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Analysis of the history and spread of HIV-1 in Uganda using phylodynamics

HIV prevalence has decreased in Uganda since the 1990s, but remains substantial within high-risk groups. Here, we reconstruct the history and spread of HIV subtypes A1 and D in Uganda and explore the transmission dynamics in high-risk populations. We analysed HIV pol sequences from female sex worker...

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Autores principales: Yebra, Gonzalo, Ragonnet-Cronin, Manon, Ssemwanga, Deogratius, Parry, Chris M., Logue, Christopher H., Cane, Patricia A., Kaleebu, Pontiano, Brown, Andrew J. Leigh
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Society for General Microbiology 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4635457/
https://www.ncbi.nlm.nih.gov/pubmed/25724670
http://dx.doi.org/10.1099/vir.0.000107
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author Yebra, Gonzalo
Ragonnet-Cronin, Manon
Ssemwanga, Deogratius
Parry, Chris M.
Logue, Christopher H.
Cane, Patricia A.
Kaleebu, Pontiano
Brown, Andrew J. Leigh
author_facet Yebra, Gonzalo
Ragonnet-Cronin, Manon
Ssemwanga, Deogratius
Parry, Chris M.
Logue, Christopher H.
Cane, Patricia A.
Kaleebu, Pontiano
Brown, Andrew J. Leigh
author_sort Yebra, Gonzalo
collection PubMed
description HIV prevalence has decreased in Uganda since the 1990s, but remains substantial within high-risk groups. Here, we reconstruct the history and spread of HIV subtypes A1 and D in Uganda and explore the transmission dynamics in high-risk populations. We analysed HIV pol sequences from female sex workers in Kampala (n = 42), Lake Victoria fisher-folk (n = 46) and a rural clinical cohort (n = 74), together with publicly available sequences from adjacent regions in Uganda (n = 412) and newly generated sequences from samples taken in Kampala in 1986 (n = 12). Of the sequences from the three Ugandan populations, 60 (37.1 %) were classified as subtype D, 54 (33.3 %) as subtype A1, 31 (19.1 %) as A1/D recombinants, six (3.7 %) as subtype C, one (0.6 %) as subtype G and 10 (6.2 %) as other recombinants. Among the A1/D recombinants we identified a new candidate circulating recombinant form. Phylodynamic and phylogeographic analyses using BEAST indicated that the Ugandan epidemics originated in 1960 (1950–1968) for subtype A1 and 1973 (1970–1977) for D, in rural south-western Uganda with subsequent spread to Kampala. They also showed extensive interconnection with adjacent countries. The sequence analysis shows both epidemics grew exponentially during the 1970s–1980s and decreased from 1992, which agrees with HIV prevalence reports in Uganda. Inclusion of sequences from the 1980s indicated the origin of both epidemics was more recent than expected and substantially narrowed the confidence intervals in comparison to previous estimates. We identified three transmission clusters and ten pairs, none of them including patients from different populations, suggesting active transmission within a structured transmission network.
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spelling pubmed-46354572015-12-15 Analysis of the history and spread of HIV-1 in Uganda using phylodynamics Yebra, Gonzalo Ragonnet-Cronin, Manon Ssemwanga, Deogratius Parry, Chris M. Logue, Christopher H. Cane, Patricia A. Kaleebu, Pontiano Brown, Andrew J. Leigh J Gen Virol Standard HIV prevalence has decreased in Uganda since the 1990s, but remains substantial within high-risk groups. Here, we reconstruct the history and spread of HIV subtypes A1 and D in Uganda and explore the transmission dynamics in high-risk populations. We analysed HIV pol sequences from female sex workers in Kampala (n = 42), Lake Victoria fisher-folk (n = 46) and a rural clinical cohort (n = 74), together with publicly available sequences from adjacent regions in Uganda (n = 412) and newly generated sequences from samples taken in Kampala in 1986 (n = 12). Of the sequences from the three Ugandan populations, 60 (37.1 %) were classified as subtype D, 54 (33.3 %) as subtype A1, 31 (19.1 %) as A1/D recombinants, six (3.7 %) as subtype C, one (0.6 %) as subtype G and 10 (6.2 %) as other recombinants. Among the A1/D recombinants we identified a new candidate circulating recombinant form. Phylodynamic and phylogeographic analyses using BEAST indicated that the Ugandan epidemics originated in 1960 (1950–1968) for subtype A1 and 1973 (1970–1977) for D, in rural south-western Uganda with subsequent spread to Kampala. They also showed extensive interconnection with adjacent countries. The sequence analysis shows both epidemics grew exponentially during the 1970s–1980s and decreased from 1992, which agrees with HIV prevalence reports in Uganda. Inclusion of sequences from the 1980s indicated the origin of both epidemics was more recent than expected and substantially narrowed the confidence intervals in comparison to previous estimates. We identified three transmission clusters and ten pairs, none of them including patients from different populations, suggesting active transmission within a structured transmission network. Society for General Microbiology 2015-07 /pmc/articles/PMC4635457/ /pubmed/25724670 http://dx.doi.org/10.1099/vir.0.000107 Text en © 2015 The Authors http://creativecommons.org/licenses/by/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/(.
spellingShingle Standard
Yebra, Gonzalo
Ragonnet-Cronin, Manon
Ssemwanga, Deogratius
Parry, Chris M.
Logue, Christopher H.
Cane, Patricia A.
Kaleebu, Pontiano
Brown, Andrew J. Leigh
Analysis of the history and spread of HIV-1 in Uganda using phylodynamics
title Analysis of the history and spread of HIV-1 in Uganda using phylodynamics
title_full Analysis of the history and spread of HIV-1 in Uganda using phylodynamics
title_fullStr Analysis of the history and spread of HIV-1 in Uganda using phylodynamics
title_full_unstemmed Analysis of the history and spread of HIV-1 in Uganda using phylodynamics
title_short Analysis of the history and spread of HIV-1 in Uganda using phylodynamics
title_sort analysis of the history and spread of hiv-1 in uganda using phylodynamics
topic Standard
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4635457/
https://www.ncbi.nlm.nih.gov/pubmed/25724670
http://dx.doi.org/10.1099/vir.0.000107
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