4.7 Article

Differential effect of p7 inhibitors on hepatitis C virus cell-to-cell transmission

期刊

ANTIVIRAL RESEARCH
卷 100, 期 3, 页码 636-639

出版社

ELSEVIER SCIENCE BV
DOI: 10.1016/j.antiviral.2013.10.006

关键词

p7; Hepatitis C; Assembly; Inhibitors; Cell-to-cell

资金

  1. Medical Research Council
  2. NIHR Centre for Liver Research
  3. Wellcome Trust
  4. MRC [G1100247, G0801976] Funding Source: UKRI
  5. Medical Research Council [G0801976, G1100247] Funding Source: researchfish

向作者/读者索取更多资源

Inhibitors targeting the hepatitis C virus (HCV) encoded viroporin, p7 prevent virus release in vitro. HCV can transmit by cell-free particle infection of new target cells and via cell-to-cell dependent contact with limited exposure to the extracellular environment. The role of assembly inhibitors in preventing HCV transmission via these pathways has not been studied. We compared the efficacy of three published p7 inhibitors to inhibit cell-free and cell-to-cell transmission of two chimeric HCV strains encoding genotype 2 (GT2) or 5 (GT5) p7 using a recently developed single cycle co-culture assay. The inhibitors reduced the infectivity of extracellular GT2 and GT5 virus by 80-90% and GT2 virus cell-to-cell transmission by 50%. However, all of the p7 inhibitors had minimal effect on GT5 cell contact dependent transmission. Screening a wider panel of diverse viral genotypes demonstrated that p7 viroporin inhibitors were significantly more effective at blocking cell-free virus than cell-to-cell transmission. These results suggest an altered assembly or trafficking of cell-to-cell transmitted compared to secreted virus. These observations have important implications for the validation, therapeutic design and testing of HCV assembly inhibitors. (C) 2013 The Authors. Published by Elsevier B.V. All rights reserved.

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