Three Novel CRF01_AE/CRF07_BC Recombinant Forms of HIV-1 Identified in Shijiazhuang City, China

Curr HIV Res. 2023;21(4):232-239. doi: 10.2174/011570162X266371231028192233.

Abstract

Background: Hebei, a province with a low Human Immunodeficiency Virus (HIV) prevalence, is also a region with the most abundant HIV-1 genetic diversity. HIV-1 recombinant forms have been the key factor influencing the effectiveness of HIV-1 control and therapy.

Objectives: We aimed to study inter-subtype recombinant structures of new HIV-1-second generation recombinant forms.

Methods: Monitoring the HIV-1 subtype by phylogenetic and recombinant breakpoint analyses are the two most frequent methods among men who have sex with men (MSM). Here, three near full-length genomes (NFLGs) were obtained from HIV-1 seropositive MSM in Shijiazhuang City, China, who have never received antiretroviral therapy in 2021.

Results: Phylogenetic analysis indicated that three NFLGs were novel inter-subtype recombinant forms between CRF07_BC and CRF01_AE. For the NFLG 21S009, four CRF07_BC gene fragments were inserted into the pol, vif-vpr, vpu-env, and nef-3` LTR gene regions within a CRF01_ AE backbone, respectively. For the NFLG 21S095, four breakpoints were identified in HIV-1 pol and vpu regions. The NFLG 21S370 contained four gene recombinant breakpoints within HIV-1 pol and vpu-env gene regions. Of these three NFLGs, the NFLG 21S009 contained the most breakpoints, distributed in the pol, vif, vpr, vpu, env, and nef regions, respectively. In the gag-pol regions, three NFLGs had only one CRF07_BC gene fragment inserted into gene points between 4250 and 4792.

Conclusion: Our findings provide strong evidence that the surveillance of novel recombinant forms is necessary for the increase in better control of HIV.

Keywords: CRF01_AE; CRF07_BC; HIV-1; MSM; near full-length genome; shijiazhuang..

MeSH terms

  • China / epidemiology
  • Genome, Viral
  • Genotype
  • HIV Infections*
  • HIV-1* / genetics
  • Homosexuality, Male
  • Humans
  • Male
  • Phylogeny
  • Recombination, Genetic
  • Sequence Analysis, DNA
  • Sexual and Gender Minorities*