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Updated: May 16, 2026

A Restriction Enzyme Based Cloning Method to Assess the In vitro Replication Capacity of HIV-1 Subtype C Gag-MJ4 Chimeric Viruses
Published on: August 31, 2014
Estimating the rate of intersubtype recombination in early HIV-1 group M strains
Melissa J Ward1, Samantha J Lycett, Marcia L Kalish
1University of Edinburgh, Institute of Evolutionary Biology, Ashworth Laboratories, Edinburgh, United Kingdom.
Abstract:
West Central Africa has been implicated as the epicenter of the HIV-1 epidemic, and almost all group M subtypes can be found there. Previous analysis of early HIV-1 group M sequences from Kinshasa in the Democratic Republic of Congo, formerly Zaire, revealed that isolates from a number of individuals fall in different positions in phylogenetic trees constructed from sequences from opposite ends of the genome as a result of recombination between viruses of different subtypes. Here, we use discrete ancestral trait mapping to develop a procedure for quantifying HIV-1 group M intersubtype recombination across phylogenies, using individuals' gag (p17) and env (gp41) subtypes. The method was applied to previously described HIV-1 group M sequences from samples obtained in Kinshasa early in the global radiation of HIV. Nine different p17 and gp41 intersubtype recombinant combinations were present in the data set. The mean number of excess ancestral subtype transitions (NEST) required to map individuals' p17 subtypes onto the gp14 phylogeny samples, compared to the number required to map them onto the p17 phylogenies, and vice versa, indicated that excess subtype transitions occurred at a rate of approximately 7 × 10(-3) to 8 × 10(-3) per lineage per year as a result of intersubtype recombination. Our results imply that intersubtype recombination may have occurred in approximately 20% of lineages evolving over a period of 30 years and confirm intersubtype recombination as a substantial force in generating HIV-1 group M diversity.
Insights
Intersubtype recombination significantly contributes to HIV-1 diversity in West Central Africa. This process, involving recombination between different human immunodeficiency virus type 1 (HIV-1) subtypes, was found in approximately 20% of lineages over 30 years.
Area of Science:
- Virology
- Molecular Epidemiology
- Genetics
Background:
- West Central Africa is the epicenter of the HIV-1 epidemic, with diverse group M subtypes present.
- Early HIV-1 group M sequences from Kinshasa show evidence of intersubtype recombination.
- Recombination between different subtypes can lead to viruses occupying different phylogenetic positions.
Purpose of the Study:
- To develop a method for quantifying HIV-1 group M intersubtype recombination.
- To apply this method to early HIV-1 sequences from Kinshasa.
- To estimate the rate and impact of intersubtype recombination on HIV-1 diversity.
Main Methods:
- Discrete ancestral trait mapping was used to quantify recombination.
- gag (p17) and env (gp41) subtypes were analyzed.
- The number of excess ancestral subtype transitions (NEST) was calculated.
Main Results:
- Nine different gag/env intersubtype recombinant combinations were identified.
- Excess subtype transitions occurred at a rate of approximately 7-8 × 10(-3) per lineage per year.
- Intersubtype recombination was present in approximately 20% of lineages over 30 years.
Conclusions:
- Intersubtype recombination is a substantial force in generating HIV-1 group M diversity.
- The developed method provides a way to quantify intersubtype recombination.
- Understanding recombination is crucial for tracking HIV-1 evolution and diversity.
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