Evidence map›Paper›PMID 18712842›Full record

ArticleJournal of medical virology2008

Biologic diversity of polyomavirus BK genomic sequences: Implications for molecular diagnostic laboratories.

C Luo, M Bueno, J Kant, P Randhawa

Open access · greenAbstract read
In one paragraph

Article in Journal of medical virology, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.7field-weighted citation impact, top 28% 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

7 citing papers in PubMed, 26 citations in OpenAlex.

  1. Trial
  2. Review
  3. Neutralizing Antibody-Mediated Response and Risk of BK Virus-Associated Nephropathy.Journal of the American Society of Nephrology : JASN · 2018
    Article
  4. Commercially available immunoglobulins contain virus neutralizing antibodies against all major genotypes of polyomavirus BK.American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons · 2015
    Article
  5. Article
  6. Review
  7. 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

4 authors at 1 institution in 1 country.

C LuoDepartment of Pathology, University of Pittsburgh, Pittsburgh, Pennsylvania 15213, USA.
M Bueno
J Kant
P Randhawa
University of Pittsburgh · 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
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 R01 AI051227NIAID NIH HHS R01 AI063360NIAID NIH HHS R01 AI 51227NIAID NIH HHS R01 AI 63360NIAID NIH HHS R56 AI063360
6 · The paper itself

Abstract

Data on polyomavirus genomic diversity has greatly expanded in the past few years. The implications of viral DNA sequence variation on the performance of molecular diagnostic assays have not been systematically examined. 716 BK, 1626 JC, and 73 SV40 virus sequences available in GenBank were aligned using Clustal-X. Five different published BKV PCR assays currently in use at major medical centers were evaluated for primer and probe mismatches with available GenBank sequences. Coverage of naturally occurring BKV strains varied amongst different assay methods. Targeted viral sequences showed major mismatch with primer or probe sequence in up to 30.7% of known BKV strains. BKV subtypes IVa, IVb, and IVc were more prone to this problem, reflecting common use of Type I Dun sequence for assay design. Despite the known polymorphism of this gene, 484 VP-1 sequences with conserved areas potentially suitable for PCR assay design are available. Assay targets in the Large T-antigen and agnogene are less subject to genetic variation, but sequence information corresponding to the latter two genes is available only for 164 and 174 published strains, respectively. Cross reactivity of appropriately selected BKV primers with JCV and SV40 sequences available in current databases was not a significant problem.

Indexed as

Polymorphism, GeneticAdolescentAdultAgedAged, 80 and overAntigens, Polyomavirus TransformingBase SequenceBK VirusCapsid ProteinsDNA PrimersFemaleGenome, ViralHumansMaleMiddle AgedPolymerase Chain Reactionagnoprotein, polyomavirusAntigens, Polyomavirus TransformingCapsid ProteinsDNA PrimersViral Regulatory and Accessory ProteinsViroporin ProteinsVP1 protein, polyomavirus

Identifiers

PMID18712842
PMCPMC2906129
OpenAlexW2031965975

What OpenQuestion holds

Textmetadata
LicenceTDM
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.