Evidence map›Paper›PMID 10482553›Full record

ArticleJournal of virology1999

Human herpesvirus 6B genome sequence: coding content and comparison with human herpesvirus 6A.

G Dominguez, T R Dambaugh, F R Stamey, S Dewhurst, N Inoue, P E Pellett

Open access · bronzeAbstract read
In one paragraph

Article in Journal of virology, 1999. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 145 papers.

0numbers the graph read from it
0cells of the map it votes in
145citing papers in PubMed
8.9field-weighted citation impact, top 2% 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

145 citing papers in PubMed, 338 citations in OpenAlex.

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  12. Virus-Induced Cell Fusion and Syncytia Formation.Results and problems in cell differentiation · 2024
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85 more citing papers are in PubMed but not listed here.

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

6 authors at 3 institutions in 1 country.

G DominguezCenters for Disease Control and Prevention, Atlanta, Georgia 30333, USA.
T R Dambaugh
F R Stamey
S Dewhurst
N Inoue
P E Pellett
Centers for Disease Control and Prevention · USUniversity of Rochester Medical Center · USWilmington University · US

Funding

PATHOGENESIS AND THERAPY FOR LENTIVIRUSESK04AI001240 · NIAID · UNIVERSITY OF ROCHESTER · PI DEWHURST, STEPHEN · 1994 to 1998
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HHV6 AND HHV7 VECTORS FOR AIDS THERAPYR21AI034231 · NIAID · UNIVERSITY OF ROCHESTER · PI DEWHURST, STEPHEN · 1998 to 1998
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NIAID NIH HHS KO4 AI01240NIAID NIH HHS R21 AI34231
6 · The paper itself

Abstract

Human herpesvirus 6 variants A and B (HHV-6A and HHV-6B) are closely related viruses that can be readily distinguished by comparison of restriction endonuclease profiles and nucleotide sequences. The viruses are similar with respect to genomic and genetic organization, and their genomes cross-hybridize extensively, but they differ in biological and epidemiologic features. Differences include infectivity of T-cell lines, patterns of reactivity with monoclonal antibodies, and disease associations. Here we report the complete genome sequence of HHV-6B strain Z29 [HHV-6B(Z29)], describe its genetic content, and present an analysis of the relationships between HHV-6A and HHV-6B. As sequenced, the HHV-6B(Z29) genome is 162,114 bp long and is composed of a 144,528-bp unique segment (U) bracketed by 8,793-bp direct repeats (DR). The genomic sequence allows prediction of a total of 119 unique open reading frames (ORFs), 9 of which are present only in HHV-6B. Splicing is predicted in 11 genes, resulting in the 119 ORFs composing 97 unique genes. The overall nucleotide sequence identity between HHV-6A and HHV-6B is 90%. The most divergent regions are DR and the right end of U, spanning ORFs U86 to U100. These regions have 85 and 72% nucleotide sequence identity, respectively. The amino acid sequences of 13 of the 17 ORFs at the right end of U differ by more than 10%, with the notable exception of U94, the adeno-associated virus type 2 rep homolog, which differs by only 2.4%. This region also includes putative cis-acting sequences that are likely to be involved in transcriptional regulation of the major immediate-early locus. The catalog of variant-specific genetic differences resulting from our comparison of the genome sequences adds support to previous data indicating that HHV-6A and HHV-6B are distinct herpesvirus species.

Indexed as

Genome, ViralSequence AnalysisBase SequenceHerpesvirus 6, HumanHumansMolecular Sequence DataSequence Alignment

Identifiers

PMID10482553
PMCPMC112820
OpenAlexW2102004866

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.