Evidence map›Paper›PMID 20869740›Full record

ArticleVirology2010

A system for the analysis of BKV non-coding control regions: application to clinical isolates from an HIV/AIDS patient.

Nicole M Broekema, Johanna R Abend, Shauna M Bennett, Janet S Butel, John A Vanchiere, Michael J Imperiale

Abstract readEvaluation Study
In one paragraph

Article in Virology, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.1field-weighted citation impact, top 24% 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

16 citing papers in PubMed, 29 citations in OpenAlex.

  1. Article
  2. Article
  3. BK polyomavirus: latency, reactivation, diseases and tumorigenesis.Frontiers in cellular and infection microbiology · 2023
    Review
  4. Article
  5. Article
  6. Biology of Polyomavirus miRNA.Frontiers in microbiology · 2021
    Review
  7. Article
  8. Article
  9. Article
  10. Review
  11. Review
  12. Article
  13. miRNA regulation of BK polyomavirus replication during early infection.Proceedings of the National Academy of Sciences of the United States of America · 2013
    Article
  14. BK polyomavirus: emerging pathogen.Microbes and infection · 2012
    Review
  15. Article
  16. 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

6 authors at 3 institutions in 1 country.

Nicole M BroekemaDepartment of Microbiology and Immunology, University of Michigan Medical School, Ann Arbor, MI 48109-5620, USA. broekenm@umich.edu
Johanna R Abend
Shauna M Bennett
Janet S Butel
John A Vanchiere
Michael J Imperiale
University of Michigan · USBaylor College of Medicine · USLouisiana State University Health Sciences Center Shreveport · US

Funding

XenograftP30CA046592 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI THEODORE S LAWRENCE · 1988 to 2026
$178.2M
PREDOCTORAL TRAINING IN GENETICST32GM007544 · NIGMS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI MORAN, JOHN V. · 1985 to 2022
$11.3M
Parameters Governing Kidney Cell Infection with BKVR01AI060584 · NIAID · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI IMPERIALE, MICHAEL J. · 2004 to 2020
$4.8M
SV40 Pathogenesis of Human InfectionsR01CA104818 · NCI · BAYLOR COLLEGE OF MEDICINE · PI BUTEL, JANET S · 2004 to 2008
$2.4M
The Role of Polyomaviruses in Pediatric Renal DiseasesK08DK062090 · NIDDK · BAYLOR COLLEGE OF MEDICINE · PI VANCHIERE, JOHN ANTHONY · 2002 to 2006
$603k
NCI NIH HHS CA046592NCI NIH HHS CA 104818NCI NIH HHS P30 CA046592NCI NIH HHS R01 CA104818NIAID NIH HHS AI060584NIAID NIH HHS R01 AI060584NIDDK NIH HHS DK62090NIDDK NIH HHS K08 DK062090NIGMS NIH HHS T32 GM007544NIGMS NIH HHS T32-GM07544
6 · The paper itself

Abstract

The human polyomavirus BK virus (BKV) is an important opportunistic pathogen whose disease prevalence continues to increase with the growing immunocompromised population. To date, the major determinant of replication in cell culture has not been formally proven. BKV exists as archetype virus and rearranged variants, which are classified based on the DNA sequence of their non-coding control regions (NCCRs). The archetype BKV NCCR is divided into five blocks of sequence and rearranged variants contain deletions and duplications of these blocks. In this study, a genetic system was developed and used to identify the major determinant of replication ability in primary renal proximal tubule epithelial cells, the natural host cell of BKV. This system was also used to analyze NCCR variants isolated from an immunocompromised patient which contain assorted rearrangement patterns and functional differences. This study solidifies the NCCR as the major genetic determinant of BKV replication ability in vitro.

Indexed as

Genetic VariationAIDS-Related Opportunistic InfectionsBK VirusCells, CulturedDNA, ViralEpithelial CellsHIV InfectionsHumansImmunocompromised HostKidney Tubules, ProximalPolyomavirus InfectionsRegulatory Sequences, Nucleic AcidSequence Analysis, DNATumor Virus InfectionsUrineVirologyDNA, Viral

Identifiers

PMID20869740
PMCPMC2957895
OpenAlexW2021048255

What OpenQuestion holds

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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.