Details

Autor(en) / Beteiligte

• Newsum, Astrid M
• Ho, Cynthia K.Y
• Lieveld, Faydra I
• van de Laar, Thijs J.W
• Koekkoek, Sylvie M
• Rebers, Sjoerd P
• van der Meer, Jan T.M
• Wensing, Anne M.J
• Boland, Greet J
• Arends, Joop E
• van Erpecum, Karel J
• Prins, Maria
• Molenkamp, Richard
• Schinkel, Janke

Titel

The hepatitis C virus nonstructural protein 3 Q80K polymorphism is frequently detected and transmitted among HIV-infected MSM in the Netherlands

Ist Teil von

• AIDS (London), 2017-01, Vol.31 (1), p.105-112

Ort / Verlag

England: Copyright Wolters Kluwer Health, Inc

Erscheinungsjahr

2017

Quelle

MEDLINE

Beschreibungen/Notizen

• OBJECTIVES:The Q80K polymorphism is a naturally occurring resistance-associated variant in the hepatitis C virus (HCV) nonstructural protein 3 (NS3) region and is likely transmissible between hosts. This study describes the Q80K origin and prevalence among HCV risk groups in the Netherlands and examines whether Q80K is linked to specific transmission networks. DESIGN AND METHODS:Stored blood samples from HCV genotype 1a-infected patients were used for PCR and sequencing to reconstruct the NS3 maximum likelihood phylogeny. The most recent common ancestor was estimated with a coalescent-based model within a Bayesian statistical framework. RESULTS:Study participants (n = 150) were either MSM (39%), people who inject drugs (17%), or patients with other (15%) or unknown/unreported (29%) risk behavior. Overall 45% was coinfected with HIV. Q80K was present in 36% (95% confidence interval 28–44%) of patients throughout the sample collection period (2000–2015) and was most prevalent in MSM (52%, 95% confidence interval 38–65%). Five MSM-specific transmission clusters were identified, of which three exclusively contained sequences with Q80K. The HCV-1a most recent common ancestor in the Netherlands was estimated in 1914 (95% higher posterior density 1879–1944) and Q80K originated in 1957 (95% higher posterior density 1942–1970) within HCV-1a clade I. All Q80K lineages could be traced back to this single origin. CONCLUSION:Q80K is a highly stable and transmissible resistance-associated variant and was present in a large part of Dutch HIV-coinfected MSM. The introduction and expansion of Q80K variants in this key population suggest a founder effect, potentially jeopardizing future treatment with simeprevir.