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Multiplex-PCR as an identity assay for Mycobacterium bovis BCG Moreau descendants
In the study, we assessed the identity of locally produced BCG vaccine via screening for the presence of genetic markers specific for particular Mycobacterium bovis BCG substrains – RD8, RD2, senX3-regX3, RD14, RD16, ΔRD1, DU2, a second copy of IS6110, mutation D322G in phoR, and deletions in fadD26...
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Published in: | Biologicals 2013-05, Vol.41 (3), p.197-200 |
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description | In the study, we assessed the identity of locally produced BCG vaccine via screening for the presence of genetic markers specific for particular Mycobacterium bovis BCG substrains – RD8, RD2, senX3-regX3, RD14, RD16, ΔRD1, DU2, a second copy of IS6110, mutation D322G in phoR, and deletions in fadD26-ppsA and Rv3887c regions. In order to increase the specificity of the multiplex-PCR test for locally produced BCG vaccine, we have modified previously developed primer sets by the introduction of a primer pair specific for deletion in Rv3887c. The modified multiplex-PCR specifically and reproducibly distinguished both BCG Moreau sublineages, and allowed, with no decrease in power, differentiation of BCG substrains of different origin. The growing knowledge of genetic differences among BCG vaccine strains enables improvements in the specificity of identity tests that will be useful both for routine release of vaccines and potential applications in clinical practice. Modified multiplex-PCR accompanied by PFGE analysis can serve as specific tools to monitor consistency in BCG manufacture.
► The Mycobacterium bovis BCG Moreau substrain used in Poland lacks of mutation Rv3887c. ► Multiplex-PCR was adopted to differentiate between descendants of BCG Moreau substrain. ► BCG working seeds and vaccine lots produced in Poland were found genetically stable. |
doi_str_mv | 10.1016/j.biologicals.2012.12.002 |
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► The Mycobacterium bovis BCG Moreau substrain used in Poland lacks of mutation Rv3887c. ► Multiplex-PCR was adopted to differentiate between descendants of BCG Moreau substrain. ► BCG working seeds and vaccine lots produced in Poland were found genetically stable.</description><identifier>ISSN: 1045-1056</identifier><identifier>EISSN: 1095-8320</identifier><identifier>DOI: 10.1016/j.biologicals.2012.12.002</identifier><identifier>PMID: 23490534</identifier><language>eng</language><publisher>England: Elsevier Ltd</publisher><subject>BCG vaccine ; BCG Vaccine - genetics ; BCG Vaccine - immunology ; DNA primers ; DNA Primers - genetics ; DNA, Bacterial - genetics ; DNA, Bacterial - immunology ; Electrophoresis, Gel, Pulsed-Field ; genetic markers ; Identity ; manufacturing ; Multiplex Polymerase Chain Reaction - methods ; Multiplex-PCR ; Mutation ; Mycobacterium bovis - classification ; Mycobacterium bovis - genetics ; Mycobacterium bovis - immunology ; Mycobacterium bovis BCG ; Mycobacterium bovis BCG Moreau ; pulsed-field gel electrophoresis ; screening ; Sequence Deletion ; Species Specificity</subject><ispartof>Biologicals, 2013-05, Vol.41 (3), p.197-200</ispartof><rights>2013 The International Alliance for Biological Standardization</rights><rights>Copyright © 2013 The International Alliance for Biological Standardization. Published by Elsevier Ltd. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c345t-d2e8a4b084e557d70beb2bd283ceb7e881a82a0ba9c7ab0c9411d9caa1dfa0753</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,777,781,27905,27906</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/23490534$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Krysztopa-Grzybowska, Katarzyna</creatorcontrib><creatorcontrib>Brzezińska, Sylwia</creatorcontrib><creatorcontrib>Augustynowicz-Kopeć, Ewa</creatorcontrib><creatorcontrib>Polak, Maciej</creatorcontrib><creatorcontrib>Lutyńska, Anna</creatorcontrib><title>Multiplex-PCR as an identity assay for Mycobacterium bovis BCG Moreau descendants</title><title>Biologicals</title><addtitle>Biologicals</addtitle><description>In the study, we assessed the identity of locally produced BCG vaccine via screening for the presence of genetic markers specific for particular Mycobacterium bovis BCG substrains – RD8, RD2, senX3-regX3, RD14, RD16, ΔRD1, DU2, a second copy of IS6110, mutation D322G in phoR, and deletions in fadD26-ppsA and Rv3887c regions. In order to increase the specificity of the multiplex-PCR test for locally produced BCG vaccine, we have modified previously developed primer sets by the introduction of a primer pair specific for deletion in Rv3887c. The modified multiplex-PCR specifically and reproducibly distinguished both BCG Moreau sublineages, and allowed, with no decrease in power, differentiation of BCG substrains of different origin. The growing knowledge of genetic differences among BCG vaccine strains enables improvements in the specificity of identity tests that will be useful both for routine release of vaccines and potential applications in clinical practice. Modified multiplex-PCR accompanied by PFGE analysis can serve as specific tools to monitor consistency in BCG manufacture.
