Superinfection exclusion of vaccinia virus in virus-infected cell cultures
Identifieur interne : 000685 ( Istex/Corpus ); précédent : 000684; suivant : 000686Superinfection exclusion of vaccinia virus in virus-infected cell cultures
Auteurs : Linda Christen ; Janny Seto ; Edward G. NilesSource :
- Virology [ 0042-6822 ] ; 1990.
English descriptors
- Teeft :
- Adsorption, Assay, Cell monolayers, Condit, Early gene expression, Early gene transcription, Exclusion, Gene, Gene expression, Host protein synthesis, Initial infection, Late gene expression, Late virus protein synthesis, Monolayer, Monolayer cultures, Monolayers, Mutant, Nonpermissive temperature, Plaque, Postinfection, Primary infection, Protein synthesis, Replication, Seto, Southern transfer analysis, Standard superinfection assay, Superinfected, Superinfecting, Superinfecting vaccinia virus, Superinfecting virus, Superinfection, Superinfection exclusion, Time point, Transcription, Vaccinia, Vaccinia virus, Vaccinia virus gene, Various times, Viral, Virology, Virus, Virus adsorption, Vsc8, Vsc9.
Abstract
Abstract: Vaccinia virus-infected BSC 40 cells do not permit the replication of superinfecting vaccinia virus. The extent of superinfecting virus propagation depends on the time of superinfection; there is 90% exclusion by 4 hr after the initial infection, and more than 99% by 6 hr. When superinfection is attempted at 6 hr after infection, the superinfecting virus is incapable of carrying out DNA replication or early gene transcription, demonstrating that an early event in the virus life cycle is inhibited. The rate of adsorption of the superinfecting virus is unaltered which shows that exclusion is affected at a point between adsorption and early gene transcription. In order to exclude superinfection, the primary infecting virus does not require replication of its DNA or expression of its late genes but it must express one or more early genes.
Url:
DOI: 10.1016/0042-6822(90)90051-R
Links to Exploration step
ISTEX:33BBF979F149D5C676FED239C107B2D1DD26B350Le document en format XML
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Niles</name><affiliation><mods:affiliation>Department of Biochemistry, State University of New York, Buffalo, New York 14214, USA</mods:affiliation></affiliation></author></analytic><monogr></monogr><series><title level="j">Virology</title><title level="j" type="abbrev">YVIRO</title><idno type="ISSN">0042-6822</idno><imprint><publisher>ELSEVIER</publisher><date type="published" when="1990">1990</date><biblScope unit="volume">174</biblScope><biblScope unit="issue">1</biblScope><biblScope unit="page" from="35">35</biblScope><biblScope unit="page" to="42">42</biblScope></imprint><idno type="ISSN">0042-6822</idno></series></biblStruct></sourceDesc><seriesStmt><idno type="ISSN">0042-6822</idno></seriesStmt></fileDesc><profileDesc><textClass><keywords scheme="Teeft" xml:lang="en"><term>Adsorption</term><term>Assay</term><term>Cell monolayers</term><term>Condit</term><term>Early gene expression</term><term>Early gene transcription</term><term>Exclusion</term><term>Gene</term><term>Gene expression</term><term>Host protein synthesis</term><term>Initial infection</term><term>Late gene expression</term><term>Late virus protein synthesis</term><term>Monolayer</term><term>Monolayer cultures</term><term>Monolayers</term><term>Mutant</term><term>Nonpermissive temperature</term><term>Plaque</term><term>Postinfection</term><term>Primary infection</term><term>Protein synthesis</term><term>Replication</term><term>Seto</term><term>Southern transfer analysis</term><term>Standard superinfection assay</term><term>Superinfected</term><term>Superinfecting</term><term>Superinfecting vaccinia virus</term><term>Superinfecting virus</term><term>Superinfection</term><term>Superinfection exclusion</term><term>Time point</term><term>Transcription</term><term>Vaccinia</term><term>Vaccinia virus</term><term>Vaccinia virus gene</term><term>Various times</term><term>Viral</term><term>Virology</term><term>Virus</term><term>Virus adsorption</term><term>Vsc8</term><term>Vsc9</term></keywords></textClass><langUsage><language ident="en">en</language></langUsage></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">Abstract: Vaccinia virus-infected BSC 40 cells do not permit the replication of superinfecting vaccinia virus. The