Hepatitis C virus
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| Hepatitis C virus | ||||||||
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Classification
Higher order taxa
Virus; ssRNA positive strand virus no DNA stage; Flaviviridae; hepacivirus
Species
Hepatitis C virus
Description and significance
The Hepatitis C virus (HCV) was discovered in 1989 at Chiron, Inc. The genome was located by using chimpanzees infected with a serum, that was from a patient with non-A, non-B Hepatitis. Through this screening they were able to discover what the virus was that was causing Hepatitis after blood transfusions that were not caused by Hepatitis A or Hepatitis B. This virus encodes a single polyprotein that is about 3,000 amino acids long. It is processed by host cells and viral proteases. This virus lives and infects the liver of its host. It reproduces in the hepatocytes of the liver. It is then spread throughout the body in the bloodstream where it can be transmitted to another host through direct blood to blood contact. It is important for its genome to be sequenced because of the lethal effects of HCV. This virus has been linked to cancer of the liver, cirrhosis, and has also been linked with many HIV patients. Also of importance because currently there are 6 different genotypes of HCV and through testing we have learned that different genotypes react differently to different methods of treatment.
Genome structure
The Genome of HCV is approximately 10,000 base pairs long. It contains single open reading frame (ORF) that encodes for a polyprotein of about 3000 amino acids. At both the 5’ and 3’ ends there are non coding regions. There are about 6 main types of genomic structure for HCV. There are thought to be many frameshift mutations during the replication of HCV, which help lead to its genetic variability. This enables the virus to become harder to track, and also leads to the difficulties in coming up with a cure for it, enhancing its life span as a virus.
Cell structure and metabolism
HCV is an enveloped icosahedral capsid. It consists of the single strand RNA, and the outside of the envelope is covered with the glycoprotein’s E1 and E2. Part of the problem with HCV is that currently they are unable to culture it in vitro, which makes it difficult for studying its structure and replication processes. With these difficulties some discoveries have been made. The E2 glycoprotein is very important because it has recently been discovered that it is this that interacts with and binds to the HCV receptor CD81 in liver cells. It is also being suggested that HCV may enter the cell bound to LDL receptors. Still we are not certain of this, but it is a theory based on the association of HCV particles and beta lipoproteins. Scientists are unsure whether entrance to the cell bound to CD81 or LDL leads to successful infection of the virus (JGV). It is known that once the virus is inside the cytoplasm of the host cell that the RNA genome is directly translated. It is believed that a –RNA strand is synthesized by a replicase composed of NS3-5B and that this will serve as the template for production of +RNA strands. Then through interactions with structural proteins it will become encapsidated, and then they are enveloped by budding in the lumen of the ER. All of this is hypothetical because without the ability to culture it in vitro, and mass produce, it is very difficult to study the virus at all.
Summary
Importing file
Ecology
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Pathology
How does this organism cause disease? Human, animal, plant hosts? Virulence factors, as well as patient symptoms.
Application to Biotechnology
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Current Research
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References
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