Recombinant viruses obtained from co-infection in vitro with a live vaccinia-vectored influenza vaccine and a naturally occurring cowpox virus display different plaque phenotypes and loss of the transgene

Some poxviruses are very attractive as transgenic vaccine vectors for humans, domestic animals and wildlife. Poxviridae family members circulate in different ecosystems and parts of the world, providing a pool of possible recombination partners for released or escaped genetically modified poxviruses...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Vaccine 2004-12, Vol.23 (4), p.499-506
Hauptverfasser: Hansen, Hilde, Okeke, Malachy Ifeanyi, Nilssen, Øivind, Traavik, Terje
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 506
container_issue 4
container_start_page 499
container_title Vaccine
container_volume 23
creator Hansen, Hilde
Okeke, Malachy Ifeanyi
Nilssen, Øivind
Traavik, Terje
description Some poxviruses are very attractive as transgenic vaccine vectors for humans, domestic animals and wildlife. Poxviridae family members circulate in different ecosystems and parts of the world, providing a pool of possible recombination partners for released or escaped genetically modified poxviruses. We performed in vitro double infections with a vaccinia virus strain Ankara (MVA) vectored influenza vaccine and a cowpox virus isolate from Norway, isolated hybrids, and further analyzed three hybrid viruses with different plaque phenotypes. One of the hybrids was genetically unstable, and during adaptation to new host cells its MVA derived influenza gene was deleted at a high frequency. This is significant in a risk assessment context, since the transgene would be the only logical tag for monitoring unwanted spread and non-target effects of a vaccine virus. Putative recombination events involving genetically modified and naturally occurring viruses should be included in health and environmental risk assessments.
doi_str_mv 10.1016/j.vaccine.2004.06.032
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_67058203</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S0264410X0400475X</els_id><sourcerecordid>17760521</sourcerecordid><originalsourceid>FETCH-LOGICAL-c502t-dd1aa92c5264edc102d023af4cc8ed660a00d5f06baa667b76cb94060c1d84293</originalsourceid><addsrcrecordid>eNqFkt-K1DAUxoso7rj6CEpA9K7jSduk7ZUsi_9gQRAF70KanO5k6CQ1abuOz-hDeYYpLHizVyHkd7585zsny15y2HLg8t1-u2hjnMdtAVBtQW6hLB5lG97UZV4I3jzONlDIKq84_LzInqW0BwBR8vZpdsGFKEG2zSb7-w1NOHTOaz-xxcU5YWKhmzQpW9bHcGAm5M73aCYXPHOeqCkGduemHdNscAuysxOn84WoEKmQCoYZ_R-9viHT3hLu9TRHPQxHFoyZY3T-lvTvxvD7_DmzLo2DPtLZ9xiRTNH114xs3KEP03EkeyepISTy2bNph2yK2qdb9Pg8e9LrIeGL9bzMfnz88P36c37z9dOX66ub3AgoptxarnVbGEHxoDUcCgtFqfvKmAatlKABrOhBdlpLWXe1NF1bgQTDbVMVbXmZvT3rjjGQtzSpg0sGh0F7DHNSsgbRFFA-CPK6liAKTuDr_8B9mKOnJhTNqgUphRREiTNlIrUfsVdjdAcdj4qDOm2F2qs1b3XaCgVS0VZQ3atVfe4OaO-r1jUg4M0K6GT00FOgxqV7Tpa8qdqKuPdnDindxWFUyTj0Bq2LNHplg3vAyj8gFN2z</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1559066565</pqid></control><display><type>article</type><title>Recombinant viruses obtained from co-infection in vitro with a live vaccinia-vectored influenza vaccine and a naturally occurring cowpox virus display different plaque phenotypes and loss of the transgene</title><source>MEDLINE</source><source>Elsevier ScienceDirect Journals</source><source>ProQuest Central UK/Ireland</source><creator>Hansen, Hilde ; Okeke, Malachy Ifeanyi ; Nilssen, Øivind ; Traavik, Terje</creator><creatorcontrib>Hansen, Hilde ; Okeke, Malachy Ifeanyi ; Nilssen, Øivind ; Traavik, Terje</creatorcontrib><description>Some poxviruses are very attractive as transgenic vaccine vectors for humans, domestic animals and wildlife. Poxviridae family members circulate in different ecosystems and parts of the world, providing a pool of possible recombination partners for released or escaped genetically modified poxviruses. We performed in vitro double infections with a vaccinia virus strain Ankara (MVA) vectored influenza vaccine and a cowpox virus isolate from Norway, isolated hybrids, and further analyzed three hybrid viruses with different plaque phenotypes. One of the hybrids was genetically unstable, and during adaptation to new host cells its MVA derived influenza gene was deleted at a high frequency. This is significant in a risk assessment context, since the transgene would be the only logical tag for monitoring unwanted spread and non-target effects of a vaccine virus. Putative recombination events involving genetically modified and naturally occurring viruses should be included in health and environmental risk assessments.