Figure 1 HCV life cycle and site of action of DAAs

Slides:



Advertisements
Similar presentations
HIV and its lifecycle Sources: Wikipedia, HIV is a retrovirus (enveloped viruses possessing an RNA genome,
Advertisements

Current Status and Benefits of Therapy for Chronic Hepatitis C Virus (HCV) Fuad AM Hasan Department Of Medicine Faculty of Medicine Kuwait University.
THE REPLICATION OF VIRUSES Virology Lecture 2 Three lectures dealing with (1) replication of DNA viruses (2) the culture, growth and recognition of virus.
Inside of cell Interior of rough endoplasmic reticulum 5' Receptor protein Signal recognition particle mRNA Ribosome Signal sequence Protein synthesis.
Associate professor in microbiology
 Hepatitis C virus (HCV) infects 170 million people worldwide  up to 80% of those infected become chronic infection.  HCV infection can cause chronic.
#LJWG2015 HEPATITIS C IN PEOPLE WHO USE DRUGS Improving Care for Hepatitis C: A Framework Approach LONDON 2015.
New Treatments of Hepatitis C
Biochemistry of Hepatitis C
 Recognition  Attachment  Penetration  Uncoating  Early protein synthesis  Nucleic acid synthesis  Late protein synthesis  Assembly  Release.
BOCEPREVIR & TELAPREVIR
The HIV virus. Objectives At the end of this session the participants will be able to: 1. Understand basic HIV structure 2. Describe the significance.
Flaviviridae Positive stranded RNA viruses. Flaviviridae Enveloped virions made up of a lipid bilayer with two or more types of envelope (E) glycoproteins.
Good teaching is more a giving of right questions than a giving of right answers. – Josef Albers Viruses Chapter 19.
Virus Replication John Goulding, Imperial College London, UK
THE INFECTIOUS PROCESS FOR A VIRUS Despite their simplicity relative to bacteria, viruses still possess various biochemical targets for potential attack.
Hepatitis C virus: life cycle in cells, infection and host response, and analysis of molecular markers influencing the outcome of infection and response.
Jean Dubuisson, François-Loïc Cosset  Journal of Hepatology 
Roles of Lipoproteins and Apolipoproteins in Particle Formation of Hepatitis C Virus  Takasuke Fukuhara, Chikako Ono, Francesc Puig-Basagoiti, Yoshiharu.
Figure 2 Genetic organization and translation of hepatitis E virus
Structural biology of hepatitis C virus
Hepatitis C Virus NS5A Protein–A Master Regulator?
VIRAL GENE EXPRESSION DR.SOBIA MANZOOR LECTURE 05.
Occult Hepatitis C Virus Infection: Are We Digging Too Deep?
Hepatitis C virus infection
Vineela Chukkapalli, Glenn Randall  Gastroenterology 
Figure 1 Patients cured of HCV infection
Hepatitis C virus: life cycle in cells, infection and host response, and analysis of molecular markers influencing the outcome of infection and response.
Mirjam B. Zeisel, Isabel Fofana, Samira Fafi-Kremer, Thomas F. Baumert 
Figure 3 Life cycle of hepatitis E virus
HCV NS5A Inhibitors: The Devil Is in the Details
Figure 5 Exosomes for delivery of RNA interference therapeutics
Figure 2 Modelling the effect of HCV treatment on reinfection in people who inject drugs Figure 2 | Modelling the effect of HCV treatment on reinfection.
Hepatitis C Virus NS5A Protein–A Master Regulator?
Hepatitis C virus entry and glucocorticosteroids
Viruses Viruses – are segments of nucleic acids
Emerging Therapeutic Targets for Hepatitis C Virus Infection
Figure 3 Mechanisms of NS5B-mediated RNA synthesis
Figure 4 Diverse molecular mechanisms of long non-coding RNAs
David Paul, Vanesa Madan, Ralf Bartenschlager  Cell Host & Microbe 
Figure 6 Possible therapeutic targets to decrease hepatic steatosis
Nat. Rev. Gastroenterol. Hepatol. doi: /nrgastro
Hepatitis C virus–cell interactions and their role in pathogenesis
Replication life cycle of HIV and sites of antiretroviral drug action.
Host-targeting agents for prevention and treatment of chronic hepatitis C – Perspectives and challenges  Mirjam B. Zeisel, Joachim Lupberger, Isabel Fofana,
Nat. Rev. Gastroenterol. Hepatol. doi: /nrgastro
Christoph Sarrazin, Stefan Zeuzem  Gastroenterology 
Replication of human astroviruses.
Protein interactions during the flavivirus life cycle elucidated by MS-based proteomics. Protein interactions during the flavivirus life cycle elucidated.
Pick up a book (pg 338) and present trp operon with your team
The Neurobiology of Zika Virus
Pathogenesis of Flavivirus Infections: Using and Abusing the Host Cell
Interferon-Free Treatment Regimens for Hepatitis C: Are We There Yet?
Hepatitis C virus: life cycle in cells, infection and host response, and analysis of molecular markers influencing the outcome of infection and response.
New therapies on the horizon for hepatitis C
Michael S. Diamond, Theodore C. Pierson  Cell 
Life cycle of HCMV in a human cell.
Nat. Rev. Gastroenterol. Hepatol. doi: /nrgastro
VIRUSES.
Good teaching is more a giving of right questions than a giving of right answers. – Josef Albers Viruses Chapter 19.
Mechanisms of drug actions during the viral life cycle.
Jean Dubuisson, François-Loïc Cosset  Journal of Hepatology 
B19V infection of human erythroid progenitor cells (B19V life cycle).
Anti−Hepatitis C Virus Drugs in Development
Terminology HIV AIDS Acquired Human Immune Immunodeficiency Deficiency
Simplified overview of the HCV life cycle and sites of direct acting antiviral therapies. Simplified overview of the HCV life cycle and sites of direct.
Philippe Metz, Antje Reuter, Silke Bender, Ralf Bartenschlager 
Understanding How Hepatitis C Virus Builds Its Unctuous Home
Production and Biomedical Application of Flavivirus-like Particles
The hantavirus life cycle.
Presentation transcript:

Figure 1 HCV life cycle and site of action of DAAs Figure 1 | HCV life cycle and site of action of DAAs. Virus entry is facilitated by a sequence of events that include particle binding to the cell surface, interactions with proteins at the junction between cells and, ultimately, receptor-mediated endocytosis. The released RNA genome is translated into a single polyprotein. This polyprotein is processed by cellular and viral proteases. Protease inhibitors target the viral NS3 enzyme. RNA replication takes place at the membranous web. NS5A and NS5B inhibitors affect replication at different stages, and NS5A inhibitors also interfere with the assembly process. DAA, direct-acting antiviral agent; ER, endoplasmic reticulum; LDLR, low-density lipoprotein receptor; RdRp, RNA-dependent RNA polymerase; SRB1, scavenger receptor class B member 1. Götte, M. & Feld, J. J. (2016) Direct-acting antiviral agents for hepatitis C: structural and mechanistic insights Nat. Rev. Gastroenterol. Hepatol. doi:10.1038/nrgastro.2016.60