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Patients infected with CRF07_BC have significantly lower viral loads than patients with HIV-1 subtype B: mechanism and impact on disease progression. | LitMetric

AI Article Synopsis

  • CRF 07_BC is the dominant HIV-1 strain in Taiwan among injection drug users and features a significant 7 amino-acid deletion in its p6gag, impacting its viral load and replication.
  • In a study comparing patients infected with CRF07_BC and subtype B, those with CRF07_BC demonstrated lower viral loads (about 58,000 copies/ml less) and reduced replicative capacity despite both strains being CCR5-tropic and non-syncytium inducing.
  • The deletion in p6gag adversely affects the viral lifecycle, resulting in slower maturation, poorer viral protein production, and less efficient interaction with the Alix protein, contributing to the lower viral loads observed

Article Abstract

The circulating recombinant form (CRF) 07_BC is the most prevalent HIV-1 strain among injection drug users (IDUs) in Taiwan. It contains a 7 amino-acid deletion in its p6gag. We conducted a cohort study to compare viral loads and CD4 cell count changes between patients infected with subtype B and CRF07_BC and to elucidate its mechanism. Twenty-one patients infected with CRF07_BC and 59 patients with subtype B were selected from a cohort of 667 HIV-1/AIDS patients whom have been followed up for 3 years. Generalized estimated equation was used to analyze their clinical data and the results showed that patients infected with CRF07_BC had significantly lower viral loads (about 58,000 copies per ml less) than patients with subtype B infection (p = 0.002). The replicative capacity of nine CRF07_BC and four subtype B isolates were compared and the results showed that the former had significantly lower replicative capacity than the latter although all of them were CCR5- tropic and non-syncytium inducing viruses. An HIV-1-NL4-3 mutant virus which contains a 7 amino-acid deletion in p6gag (designated as 7d virus) was generated and its live cycle was investigated. The results showed that 7d virus had significantly lower replication capacity, poorer protease-mediated processing and viral proteins production. Electron microscopic examination of cells infected with wild-type or 7d virus demonstrated that the 7d virus had poorer and slower viral maturation processes: more viruses attached to the cell membrane and higher proportion of immature virions outside the cells. The interaction between p6gag and Alix protein was less efficient in cells infected with 7d virus. In conclusion, patients infected with CRF07_BC had significantly lower viral loads than patients infected with subtype B and it may due to the deletion of 7 amino acids which overlaps with Alix protein-binding domain of the p6gag.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4263662PMC
http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0114441PLOS

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