</description><identifier>ISSN: 0264-410X</identifier><identifier>EISSN: 1873-2518</identifier><identifier>DOI: 10.1016/j.vaccine.2004.06.032</identifier><identifier>PMID: 15530698</identifier><identifier>CODEN: VACCDE</identifier><language>eng</language><publisher>Oxford: Elsevier Ltd</publisher><subject>Animals ; Applied microbiology ; Biological and medical sciences ; Blotting, Southern ; Cell Line ; Cercopithecus aethiops ; Cowpox virus ; Cowpox virus - genetics ; Cowpox virus - growth &amp; development ; DNA, Viral - isolation &amp; purification ; Domestic animals ; Environmental assessment ; Environmental risk ; Fundamental and applied biological sciences. Psychology ; Genes ; Genomes ; Hybrids ; Immunization ; Infections ; Influenza ; Influenza Vaccines - genetics ; Influenza virus ; Microbiology ; Miscellaneous ; MVA recombinant vaccines ; Organisms, Genetically Modified ; Orthopoxvirus ; Phenotype ; Polymerase Chain Reaction ; Poxvirus ; Proteins ; Reassortant Viruses - genetics ; Reassortant Viruses - physiology ; Recombination, Genetic ; Risk assessment ; Safety ; Vaccines ; Vaccines, antisera, therapeutical immunoglobulins and monoclonal antibodies (general aspects) ; Vaccinia virus ; Vaccinia virus - genetics ; Vaccinia virus - growth &amp; development ; Vero Cells ; Viral Plaque Assay ; Viral Vaccines - genetics ; Virology ; Viruses ; Wildlife</subject><ispartof>Vaccine, 2004-12, Vol.23 (4), p.499-506</ispartof><rights>2004 Elsevier Ltd</rights><rights>2005 INIST-CNRS</rights><rights>Copyright Elsevier Limited Dec 9, 2004</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c502t-dd1aa92c5264edc102d023af4cc8ed660a00d5f06baa667b76cb94060c1d84293</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.proquest.com/docview/1559066565?pq-origsite=primo$$EHTML$$P50$$Gproquest$$H</linktohtml><link.rule.ids>314,776,780,3536,27903,27904,64361,64363,64365,65309,72215</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=16318494$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/15530698$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Hansen, Hilde</creatorcontrib><creatorcontrib>Okeke, Malachy Ifeanyi</creatorcontrib><creatorcontrib>Nilssen, Øivind</creatorcontrib><creatorcontrib>Traavik, Terje</creatorcontrib><title>Recombinant viruses obtained from co-infection in vitro with a live vaccinia-vectored influenza vaccine and a naturally occurring cowpox virus display different plaque phenotypes and loss of the transgene</title><title>Vaccine</title><addtitle>Vaccine</addtitle><description>Some poxviruses are very attractive as transgenic vaccine vectors for humans, domestic animals and wildlife. Poxviridae family members circulate in different ecosystems and parts of the world, providing a pool of possible recombination partners for released or escaped genetically modified poxviruses. We performed in vitro double infections with a vaccinia virus strain Ankara (MVA) vectored influenza vaccine and a cowpox virus isolate from Norway, isolated hybrids, and further analyzed three hybrid viruses with different plaque phenotypes. One of the hybrids was genetically unstable, and during adaptation to new host cells its MVA derived influenza gene was deleted at a high frequency. This is significant in a risk assessment context, since the transgene would be the only logical tag for monitoring unwanted spread and non-target effects of a vaccine virus. Putative recombination events involving genetically modified and naturally occurring viruses should be included in health and environmental risk assessments.