Prevalence of transmitted HIV drug resistance in Iran between 2010 and 2011

PLoS One. 2013 Apr 23;8(4):e61864. doi: 10.1371/journal.pone.0061864. Print 2013.

Abstract

Objective: Drug-resistant (DR) HIV emerges during combined antiretroviral treatment (cART), creating concern about widespread transmission of DR-HIV as cART is expanded in resource-limited countries. The aim of this study was to determine the predominant HIV-1 subtypes and prevalence of transmitted DR mutations among antiretroviral-naïve patients in Iran.

Design: To monitor transmission of DR HIV, a threshold surveillance based on the world health organization (WHO) guidelines was implemented in Iran.

Methods: For this HIVDR threshold surveillance study, blood samples were collected from 50 antiretroviral-naïve HIV-1-infected patients. Antiretroviral-resistant mutations were determined by sequencing HIV-1 protease, reverse transcriptase and integrase regions. The HIV-1 subtype was determined by sequencing the p17 and C2-V5 regions of the gag and env genes, respectively.

Results: Phylogenetic analyses of the sequenced regions revealed that 45 (95.7%) of 47 samples that were successfully obtained were CRF35_AD. The remaining two cases were subtype B (2.1%) and CRF01_AE (2.1%). Consistent results were obtained also from Env and Gag sequences. Regarding prevalence of transmitted DR viruses, two cases were found to harbor reverse transcriptase-inhibitor-resistant mutations (4.3%). In addition, although not in the WHO list for surveillance of transmitted mutations, 13 minor protease-inhibitor-resistant mutations listed in the International AIDS Society-USA panel of drug resistance mutations were found. No DR mutations were detected in the integrase region.

Conclusions: Our study clarified that CRF35_AD is the major subtype among HIV-1-infected patients in Iran. According to the WHO categorization method of HIVDR threshold survey, the prevalence of transmitted drug resistant HIV in Iran was estimated as moderate (5-15%).

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adolescent
  • Adult
  • Anti-HIV Agents / therapeutic use
  • Drug Resistance, Viral / drug effects
  • Drug Resistance, Viral / genetics
  • Female
  • Genes, env*
  • HIV Infections / epidemiology*
  • HIV Infections / virology
  • HIV Integrase / classification
  • HIV Integrase / genetics*
  • HIV Protease / classification
  • HIV Protease / genetics*
  • HIV Reverse Transcriptase / classification
  • HIV Reverse Transcriptase / genetics*
  • HIV-1 / classification
  • HIV-1 / drug effects
  • HIV-1 / genetics*
  • Humans
  • Iran / epidemiology
  • Male
  • Mutation
  • Peptide Fragments / classification
  • Peptide Fragments / genetics*
  • Phylogeny
  • Prevalence
  • Retrospective Studies
  • Sequence Analysis, DNA
  • env Gene Products, Human Immunodeficiency Virus / classification
  • env Gene Products, Human Immunodeficiency Virus / genetics*

Substances

  • Anti-HIV Agents
  • Peptide Fragments
  • env Gene Products, Human Immunodeficiency Virus
  • p17 gag peptide, human immunodeficiency virus
  • HIV Integrase
  • reverse transcriptase, Human immunodeficiency virus 1
  • HIV Reverse Transcriptase
  • HIV Protease
  • p16 protease, Human immunodeficiency virus 1

Grants and funding

This study was supported by grants from the World Health Organization (APW/09/00252), Iranian Ministry of Health and Medical Education, and a Grant-in-Aid for AIDS research from the Ministry of Health,Labour and Welfare of Japan (H22-AIDS-004). The stipendiary of Fatemeh Jahanbakhsh’s Ph.D. sabbatical leave in Japan, at Nagoya Medical Center was funded by Ministry of Health and Medical Education of Iran. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.