Evidence map›Paper›PMID 19770693›Full record

ArticleAIDS (London, England)2009

Evolution and molecular epidemiology of subtype C HIV-1 in Zimbabwe.

Sudeb C Dalai, Tulio de Oliveira, Gordon W Harkins, Seble G Kassaye, Jennifer Lint, Justen Manasa, Elizabeth Johnston, David Katzenstein

Abstract read
In one paragraph

Article in AIDS (London, England), 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed, 1 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

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3 · Its place in the literature

Who cites it

30 citing papers in PubMed, 1 synthesis or guideline 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.

Sudeb C DalaiStanford University School of Medicine, Stanford University Medical Center, Stanford, CA 94305, USA. sdalai@stanford.edu
Tulio de Oliveira
Gordon W Harkins
Seble G Kassaye
Jennifer Lint
Justen Manasa
Elizabeth Johnston
David Katzenstein

Funding

HIV-1 Drug Resistance in Different SubtypesR01AI066922 · NIAID · STANFORD UNIVERSITY · PI KANTOR, RAMI, KATZENSTEIN, DAVID ALLENBERG · 2008 to 2012
$3.6M
Drug Resistance and Pathogenesis in Subtype C HIV-1R01AI060399 · NIAID · STANFORD UNIVERSITY · PI KATZENSTEIN, DAVID ALLENBERG · 2005 to 2008
$1.2M
African Program for Research training in HIV, TB and associated opportunistic infU2RTW006878 · FIC · STANFORD UNIVERSITY · PI KATZENSTEIN, DAVID ALLENBERG · 2005 to 2009
$747k
FIC NIH HHS U2R TW006878FIC NIH HHS U2R TW006878-4Howard Hughes Medical InstituteNIAID NIH HHS R01 AI060399NIAID NIH HHS R01 AI066922Wellcome TrustWellcome Trust 082384/Z/07/Z
6 · The paper itself

Abstract

objectiveTo investigate the origins and evolutionary history of subtype C HIV-1 in Zimbabwe in a context of regional conflict and migration.

designHIV-1C pol sequence datasets were generated from four sequential cohorts of antenatal women in Harare, Zimbabwe sampled over 15 years (1991-2006).

methodsOne hundred and seventy-seven HIV-1C pol sequences were obtained from four successive cohorts in Zimbabwe. Maximum-likelihood methods were used to explore phylogenetic relationships between Zimbabwean HIV-1C sequences and subtype C strains from other regions. A Bayesian coalescent-based framework was used to estimate evolutionary parameters for HIV-1C in Zimbabwe, including origin and demographic growth patterns.

resultsZimbabwe HIV-1C pol demonstrated increasing sequence divergence over the 15-year period. Nearly all Zimbabwe sequences clustered phylogenetically with subtype C strains from neighboring countries. Bayesian evolutionary analysis indicated a most recent common ancestor date of 1973 with three epidemic growth phases: an initial, slow phase (1970s) followed by exponential growth (1980s), and a linearly expanding epidemic to the present. Bayesian trees provided evidence for multiple HIV-1C introductions into Zimbabwe during 1979-1981, corresponding with Zimbabwean national independence following a period of socio-political instability.

conclusionThe Zimbabwean HIV-1C epidemic likely originated from multiple introductions in the late 1970s and grew exponentially during the 1980s, corresponding to changing political boundaries and rapid population influx from neighboring countries. The timing and phylogenetic clustering of the Zimbabwean sequences is consistent with an origin in southern Africa and subsequent expansion. HIV-1 sequence data contain important epidemiological information, which can help focus treatment and prevention strategies in light of more recent political volatility in Zimbabwe.

Indexed as

AdultEvolution, MolecularFemaleHIV-1HIV InfectionsHumansMolecular EpidemiologyPhylogenyZimbabwe

Identifiers

PMID19770693
PMCPMC2923658

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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.