Transmission Networks of HCV Genotype 1a Enriched With Pre-existing Polymorphism Q80K Among HIV-Infected Patients With Acute Hepatitis C in Poland

BACKGROUND:Hepatitis C virus (HCV) resistance–associated variants (RAVs) have been shown to adversely affect treatment response of direct-acting antivirals. Identifying pre-existing RAVs and transmission networks among HIV/HCV genotype 1 (G1)–infected patients from Poland will assist in shaping surv...

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Veröffentlicht in:Journal of acquired immune deficiency syndromes (1999) 2018-04, Vol.77 (5), p.514-522
Hauptverfasser: Parczewski, Miłosz, Cielniak, Iwona, Kordek, Justyna, Aksak-Wąs, Bogusz, Urbańska, Anna, Leszczyszyn-Pynka, Magdalena, Siwak, Ewa, Bociąga-Jasik, Monika, Nowak, Anna, Szymczak, Aleksandra, Zalewska, Małgorzata, Łojewski, Władysław, Vandamme, Anne-Mieke, Lübke, Nadine, Cuypers, Lize
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Sprache:eng
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Zusammenfassung:BACKGROUND:Hepatitis C virus (HCV) resistance–associated variants (RAVs) have been shown to adversely affect treatment response of direct-acting antivirals. Identifying pre-existing RAVs and transmission networks among HIV/HCV genotype 1 (G1)–infected patients from Poland will assist in shaping surveillance strategies for HCV. METHODS:NS3 and NS5A sequences were obtained from samples of 112 direct-acting antiviral–naive G1 patients (45 G1a and 67 G1b), of which 74 were chronically infected and 38 were diagnosed with acute hepatitis C (AHC). RAVs were identified using geno2pheno, and 98 concatenated NS3/NS5A alignments were constructed to identify transmission clusters using a maximum likelihood approach. RESULTS:G1a was notably more prevalent compared with G1b among men-having-sex-with-men (MSM) (60.0% vs. 31.3%, P = 0.004), AHC cases (46.7% vs. 25.4%, P = 0.019), and patients diagnosed with syphilis (52.2% vs. 24.5%, P = 0.009). The overall NS3/NS5A RAVs frequency was 14.3% with variants occurring more often in G1a compared with G1b (27.5% vs. 5.2%, P = 0.005), mostly for NS3 due to the high prevalence of polymorphism Q80K. NS5A RAVs were only found in 2.9% of sequences. Significant clustering was observed for 73.5% of the Polish sequences, however, more common in G1a MSM compared with G1b (50.0% vs. 25.9%, P = 0.02). The identified clusters contained sequences originating from up to 5 Polish cities, located within a mean distance of 370 km. CONCLUSIONS:Close clustering of Polish strains suggests the presence of compartmentalized epidemics of MSM that fuel the spread of G1a variants. Particularly patients with AHC form a national transmission network, including clusters enriched with the NS3 Q80K polymorphism.
ISSN:1525-4135
1944-7884
DOI:10.1097/QAI.0000000000001628