Identification, Genetic Characterization and Validation of Highly Diverse HIV-1 Viruses for Reference Panel Development

• Published in: Viruses Vol. 13; no. 7; p. 1417
• Main Authors: Zhao, Jiangqin, Huang, Hanxia, Lee, Sherwin, Ragupathy, Viswanath, Biswas, Santanu, Mbondji-wonje, Christelle, Wang, Xue, Jiang, Alex, Hewlett, Indira
• Format: Journal Article
• Language: English
• Published: Basel MDPI AG 20-07-2021; MDPI
• Subjects: Antigens; Blood & organ donations; Divergence; Epidemiology; Genetic diversity; HIV; Human immunodeficiency virus; Infections; Laboratories; Leukocytes (mononuclear); p24; Pandemics; Peripheral blood mononuclear cells; phylogenetic analysis; Phylogenetics; Phylogeny; recombinant; Recombinants; Software; subtype; Viruses; United States > US; Cameroon
• ISSN: 1999-4915; 1999-4915
• DOI: 10.3390/v13071417

The continued diversification of HIV poses potentially significant challenges to HIV diagnostics and therapeutics. The dynamic evolution of emerging variants is highlighted in countries such as Cameroon in West Central Africa, where all known subtypes and circulating recombinant forms (CRFs) have been shown to be prevalent. We obtained several hundred HIV-positive plasma and viruses from this region for characterization and identification of highly divergent HIV strains. A total of 163 viral strains were cultured to high titers and high volumes using donor peripheral blood mononuclear cells (PBMCs). Initially, 101 viruses representing 59 strains were well characterized and categorized. Results showed that the viral load (VL) range was 0.36–398.9 × 107 copies/mL, p24 values was 0.2–1134 ng/mL. Phylogenetic analysis of thirty-six near full-length HIV-1 genomic sequences demonstrated that most recombinants were highly diverse CRF02 containing unique recombinant forms (URFs). There were seven viral isolates identified as pure subtype/sub-subtypes (F2, A1, G, and D), six as CRFs (CRF06, CRF18, and CRF22), and ten as URFs. These extensively characterized reagents reflect the current dynamic and complex HIV epidemic in Cameroon and provide valuable insights into the potential phylogenetic evolutionary trend of global HIV molecular epidemiology in the future. These materials may be useful for development of HIV validation and reference panels to evaluate the performance of serologic antigen and nucleic acid assays for their ability to detect and quantitate highly divergent HIV strains.