Evidence map›Paper›PMID 30733546›Full record

ArticleScientific reports2019

Plasmid DNA contaminant in molecular reagents.

N Wally, M Schneider, J Thannesberger, M T Kastner, T Bakonyi, S Indik, T Rattei, J Bedarf, F Hildebrand, J Law and 2 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed, 2 pooled it
1.7field-weighted citation impact, top 16% 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

17 citing papers in PubMed, 2 syntheses or guidelines pooled it, 26 citations in OpenAlex.

  1. Pooled it
  2. Towards an understanding of the avian virome.The Journal of general virology · 2020
    Pooled it
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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

12 authors at 6 institutions in 3 countries.

N WallyDivision of Infectious Diseases, Department of Medicine 1, Medical University of Vienna, Vienna, Austria.ORCID 0000-0003-2573-8530
M SchneiderDivision of Infectious Diseases, Department of Medicine 1, Medical University of Vienna, Vienna, Austria.
J ThannesbergerDivision of Infectious Diseases, Department of Medicine 1, Medical University of Vienna, Vienna, Austria.
M T KastnerDivision of Infectious Diseases, Department of Medicine 1, Medical University of Vienna, Vienna, Austria.
T BakonyiUniversity of Veterinary Medicine, Department of Virology, Vienna, Austria.
S IndikUniversity of Veterinary Medicine, Department of Virology, Vienna, Austria.
T RatteiCUBE-Division of Computational Systems Biology, Department of Microbiology and Ecosystem Science, University of Vienna, Vienna, Austria.ORCID 0000-0002-0592-7791
J BedarfGerman Centre for neurodegenerative disease research (DZNE), Department of Neurology, University of Bonn, Bonn, Germany.
F HildebrandEuropean Molecular Biology Laboratory, EMBL, Heidelberg, Germany.ORCID 0000-0002-0078-8948
J LawDepartment of Medicine, University of Alberta, Edmonton, Alberta, Canada.
J JovelDepartment of Medicine, University of Alberta, Edmonton, Alberta, Canada.
C SteiningerDivision of Infectious Diseases, Department of Medicine 1, Medical University of Vienna, Vienna, Austria. christoph.steininger@meduniwien.ac.at.ORCID 0000-0003-3500-7205
Medical University of Vienna · ATUniversity of Alberta · CAUniversity of Veterinary Medicine Vienna · ATEuropean Molecular Biology Laboratory · DEUniversity of Bonn · DEUniversity of Vienna · AT

Funding

Austrian Science Fund FWF P 25353Austrian Science Fund FWF P 28102
6 · The paper itself

Abstract

Background noise in metagenomic studies is often of high importance and its removal requires extensive post-analytic, bioinformatics filtering. This is relevant as significant signals may be lost due to a low signal-to-noise ratio. The presence of plasmid residues, that are frequently present in reagents as contaminants, has not been investigated so far, but may pose a substantial bias. Here we show that plasmid sequences from different sources are omnipresent in molecular biology reagents. Using a metagenomic approach, we identified the presence of the (pol) of equine infectious anemia virus in human samples and traced it back to the expression plasmid used for generation of a commercial reverse transcriptase. We found fragments of multiple other expression plasmids in human samples as well as commercial polymerase preparations. Plasmid contamination sources included production chain of molecular biology reagents as well as contamination of reagents from environment or human handling of samples and reagents. Retrospective analyses of published metagenomic studies revealed an inaccurate signal-to-noise differentiation. Hence, the plasmid sequences that seem to be omnipresent in molecular biology reagents may misguide conclusions derived from genomic/metagenomics datasets and thus also clinical interpretations. Critical appraisal of metagenomic data sets for the possibility of plasmid background noise is required to identify reliable and significant signals.

Indexed as

DNA ContaminationMetagenomicsComputational BiologyDiagnostic ErrorsDNA, ViralGenes, polHigh-Throughput Nucleotide SequencingHumansIndicators and ReagentsInfectious Anemia Virus, EquinePlasmidsRetrospective StudiesSequence Analysis, DNADNA, ViralIndicators and Reagents

Identifiers

PMID30733546
PMCPMC6367390
OpenAlexW2912851663

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.