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A Protocol for Analyzing Hepatitis C Virus Replication
Published on: June 26, 2014
The long and winding road leading to the identification of the hepatitis C virus
1Epiphany Biosciences Inc., San Francisco, CA 94111, USA. ceevirfind@yahoo.com
Insights
Researchers identified the hepatitis C virus (HCV) using a novel immunoscreening approach. This breakthrough enabled the development of diagnostics and treatments for this global pathogen.
Area of Science:
- Virology
- Molecular Biology
- Immunology
Background:
- Non-A, Non-B Hepatitis (NANBH) posed a significant diagnostic challenge prior to viral identification.
- Early genomic approaches failed to identify infectious agents responsible for NANBH.
- Hepatitis delta virus characterization did not provide a molecular handle for HCV identification.
Observation:
- A blind cDNA immunoscreening strategy was employed, utilizing patient sera to probe viral cDNA libraries.
- Millions of bacterial cDNA clones were screened from NANBH-infectious chimpanzee materials.
- This approach predated the widespread use of Polymerase Chain Reaction (PCR) technology.
Findings:
- A single small cDNA clone was isolated and confirmed to be derived from the hepatitis C virus (HCV) genome.
- Molecular and serological criteria validated the HCV identification.
- The discovery marked a pivotal moment in understanding and combating HCV.
Implications:
- Facilitated the development of effective HCV diagnostics and blood screening tests.
- Enabled the identification of drug and vaccine targets for HCV control.
- Paved the way for managing HCV as a global health concern.
Abstract:
This review describes work conducted largely in my laboratory at the Chiron Corporation between 1982 and 1989 that led to the identification of the hepatitis C virus (HCV). Key colleagues included Dr. Qui-Lim Choo in my laboratory and Dr. George Kuo also of Chiron as well as my collaborator Dr. Daniel Bradley at the CDC who provided many biological samples from the NANBH chimpanzee model. Numerous molecular approaches were explored including the screening of tens of millions of bacterial cDNA clones derived from these materials. While this early genomics approach resulted in the identification of many host gene activities associated with NANBH, no genes of proven infectious etiology could be identified. A separate avenue of our research led to the molecular characterization of the complete hepatitis delta viral genome but unfortunately, this could not be used as a molecular handle for HCV. Largely following input from Dr. Kuo, I initiated a blind cDNA immunoscreening approach involving the large-scale screening of bacterial proteomic cDNA libraries derived from NANBH-infectious chimpanzee materials (prior to the development of PCR technology) using sera from NANBH patients as a presumptive source of viral antibodies. Eventually, this novel approach to identifying agents of infectious etiology led to the isolation of a single small cDNA clone that was proven to be derived from the HCV genome using various molecular and serological criteria. This discovery has facilitated the development of effective diagnostics, blood screening tests and the elucidation of promising drug and vaccine targets to control this global pathogen.
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