Geographic Distribution of HCV-GT3 Subtypes and Naturally Occurring Resistance Associated Substitutions

Viruses. 2019 Feb 11;11(2):148. doi: 10.3390/v11020148.

Abstract

Background: Little is known about the frequency or geographic distributions of naturally occurring resistance-associated substitutions (RASs) in the nonstructural protein 5A (NS5A) domain of hepatitis-C virus (HCV) genotype-3 (GT-3) different subtypes. We investigated naturally occurring GT-3 RASs that confer resistance to NS5A inhibitors.

Methods: From a publicly accessible database, we retrieved 58 complete GT-3 genomes and an additional 731 worldwide NS5A sequences from patients infected with GT-3 that were naive to direct-acting antiviral treatment.

Results: We performed a phylogenetic analysis of NS5A domains in complete HCV genomes to determine more precisely HCV-GT-3 subtypes, based on commonly used target regions (e.g., 5'untranslated region and NS5B partial domain). Among 789 NS5A sequences, GT-3nonA subtypes were more prevalent in Asia than in other geographic regions (P<0.0001). The A30K RAS was detected more frequently in HCV GT3nonA (84.6%) than in GT-3A subtypes (0.8%), and the amino acid change was polymorphic in isolates from Asia.

Conclusions: These results provided information on the accuracy of HCV-3 subtyping with a phylogenetic analysis of the NS5A domain with data from the Los Alamos HCV genome database. This information and the worldwide geographic distribution of RASs according to HCV GT-3 subtypes are crucial steps in meeting the challenges of treating HCV GT-3.

Keywords: HCV genotype 3 subtypes; NS5A replication complex inhibitors; geographic distribution; natural polymorphisms; resistance-associated substitutions (RASs).

MeSH terms

  • Amino Acid Substitution
  • Databases, Genetic
  • Drug Resistance, Viral / genetics*
  • Genome, Viral*
  • Genotype
  • Geography
  • Hepacivirus / classification
  • Hepacivirus / genetics*
  • Phylogeny*
  • Prevalence
  • Sequence Analysis, DNA
  • Viral Nonstructural Proteins / genetics*

Substances

  • Viral Nonstructural Proteins
  • NS-5 protein, hepatitis C virus