Forskning ved Københavns Universitet - Københavns Universitet


Advantages of a single-cycle production assay to study cell culture-adaptive mutations of hepatitis C virus

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

  • Rodney S Russell
  • Jean-Christophe Meunier
  • Shingo Takikawa
  • Kristina Faulk
  • Ronald E Engle
  • Bukh, Jens
  • Robert H Purcell
  • Suzanne U Emerson
The JFH1 strain of hepatitis C virus (HCV) is unique among HCV isolates, in that the wild-type virus can traverse the entire replication cycle in cultured cells. However, without adaptive mutations, only low levels of infectious virus are produced. In the present study, the effects of five mutations that were selected during serial passage in Huh-7.5 cells were studied. Recombinant genomes containing all five mutations produced 3-4 logs more infectious virions than did wild type. Neither a coding mutation in NS5A nor a silent mutation in E2 was adaptive, whereas coding mutations in E2, p7, and NS2 all increased virus production. A single-cycle replication assay in CD81-deficient cells was developed to study more precisely the effect of the adaptive mutations. The E2 mutation had minimal effect on the amount of infectious virus released but probably enhanced entry into cells. In contrast, both the p7 and NS2 mutations independently increased the amount of virus released.
TidsskriftPNAS Early Edition
Udgave nummer11
Sider (fra-til)4370-5
Antal sider6
StatusUdgivet - 18 mar. 2008

ID: 32949214