IST, Genoa, 16132,
Italy
Abstract :
Introduction Hepatitis C virus (HCV) multiple infections can
influence the course of the disease, either by boosting hepatocellular
injury or by increasing the frequency of exacerbations. Their prevalence
ranges from 5% to 39% in individuals with HCV infection, with a higher
impact on injection drug users (IDUs), or in prison settings. Case
Presentation The current paper reported a case of dual HCV infection in
a 31-year-old female, with a referred vertical transmission of HCV
infection and also a history of IDU, who harbored a subtype 4d since
youth. Treatment failure, after a 24-week course of
sofosbuvir/ledipasvir, prompted a reevaluation of present and past HCV
status. HCV genotype was determined by
INNO-LiPATM HCV II kit (LiPA II) (Innogenetics,
Ghent, Belgium) and sequencing of NS5B region (nucleotide 8281 - 8679).
Direct-acting antivirals (DAAs) resistance profile was investigated by
NS3/4, NS5A and NS5B sequencing with specific primers. The Sentosa® SQ
next generation sequencing (NGS) workflow was further performed in the
baseline and failure samples. Unexpectedly, a subtype 4d in the
pretreatment sample and a subtype 1a in the posttreatment were
identified. No resistance associated mutations (RAS) were detected in
the subtype 4d, although the 170AV and 174S in the NS3/4 gene, the 30R
in the NS5A gene, and the 444D in the NS5B gene were detected in the
subtype 1a virus from the failure sample. Conclusions Two main
hypotheses were raised: a reinfection with a new subtype 1a virus during
the treatment with a wild type strain, which developed RAS after
infection or with an already mutated virus; and a pretreatment hidden
dual subtype 4d plus 1a infection.