Evidence map›Paper›PMID 33827948›Full record

ArticleJournal of virology2021

Amin Addetia, Quynh Phung, Benjamin T Bradley, Michelle J Lin, Haiying Zhu, Hong Xie, Meei-Li Huang, Alexander L Greninger

Open access · hybridAbstract read
In one paragraph

Article in Journal of virology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
0.9field-weighted citation impact, top 23% 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

10 citing papers in PubMed, 14 citations in OpenAlex.

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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

8 authors at 1 institution in 1 country.

Amin Addetia *Department of Laboratory Medicine and Pathology, University of Washington, Seattle, Washington, USA.
Quynh Phung *Department of Laboratory Medicine and Pathology, University of Washington, Seattle, Washington, USA.
Benjamin T BradleyDepartment of Laboratory Medicine and Pathology, University of Washington, Seattle, Washington, USA.
Michelle J LinDepartment of Laboratory Medicine and Pathology, University of Washington, Seattle, Washington, USA.
Haiying ZhuDepartment of Laboratory Medicine and Pathology, University of Washington, Seattle, Washington, USA.
Hong XieDepartment of Laboratory Medicine and Pathology, University of Washington, Seattle, Washington, USA.
Meei-Li HuangDepartment of Laboratory Medicine and Pathology, University of Washington, Seattle, Washington, USA.
Alexander L GreningerDepartment of Laboratory Medicine and Pathology, University of Washington, Seattle, Washington, USA agrening@uw.edu.ORCID 0000-0002-7443-0527
University of Washington · US

Funding

Fragment Size-Based Pathogen Enrichment in cfDNAR21AI153581 · NIAID · UNIVERSITY OF WASHINGTON · PI GRENINGER, ALEXANDER L · 2020 to 2021
$428k
NIAID NIH HHS R21 AI153581
6 · The paper itself

Abstract

Defective viral genomes (DVGs) are parasitic viral sequences containing point mutations, deletions, or duplications that might interfere with replication. DVGs are often associated with viral passage at high multiplicities of infection in culture systems but have been increasingly reported in clinical specimens. To date however, only RNA viruses have been shown to contain DVGs in clinical specimens. Here, using direct deep sequencing with multiple library preparation strategies and confirmatory digital droplet PCR (ddPCR) of urine samples taken from immunosuppressed individuals, we show that clinical BK polyomavirus (BKPyV) and JC polyomavirus (JCPyV) strains contain widespread genomic rearrangements across multiple loci that likely interfere with viral replication. BKPyV DVGs were derived from BKPyV genotypes Ia, Ib-1, and Ic. The presence of DVGs was associated with specimens containing higher viral loads but never reached clonality, consistent with a model of parasitized replication. These DVGs persisted during clinical infection as evidenced in two separate pairs of samples containing BK virus collected from the same individual up to 302 days apart. In a separate individual, we observed the generation of DVGs after a 57.5-fold increase in viral load. In summary, by extending the presence of DVGs in clinical specimens to DNA viruses, we demonstrate the ubiquity of DVGs in clinical virology.

Indexed as

Genome, ViralBK VirusFemaleGene RearrangementHumansImmunocompromised HostJC VirusMaleMiddle AgedMutationPolyomavirus InfectionsSequence DeletionTumor Virus InfectionsUrineViral LoadVirus ReplicationBK virusddPCRdefectivedefective interfering genomedefective interfering particledefective viral genomeDNA virusJC viruspolyomavirusrearrangement

Identifiers

PMID33827948
PMCPMC8316075
OpenAlexW3130574797

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.