Evidence map›Paper›PMID 19187529›Full record

ArticleRetrovirology2009

Ancient, independent evolution and distinct molecular features of the novel human T-lymphotropic virus type 4.

William M Switzer, Marco Salemi, Shoukat H Qari, Hongwei Jia, Rebecca R Gray, Aris Katzourakis, Susan J Marriott, Kendle N Pryor, Nathan D Wolfe, Donald S Burke and 2 more

Open access · goldAbstract read
In one paragraph

Article in Retrovirology, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 38 papers.

0numbers the graph read from it
0cells of the map it votes in
38citing papers in PubMed
4.0field-weighted citation impact, top 6% 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

38 citing papers in PubMed, 76 citations in OpenAlex.

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  10. Discovery of an endogenous Deltaretrovirus in the genome of long-fingered bats (Chiroptera: Miniopteridae).Proceedings of the National Academy of Sciences of the United States of America · 2017
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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

12 authors at 7 institutions in 2 countries.

William M SwitzerLaboratory Branch, Division of HIV/AIDS Prevention, National Center for HIV/AIDS, Viral Hepatitis, STD, and TB Prevention, Centers for Disease Control and Prevention, Atlanta, GA 30333, USA. bis3@cdc.gov
Marco Salemi
Shoukat H Qari
Hongwei Jia
Rebecca R Gray
Aris Katzourakis
Susan J Marriott
Kendle N Pryor
Nathan D Wolfe
Donald S Burke
Thomas M Folks
Walid Heneine
National Center for HIV/AIDS Viral Hepatitis STD and TB Prevention · USBaylor College of Medicine · USUniversity of Florida · USStanford University · USTexas Biomedical Research Institute · USUniversity of Oxford · GBUniversity of Pittsburgh · US

Funding

NIH Director's Pioneer Award (RMI)DP1OD000370 · OD · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI WOLFE, NATHAN D · 2005 to 2009
$3.4M
THE EMERGENCE OF HIV GENETIC DIVERSITY IN CAMEROONK01TW000003 · FIC · JOHNS HOPKINS UNIVERSITY · PI WOLFE, NATHAN D · 1999 to 2005
$634k
Transforming Potential of Emerging Human RetrovirusesR21AI078307 · NIAID · BAYLOR COLLEGE OF MEDICINE · PI MARRIOTT, SUSAN J · 2008 to 2009
$415k
FIC NIH HHS K01 TW000003FIC NIH HHS K01 TW00003-1NIAID NIH HHS #R21 AI078307NIAID NIH HHS R21 AI078307NIH HHS DP1 OD000370NIH HHS DP1-OD000370PHS HHS #R25 M 69234
6 · The paper itself

Abstract

backgroundHuman T-lymphotropic virus type 4 (HTLV-4) is a new deltaretrovirus recently identified in a primate hunter in Cameroon. Limited sequence analysis previously showed that HTLV-4 may be distinct from HTLV-1, HTLV-2, and HTLV-3, and their simian counterparts, STLV-1, STLV-2, and STLV-3, respectively. Analysis of full-length genomes can provide basic information on the evolutionary history and replication and pathogenic potential of new viruses.

resultsWe report here the first complete HTLV-4 sequence obtained by PCR-based genome walking using uncultured peripheral blood lymphocyte DNA from an HTLV-4-infected person. The HTLV-4(1863LE) genome is 8791-bp long and is equidistant from HTLV-1, HTLV-2, and HTLV-3 sharing only 62-71% nucleotide identity. HTLV-4 has a prototypic genomic structure with all enzymatic, regulatory, and structural proteins preserved. Like STLV-2, STLV-3, and HTLV-3, HTLV-4 is missing a third 21-bp transcription element found in the long terminal repeats of HTLV-1 and HTLV-2 but instead contains unique c-Myb and pre B-cell leukemic transcription factor binding sites. Like HTLV-2, the PDZ motif important for cellular signal transduction and transformation in HTLV-1 and HTLV-3 is missing in the C-terminus of the HTLV-4 Tax protein. A basic leucine zipper (b-ZIP) region located in the antisense strand of HTLV-1 and believed to play a role in viral replication and oncogenesis, was also found in the complementary strand of HTLV-4. Detailed phylogenetic analysis shows that HTLV-4 is clearly a monophyletic viral group. Dating using a relaxed molecular clock inferred that the most recent common ancestor of HTLV-4 and HTLV-2/STLV-2 occurred 49,800 to 378,000 years ago making this the oldest known PTLV lineage. Interestingly, this period coincides with the emergence of Homo sapiens sapiens during the Middle Pleistocene suggesting that early humans may have been susceptible hosts for the ancestral HTLV-4.

conclusionThe inferred ancient origin of HTLV-4 coinciding with the appearance of Homo sapiens, the propensity of STLVs to cross-species into humans, the fact that HTLV-1 and -2 spread globally following migrations of ancient populations, all suggest that HTLV-4 may be prevalent. Expanded surveillance and clinical studies are needed to better define the epidemiology and public health importance of HTLV-4 infection.

Indexed as

Evolution, MolecularAmino Acid SequenceBase SequenceCell LineDeltaretrovirusGenome, ViralHumansMolecular Sequence DataPhylogenySequence Homology, Amino AcidTerminal Repeat SequencesViral ProteinsViral Proteins

Identifiers

PMID19187529
PMCPMC2647524
OpenAlexW1991302498

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.