Global Origin and Spatiotemporal Spread of Hepatitis C Virus Epidemic Genotypes/Subtypes: A Complete Genome-Based

Sakshi Kamboj1,2, Manoj Kumar1,2

  • 1Virology Unit and Bioinformatics Centre, Institute of Microbial Technology (IMTECH), Council of Scientific and Industrial Research (CSIR), Chandigarh, India.

Journal of Medical Virology
|December 19, 2024
PubMed

Insights

This study reveals the global origins and spread of Hepatitis C virus (HCV) genotypes 1a, 1b, 2, and 3. It identifies new origins for genotype 2 and links HCV spread to historical events and behaviors.

Area of Science:

  • Virology
  • Epidemiology
  • Evolutionary Biology

Background:

  • Hepatitis C virus (HCV) poses a global health challenge.
  • Previous studies on HCV phylodynamics were geographically limited.
  • The global origin and spread of major HCV genotypes remain underexplored.

Purpose of the Study:

  • To investigate the global origin and spatiotemporal spread of epidemic HCV genotypes/subtypes.
  • To conduct the first global phylogeographic analysis of HCV genotype 2.
  • To elucidate the evolutionary rates and migration patterns of key HCV genotypes.

Main Methods:

  • Screened 2744 HCV complete genome sequences from 27 countries over four decades.
  • Utilized phylodynamic and phylogeographic analyses on 516 representative sequences.
  • Calculated evolutionary rates and estimated time to the most recent common ancestor (tMRCA) and origin locations.

Main Results:

  • Estimated evolutionary rates: 1a (1.109×10-3), 1b (1.096×10-3), 2 (5.013×10-3), and 3 (1.483×10-3) substitutions/site/year.
  • Identified origins: genotype 1a (United States, 1909.21), 1b (Japan, 1893.36), 2 (France, 981.76), and 3 (India, 1714.89).
  • Revealed genotype 2 originated in France, contradicting previous assumptions of an African origin.

Conclusions:

  • HCV spread is influenced by historical factors like World War II, medical practices, and drug use.
  • The study provides comprehensive insights into the evolutionary history and global dissemination of major HCV genotypes.
  • Identified origins and spread patterns offer crucial data for public health interventions and future research.

Related Concept Videos

Retroviruses02:33

Retroviruses

Retroviruses and retrotransposons both insert copies of their genetic elements into the genome of the host cell. Thus, the viral genes are passed on when the host genome is replicated or translated. A typical retroviral DNA sequence contains 3-4 genes that encode the different proteins required for its structural assembly and function as a molecular parasite. This DNA is transcribed into a single mRNA, which is very similar in structure to conventional mRNAs, i.e., it is capped at the 5’...
12.2K
Viral Mutations00:36

Viral Mutations

A mutation is a change in the sequence of bases of DNA or RNA in a genome. Some mutations occur during replication of the genome due to errors made by the polymerase enzymes that replicate DNA or RNA. Unlike DNA polymerase, RNA polymerase is prone to errors because it is not capable of “proofreading” its work. Viruses with RNA-based genomes, like HIV, therefore accrue mutations faster than viruses with DNA-based genomes. Because mutation and recombination provide the raw material...
32.1K
Viral Recombination00:57

Viral Recombination

Cells are sometimes infected by more than one virus at once. When two viruses disassemble to expose their genomes for replication in the same cell, similar regions of their genomes can pair together and exchange sequences in a process called recombination. Alternatively, viruses with segmented genomes can swap segments in a process called reassortment.
23.2K
Single Nucleotide Polymorphisms-SNPs01:05

Single Nucleotide Polymorphisms-SNPs

A single nucleotide polymorphism or SNP is a single nucleotide variation at a specific genomic position in a large population. It is the most prevalent type of sequence variation found in the human genome. Point mutations that occur in more than 1% of the population qualify as SNPs. These are present once every 1000 nucleotides on an average in the human genome. Replacement of a purine with another purine (A/G) or a pyrimidine with another pyrimidine (C/T) is known as a transition. In contrast,...
14.0K