» Articles » PMID: 20426823

HIV-1 Recombinants with Multiple Parental Strains in Low-prevalence, Remote Regions of Cameroon: Evolutionary Relics?

Overview
Journal Retrovirology
Publisher Biomed Central
Specialty Microbiology
Date 2010 Apr 30
PMID 20426823
Citations 27
Authors
Affiliations
Soon will be listed here.
Abstract

Background: The HIV pandemic disseminated globally from Central West Africa, beginning in the second half of the twentieth century. To elucidate the virologic origins of the pandemic, a cross-sectional study was conducted of the genetic diversity of HIV-1 strains in villagers in 14 remote locations in Cameroon and in hospitalized and STI patients. DNA extracted from PBMC was PCR amplified from HIV(+) subjects. Partial pol amplicons (N = 164) and nearly full virus genomes (N = 78) were sequenced. Among the 3956 rural villagers studied, the prevalence of HIV infection was 4.9%; among the hospitalized and clinic patients, it was 8.6%.

Results: Virus genotypes fell into two distinctive groups. A majority of the genotyped strains (109/164) were the circulating recombinant form (CRF) known to be endemic in West Africa and Central West Africa, CRF02_AG. The second most common genetic form (9/164) was the recently described CRF22_01A1, and the rest were a collection of 4 different subtypes (A2, D, F2, G) and 6 different CRFs (-01, -11, -13, -18, -25, -37). Remarkably, 10.4% of HIV-1 genomes detected (17/164) were heretofore undescribed unique recombinant forms (URF) present in only a single person. Nearly full genome sequencing was completed for 78 of the viruses of interest. HIV genetic diversity was commonplace in rural villages: 12 villages each had at least one newly detected URF, and 9 villages had two or more.

Conclusions: These results show that while CRF02_AG dominated the HIV strains in the rural villages, the remainder of the viruses had tremendous genetic diversity. Between the trans-species transmission of SIVcpz and the dispersal of pandemic HIV-1, there was a time when we hypothesize that nascent HIV-1 was spreading, but only to a limited extent, recombining with other local HIV-1, creating a large variety of recombinants. When one of those recombinants began to spread widely (i.e. became epidemic), it was recognized as a subtype. We hypothesize that the viruses in these remote Cameroon villages may represent that pre-epidemic stage of viral evolution.

Citing Articles

Differences in HIV infection trends in two regions of Cameroon with a longstanding HIV epidemic: insights from 2012 and 2022.

Ngoume Y, Teagho U, Eselacha B, Goni O, Kenfack D, Tchakoute M Front Public Health. 2025; 13.

PMID: 40008148 PMC: 7617435. DOI: 10.3389/fpubh.2025.1517213.


Phylogenetic evidence of extensive spatial mixing of diverse HIV-1 group M lineages within Cameroon but not between its neighbours.

Godwe C, Goni O, San J, Sonela N, Tchakoute M, Nanfack A Virus Evol. 2024; 10(1):veae070.

PMID: 39386075 PMC: 11463025. DOI: 10.1093/ve/veae070.


No detectable differences in Nef-mediated downregulation of HLA-I and CD4 molecules among HIV-1 group M lineages circulating in Cameroon, where the pandemic originated.

Sonela N, Mann J, Godwe C, Goni O, Tchakoute M, Nkoue N Front Virol. 2024; 4.

PMID: 38883214 PMC: 7616105. DOI: 10.3389/fviro.2024.1379217.


Elucidation of Early Evolution of HIV-1 Group M in the Congo Basin Using Computational Methods.

Tongo M, Martin D, Dorfman J Genes (Basel). 2021; 12(4).

PMID: 33918115 PMC: 8065694. DOI: 10.3390/genes12040517.


Phylogeny of partial , and genes show predominance of HIV-1G and CRF02_AG with emerging recombinants in south-eastern Nigeria.

Udeze A, Olaleye D, Odaibo G Heliyon. 2020; 6(8):e04310.

PMID: 32775738 PMC: 7403892. DOI: 10.1016/j.heliyon.2020.e04310.


References
1.
Worobey M, Gemmel M, Teuwen D, Haselkorn T, Kunstman K, Bunce M . Direct evidence of extensive diversity of HIV-1 in Kinshasa by 1960. Nature. 2008; 455(7213):661-4. PMC: 3682493. DOI: 10.1038/nature07390. View

2.
Brennan C, Bodelle P, Coffey R, Devare S, Golden A, Hackett Jr J . The prevalence of diverse HIV-1 strains was stable in Cameroonian blood donors from 1996 to 2004. J Acquir Immune Defic Syndr. 2008; 49(4):432-9. DOI: 10.1097/QAI.0b013e31818a6561. View

3.
Carr J, Laukkanen T, Salminen M, Albert J, Alaeus A, Kim B . Characterization of subtype A HIV-1 from Africa by full genome sequencing. AIDS. 1999; 13(14):1819-26. DOI: 10.1097/00002030-199910010-00003. View

4.
Chohan B, Lang D, Sagar M, Korber B, Lavreys L, Richardson B . Selection for human immunodeficiency virus type 1 envelope glycosylation variants with shorter V1-V2 loop sequences occurs during transmission of certain genetic subtypes and may impact viral RNA levels. J Virol. 2005; 79(10):6528-31. PMC: 1091724. DOI: 10.1128/JVI.79.10.6528-6531.2005. View

5.
Keele B, Van Heuverswyn F, Li Y, Bailes E, Takehisa J, Santiago M . Chimpanzee reservoirs of pandemic and nonpandemic HIV-1. Science. 2006; 313(5786):523-6. PMC: 2442710. DOI: 10.1126/science.1126531. View