001     140475
005     20240501120108.0
024 7 _ |a 10.1038/s41598-019-38733-1
|2 doi
024 7 _ |a pmid:30733546
|2 pmid
024 7 _ |a pmc:PMC6367390
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037 _ _ |a DZNE-2020-06797
041 _ _ |a English
082 _ _ |a 600
100 1 _ |a Wally, N.
|b 0
245 _ _ |a Plasmid DNA contaminant in molecular reagents.
260 _ _ |a [London]
|c 2019
|b Macmillan Publishers Limited, part of Springer Nature
264 _ 1 |3 online
|2 Crossref
|b Society for Mining, Metallurgy and Exploration Inc.
|c 2019-02-07
264 _ 1 |3 print
|2 Crossref
|b Society for Mining, Metallurgy and Exploration Inc.
|c 2019-12-01
336 7 _ |a article
|2 DRIVER
336 7 _ |a Output Types/Journal article
|2 DataCite
336 7 _ |a Journal Article
|b journal
|m journal
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|s 1714473742_8221
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336 7 _ |a ARTICLE
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336 7 _ |a JOURNAL_ARTICLE
|2 ORCID
336 7 _ |a Journal Article
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|2 EndNote
520 _ _ |a 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.
536 _ _ |a 342 - Disease Mechanisms and Model Systems (POF3-342)
|0 G:(DE-HGF)POF3-342
|c POF3-342
|f POF III
|x 0
542 _ _ |i 2019-02-07
|2 Crossref
|u https://creativecommons.org/licenses/by/4.0
588 _ _ |a Dataset connected to CrossRef, PubMed,
650 _ 2 |a Computational Biology
|2 MeSH
650 _ 2 |a DNA Contamination
|2 MeSH
650 _ 2 |a DNA, Viral: analysis
|2 MeSH
650 _ 2 |a DNA, Viral: genetics
|2 MeSH
650 _ 2 |a Diagnostic Errors: prevention & control
|2 MeSH
650 _ 2 |a Genes, pol: genetics
|2 MeSH
650 _ 2 |a High-Throughput Nucleotide Sequencing
|2 MeSH
650 _ 2 |a Humans
|2 MeSH
650 _ 2 |a Indicators and Reagents: analysis
|2 MeSH
650 _ 2 |a Infectious Anemia Virus, Equine: genetics
|2 MeSH
650 _ 2 |a Metagenomics
|2 MeSH
650 _ 2 |a Plasmids: analysis
|2 MeSH
650 _ 2 |a Plasmids: genetics
|2 MeSH
650 _ 2 |a Retrospective Studies
|2 MeSH
650 _ 2 |a Sequence Analysis, DNA: methods
|2 MeSH
700 1 _ |a Schneider, M.
|b 1
700 1 _ |a Thannesberger, J.
|b 2
700 1 _ |a Kastner, M. T.
|b 3
700 1 _ |a Bakonyi, T.
|b 4
700 1 _ |a Indik, S.
|b 5
700 1 _ |a Rattei, T.
|b 6
700 1 _ |a Bedarf, J.
|0 P:(DE-2719)2811747
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700 1 _ |a Hildebrand, F.
|b 8
700 1 _ |a Law, J.
|b 9
700 1 _ |a Jovel, J.
|b 10
700 1 _ |a Steininger, C.
|0 P:(DE-HGF)0
|b 11
|e Corresponding author
773 1 8 |a 10.1038/s41598-019-38733-1
|b : Society for Mining, Metallurgy and Exploration Inc., 2019-02-07
|n 1
|p 1652
|3 journal-article
|2 Crossref
|t Scientific Reports
|v 9
|y 2019
|x 2045-2322
773 _ _ |a 10.1038/s41598-019-38733-1
|g Vol. 9, no. 1, p. 1652
|0 PERI:(DE-600)2615211-3
|n 1
|q 9:1<1652
|p 1652
|t Scientific reports
|v 9
|y 2019
|x 2045-2322
856 4 _ |y OpenAccess
|u https://pub.dzne.de/record/140475/files/DZNE-2020-06797.pdf
856 4 _ |y OpenAccess
|x pdfa
|u https://pub.dzne.de/record/140475/files/DZNE-2020-06797.pdf?subformat=pdfa
856 7 _ |2 Pubmed Central
|u http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6367390
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910 1 _ |a Deutsches Zentrum für Neurodegenerative Erkrankungen
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913 1 _ |a DE-HGF
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|0 G:(DE-HGF)POF3-342
|3 G:(DE-HGF)POF3
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|v Disease Mechanisms and Model Systems
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914 1 _ |y 2019
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LibraryCollectionCLSMajorCLSMinorLanguageAuthor
Marc 21