</description><subject>Animals</subject><subject>Applied microbiology</subject><subject>Biological and medical sciences</subject><subject>Blotting, Southern</subject><subject>Cell Line</subject><subject>Cercopithecus aethiops</subject><subject>Cowpox virus</subject><subject>Cowpox virus - genetics</subject><subject>Cowpox virus - growth &amp; development</subject><subject>DNA, Viral - isolation &amp; purification</subject><subject>Domestic animals</subject><subject>Environmental assessment</subject><subject>Environmental risk</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Genes</subject><subject>Genomes</subject><subject>Hybrids</subject><subject>Immunization</subject><subject>Infections</subject><subject>Influenza</subject><subject>Influenza Vaccines - genetics</subject><subject>Influenza virus</subject><subject>Microbiology</subject><subject>Miscellaneous</subject><subject>MVA recombinant vaccines</subject><subject>Organisms, Genetically Modified</subject><subject>Orthopoxvirus</subject><subject>Phenotype</subject><subject>Polymerase Chain Reaction</subject><subject>Poxvirus</subject><subject>Proteins</subject><subject>Reassortant Viruses - genetics</subject><subject>Reassortant Viruses - physiology</subject><subject>Recombination, Genetic</subject><subject>Risk assessment</subject><subject>Safety</subject><subject>Vaccines</subject><subject>Vaccines, antisera, therapeutical immunoglobulins and monoclonal antibodies (general aspects)</subject><subject>Vaccinia virus</subject><subject>Vaccinia virus - genetics</subject><subject>Vaccinia virus - growth &amp; development</subject><subject>Vero Cells</subject><subject>Viral Plaque Assay</subject><subject>Viral Vaccines - genetics</subject><subject>Virology</subject><subject>Viruses</subject><subject>Wildlife</subject><issn>0264-410X</issn><issn>1873-2518</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2004</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>8G5</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><sourceid>GUQSH</sourceid><sourceid>M2O</sourceid><recordid>eNqFkt-K1DAUxoso7rj6CEpA9K7jSduk7ZUsi_9gQRAF70KanO5k6CQ1abuOz-hDeYYpLHizVyHkd7585zsny15y2HLg8t1-u2hjnMdtAVBtQW6hLB5lG97UZV4I3jzONlDIKq84_LzInqW0BwBR8vZpdsGFKEG2zSb7-w1NOHTOaz-xxcU5YWKhmzQpW9bHcGAm5M73aCYXPHOeqCkGduemHdNscAuysxOn84WoEKmQCoYZ_R-9viHT3hLu9TRHPQxHFoyZY3T-lvTvxvD7_DmzLo2DPtLZ9xiRTNH114xs3KEP03EkeyepISTy2bNph2yK2qdb9Pg8e9LrIeGL9bzMfnz88P36c37z9dOX66ub3AgoptxarnVbGEHxoDUcCgtFqfvKmAatlKABrOhBdlpLWXe1NF1bgQTDbVMVbXmZvT3rjjGQtzSpg0sGh0F7DHNSsgbRFFA-CPK6liAKTuDr_8B9mKOnJhTNqgUphRREiTNlIrUfsVdjdAcdj4qDOm2F2qs1b3XaCgVS0VZQ3atVfe4OaO-r1jUg4M0K6GT00FOgxqV7Tpa8qdqKuPdnDindxWFUyTj0Bq2LNHplg3vAyj8gFN2z</recordid><startdate>20041209</startdate><enddate>20041209</enddate><creator>Hansen, Hilde</creator><creator>Okeke, Malachy Ifeanyi</creator><creator>Nilssen, Øivind</creator><creator>Traavik, Terje</creator><general>Elsevier Ltd</general><general>Elsevier</general><general>Elsevier Limited</general><scope>IQODW</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>3V.</scope><scope>7QL</scope><scope>7RV</scope><scope>7T2</scope><scope>7T5</scope><scope>7U9</scope><scope>7X7</scope><scope>7XB</scope><scope>88C</scope><scope>88E</scope><scope>8AO</scope><scope>8C1</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>8G5</scope><scope>ABUWG</scope><scope>AEUYN</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>C1K</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>H94</scope><scope>HCIFZ</scope><scope>K9-</scope><scope>K9.