Evidence map›Paper›PMID 9188555›Full record

ArticleJournal of virology1997

Localized sequence heterogeneity in the long terminal repeats of in vivo isolates of equine infectious anemia virus.

W Maury, S Perryman, J L Oaks, B K Seid, T Crawford, T McGuire, S Carpenter

Open access · bronzeAbstract read
In one paragraph

Article in Journal of virology, 1997. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.0field-weighted citation impact, top 25% 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

11 citing papers in PubMed, 35 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
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

7 authors at 1 institution in 1 country.

W MauryDepartment of Microbiology, University of South Dakota, Vermillion 57069, USA. wmaury@charlie.usd.edu
S Perryman
J L Oaks
B K Seid
T Crawford
T McGuire
S Carpenter
University of South Dakota · US

Funding

VACCINE FOR EQUINE INFECTIOUS ANEMIA VIRUS VARIANTSR01AI024291 · NIAID · WASHINGTON STATE UNIVERSITY · PI MCGUIRE, TRAVIS C. · 1986 to 2002
$726k
LTR VARIATION REGULATES EIA EXPRESSION IN MACROPHAGESR29CA072063 · NCI · UNIVERSITY OF SOUTH DAKOTA · PI MAURY, WENDY JEAN · 1996 to 2000
$197k
BIOLOGICAL VARIATION OF EQUINE INFECTIOUS ANEMIA VIRUSR01AI030025 · NIAID · IOWA STATE UNIVERSITY · PI CARPENTER, SUSAN L · 1991 to 1993
–
NCI NIH HHS CA72063NIAID NIH HHS AI24291NIAID NIH HHS AI30025
6 · The paper itself

Abstract

The role of in vivo long terminal repeat (LTR) sequence variation of the lentivirus equine infectious anemia virus (EIAV) has not been explored. In this study, we investigated the heterogeneity found in the LTR sequences from seven EIAV-seropositive horses: three horses with clinical disease and four horses without any detectable signs of disease. LTR sequences were targeted in this study because the LTR U3 enhancer region of tissue culture-derived isolates has been identified as one of the few hypervariable regions of the EIAV genome. Furthermore, LTR variation may regulate EIAV expression in vivo. Both intra- and interanimal sequence variations were investigated. The intra-animal variation was low in seropositive, healthy horses (on average 0.44%). Intra-animal variation was consistently higher in clinically ill horses (0.99%), suggesting that greater numbers of quasispecies of EIAV are present when active virus replication is ongoing. Interanimal comparisons of consensus sequences generated from each horse demonstrated that the enhancer region is a hotspot of sequence variation in vivo. Thirty-seven of the 83 nucleotides that compose the U3 enhancer region were variable between the different in vivo-derived LTRs. The remainder of the LTR that was analyzed was more conserved, 8 of 195 nucleotide positions being variable. Results of electrophoretic mobility shift assays demonstrated that some nucleotide substitutions that occurred in the enhancer region eliminated or altered transcription factor binding motifs that are known to be important for EIAV LTR expression. These data suggested that the selective pressures exerted on the EIAV LTR enhancer sequences are different from those exerted on the remainder of the LTR. Our findings are consistent with the possibility that enhancer sequence hypervariability can alter expression of the virus in tissue macrophages and therefore contribute to clinical disease in infected horses.

Indexed as

Genetic VariationRepetitive Sequences, Nucleic AcidAnimalsBase SequenceBinding SitesDNA, ViralEnhancer Elements, GeneticEquine Infectious AnemiaGenetic HeterogeneityHorsesMolecular Sequence DataPolymerase Chain ReactionSequence Homology, Nucleic AcidTranscription FactorsDNA, ViralTranscription Factors

Identifiers

PMID9188555
PMCPMC191723
OpenAlexW2096607681

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.