Evidence map›Paper›PMID 16940499›Full record

ArticleJournal of virology2006

Phylogenetic analysis of polyomavirus BK sequences.

Preety M Sharma, Gaurav Gupta, Abhay Vats, Ron Shapiro, Parmjeet Randhawa

Erratum issuedOpen access · greenAbstract read
In one paragraph

Article in Journal of virology, 2006. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
1.7field-weighted citation impact, top 17% 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

26 citing papers in PubMed, 62 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Review
  7. Observational
  8. Article
  9. Polyoma virus nephropathy in kidney transplantation.World journal of transplantation · 2017
    Review
  10. Review
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Review
  18. BK polyomavirus: emerging pathogen.Microbes and infection · 2012
    Review
  19. Article
  20. Article
4 · The record

Corrections and comments

  • Erratum issued
5 · Who and what money

Authors and funding

5 authors at 2 institutions in 1 country.

Preety M SharmaDivision of Transplant Pathology, E737 UPMC-Montefiore Hospital, 3459 Fifth Ave., Pittsburgh, PA 15213, USA.
Gaurav Gupta
Abhay Vats
Ron Shapiro
Parmjeet Randhawa
Children's Hospital of Pittsburgh · USUniversity of Pittsburgh Medical Center · US

Funding

Polyomavirus Infection after Kidney TransplantationR01AI051227 · NIAID · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI RANDHAWA, PARMJEET S · 2003 to 2011
$2.3M
Immune Response to Polyomavirus InfectionR01AI063360 · NIAID · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI RANDHAWA, PARMJEET S · 2006 to 2010
$2.0M
Biomarkers Based Studies of PolyomavirusesR01AI060602 · NIAID · CHILDREN'S HOSP PITTSBURGH/UPMC HLTH SYS · PI VATS, ABHAY N. · 2004 to 2008
$1.7M
Immune Response to Polyomavirus InfectionR56AI063360 · NIAID · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI RANDHAWA, PARMJEET S, VISCIDI, RAPHAEL PAUL · 2012 to 2012
$379k
NIAID NIH HHS AI 060602NIAID NIH HHS AI 063360NIAID NIH HHS R01 AI051227NIAID NIH HHS R01 AI060602NIAID NIH HHS R01 AI063360NIAID NIH HHS R01 AI 51227-01NIAID NIH HHS R56 AI063360
6 · The paper itself

Abstract

Polyomavirus BK (BKV) has emerged as an important pathogen in kidney transplant patients. Existing taxonomic classifications of BKV come from conventional DNA sequence alignments based on limited data derived from the VP1 gene. We have used a phylogenetic whole-genome approach to examine the pattern of diversity and evolutionary relationships between 45 BKV strains isolated from multiple clinical settings. This analysis supports the classification of BKV into six genotypes, of which types V and VI have not been previously recognized. BKV strains hitherto classified as type I are, in fact, quite heterogeneous, and several cluster with our newly defined genotypes V and VI. The sequence information needed for assigning genotypes can be captured by VP1, VP2, VP3, or large T-gene sequencing. The most polymorphic coding region in the viral genome is VP1, but significant variation is also present in the large T-antigen gene, wherein polymorphisms are found in 11.39% of all nucleotide sites, 46.22% of which are cluster specific. Type-specific amino acid changes within the VP1 region are predicted to map to the BC and DE loops. The number of taxonomically informative amino acid changes in the large T antigen exceeds even that of the VP1 region. Viral strains isolated from healthy subjects and from patients with human immunodeficiency virus infection, Wiskott-Aldrich syndrome, and vasculopathy with capillary leak syndrome formed distinct subclusters. However, within the kidney transplant population, BKV strains derived from patients with asymptomatic viruria did not show complete separation from strains associated with allograft nephropathy.

Indexed as

Antigens, Viral, TumorBK VirusCluster AnalysisGenomeGenome, ViralGenotypeHumansKidneyKidney TransplantationPhylogenyPolymerase Chain ReactionPolymorphism, GeneticPolyomavirus InfectionsSequence Analysis, DNAAntigens, Viral, Tumor

Identifiers

PMID16940499
PMCPMC1563921
OpenAlexW2027849233

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.