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Small RNA profiling of low biomass samples: identification and removal of contaminants

BACKGROUND: Sequencing-based analyses of low-biomass samples are known to be prone to misinterpretation due to the potential presence of contaminating molecules derived from laboratory reagents and environments. DNA contamination has been previously reported, yet contamination with RNA is usually co...

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Autores principales: Heintz-Buschart, Anna, Yusuf, Dilmurat, Kaysen, Anne, Etheridge, Alton, Fritz, Joëlle V., May, Patrick, de Beaufort, Carine, Upadhyaya, Bimal B., Ghosal, Anubrata, Galas, David J., Wilmes, Paul
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5952572/
https://www.ncbi.nlm.nih.gov/pubmed/29759067
http://dx.doi.org/10.1186/s12915-018-0522-7
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author Heintz-Buschart, Anna
Yusuf, Dilmurat
Kaysen, Anne
Etheridge, Alton
Fritz, Joëlle V.
May, Patrick
de Beaufort, Carine
Upadhyaya, Bimal B.
Ghosal, Anubrata
Galas, David J.
Wilmes, Paul
author_facet Heintz-Buschart, Anna
Yusuf, Dilmurat
Kaysen, Anne
Etheridge, Alton
Fritz, Joëlle V.
May, Patrick
de Beaufort, Carine
Upadhyaya, Bimal B.
Ghosal, Anubrata
Galas, David J.
Wilmes, Paul
author_sort Heintz-Buschart, Anna
collection PubMed
description BACKGROUND: Sequencing-based analyses of low-biomass samples are known to be prone to misinterpretation due to the potential presence of contaminating molecules derived from laboratory reagents and environments. DNA contamination has been previously reported, yet contamination with RNA is usually considered to be very unlikely due to its inherent instability. Small RNAs (sRNAs) identified in tissues and bodily fluids, such as blood plasma, have implications for physiology and pathology, and therefore the potential to act as disease biomarkers. Thus, the possibility for RNA contaminants demands careful evaluation. RESULTS: Herein, we report on the presence of small RNA (sRNA) contaminants in widely used microRNA extraction kits and propose an approach for their depletion. We sequenced sRNAs extracted from human plasma samples and detected important levels of non-human (exogenous) sequences whose source could be traced to the microRNA extraction columns through a careful qPCR-based analysis of several laboratory reagents. Furthermore, we also detected the presence of artefactual sequences related to these contaminants in a range of published datasets, thereby arguing in particular for a re-evaluation of reports suggesting the presence of exogenous RNAs of microbial and dietary origin in blood plasma. To avoid artefacts in future experiments, we also devise several protocols for the removal of contaminant RNAs, define minimal amounts of starting material for artefact-free analyses, and confirm the reduction of contaminant levels for identification of bona fide sequences using ‘ultra-clean’ extraction kits. CONCLUSION: This is the first report on the presence of RNA molecules as contaminants in RNA extraction kits. The described protocols should be applied in the future to avoid confounding sRNA studies. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12915-018-0522-7) contains supplementary material, which is available to authorized users.
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spelling pubmed-59525722018-05-21 Small RNA profiling of low biomass samples: identification and removal of contaminants Heintz-Buschart, Anna Yusuf, Dilmurat Kaysen, Anne Etheridge, Alton Fritz, Joëlle V. May, Patrick de Beaufort, Carine Upadhyaya, Bimal B. Ghosal, Anubrata Galas, David J. Wilmes, Paul BMC Biol Research Article BACKGROUND: Sequencing-based analyses of low-biomass samples are known to be prone to misinterpretation due to the potential presence of contaminating molecules derived from laboratory reagents and environments. DNA contamination has been previously reported, yet contamination with RNA is usually considered to be very unlikely due to its inherent instability. Small RNAs (sRNAs) identified in tissues and bodily fluids, such as blood plasma, have implications for physiology and pathology, and therefore the potential to act as disease biomarkers. Thus, the possibility for RNA contaminants demands careful evaluation. RESULTS: Herein, we report on the presence of small RNA (sRNA) contaminants in widely used microRNA extraction kits and propose an approach for their depletion. We sequenced sRNAs extracted from human plasma samples and detected important levels of non-human (exogenous) sequences whose source could be traced to the microRNA extraction columns through a careful qPCR-based analysis of several laboratory reagents. Furthermore, we also detected the presence of artefactual sequences related to these contaminants in a range of published datasets, thereby arguing in particular for a re-evaluation of reports suggesting the presence of exogenous RNAs of microbial and dietary origin in blood plasma. To avoid artefacts in future experiments, we also devise several protocols for the removal of contaminant RNAs, define minimal amounts of starting material for artefact-free analyses, and confirm the reduction of contaminant levels for identification of bona fide sequences using ‘ultra-clean’ extraction kits. CONCLUSION: This is the first report on the presence of RNA molecules as contaminants in RNA extraction kits. The described protocols should be applied in the future to avoid confounding sRNA studies. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12915-018-0522-7) contains supplementary material, which is available to authorized users. BioMed Central 2018-05-14 /pmc/articles/PMC5952572/ /pubmed/29759067 http://dx.doi.org/10.1186/s12915-018-0522-7 Text en © Wilmes et al. 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Heintz-Buschart, Anna
Yusuf, Dilmurat
Kaysen, Anne
Etheridge, Alton
Fritz, Joëlle V.
May, Patrick
de Beaufort, Carine
Upadhyaya, Bimal B.
Ghosal, Anubrata
Galas, David J.
Wilmes, Paul
Small RNA profiling of low biomass samples: identification and removal of contaminants
title Small RNA profiling of low biomass samples: identification and removal of contaminants
title_full Small RNA profiling of low biomass samples: identification and removal of contaminants
title_fullStr Small RNA profiling of low biomass samples: identification and removal of contaminants
title_full_unstemmed Small RNA profiling of low biomass samples: identification and removal of contaminants
title_short Small RNA profiling of low biomass samples: identification and removal of contaminants
title_sort small rna profiling of low biomass samples: identification and removal of contaminants
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5952572/
https://www.ncbi.nlm.nih.gov/pubmed/29759067
http://dx.doi.org/10.1186/s12915-018-0522-7
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