Evidence map›Paper›PMID 25724670›Full record

ArticleThe Journal of general virology2015

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

Gonzalo Yebra, Manon Ragonnet-Cronin, Deogratius Ssemwanga, Chris M Parry, Christopher H Logue, Patricia A Cane, Pontiano Kaleebu, Andrew J Leigh Brown

Abstract read
In one paragraph

Article in The Journal of general virology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed, 2 pooled it
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

29 citing papers in PubMed, 2 syntheses or guidelines pooled it.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors.

Gonzalo Yebra1Institute of Evolutionary Biology, University of Edinburgh, Edinburgh, UK.
Manon Ragonnet-Cronin1Institute of Evolutionary Biology, University of Edinburgh, Edinburgh, UK.
Deogratius Ssemwanga2MRC/UVRI, Uganda Research Unit on AIDS, Entebbe, Uganda.
Chris M Parry2MRC/UVRI, Uganda Research Unit on AIDS, Entebbe, Uganda.
Christopher H Logue3NADP Training, Public Health England, Porton, UK.
Patricia A Cane3NADP Training, Public Health England, Porton, UK.
Pontiano Kaleebu2MRC/UVRI, Uganda Research Unit on AIDS, Entebbe, Uganda.
Andrew J Leigh Brown1Institute of Evolutionary Biology, University of Edinburgh, Edinburgh, UK.

Funding

Modeling Epidemic Infectious Diseases Using Sequence AnalysisU01GM110749 · NIGMS · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI POND, SERGEI L KOSAKOVSKY · 2014 to 2018
$3.0M
Medical Research Council MC_U950097144Medical Research Council MC_UP_1204/1NIGMS NIH HHS U01 GM110749Wellcome Trust 095831
6 · The paper itself

Abstract

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.

Indexed as

PhylogenyCohort StudiesFemaleGenotypeHIV-1HIV InfectionsHumansMolecular EpidemiologyMolecular Sequence Datapol Gene Products, Human Immunodeficiency VirusSequence Analysis, DNASequence HomologyUgandapol Gene Products, Human Immunodeficiency Virus

Identifiers

PMID25724670
PMCPMC4635457

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.