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DOI 10.1086/657317

Медицинская библиотека · The Journal of infectious diseases · 2010

Dynamic coinfection with multiple viral subtypes in acute hepatitis C.

Smith Jennifer A, Aberle Judith H, Fleming Vicki M, Ferenci Peter, Thomson Emma C, Karayiannis Peter, McLean Angela R, Holzmann Heidemarie, Klenerman Paul

СтатьяПоддержка NIH: внешняя программаПоддержка исследования: вне правительства СШАПеревод требует повторной обработки

Аннотация

INTRODUCTION

Acute hepatitis C virus (HCV) infection is rarely studied, but virus sequence evolution and host-virus dynamics during this early stage may influence the outcome of infection. Hypervariable region 1 (HVR1) is genetically diverse and under selective pressure from the host immune response. We analyzed HVR1 evolution by frequent sampling of an acutely infected HCV cohort.

METHODS

Three or more pretreatment samples were obtained from each of 10 acutely infected subjects. Polymerase chain reaction amplification was performed with multiple primer combinations to identify the full range of sequences present. Positive samples were cloned and sequenced. Phylogenetic analyses were used to assess viral diversity.

RESULTS

Eight of the 10 subjects were coinfected with at least 2 HCV subtypes. Multiple subtypes were detected in individual samples, and their relative proportions changed through acute infection. The subjects with the most complex subtype structure also had a dynamic viral load; however, changes in viral load were not directly linked to changes in subtype.

CONCLUSIONS

This well-sampled cohort with acute HCV infection was characterized by dynamic coinfection with multiple viral subtypes, representing a highly complex virologic landscape extremely early in infection.

Для цитирования: Smith Jennifer A, Aberle Judith H, Fleming Vicki M, Ferenci Peter, Thomson Emma C, Karayiannis Peter, McLean Angela R, Holzmann Heidemarie, Klenerman Paul. Dynamic coinfection with multiple viral subtypes in acute hepatitis C.. The Journal of infectious diseases. 2010. DOI: 10.1086/657317.

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