Prevalence of resistance to integrase strand-transfer inhibitors (INSTIs) among untreated HIV-1 infected patients in Morocco

BMC Res Notes. 2018 Jun 8;11(1):369. doi: 10.1186/s13104-018-3492-5.

Abstract

Objective: The integrase strand-transfer inhibitors (INSTIs) are an important class in the arsenal of antiretroviral drugs designed to block the integration of HIV-1 cDNA into the host DNA through the inhibition of DNA strand transfer. In this study for the first time in Morocco, the complete HIV-1 integrase gene was analysed from newly diagnosed patients to evaluate the prevalence of natural polymorphisms and INSTIs resistance-associated mutations in the integrase gene.

Results: The 864pb IN coding region was successfully sequenced from plasma sample for 77 among 80 antiretroviral naïve patients. The sequences were interpreted for drug resistance according to the Stanford algorithm. Sixty samples were HIV-1 subtype B (78%), fourteen CRF02_AG (18%), two subtype C and one subtype A. Overall 81 of 288 (28%) amino acid IN positions presented at least one polymorphism each. We found 18 (36.73%), 42 (25.76%) and 21 (27.27%) of polymorphic residues assigned to the N-Terminal Domain, Catalytic Core Domaine and the C-Terminal Domain positions respectively. Primary INSTIs resistance mutation were absent, however secondary mutations L74IM, T97A were detected in four samples (5.2%). These results demonstrate that untreated HIV-1 infected Moroccans will be susceptible to INSTIs.

Keywords: HIV-1; INSTIs; Integrase; Morocco; Naïve patients; Resistance mutations.

MeSH terms

  • Adolescent
  • Adult
  • Amino Acid Sequence
  • Child
  • Demography
  • Drug Resistance, Viral*
  • Female
  • HIV Infections / drug therapy*
  • HIV Infections / epidemiology*
  • HIV Integrase Inhibitors / therapeutic use*
  • HIV-1 / physiology*
  • Humans
  • Integrases / chemistry
  • Integrases / genetics
  • Likelihood Functions
  • Male
  • Morocco / epidemiology
  • Phylogeny
  • Prevalence
  • Young Adult

Substances

  • HIV Integrase Inhibitors
  • Integrases