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Updated: Jun 28, 2026

A Restriction Enzyme Based Cloning Method to Assess the In vitro Replication Capacity of HIV-1 Subtype C Gag-MJ4 Chimeric Viruses
Published on: August 31, 2014
Polymorphism, recombination, and mutations in HIV type 1 gag-infecting Peruvian male sex workers
Carlos Augusto Yabar1, Javier Salvatierra, Eberth Quijano
1Laboratorio de Biotecnología y Biología Molecular, Instituto Nacional de Salud, Lima, Peru. cyabar@ins.gob-pe
Abstract:
HIV genetic diversity in female sex workers (FSW) has been previously described in Peru; however this information is not yet available for male sex workers (MSW). Therefore, purified peripheral blood mononuclear cell DNA from 147 HIV-infected subjects identified as MSW and FSW was used to amplify a 460-bp fragment corresponding to the p24-p7 region of the gag gene. The PCR product was digested with restriction enzymes to identify genetic polymorphism. Later, a random group of samples (n = 19) was sequenced to perform phylogenetic analysis, intragenic recombination analysis, and deleterious mutations leading to a nonfunctional protein in conservative regions of the Gag protein. RFLP analysis revealed 11 genetic variants for AluI and five for MspI. A group of nonsex workers (NSW) used for comparison showed different RFLP genetic variant distributions. Of interest, nine cases of mixed genetic variants were observed for MSW, one case for FSW, and none for NSW. Phylogenetic analysis revealed that all HIV-1 species were subtype B. Intragenic recombination analysis showed a B/C recombination case from an FSW (boostrap = 1000; p value < 0.05). Of interest, deleterious mutations were observed in three cases of conservative D2 zinc domains for Gag 3/19 and one case of the high homology region (1/19). This study shows that gag of HIV circulating from MSW has high genetic polymorphism involving deleterious mutations in conserved domains from the p24-p7 gag region.
Insights
This study reveals significant genetic diversity in the HIV gag gene among male sex workers in Peru, including unique mixed variants and deleterious mutations. This highlights the need for targeted HIV prevention and treatment strategies for this population.
Area of Science:
- Virology
- Molecular Biology
- Public Health
Background:
- Previous studies documented HIV genetic diversity in female sex workers (FSW) in Peru.
- Genetic diversity data for male sex workers (MSW) was lacking.
- Understanding HIV genetic diversity is crucial for effective public health interventions.
Purpose of the Study:
- To characterize the genetic diversity of the HIV gag gene in Peruvian male sex workers (MSW).
- To compare HIV genetic profiles between MSW, FSW, and non-sex workers (NSW).
- To identify potential deleterious mutations in conserved regions of the Gag protein.
Main Methods:
- DNA was extracted from 147 HIV-infected MSW and FSW.
- A fragment of the gag gene (p24-p7 region) was amplified and analyzed using Restriction Fragment Length Polymorphism (RFLP).
- Phylogenetic and intragenic recombination analyses were performed on a subset of samples.
Main Results:
- RFLP identified 11 genetic variants for AluI and 5 for MspI, with distinct distributions between MSW, FSW, and NSW.
- Nine cases of mixed genetic variants were found in MSW, one in FSW, and none in NSW.
- Phylogenetic analysis confirmed all HIV-1 strains as subtype B, with one B/C recombination case identified in an FSW.
- Deleterious mutations were observed in conserved Gag domains in three MSW and one FSW.
Conclusions:
- HIV circulating in Peruvian MSW exhibits high genetic polymorphism in the gag gene's p24-p7 region.
- The presence of mixed genetic variants and deleterious mutations in MSW warrants further investigation.
- Findings underscore the importance of considering genetic diversity in HIV control programs targeting key populations.
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