</scope><scope>KB0</scope><scope>LK8</scope><scope>M0R</scope><scope>M0S</scope><scope>M0T</scope><scope>M1P</scope><scope>M2O</scope><scope>M7N</scope><scope>M7P</scope><scope>MBDVC</scope><scope>NAPCQ</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>Q9U</scope><scope>7QO</scope><scope>8FD</scope><scope>FR3</scope><scope>P64</scope><scope>7X8</scope></search><sort><creationdate>20041209</creationdate><title>Recombinant viruses obtained from co-infection in vitro with a live vaccinia-vectored influenza vaccine and a naturally occurring cowpox virus display different plaque phenotypes and loss of the transgene</title><author>Hansen, Hilde ; Okeke, Malachy Ifeanyi ; Nilssen, Øivind ; Traavik, Terje</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c502t-dd1aa92c5264edc102d023af4cc8ed660a00d5f06baa667b76cb94060c1d84293</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2004</creationdate><topic>Animals</topic><topic>Applied microbiology</topic><topic>Biological and medical sciences</topic><topic>Blotting, Southern</topic><topic>Cell Line</topic><topic>Cercopithecus aethiops</topic><topic>Cowpox virus</topic><topic>Cowpox virus - genetics</topic><topic>Cowpox virus - growth &amp; development</topic><topic>DNA, Viral - isolation &amp; purification</topic><topic>Domestic animals</topic><topic>Environmental assessment</topic><topic>Environmental risk</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Genes</topic><topic>Genomes</topic><topic>Hybrids</topic><topic>Immunization</topic><topic>Infections</topic><topic>Influenza</topic><topic>Influenza Vaccines - genetics</topic><topic>Influenza virus</topic><topic>Microbiology</topic><topic>Miscellaneous</topic><topic>MVA recombinant vaccines</topic><topic>Organisms, Genetically Modified</topic><topic>Orthopoxvirus</topic><topic>Phenotype</topic><topic>Polymerase Chain Reaction</topic><topic>Poxvirus</topic><topic>Proteins</topic><topic>Reassortant Viruses - genetics</topic><topic>Reassortant Viruses - physiology</topic><topic>Recombination, Genetic</topic><topic>Risk assessment</topic><topic>Safety</topic><topic>Vaccines</topic><topic>Vaccines, antisera, therapeutical immunoglobulins and monoclonal antibodies (general aspects)</topic><topic>Vaccinia virus</topic><topic>Vaccinia virus - genetics</topic><topic>Vaccinia virus - growth &amp; development</topic><topic>Vero Cells</topic><topic>Viral Plaque Assay</topic><topic>Viral Vaccines - genetics</topic><topic>Virology</topic><topic>Viruses</topic><topic>Wildlife</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Hansen, Hilde</creatorcontrib><creatorcontrib>Okeke, Malachy Ifeanyi</creatorcontrib><creatorcontrib>Nilssen, Øivind</creatorcontrib><creatorcontrib>Traavik, Terje</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Nursing &amp; Allied Health Database</collection><collection>Health and Safety Science Abstracts (Full archive)</collection><collection>Immunology Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Health &amp; Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Healthcare Administration Database (Alumni)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Public Health Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Research Library (Alumni Edition)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest One Sustainability</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>Research Library Prep</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>SciTech Premium Collection</collection><collection>Consumer Health Database (Alumni Edition)</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>Nursing &amp; Allied Health Database (Alumni Edition)</collection><collection>ProQuest Biological Science Collection</collection><collection>Consumer Health Database</collection><collection>Health &amp; Medical Collection (Alumni Edition)</collection><collection>Healthcare Administration Database</collection><collection>Medical Database</collection><collection>Research Library</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biological Science Database</collection><collection>Research Library (Corporate)</collection><collection>Nursing &amp; Allied Health Premium</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central Basic</collection><collection>Biotechnology Research Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Vaccine</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Hansen, Hilde</au><au>Okeke, Malachy