Evaluation of mycoplasma removal reagents using qPCR-based quantification

In this study, we evaluated the efficacy of various mycoplasma removal reagents using nuclear staining, DNA gel electrophoresis, and qPCR-based quantification. Our results showed Plasmocure and Plasmocin are two effective anti-mycoplasma reagents whose effects can be observed within a week. However,...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Analytical biochemistry 2019-01, Vol.564-565, p.88-95
Hauptverfasser: Lai, Yueyang, Xu, Xuebo, Yan, Ruiying, Hua, Zichun
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 95
container_issue
container_start_page 88
container_title Analytical biochemistry
container_volume 564-565
creator Lai, Yueyang
Xu, Xuebo
Yan, Ruiying
Hua, Zichun
description In this study, we evaluated the efficacy of various mycoplasma removal reagents using nuclear staining, DNA gel electrophoresis, and qPCR-based quantification. Our results showed Plasmocure and Plasmocin are two effective anti-mycoplasma reagents whose effects can be observed within a week. However, prolonged treatment with Plasmocin led to development of resistance. Withdrawal of anti-mycoplasma reagents led to reoccurrence of mycoplasma contamination, but addition of prevention reagent, such as Primocin, prevented recontamination. Therefore, sequential treatment by Plasmocure and Primocin is the best course of action against mycoplasma contamination. Lastly, we developed methods based on qPCR to estimate the average number of mycoplasma associated with a single contaminated cell. We have shown, for the first time, that untreated contaminated BEAS-2B cells have approximately 300–400 mycoplasma contaminants per cell in the cytoplasm or attached to the cell membrane. Furthermore, withdrawal of anti-mycoplasma reagents led to reoccurrence of mycoplasma contamination within two days, and therefore continued use of prevention reagent is imperative. •Employed DNA gel electrophoresis and nuclear staining to preliminarily determine the level of mycoplasma contamination in cultured cells.•Assayed for five anti-mycoplasma reagents using DNA gel electrophoresis and nuclear staining and discovered an efficient and effective treatment using Plasmocure and Primocin.•Prolonged treatment with reagent containing single antibiotic, i.e. Plasmocin in this study, led to development of bacterial resistance and therefore should be avoided. Reagents containing more than one antibiotic or peptides are recommended.•Recontamination of mycoplasma is highly likely following withdrawal of reagents. Therefore, use of prevention reagent is mandatory.•qPCR-based quantification of mycoplasma in contaminated cultured cells was able to determine the number of mycoplasma in a single contaminated cell.
doi_str_mv 10.1016/j.ab.2018.10.014
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_2123715341</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S0003269718307036</els_id><sourcerecordid>2123715341</sourcerecordid><originalsourceid>FETCH-LOGICAL-c350t-88ae0ddbd2a5003c485698497180e5570c602eaad9fd878d03a14a658c46e5953</originalsourceid><addsrcrecordid>eNp1kMtLxDAQxoMouj7unqRHL10nTZOm3mTxBYIieg7TZCpZ-thtWmH_e7OuevM0zMz3fcz8GDvnMOfA1dVyjtU8A65jOwee77EZh1KlIKDcZzMAEGmmyuKIHYewBOA8l-qQHQkQQvFMztjj7Sc2E46-75K-TtqN7VcNhhaTgdo-7mLFD-rGkEzBdx_J-mXxmlYYyCXrCbvR195-20_ZQY1NoLOfesLe727fFg_p0_P94-LmKbVCwphqjQTOVS5DGc-zuZaq1HlZcA0kZQFWQUaIrqydLrQDgTxHJbXNFclSihN2uctdDf16ojCa1gdLTYMd9VMwGc9EwaXIeZTCTmqHPoSBarMafIvDxnAwW4BmabAyW4DbSQQYLRc_6VPVkvsz_BKLguudgOKPn54GE6ynzpLzA9nRuN7_n_4FjpF_EA</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2123715341</pqid></control><display><type>article</type><title>Evaluation of mycoplasma removal reagents using qPCR-based quantification</title><source>Elsevier ScienceDirect Journals</source><creator>Lai, Yueyang ; Xu, Xuebo ; Yan, Ruiying ; Hua, Zichun</creator><creatorcontrib>Lai, Yueyang ; Xu, Xuebo ; Yan, Ruiying ; Hua, Zichun</creatorcontrib><description>In this study, we evaluated the efficacy of various mycoplasma removal reagents using nuclear staining, DNA gel electrophoresis, and qPCR-based quantification. Our results showed Plasmocure and Plasmocin are two effective anti-mycoplasma reagents whose effects can be observed within a week. However, prolonged treatment with Plasmocin led to development of resistance. Withdrawal of anti-mycoplasma reagents led to reoccurrence of mycoplasma contamination, but addition of prevention reagent, such as Primocin, prevented recontamination. Therefore, sequential treatment by Plasmocure and Primocin is the best course of action against mycoplasma contamination. Lastly, we developed methods based on qPCR to estimate the average number of mycoplasma associated with a single contaminated cell. We have shown, for the first time, that untreated contaminated BEAS-2B cells have approximately 300–400 mycoplasma contaminants per cell in the cytoplasm or attached to the cell membrane. Furthermore, withdrawal of anti-mycoplasma reagents led to reoccurrence of mycoplasma contamination within two days, and therefore continued use of prevention reagent is imperative. •Employed DNA gel electrophoresis and nuclear staining to preliminarily determine the level of mycoplasma contamination in cultured cells.