► The Mycobacterium bovis BCG Moreau substrain used in Poland lacks of mutation Rv3887c. ► Multiplex-PCR was adopted to differentiate between descendants of BCG Moreau substrain. ► BCG working seeds and vaccine lots produced in Poland were found genetically stable.</description><subject>BCG vaccine</subject><subject>BCG Vaccine - genetics</subject><subject>BCG Vaccine - immunology</subject><subject>DNA primers</subject><subject>DNA Primers - genetics</subject><subject>DNA, Bacterial - genetics</subject><subject>DNA, Bacterial - immunology</subject><subject>Electrophoresis, Gel, Pulsed-Field</subject><subject>genetic markers</subject><subject>Identity</subject><subject>manufacturing</subject><subject>Multiplex Polymerase Chain Reaction - methods</subject><subject>Multiplex-PCR</subject><subject>Mutation</subject><subject>Mycobacterium bovis - classification</subject><subject>Mycobacterium bovis - genetics</subject><subject>Mycobacterium bovis - immunology</subject><subject>Mycobacterium bovis BCG</subject><subject>Mycobacterium bovis BCG Moreau</subject><subject>pulsed-field gel electrophoresis</subject><subject>screening</subject><subject>Sequence Deletion</subject><subject>Species Specificity</subject><issn>1045-1056</issn><issn>1095-8320</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><recordid>eNqNkE1v1DAQhi0EoqXwFyDcuGQZO_Y6OUJUWqSu-OzZGtuTyqtsvNhJxf57vNoWcUQaybb0zMzrh7G3HFYc-Pr9dmVDHONdcDjmlQAuVqUAxBN2zqFTddsIeHq8S1VzUOsz9iLnLQDnUsvn7Ew0sgPVyHP2bbOMc9iP9Lv-2n-vMFc4VcHTNIf5UJ4ZD9UQU7U5uGjRzZTCsqtsvA-5-thfVZuYCJfKU3Y0eZzm_JI9G0osevVwXrDbT5c_--v65svV5_7DTe0aqebaC2pRWmglKaW9BktWWC_axpHV1LYcW4FgsXMaLbhOcu47h8j9gKBVc8HenebuU_y1UJ7NLpQQ44gTxSUbXv6oQUgNBe1OqEsx50SD2aeww3QwHMzRqNmaf4yao1FTqhgtva8f1ix2R_5v56PCArw5AQNGg3cpZHP7o0xQRfdacd0Woj8RVHTcB0omu0CTIx8Sudn4GP4jyB8Kp5cA</recordid><startdate>20130501</startdate><enddate>20130501</enddate><creator>Krysztopa-Grzybowska, Katarzyna</creator><creator>Brzezińska, Sylwia</creator><creator>Augustynowicz-Kopeć, Ewa</creator><creator>Polak, Maciej</creator><creator>Lutyńska, Anna</creator><general>Elsevier Ltd</general><scope>FBQ</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20130501</creationdate><title>Multiplex-PCR as an identity assay for Mycobacterium bovis BCG Moreau descendants</title><author>Krysztopa-Grzybowska, Katarzyna ; Brzezińska, Sylwia ; Augustynowicz-Kopeć, Ewa ; Polak, Maciej ; Lutyńska, Anna</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c345t-d2e8a4b084e557d70beb2bd283ceb7e881a82a0ba9c7ab0c9411d9caa1dfa0753</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>BCG vaccine</topic><topic>BCG Vaccine - genetics</topic><topic>BCG Vaccine - immunology</topic><topic>DNA primers</topic><topic>DNA Primers - genetics</topic><topic>DNA, Bacterial - genetics</topic><topic>DNA, Bacterial - immunology</topic><topic>Electrophoresis, Gel, Pulsed-Field</topic><topic>genetic markers</topic><topic>Identity</topic><topic>manufacturing</topic><topic>Multiplex Polymerase Chain Reaction - methods</topic><topic>Multiplex-PCR</topic><topic>Mutation</topic><topic>Mycobacterium bovis - classification</topic><topic>Mycobacterium bovis - genetics</topic><topic>Mycobacterium bovis - immunology</topic><topic>Mycobacterium bovis BCG</topic><topic>Mycobacterium bovis BCG Moreau</topic><topic>pulsed-field gel