Evidence map›Paper›PMID 24077364›Full record

ArticleThe Journal of general virology2013

Deep sequencing identifies two genotypes and high viral genetic diversity of human pegivirus (GB virus C) in rural Ugandan patients.

Ria R Ghai, Samuel D Sibley, Michael Lauck, Jorge M Dinis, Adam L Bailey, Colin A Chapman, Patrick Omeja, Thomas C Friedrich, David H O'Connor, Tony L Goldberg

Open access · greenAbstract read
In one paragraph

Article in The Journal of general virology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.6field-weighted citation impact, top 15% of its field
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

10 citing papers in PubMed, 17 citations in OpenAlex.

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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

10 authors at 4 institutions in 3 countries.

Ria R GhaiDepartment of Biology, McGill University, Montreal, QC, Canada.
Samuel D SibleyDepartment of Pathobiological Sciences, University of Wisconsin-Madison, Madison, WI, USA.
Michael LauckDepartment of Pathology and Laboratory Medicine, University of Wisconsin-Madison, Madison, WI, USA.
Jorge M DinisDepartment of Pathobiological Sciences, University of Wisconsin-Madison, Madison, WI, USA.
Adam L BaileyDepartment of Pathology and Laboratory Medicine, University of Wisconsin-Madison, Madison, WI, USA.
Colin A ChapmanDepartment of Anthropology and McGill School of Environment, Montreal, QC, Canada, and Wildlife Conservation Society, NY, USA.
Patrick OmejaMakerere University Biological Field Station, Fort Portal, Uganda.
Thomas C FriedrichWisconsin National Primate Research Center, Madison, WI, USA.
David H O'ConnorSchool of Medicine and Public Health, University of Wisconsin-Madison, Madison, WI, USA.
Tony L GoldbergWisconsin National Primate Research Center, Madison, WI, USA.
University of Wisconsin–Madison · USMakerere University · UGMcGill University · CAWildlife Conservation Society · US

Funding

INTEGRATED TRAINING FOR PHYSICIAN-SCIENTISTST32GM008692 · NIGMS · UNIVERSITY OF WISCONSIN-MADISON · PI BURKARD, MARK E · 1998 to 2020
$10.3M
Biological and Human Dimensions of Primate Retroviral TransmissionR01AI098420 · NIAID · UNIVERSITY OF WISCONSIN-MADISON · PI GOLDBERG, TONY L. · 2011 to 2015
$2.3M
The Impact and Society Ecology of Bacterial Zoonoses in Northern Tanzania: UnderR01TW009237 · FIC · DUKE UNIVERSITY · PI CRUMP, JOHN ANDREW · 2011 to 2014
$1.7M
FIC NIH HHS R01 TW009237FIC NIH HHS TW009237NIAID NIH HHS R01 AI098420NIGMS NIH HHS T32 GM008692
6 · The paper itself

Abstract

Human pegivirus (HPgV), formerly 'GB virus C' or 'hepatitis G virus', is a member of the genus Flavivirus (Flaviviridae) that has garnered significant attention due to its inhibition of HIV, including slowing disease progression and prolonging survival in HIV-infected patients. Currently, there are six proposed HPgV genotypes that have roughly distinct geographical distributions. Genotypes 2 and 3 are the most comprehensively characterized, whereas those genotypes occurring on the African continent, where HPgV prevalence is highest, are less well studied. Using deep sequencing methods, we identified complete coding HPgV sequences in four of 28 patients (14.3%) in rural Uganda, east Africa. One of these sequences corresponds to genotype 1 and is the first complete genome of this genotype from east Africa. The remaining three sequences correspond to genotype 5, a genotype that was previously considered exclusively South African. All four positive samples were collected within a geographical area of less than 25 km(2), showing that multiple HPgV genotypes co-circulate in this area. Analysis of intra-host viral genetic diversity revealed that total single-nucleotide polymorphism frequency was approximately tenfold lower in HPgV than in hepatitis C virus. Finally, one patient was co-infected with HPgV and HIV, which, in combination with the high prevalence of HIV, suggests that this region would be a useful locale to study the interactions and co-evolution of these viruses.

Indexed as

Genetic VariationAdolescentAdultAnimalsFemaleFlaviviridae InfectionsGB virus CGenome, ViralGenotypeHepatitis, Viral, HumanHigh-Throughput Nucleotide SequencingHIV InfectionsHumansMaleMiddle AgedMolecular Sequence Data

Identifiers

PMID24077364
PMCPMC3836497
OpenAlexW2101779010

What OpenQuestion holds

Textmetadata
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Registered trials

None linked

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.