Project TP 5


(S. Urban)

Mechanisms of Hepatitis B virus X-protein (HBx)-mediated regulation of viral transcription in authentic cell culture systems

The failure to resolve an acute HBV infection can be regarded as the consequence of insufficient innate and adaptive immune responses resulting in lifelong persistence of a tightly regulated replication competent cccDNA template in hepatocytes. To escape innate immune surveillance of HBV in infected cells, passive and active mechanisms are supposed to be involved. Reverse transcription of viral pregenomic (pg)RNA within fully assembled nucleocapsids creates a physical barrier for the recognition by cellular pattern recognition receptors (PRRs). In addition although minimalistic in its genetic repertoire, HBV might use strategies to counteract surveillance by the immune system. Understanding of such mechanisms in molecular terms will have profound implications for more successful treatment strategies. We applied primary human hepatocytes (PHHs) and HepaRG cells to investigate two questions related to the control of HBV infection within the first funding period: (1) Does the regulatory protein HBx modulate transcription of viral RNAs and if so, what is the mechanism underlying this process? (2) Which role does the Interferon (IFN) response play in the establishment and chronification of HBV infection? We showed that HBx is the viral key player for regulating HBV transcription from its authentic template, the cccDNA. HBx-protein is not part of the viral particle and displays a strong and selective effect on histone-associated cccDNA, but not on artificial templates. Through biochemical analyses we detected HBx expressed from its endogenous promoter in the nucleus of hepatocytes and identified phosphorylation and acetylation sites. We established a lentiviral complementation assay, which will allow the functional mapping of the essential domains required for HBx-regulated HBV transcription. Regarding the effect of IFN on HBV replication, we found that both, type I and type III IFNs efficiently control HBV replication, predominantly at a late replication step. Compared to other viruses, HBV infection does not induce robust IFN-responses arguing for a mechanism to counteract the sensors of infection.

The overall goal of this follow up application is the molecular understanding of the mechanism of HBx-mediated regulation of cccDNA-dependent gene expression. Particularly we will (i) use the previously established lentiviral transduction system to functionally allocate HBx subdomains required to control cccDNA-dependent transcription, (ii) investigate the role of phosphorylation and acetylation, (iii) attempt to identify the participating cellular enzymes and finally (iv) assess the pathway(s) involved in shutting down HBx-dependent HBV gene transcription. The employment of the most authentic infection systems will provide us with the most relevant molecular details of the early steps in the establishment of persistent HBV infection.
© Dep. of Infectious Diseases, Molecular Virology. University of Heidelberg
NEWS
26.11.2015
Activation of Type I and III Interferon Response by Mitochondrial and Peroxisomal MAVS and Inhibition by Hepatitis C Virus.Bender S, Reuter A, Eberle F, Einhorn E, Binder M, Bartenschlager R. PLoS Pathog. 2015 Nov 20;11(11):e1005264.

Virus-specific CD4+ T Cells Have Functional and Phenotypic Characteristics of Follicular T-helper Cells in Patients With Acute and Chronic HCV Infections. Raziorrouh B, Sacher K, Tawar RG, Emmerich F, Neumann-Haefelin C, Baumert TF, Thimme R, Boettler T. Gastroenterology. 2015 Nov 13. pii: S0016-5085(15)01622-4.

Evidence that hepatitis B virus replication in mouse cells is limited by the lack of a host cell dependency factor. Lempp FA, Mutz P, Lipps C, Wirth D, Bartenschlager R, Urban S. J Hepatol. 2015 Nov 11. pii: S0168-8278(15)00736-9. doi: 10.1016/j.jhep.2015.10.030. [Epub ahead of print]