Genetic Diversity and Antiretroviral Resistance in HIV-1-Infected Patients Newly Diagnosed in Cabo Verde

Silvânia Da Veiga Leal1,2, Victor Pimentel2, Paloma Gonçalves3

  • 1Instituto Nacional de Saúde Pública de Cabo Verde, Largo do Desastre da Assistência, Chã de Areia, Praia CP 7943-010, Cape Verde.

Viruses
|January 8, 2025
PubMed

Insights

Transmitted drug resistance (TDR) in Cabo Verde shows 9.6% prevalence, with Non-Nucleoside Reverse Transcriptase Inhibitor (NNRTI) resistance being most common. This highlights the need for ongoing HIV-1 resistance surveillance.

Area of Science:

  • Virology
  • Epidemiology
  • Genetics

Background:

  • Human Immunodeficiency Virus type 1 (HIV-1) genetic diversity and transmitted drug resistance (TDR) pose challenges to effective treatment.
  • Understanding HIV-1 genotypes and resistance mutations is crucial for optimizing antiretroviral therapy.

Purpose of the Study:

  • To investigate prevalent HIV-1 genotypes and drug-resistance-associated mutations in drug-naïve individuals in Cabo Verde.
  • To assess the prevalence of TDR and specific resistance mutations within the study population.

Main Methods:

  • Sequencing of the HIV-1 pol gene from drug-naïve individuals using Sanger sequencing.
  • Identification of TDR with the Stanford Calibrated Population Resistance tool and interpretation using the Stanford HIV database.
  • Phylogenetic analysis for HIV-1 genetic diversity and collection of epidemiological data via questionnaires.

Main Results:

  • The predominant HIV-1 genotype was CRF02_AG (41.1%), followed by subtype G (37.0%).
  • Overall TDR prevalence was 9.6%, with Non-Nucleoside Reverse Transcriptase Inhibitor (NNRTI) mutations found in 9.6% of individuals.
  • The most frequent mutations were K103N (5.5%) and M184V (2.7%); no protease or integrase mutations were detected.

Conclusions:

  • The study identified a significant prevalence of TDR, particularly NNRTIs, in drug-naïve individuals in Cabo Verde.
  • Findings underscore the necessity for continuous surveillance of HIV-1 resistance mutations to maintain the efficacy of current antiretroviral regimens, including Dolutegravir.