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High-throughput sequencing for species authentication and contamination detection of 63 cell lines
Cell lines are widely used in research and for diagnostic tests and are often shared between laboratories. Lack of cell line authentication can result in the use of contaminated or misidentified cell lines, potentially affecting the results from research and diagnostic activities. Cell line authenti...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8569163/ https://www.ncbi.nlm.nih.gov/pubmed/34737324 http://dx.doi.org/10.1038/s41598-021-00779-5 |
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author | Lung, Oliver Candlish, Rebecca Nebroski, Michelle Kruckiewicz, Peter Buchanan, Cody Moniwa, Mariko |
author_facet | Lung, Oliver Candlish, Rebecca Nebroski, Michelle Kruckiewicz, Peter Buchanan, Cody Moniwa, Mariko |
author_sort | Lung, Oliver |
collection | PubMed |
description | Cell lines are widely used in research and for diagnostic tests and are often shared between laboratories. Lack of cell line authentication can result in the use of contaminated or misidentified cell lines, potentially affecting the results from research and diagnostic activities. Cell line authentication and contamination detection based on metagenomic high-throughput sequencing (HTS) was tested on DNA and RNA from 63 cell lines available at the Canadian Food Inspection Agency’s National Centre for Foreign Animal Disease. Through sequence comparison of the cytochrome c oxidase subunit 1 (COX1) gene, the species identity of 53 cell lines was confirmed, and eight cell lines were found to show a greater pairwise nucleotide identity in the COX1 sequence of a different species within the same expected genus. Two cell lines, LFBK-αvβ6 and SCP-HS, were determined to be composed of cells from a different species and genus. Mycoplasma contamination was not detected in any cell lines. However, several expected and unexpected viral sequences were detected, including part of the classical swine fever virus genome in the IB-RS-2 Clone D10 cell line. Metagenomics-based HTS is a useful laboratory QA tool for cell line authentication and contamination detection that should be conducted regularly. |
format | Online Article Text |
id | pubmed-8569163 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-85691632021-11-05 High-throughput sequencing for species authentication and contamination detection of 63 cell lines Lung, Oliver Candlish, Rebecca Nebroski, Michelle Kruckiewicz, Peter Buchanan, Cody Moniwa, Mariko Sci Rep Article Cell lines are widely used in research and for diagnostic tests and are often shared between laboratories. Lack of cell line authentication can result in the use of contaminated or misidentified cell lines, potentially affecting the results from research and diagnostic activities. Cell line authentication and contamination detection based on metagenomic high-throughput sequencing (HTS) was tested on DNA and RNA from 63 cell lines available at the Canadian Food Inspection Agency’s National Centre for Foreign Animal Disease. Through sequence comparison of the cytochrome c oxidase subunit 1 (COX1) gene, the species identity of 53 cell lines was confirmed, and eight cell lines were found to show a greater pairwise nucleotide identity in the COX1 sequence of a different species within the same expected genus. Two cell lines, LFBK-αvβ6 and SCP-HS, were determined to be composed of cells from a different species and genus. Mycoplasma contamination was not detected in any cell lines. However, several expected and unexpected viral sequences were detected, including part of the classical swine fever virus genome in the IB-RS-2 Clone D10 cell line. Metagenomics-based HTS is a useful laboratory QA tool for cell line authentication and contamination detection that should be conducted regularly. Nature Publishing Group UK 2021-11-04 /pmc/articles/PMC8569163/ /pubmed/34737324 http://dx.doi.org/10.1038/s41598-021-00779-5 Text en © Crown 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Lung, Oliver Candlish, Rebecca Nebroski, Michelle Kruckiewicz, Peter Buchanan, Cody Moniwa, Mariko High-throughput sequencing for species authentication and contamination detection of 63 cell lines |
title | High-throughput sequencing for species authentication and contamination detection of 63 cell lines |
title_full | High-throughput sequencing for species authentication and contamination detection of 63 cell lines |
title_fullStr | High-throughput sequencing for species authentication and contamination detection of 63 cell lines |
title_full_unstemmed | High-throughput sequencing for species authentication and contamination detection of 63 cell lines |
title_short | High-throughput sequencing for species authentication and contamination detection of 63 cell lines |
title_sort | high-throughput sequencing for species authentication and contamination detection of 63 cell lines |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8569163/ https://www.ncbi.nlm.nih.gov/pubmed/34737324 http://dx.doi.org/10.1038/s41598-021-00779-5 |
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