Widespread hepatitis C virus transmission network among people who inject drugs in Kenya

Int J Infect Dis. 2024 Oct:147:107215. doi: 10.1016/j.ijid.2024.107215. Epub 2024 Sep 7.

Abstract

Objectives: Hepatitis C virus (HCV) disproportionately affects people who inject drugs (PWID) worldwide. Despite carrying a high HCV burden, little is known about transmission dynamics in low- and middle-income countries.

Methods: We recruited PWID from Nairobi and coastal cities and towns of Mombasa, Kilifi, and Malindi in Kenya at needle and syringe programs. Next-generation sequencing data from HCV hypervariable region 1 were analyzed using Global Hepatitis Outbreak and Surveillance Technology to identify transmission clusters.

Results: HCV strains belonged to genotype 1a (n = 64, 46.0%), 4a (n = 72, 51.8%) and mixed HCV/1a/4a (n = 3, 2.2%). HCV/1a was dominant (61.2%) in Nairobi, whereas HCV/4a was dominant in Malindi (85.7%) and Kilifi (60.9%), and both genotypes were evenly identified in Mombasa (45.3% for HCV/1a and 50.9% for HCV/4a). Global Hepatitis Outbreak and Surveillance Technology identified 11 transmission clusters involving 90 cases. Strains in the two largest clusters (n = 38 predominantly HCV/4a and n = 32 HCV/1a) were sampled from all four sites.

Conclusions: Transmission clusters involving 64.7% of cases indicate an effective sampling of major HCV strains circulating among PWID. Large clusters involving 77.8% of clustered strains from Nairobi and Coast suggest successful introduction of two ancestral HCV/1a and HCV/4a strains to PWID and the existence of a widespread transmission network in the country. The disruption of this network is essential for HCV elimination.

Keywords: GHOST; Hepatitis C; Kenya; Next-generation sequencing (NGS); People who inject drugs (PWID); Transmission network.

MeSH terms

  • Adult
  • Disease Outbreaks
  • Female
  • Genotype*
  • Hepacivirus* / classification
  • Hepacivirus* / genetics
  • Hepacivirus* / isolation & purification
  • Hepatitis C* / epidemiology
  • Hepatitis C* / transmission
  • Hepatitis C* / virology
  • High-Throughput Nucleotide Sequencing
  • Humans
  • Kenya / epidemiology
  • Male
  • Middle Aged
  • Phylogeny
  • Substance Abuse, Intravenous* / complications
  • Substance Abuse, Intravenous* / epidemiology
  • Young Adult