Origin, prevalence and response to therapy of hepatitis C virus genotype 2k/1b chimeras

被引:21
|
作者
Susser, Simone [1 ]
Dietz, Julia [1 ]
Schlevogt, Bernhard [3 ]
Zuckerman, Eli [5 ,6 ]
Barak, Mira [7 ]
Piazzolla, Valeria [8 ]
Howe, Anita [9 ]
Hinrichsen, Holger [10 ]
Passmann, Sandra [1 ]
Daniel, Rasha [7 ]
Cornberg, Markus [3 ,4 ]
Mangia, Alessandra [8 ]
Zeuzem, Stefan [1 ]
Sarrazin, Christoph [1 ,2 ]
机构
[1] Goethe Univ Hosp, Med Clin 1, Theodor Stern Kai 7, D-60590 Frankfurt, Germany
[2] St Josefs Hosp, Med Clin 2, Wiesbaden, Germany
[3] Hannover Med Sch, Dept Gastroenterol Hepatol & Endocrinol, Hannover, Germany
[4] German Ctr Infect Res DZIF, Partner Site Hannover Braunschweig, Hannover, Germany
[5] Carmel Hosp, Liver Unit, Haifa, Israel
[6] Technion, Rappaport Fac Med, Haifa, Israel
[7] Clalit Hlth Serv, Haifa & Western Galilee Lab, Nesher, Israel
[8] IRCCS Casa Sollievo della Sofferenza Hosp, Liver Unit, San Giovanni Rotondo, Italy
[9] British Columbia Ctr Excellence HIV AIDS, Vancouver, BC, Canada
[10] Gastroenterol Schwerpunkt Praxis, Gastroenterol, Kiel, Germany
关键词
HCV genotype; Chimeras; Phylogeny; Epidemiology; DAA-treatment; SVR; INTERGENOTYPIC RECOMBINANT; STRAINS; WEB; CLASSIFICATION; IDENTIFICATION; EPIDEMIOLOGY; EVOLUTION;
D O I
10.1016/j.jhep.2017.05.027
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background & Aims: Little is known about the epidemiology and frequency of recombinant HCV genotype 2/1 strains, which may represent a challenge for direct antiviral therapy (DAA). This study aims to identify the epidemiology and phylogeny of HCV genotype 2/1 strains and encourages genotype screening, to select the DAA-regimen that achieves the optimal sustained virologic response. Methods: Consecutive samples from HCV genotype 2 infected patients, according to commercial genotyping, from Germany, Italy and Israel were re-genotyped by Sanger-based sequencing. Virologic, epidemiological, and phylogenetic analyses including other published chimeras were performed. Results: Sequence analysis of 442 supposed HCV genotype 2 isolates revealed 61 (genotype 2k/1b (n = 59), 2a/1b (n = 1) or 2b/1a (n = 1)) chimeras. No chimeras were observed in Italy, but the frequency was 14% and 25% in Germany and Israel. Treatment of viral chimera with sofosbuvir/ribavirin led to virologic relapse in 25/27 patients (93%). Nearly all patients treated with genotype 1-based DAA-regimens initially (n = 8/9), or after relapse (n = 13/13), achieved a sustained virologic response. Most patients with 2k/1b chimeras (88%) were originally from eight different areas of the former Soviet Union. All known 2k/1b chimeras harbour the same recombination breakpoint and build one phylogenetic cluster, while all other chimeras have different phylogenies. Conclusions: The HCV genotype 2k/1b variant derives from one single recombination event most likely in the former Soviet Union, while other chimeras are unique and develop independently. A relatively high frequency has been observed along the migration flows, in Germany and Israel. In countries with little migration from the former Soviet Union the prevalence of 2k/1b chimeras is expected to be low. Treatment with sofosbuvir plus ribavirin is insufficient, but genotype 1-based regimens seem to be effective. Lay summary: The frequency of recombinant HCV is higher than expected. A novel recombinant variant (HCV genotype 2a/1b) was identified. Screening for recombinant viruses would contribute to increased response rates to direct antiviral therapy. (C) 2017 European Association for the Study of the Liver. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:680 / 686
页数:7
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