Evidence map›Paper›PMID 17690010›Full record

ArticleJournal of clinical virology : the official publication of the Pan American Society for Clinical Virology2007

Evaluation of global clustering patterns and strain variation over an extended ORF26 gene locus from Kaposi's sarcoma herpesvirus.

Jian-Chao Zong, Henry Kajumbula, William Boto, Gary S Hayward

Open access · greenAbstract read
In one paragraph

Article in Journal of clinical virology : the official publication of the Pan American Society for Clinical Virology, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.6field-weighted citation impact, top 30% 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

6 citing papers in PubMed, 20 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Article
  5. Reflections on the interpretation of heterogeneity and strain differences based on very limited PCR sequence data from Kaposi's sarcoma-associated herpesvirus genomes.Journal of clinical virology : the official publication of the Pan American Society for Clinical Virology · 2007
    Review
  6. Review
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

4 authors at 2 institutions in 2 countries.

Jian-Chao ZongViral Oncology Program, Department of Oncology, Blunting Blaustein Cancer Research Building, Sydney Kimmel Comprehensive Cancer Center, Johns Hopkins School of Medicine, Baltimore, MD 21231-1000, United States.
Henry Kajumbula
William Boto
Gary S Hayward
Makerere University · UGSidney Kimmel Comprehensive Cancer Center · US

Funding

Regulation of Cellular Proteins by KSHV RAP and RTAR01CA073585 · NCI · JOHNS HOPKINS UNIVERSITY · PI HAYWARD, GARY S · 1996 to 2011
$4.4M
Treatment of herpesvirus-associated AIDS malignanciesP01CA081400 · NCI · JOHNS HOPKINS UNIVERSITY · PI AMBINDER, RICHARD F. · 2000 to 2003
$3.0M
IMMEDIATE-EARLY REGULATORY GENES OF CYTOMEGALOVIRUSR01AI024576 · NIAID · JOHNS HOPKINS UNIVERSITY · PI HAYWARD, GARY S · 1987 to 2007
$2.0M
HYPERVARIABLE ORF-K1 SIGNALING PROTEIN OF KSHV/HHV8R01CA081422 · NCI · JOHNS HOPKINS UNIVERSITY · PI HAYWARD, GARY S · 1999 to 2003
$1.1M
NCI NIH HHS CA73585NCI NIH HHS CA81400NCI NIH HHS CA81422NCI NIH HHS P01 CA081400NCI NIH HHS R01 CA073585NCI NIH HHS R01 CA081422NIAID NIH HHS R01 AI024576
6 · The paper itself

Abstract

backgroundSmall 233-bp or 330-bp DNA fragments of the ORF26 gene of human Kaposi's sarcoma herpesvirus (KSHV) have been used extensively to identify KSHV by PCR in clinical samples; to associate KSHV with novel diseases and to correlate KSHV strain differences with pathogenicity.

objectivesWe evaluated the nature, extent and source of nucleotide sequence variability among a large and diverse set of known KSHV-positive DNA samples. STUDY

designDirect DNA PCR sequencing was carried out on 136 distinct Kaposi's sarcoma and primary effusion lymphoma-related samples from different geographic locations.

resultsThe presence of 26 diagnostic nucleotide polymorphisms across an expanded 965-bp PCR locus define eight distinct ORF26E genotypes, three being of Eurasian origin, one from the Pacific Rim, and five from Sub-Saharan Africa. Previous ambiguities between some genotype patterns in the 330-bp locus data are fully resolved.

conclusionsThis analysis provides an expanded database for understanding and evaluating ORF26 polymorphisms. In particular, the eight genotype clusters correlated with specific ethnic and geographic origins of the patients. Furthermore, the very low level of additional sporadic nucleotide variation found permits detection of spurious sequence errors or contamination present in some published data.

Indexed as

Open Reading FramesPolymorphism, GeneticAIDS-Related Opportunistic InfectionsBase SequenceCluster AnalysisDemographyGenome, ViralGenotypeHerpesviridae InfectionsHerpesvirus 8, HumanHumansMolecular Sequence DataSarcoma, Kaposi

Identifiers

PMID17690010
PMCPMC2043355
OpenAlexW2108577459

What OpenQuestion holds

Textmetadata
Read underepoch 390

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.