Using a gene silencing approach, the authors

convincingly show that cellular DGAT1 depletion results in a marked decrease of infection and viral spread in the HCV cell culture (HCVcc) model system. Interestingly, this effect was not observed when viral spreading was analyzed following DGAT2 depletion in the same conditions. Similarly, the treatment of HCV-producing cells with a well characterized DGAT1 inhibitor,11 conferred a marked decrease in viral spread in HCV permissive cells. Because the DGAT1 inhibitor had no effect on HCV protein expression and RNA synthesis, the authors conclude that this molecule affects a life cycle step following viral replication. Additional functional studies uncovered that DGAT1 is this website involved in the very early steps of viral assembly. To further elucidate the molecular mechanism of DGAT1-mediated HCV production, Herker et al. performed coimmunoprecipitation and colocalization assays. In their mechanistic studies, the authors observed that DGAT1 interacts with HCV core protein at the ER and that

DGAT1 is required for the trafficking of core to LD surface, allowing early steps of viral assembly to occur. These observations support a model where packaging of viral genomes into progeny virions requires DGAT1 (Fig. 1). What are the clinical implications of this important study? First, the results of Herker et al.9 identify DGAT1 as an important host factor for HCV infection. This discovery does not only advance our understanding of the viral life cycle but may selleckchem also have implications for the understanding of pathogenesis of HCV-induced liver disease. Further studies are needed to investigate the relevance of the uncovered virus-host MCE公司 interactions for HCV-associated steatosis and modulation of treatment response. In this regard it is of interest to note that DGAT1 has been previously identified as a specific

factor for hepatic steatosis12 and the HCV core protein has been suggested to modulate triglyceride accumulation in hepatocytes (for review, see Negro1). Second, by demonstrating that a DGAT1 inhibitor decreases HCV particle assembly and production, the results of Herker et al. have uncovered a promising novel target for antiviral therapy. Because specific DGAT1-inhibitors do not affect LD composition, their further development might not be limited by potential off-target effects. As shown previously for micro-RNA122, cyclophilin A, and claudin-1, targeting host factors is an attractive antiviral strategy which may increase the genetic barrier for viral resistance (for review see Georgel et al.2). Proof-of-concept studies in HCV animal models are clearly the next step to demonstrate the efficacy and the antiviral resistance profile for the DGAT1-inhibitor in vivo. Clinical trials in HCV-infected patients may ultimately address its clinical relevance within the widening arsenal of antiviral strategies for HCV infection.