electrophoresis</topic><topic>screening</topic><topic>Sequence Deletion</topic><topic>Species Specificity</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Krysztopa-Grzybowska, Katarzyna</creatorcontrib><creatorcontrib>Brzezińska, Sylwia</creatorcontrib><creatorcontrib>Augustynowicz-Kopeć, Ewa</creatorcontrib><creatorcontrib>Polak, Maciej</creatorcontrib><creatorcontrib>Lutyńska, Anna</creatorcontrib><collection>AGRIS</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Biologicals</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Krysztopa-Grzybowska, Katarzyna</au><au>Brzezińska, Sylwia</au><au>Augustynowicz-Kopeć, Ewa</au><au>Polak, Maciej</au><au>Lutyńska, Anna</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Multiplex-PCR as an identity assay for Mycobacterium bovis BCG Moreau descendants</atitle><jtitle>Biologicals</jtitle><addtitle>Biologicals</addtitle><date>2013-05-01</date><risdate>2013</risdate><volume>41</volume><issue>3</issue><spage>197</spage><epage>200</epage><pages>197-200</pages><issn>1045-1056</issn><eissn>1095-8320</eissn><abstract>In the study, we assessed the identity of locally produced BCG vaccine via screening for the presence of genetic markers specific for particular Mycobacterium bovis BCG substrains – RD8, RD2, senX3-regX3, RD14, RD16, ΔRD1, DU2, a second copy of IS6110, mutation D322G in phoR, and deletions in fadD26-ppsA and Rv3887c regions. In order to increase the specificity of the multiplex-PCR test for locally produced BCG vaccine, we have modified previously developed primer sets by the introduction of a primer pair specific for deletion in Rv3887c. The modified multiplex-PCR specifically and reproducibly distinguished both BCG Moreau sublineages, and allowed, with no decrease in power, differentiation of BCG substrains of different origin. The growing knowledge of genetic differences among BCG vaccine strains enables improvements in the specificity of identity tests that will be useful both for routine release of vaccines and potential applications in clinical practice. Modified multiplex-PCR accompanied by PFGE analysis can serve as specific tools to monitor consistency in BCG manufacture.
► The Mycobacterium bovis BCG Moreau substrain used in Poland lacks of mutation Rv3887c. ► Multiplex-PCR was adopted to differentiate between descendants of BCG Moreau substrain. ► BCG working seeds and vaccine lots produced in Poland were found genetically stable.</abstract><cop>England</cop><pub>Elsevier Ltd</pub><pmid>23490534</pmid><doi>10.1016/j.biologicals.2012.12.002</doi><tpages>4</tpages></addata></record> |
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subjects | BCG vaccine BCG Vaccine - genetics BCG Vaccine - immunology DNA primers DNA Primers - genetics DNA, Bacterial - genetics DNA, Bacterial - immunology Electrophoresis, Gel, Pulsed-Field genetic markers Identity manufacturing Multiplex Polymerase Chain Reaction - methods Multiplex-PCR Mutation Mycobacterium bovis - classification Mycobacterium bovis - genetics Mycobacterium bovis - immunology Mycobacterium bovis BCG Mycobacterium bovis BCG Moreau pulsed-field gel electrophoresis screening Sequence Deletion Species Specificity |
title | Multiplex-PCR as an identity assay for Mycobacterium bovis BCG Moreau descendants |
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