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. 2019 Nov 26;14(11):e0225251.
doi: 10.1371/journal.pone.0225251. eCollection 2019.

Genetic diversity and drug resistance of HIV-1 among infected pregnant women newly diagnosed in Luanda, Angola

Affiliations

Genetic diversity and drug resistance of HIV-1 among infected pregnant women newly diagnosed in Luanda, Angola

Cruz S Sebastião et al. PLoS One. .

Abstract

Monitoring genetic diversity and drug resistance mutations (DRMs) is critical for understanding HIV epidemiology. Here, we report HIV-1 genetic diversity and DRMs in blood samples from 42 HIV-positive pregnant women naive to antiretroviral therapy (ART), in Luanda. The samples were subjected to nested-PCR, followed by sequencing of HIV-1 pol gene, targeting the protease and reverse transcriptase fragments. HIV-1 diversity was analyzed using the REGA HIV-1 subtyping tool and DRMs were identified using the Calibrated Population Resistance tool. A total of 34 sequences were obtained. The data revealed wide HIV-1 subtypes heterogeneity, with subtype C (38%, 13/34) the most frequent, followed by the subtypes F1 (18%, 6/34), A1 (9%, 3/34), G (9%, 3/34), D (6%, 2/34) and H (3%, 1/34). In addition, recombinants strains were detected, with CRF02_AG (6%, 2/34) the most frequent, followed by CRF37_cpx, F1/C, A1/G and H/G, all with 3% (1/34). A total of 6/34 (18%) of the sequences presented DRMs. The non-nucleoside reverse transcriptase inhibitors presented 15% (5/34) of resistance. Moreover, 1/34 (3%) sequence presented resistance against both non-nucleoside reverse transcriptase inhibitors and nucleoside reverse transcriptase inhibitors, simultaneously. Despite the small sample size, our results suggest the need to update currently used ART regimens. Surveillance of HIV-1 subtypes and DRMs are necessary to understand HIV epidemiology and to guide modification of ART guidelines in Angola.

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Conflict of interest statement

The authors have declared that no competing interests exist.

Figures

Fig 1
Fig 1. HIV-1 diversity among infected pregnant women in Luanda, Angola, 2018.
The analysis involved 34 nucleotide sequences. (A) Frequency of HIV-1 subtypes and recombinants. (B) Recombinants distribution. The subtypes were identified by the REGA v3.0, and recombinants strains by SimPlot.
Fig 2
Fig 2. Evolutionary relationships of HIV-1 subtypes among infected pregnant women in Luanda, Angola, 2018.
The analysis involved 56 nucleotide sequences. All HIV-1 strains identified in this study were from M-group. The phylogenetic tree was inferred using the NJ method, and Tamura-Nei genetic distances with 1000 bootstrap replicates. Analyses were conducted in MEGA v7.0. Bootstrap values more than 70% and recombinants strains are indicated.

References

    1. United Nations. Political Declaration on HIV and AIDS: On the Fast Track to Accelerating the Fight against HIV and to Ending the AIDS Epidemic by 2030. 2016;17020: 1–26.
    1. United Nations Joint Programme on HIV/AIDS (UNAIDS). Unaids Data 2018. 2018.
    1. Leitner T, Hahn B, Mullins J, Wolinsky S, Foley B, Apetrei C, et al. HIV Sequence Compendium 2015 Editors. Theor Biol Biophys Los Alamos Natl Lab. 2015.
    1. Sharp PM, Hahn BH. Origins of HIV and the AIDS pandemic. Cold Spring Harb Perspect Med. 2011;1: a006841. 10.1101/cshperspect.a006841 - DOI - PMC - PubMed
    1. Afonso JM, Bello G, Monick GL, Sojka M, Morgado MG. HIV-1 Genetic Diversity and Transmitted Drug Resistance Mutations among Patients from the North, Central and South Regions of Angola. PLoS One. 2012;7: 11 10.1371/journal.pone.0042996 - DOI - PMC - PubMed

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