Casein kinase II inhibitor enhances production of infectious genotype 1a hepatitis C virus (H77S)

Seungtaek Kim, Bora Jin, Sung Hoon Choi, Kwang Hyub Han, Sang Hoon Ahn

Research output: Contribution to journalArticlepeer-review

7 Citations (Scopus)


Genotype 2a JFH1 virus has substantially contributed to the progress of HCV biology by allowing entire viral life cycle of HCV in cell culture. Using this genotype 2a virus, casein kinase II (CKII) was previously identified as a crucial host factor in virus assembly by phosphorylating NS5A. Since most of the prior studies employed genotype 2a JFH1 or JFH1-based intragenotypic chimera, we used genotype 1a H77S to study virus assembly. CKII inhibition by chemical inhibitors enhanced H77S virus production in contrast to that of JFH1 virus, but genetic inhibition of CKII by siRNA did not change H77S virus titer significantly. The different outcomes from these two approaches of CKII inhibition suggested that nonspecific target kinase of CKII inhibitors plays a role in increasing H77S virus production and both viral and host factors were investigated in this study. Our results emphasize substantial differences among the HCV genotypes that should be considered in both basic research and clinical practices.

Original languageEnglish
Article numbere113938
JournalPloS one
Issue number12
Publication statusPublished - 2014 Dec 2

Bibliographical note

Publisher Copyright:
© 2014 Kim et al.

All Science Journal Classification (ASJC) codes

  • Biochemistry, Genetics and Molecular Biology(all)
  • Agricultural and Biological Sciences(all)
  • General

Fingerprint Dive into the research topics of 'Casein kinase II inhibitor enhances production of infectious genotype 1a hepatitis C virus (H77S)'. Together they form a unique fingerprint.

Cite this