Genomic characterization of hepatitis C virus transmitted founder variants with deep sequencing

Infect Genet Evol. 2019 Jul:71:36-41. doi: 10.1016/j.meegid.2019.02.032. Epub 2019 Mar 8.

Abstract

Transfer of hepatitis C virus (HCV) infection from a donor to a new recipient is associated with a bottleneck of genetic diversity in the transmitted viral variants. Existing data suggests that one, or very few, variants emerge from this bottleneck to establish the infection (transmitted founder [T/F] variants). In HCV, very few T/F variants have been characterized due to the challenges of obtaining early infection samples and of high throughput viral genome sequencing. This study used a large, acute HCV, deep-sequenced dataset from first viremia samples collected in nine prospective cohorts across four countries, to estimate the prevalence of single T/F viruses, and to identify host and virus-related factors associated with infections initiated by a single T/F variant. The short reads generated by Illumina sequencing were used to reconstruct viral haplotypes with two haplotype reconstruction algorithms. The haplotypes were examined for random mutations (Poisson distribution) and a star-like phylogeny to identify T/F viruses. The findings were cross-validated by haplotype reconstructions across three regions of the genome (Core-E2, NS3, NS5A) to minimize the possibility of spurious overestimation of single T/F variants. Of 190 acute infection samples examined, 54 were very early acute infections (HCV antibody negative, RNA positive), and single transmitted founders were identified in 14 (26%, 95% CI: 16-39%) after cross validation across multiple regions of the genome with two haplotype reconstruction algorithms. The presence of a single T/F virus was not associated with any host or virus-related factors, notably viral genotype or spontaneous clearance. In conclusion, approximately one in four new HCV infections originates from a single T/F virus. Resolution of genomic sequences of single T/F variants is the first step in exploring unique properties of these variants in the infection of host hepatocytes.

Keywords: Hepatitis C virus; InC3 study; Next generation sequencing; People who inject drugs; Transmitted-founder virus.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Disease Transmission, Infectious
  • Drug Users
  • Female
  • Genetic Variation
  • Genome, Viral / genetics*
  • Genomics
  • Hepacivirus / genetics*
  • Hepatitis C / transmission*
  • Hepatitis C / virology
  • High-Throughput Nucleotide Sequencing
  • Humans
  • Male
  • Phylogeny
  • Prospective Studies
  • Young Adult