4.6 Article

Phylogenetic Characterization of HIV-1 Sub-Subtype A1 in Karachi, Pakistan

Journal

VIRUSES-BASEL
Volume 14, Issue 10, Pages -

Publisher

MDPI
DOI: 10.3390/v14102307

Keywords

HIV-1; sub-subtype A1; phylogenetics; phylodynamics; epitopes; gag; Pakistan

Categories

Funding

  1. HIV Research Trust [HIVRT 3927290]
  2. Aga Khan University Seed Money Grant [PF84/0716]
  3. Higher Education Commission, Pakistan [5217/Sindh/NRPU/RD/HEC/2016]
  4. Pakistan Science Foundation Grant [PSF/Res/S-AKU/Med (488)]
  5. Swedish Research Council [2016-01417]
  6. Swedish Society for Medical Research [SA-2016]

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This study provides a detailed characterization of the HIV-1 sub-subtype A1 epidemic in Pakistan. It reveals that the majority of the Pakistan HIV-1 sub-subtype A1 strains are unique to Pakistan and exhibit a specific mutation pattern in the Gag protein. The study also establishes a link between these signature variations and alterations in Gag protein structure and Gag-specific T-cell epitopes.
(1) Background: HIV-1 sub-subtype A1 is common in parts of Africa, Russia, former Soviet Union countries, and Eastern Europe. In Pakistan, sub-subtype A1 is the predominant HIV-1 subtype. Preliminary evidence suggests that distinct strains of HIV-1 sub-subtype A1 are circulating in Pakistan; however, an in-depth molecular phylogenetic characterization of HIV-1 sub-subtype A1 strains in Pakistan have not been presented. We performed a detailed characterization of the HIV-1 sub-subtype A1 epidemic in Pakistan using state-of-the-art molecular epidemiology and phylodynamics. (2) Methods: A total of 143 HIV-1 sub-subtype A1 gag sequences, including 61 sequences generated specifically for this study from PLHIVs part of our cohort, representing all sub-subtype A1 gag sequences from Pakistan, were analyzed. Maximum-likelihood phylogenetic cluster analysis was used to determine the relationship between Pakistani sub-subtype A1 strains and pandemic sub-subtype A1 strains. Furthermore, we used signature variation, charge distribution, selection pressures, and epitope prediction analyses to characterize variations unique to Pakistani HIV-1 strains and establish the association between signature variations and Gag epitope profile. (3) Results: The HIV-1 sub-subtype A1 sequences from Pakistan formed three main clusters: two that clustered with Kenyan sequences (7 and 10 sequences, respectively) and one that formed a Pakistan-specific cluster of 123 sequences that were much less related to other sub-subtype A1 sequences available in the database. The sequences in the Pakistan-specific cluster and the Kenyan reference strains exhibited several signature variations, especially at amino acid positions 312, 319, 331, 372, 373, 383, and 402. Structural protein modeling suggested that amino acid changes in these positions result in alterations of the Gag protein structure as well as in Gag-specific T-cell epitopes. (4) Conclusions: Our results suggest that the majority of the Pakistan HIV-1 sub-subtype A1 strains were unique to Pakistan and with a specific mutation pattern in Gag.

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