•Assayed for five anti-mycoplasma reagents using DNA gel electrophoresis and nuclear staining and discovered an efficient and effective treatment using Plasmocure and Primocin.•Prolonged treatment with reagent containing single antibiotic, i.e. Plasmocin in this study, led to development of bacterial resistance and therefore should be avoided. Reagents containing more than one antibiotic or peptides are recommended.•Recontamination of mycoplasma is highly likely following withdrawal of reagents. Therefore, use of prevention reagent is mandatory.•qPCR-based quantification of mycoplasma in contaminated cultured cells was able to determine the number of mycoplasma in a single contaminated cell.</description><identifier>ISSN: 0003-2697</identifier><identifier>EISSN: 1096-0309</identifier><identifier>DOI: 10.1016/j.ab.2018.10.014</identifier><identifier>PMID: 30336125</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Cell culture contaminant ; DNA gel electrophoresis ; Mycoplasma ; Nuclear staining ; qPCR-based quantification</subject><ispartof>Analytical biochemistry, 2019-01, Vol.564-565, p.88-95</ispartof><rights>2018 Elsevier Inc.</rights><rights>Copyright © 2018 Elsevier Inc. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c350t-88ae0ddbd2a5003c485698497180e5570c602eaad9fd878d03a14a658c46e5953</citedby><cites>FETCH-LOGICAL-c350t-88ae0ddbd2a5003c485698497180e5570c602eaad9fd878d03a14a658c46e5953</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0003269718307036$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/30336125$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Lai, Yueyang</creatorcontrib><creatorcontrib>Xu, Xuebo</creatorcontrib><creatorcontrib>Yan, Ruiying</creatorcontrib><creatorcontrib>Hua, Zichun</creatorcontrib><title>Evaluation of mycoplasma removal reagents using qPCR-based quantification</title><title>Analytical biochemistry</title><addtitle>Anal Biochem</addtitle><description>In this study, we evaluated the efficacy of various mycoplasma removal reagents using nuclear staining, DNA gel electrophoresis, and qPCR-based quantification. Our results showed Plasmocure and Plasmocin are two effective anti-mycoplasma reagents whose effects can be observed within a week. However, prolonged treatment with Plasmocin led to development of resistance. Withdrawal of anti-mycoplasma reagents led to reoccurrence of mycoplasma contamination, but addition of prevention reagent, such as Primocin, prevented recontamination. Therefore, sequential treatment by Plasmocure and Primocin is the best course of action against mycoplasma contamination. Lastly, we developed methods based on qPCR to estimate the average number of mycoplasma associated with a single contaminated cell. We have shown, for the first time, that untreated contaminated BEAS-2B cells have approximately 300–400 mycoplasma contaminants per cell in the cytoplasm or attached to the cell membrane. Furthermore, withdrawal of anti-mycoplasma reagents led to reoccurrence of mycoplasma contamination within two days, and therefore continued use of prevention reagent is imperative. •Employed DNA gel electrophoresis and nuclear staining to preliminarily determine the level of mycoplasma contamination in cultured cells.•Assayed for five anti-mycoplasma reagents using DNA gel electrophoresis and nuclear staining and discovered an efficient and effective treatment using Plasmocure and Primocin.•Prolonged treatment with reagent containing single antibiotic, i.e. Plasmocin in this study, led to development of bacterial resistance and therefore should be avoided. Reagents containing more than one antibiotic or peptides are recommended.•Recontamination of mycoplasma is highly likely following withdrawal of reagents. Therefore, use of prevention reagent is mandatory.•qPCR-based quantification of mycoplasma in contaminated cultured cells was able to determine the number of mycoplasma in a single contaminated cell.