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Silibinin inhibits hepatitis C virus entry into hepatocytes by hindering clathrin‐dependent trafficking
Authors:Julie Blaising  Pierre L Lévy  Claire Gondeau  Capucine Phelip  Mihayl Varbanov  Elodie Teissier  Florence Ruggiero  Stephen J Polyak  Nicholas H Oberlies  Tijana Ivanovic  Eve‐Isabelle Pécheur
Institution:1. UMR CNRS 5086, IBCP, , Lyon, France;2. UMR Inserm U1052/CNRS 5286, Cancer Research Center of Lyon, University of Lyon, , Lyon, France;3. Inserm U1040, Institut de Recherche en Biothérapie, H?pital St Eloi, , Montpellier, France;4. IGFL, ENS de Lyon, , Lyon, France;5. Department of Laboratory Medicine, University of Washington, , Seattle, WA, USA;6. Department of Chemistry and Biochemistry, University of North Carolina at Greensboro, , Greensboro, NC, USA;7. Department of Biological Chemistry and Molecular Pharmacology, Harvard Medical School, , Boston, MA, 02115 USA;8. Department of Molecular, Cellular and Developmental Biology, University of Colorado, , Boulder, CO, 80309 USA
Abstract:Hepatitis C virus (HCV) is a global health concern infecting 170 million people worldwide. Previous studies indicate that the extract from milk thistle known as silymarin and its main component silibinin inhibit HCV infection. Here we investigated the mechanism of anti‐HCV action ofsilymarin‐derived compounds at the molecular level. By using live‐cell confocal imaging, single particle tracking, transmission electron microscopy and biochemical approaches on HCV‐infected human hepatoma cells and primary hepatocytes, we show that silibinin potently inhibits HCV infection and hinders HCV entry by slowing down trafficking through clathrin‐coated pits and vesicles. Detailed analyses revealed that silibinin altered the formation of both clathrin‐coated pits and vesicles in cells and caused abnormal uptake and trafficking of transferrin, a well‐known cargo of the clathrin endocytic pathway. Silibinin also inhibited infection by other viruses that enter cells by clathrin‐mediated endocytosis including reovirus, vesicular stomatitis and influenza viruses. Our study demonstrates that silibinin inhibits HCV early steps of infection by affecting endosomal trafficking of virions. It provides new insights into the molecular mechanisms of action of silibinin against HCV entry and also suggests that silibinin is a potential broad‐spectrum antiviral therapy.
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