Ifeanyi</au><au>Nilssen, Øivind</au><au>Traavik, Terje</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Recombinant viruses obtained from co-infection in vitro with a live vaccinia-vectored influenza vaccine and a naturally occurring cowpox virus display different plaque phenotypes and loss of the transgene</atitle><jtitle>Vaccine</jtitle><addtitle>Vaccine</addtitle><date>2004-12-09</date><risdate>2004</risdate><volume>23</volume><issue>4</issue><spage>499</spage><epage>506</epage><pages>499-506</pages><issn>0264-410X</issn><eissn>1873-2518</eissn><coden>VACCDE</coden><abstract>Some poxviruses are very attractive as transgenic vaccine vectors for humans, domestic animals and wildlife. Poxviridae family members circulate in different ecosystems and parts of the world, providing a pool of possible recombination partners for released or escaped genetically modified poxviruses. We performed in vitro double infections with a vaccinia virus strain Ankara (MVA) vectored influenza vaccine and a cowpox virus isolate from Norway, isolated hybrids, and further analyzed three hybrid viruses with different plaque phenotypes. One of the hybrids was genetically unstable, and during adaptation to new host cells its MVA derived influenza gene was deleted at a high frequency. This is significant in a risk assessment context, since the transgene would be the only logical tag for monitoring unwanted spread and non-target effects of a vaccine virus. Putative recombination events involving genetically modified and naturally occurring viruses should be included in health and environmental risk assessments.</abstract><cop>Oxford</cop><pub>Elsevier Ltd</pub><pmid>15530698</pmid><doi>10.1016/j.vaccine.2004.06.032</doi><tpages>8</tpages></addata></record>
fulltext fulltext
identifier ISSN: 0264-410X
ispartof Vaccine, 2004-12, Vol.23 (4), p.499-506
issn 0264-410X
1873-2518
language eng
recordid cdi_proquest_miscellaneous_67058203
source MEDLINE; Elsevier ScienceDirect Journals; ProQuest Central UK/Ireland
subjects Animals
Applied microbiology
Biological and medical sciences
Blotting, Southern
Cell Line
Cercopithecus aethiops
Cowpox virus
Cowpox virus - genetics
Cowpox virus - growth & development
DNA, Viral - isolation & purification
Domestic animals
Environmental assessment
Environmental risk
Fundamental and applied biological sciences. Psychology
Genes
Genomes
Hybrids
Immunization
Infections
Influenza
Influenza Vaccines - genetics
Influenza virus
Microbiology
Miscellaneous
MVA recombinant vaccines
Organisms, Genetically Modified
Orthopoxvirus
Phenotype
Polymerase Chain Reaction
Poxvirus
Proteins
Reassortant Viruses - genetics
Reassortant Viruses - physiology
Recombination, Genetic
Risk assessment
Safety
Vaccines
Vaccines, antisera, therapeutical immunoglobulins and monoclonal antibodies (general aspects)
Vaccinia virus
Vaccinia virus - genetics
Vaccinia virus - growth & development
Vero Cells
Viral Plaque Assay
Viral Vaccines - genetics
Virology
Viruses
Wildlife
title Recombinant viruses obtained from co-infection in vitro with a live vaccinia-vectored influenza vaccine and a naturally occurring cowpox virus display different plaque phenotypes and loss of the transgene
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-25T18%3A37%3A03IST&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=Recombinant%20viruses%20obtained%20from%20co-infection%20in%20vitro%20with%20a%20live%20vaccinia-vectored%20influenza%20vaccine%20and%20a%20naturally%20occurring%20cowpox%20virus%20display%20different%20plaque%20phenotypes%20and%20loss%20of%20the%20transgene&rft.jtitle=Vaccine&rft.au=Hansen,%20Hilde&rft.date=2004-12-09&rft.volume=23&rft.issue=4&rft.spage=499&rft.epage=506&rft.pages=499-506&rft.issn=0264-410X&rft.eissn=1873-2518&rft.coden=VACCDE&rft_id=info:doi/10.1016/j.vaccine.2004.06.032&rft_dat=%3Cproquest_cross%3E17760521%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=1559066565&rft_id=info:pmid/15530698&rft_els_id=S0264410X0400475X&rfr_iscdi=true