</description><subject>Cell culture contaminant</subject><subject>DNA gel electrophoresis</subject><subject>Mycoplasma</subject><subject>Nuclear staining</subject><subject>qPCR-based quantification</subject><issn>0003-2697</issn><issn>1096-0309</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><recordid>eNp1kMtLxDAQxoMouj7unqRHL10nTZOm3mTxBYIieg7TZCpZ-thtWmH_e7OuevM0zMz3fcz8GDvnMOfA1dVyjtU8A65jOwee77EZh1KlIKDcZzMAEGmmyuKIHYewBOA8l-qQHQkQQvFMztjj7Sc2E46-75K-TtqN7VcNhhaTgdo-7mLFD-rGkEzBdx_J-mXxmlYYyCXrCbvR195-20_ZQY1NoLOfesLe727fFg_p0_P94-LmKbVCwphqjQTOVS5DGc-zuZaq1HlZcA0kZQFWQUaIrqydLrQDgTxHJbXNFclSihN2uctdDf16ojCa1gdLTYMd9VMwGc9EwaXIeZTCTmqHPoSBarMafIvDxnAwW4BmabAyW4DbSQQYLRc_6VPVkvsz_BKLguudgOKPn54GE6ynzpLzA9nRuN7_n_4FjpF_EA</recordid><startdate>20190101</startdate><enddate>20190101</enddate><creator>Lai, Yueyang</creator><creator>Xu, Xuebo</creator><creator>Yan, Ruiying</creator><creator>Hua, Zichun</creator><general>Elsevier Inc</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20190101</creationdate><title>Evaluation of mycoplasma removal reagents using qPCR-based quantification</title><author>Lai, Yueyang ; Xu, Xuebo ; Yan, Ruiying ; Hua, Zichun</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c350t-88ae0ddbd2a5003c485698497180e5570c602eaad9fd878d03a14a658c46e5953</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>Cell culture contaminant</topic><topic>DNA gel electrophoresis</topic><topic>Mycoplasma</topic><topic>Nuclear staining</topic><topic>qPCR-based quantification</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Lai, Yueyang</creatorcontrib><creatorcontrib>Xu, Xuebo</creatorcontrib><creatorcontrib>Yan, Ruiying</creatorcontrib><creatorcontrib>Hua, Zichun</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Analytical biochemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Lai, Yueyang</au><au>Xu, Xuebo</au><au>Yan, Ruiying</au><au>Hua, Zichun</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Evaluation of mycoplasma removal reagents using qPCR-based quantification</atitle><jtitle>Analytical biochemistry</jtitle><addtitle>Anal Biochem</addtitle><date>2019-01-01</date><risdate>2019</risdate><volume>564-565</volume><spage>88</spage><epage>95</epage><pages>88-95</pages><issn>0003-2697</issn><eissn>1096-0309</eissn><abstract>In this study, we evaluated the efficacy of various mycoplasma removal reagents using nuclear staining, DNA gel electrophoresis, and qPCR-based quantification. Our results showed Plasmocure and Plasmocin are two effective anti-mycoplasma reagents whose effects can be observed within a week. However, prolonged treatment with Plasmocin led to development of resistance. Withdrawal of anti-mycoplasma reagents led to reoccurrence of mycoplasma contamination, but addition of prevention reagent, such as Primocin, prevented recontamination. Therefore, sequential treatment by Plasmocure and Primocin is the best course of action against mycoplasma contamination. Lastly, we developed methods based on qPCR to estimate the average number of mycoplasma associated with a single contaminated cell. We have shown, for the first time, that untreated contaminated BEAS-2B cells have approximately 300–400 mycoplasma contaminants per cell in the cytoplasm or attached to the cell membrane. Furthermore, withdrawal of anti-mycoplasma reagents led to reoccurrence of mycoplasma contamination within two days, and therefore continued use of prevention reagent is imperative. •Employed DNA gel electrophoresis and nuclear staining to preliminarily determine the level of mycoplasma contamination in cultured cells.•Assayed for five anti-mycoplasma reagents using DNA gel electrophoresis and nuclear staining and discovered an efficient and effective treatment using Plasmocure and Primocin.•Prolonged treatment with reagent containing single antibiotic, i.e. Plasmocin in this study, led to development of bacterial resistance and therefore should be avoided. Reagents containing more than one antibiotic or peptides are recommended.•Recontamination of mycoplasma is highly likely following withdrawal of reagents. Therefore, use of prevention reagent is mandatory.•qPCR-based quantification of mycoplasma in contaminated cultured cells was able to determine the number of mycoplasma in a single contaminated cell.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>30336125</pmid><doi>10.1016/j.ab.2018.10.014</doi><tpages>8</tpages></addata></record>
fulltext fulltext
identifier ISSN: 0003-2697
ispartof Analytical biochemistry, 2019-01, Vol.564-565, p.88-95
issn 0003-2697
1096-0309
language eng
recordid cdi_proquest_miscellaneous_2123715341
source Elsevier ScienceDirect Journals
subjects Cell culture contaminant
DNA gel electrophoresis
Mycoplasma
Nuclear staining
qPCR-based quantification
title Evaluation of mycoplasma removal reagents using qPCR-based quantification
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-07T22%3A07%3A21IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Evaluation%20of%20mycoplasma%20removal%20reagents%20using%20qPCR-based%20quantification&rft.jtitle=Analytical%20biochemistry&rft.au=Lai,%20Yueyang&rft.date=2019-01-01&rft.volume=564-565&rft.spage=88&rft.epage=95&rft.pages=88-95&rft.issn=0003-2697&rft.eissn=1096-0309&rft_id=info:doi/10.1016/j.ab.2018.10.014&rft_dat=%3Cproquest_cross%3E2123715341%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=2123715341&rft_id=info:pmid/30336125&rft_els_id=S0003269718307036&rfr_iscdi=true