extent of superinfecting virus propagation depends on the time of superinfection; there is 90% exclusion by 4 hr after the initial infection, and more than 99% by 6 hr. When superinfection is attempted at 6 hr after infection, the superinfecting virus is incapable of carrying out DNA replication or early gene transcription, demonstrating that an early event in the virus life cycle is inhibited. The rate of adsorption of the superinfecting virus is unaltered which shows that exclusion is affected at a point between adsorption and early gene transcription. In order to exclude superinfection, the primary infecting virus does not require replication of its DNA or expression of its late genes but it must express one or more early genes.</div></front></TEI><istex><corpusName>elsevier</corpusName><keywords><teeft><json:string>superinfection</json:string><json:string>vaccinia</json:string><json:string>superinfecting</json:string><json:string>superinfecting virus</json:string><json:string>viral</json:string><json:string>replication</json:string><json:string>vsc8</json:string><json:string>vaccinia virus</json:string><json:string>condit</json:string><json:string>mutant</json:string><json:string>adsorption</json:string><json:string>seto</json:string><json:string>early gene expression</json:string><json:string>monolayer</json:string><json:string>postinfection</json:string><json:string>superinfected</json:string><json:string>early gene transcription</json:string><json:string>monolayers</json:string><json:string>vsc9</json:string><json:string>virology</json:string><json:string>initial infection</json:string><json:string>superinfection exclusion</json:string><json:string>virus</json:string><json:string>cell monolayers</json:string><json:string>host protein synthesis</json:string><json:string>nonpermissive temperature</json:string><json:string>various times</json:string><json:string>primary infection</json:string><json:string>late gene expression</json:string><json:string>superinfecting vaccinia virus</json:string><json:string>assay</json:string><json:string>transcription</json:string><json:string>southern transfer analysis</json:string><json:string>vaccinia virus gene</json:string><json:string>monolayer cultures</json:string><json:string>late virus protein synthesis</json:string><json:string>gene expression</json:string><json:string>time point</json:string><json:string>virus adsorption</json:string><json:string>standard superinfection assay</json:string><json:string>protein synthesis</json:string><json:string>gene</json:string><json:string>exclusion</json:string><json:string>plaque</json:string></teeft></keywords><author><json:item><name>Linda Christen</name><affiliations><json:string>Department of Biochemistry, State University of New York, Buffalo, New York 14214, USA</json:string></affiliations></json:item><json:item><name>Janny Seto</name><affiliations><json:string>Department of Biochemistry, State University of New York, Buffalo, New York 14214, USA</json:string></affiliations></json:item><json:item><name>Edward G. Niles</name><affiliations><json:string>Department of Biochemistry, State University of New York, Buffalo, New York 14214, USA</json:string></affiliations></json:item></author><arkIstex>ark:/67375/6H6-ZHH760W7-V</arkIstex><language><json:string>eng</json:string></language><originalGenre><json:string>Full-length article</json:string></originalGenre><abstract>Abstract: Vaccinia virus-infected BSC 40 cells do not permit the replication of superinfecting vaccinia virus. The extent of superinfecting virus propagation depends on the time of superinfection; there is 90% exclusion by 4 hr after the initial infection, and more than 99% by 6 hr. When superinfection is attempted at 6 hr after infection, the superinfecting virus is incapable of carrying out DNA replication or early gene transcription, demonstrating that an early event in the virus life cycle is inhibited. The rate of adsorption of the superinfecting virus is unaltered which shows that exclusion is affected at a point between adsorption and early gene transcription. In order to exclude superinfection, the primary infecting virus does not require replication of its DNA or expression of its late genes but it must express one or more early genes.</abstract><qualityIndicators><refBibsNative>true</refBibsNative><abstractWordCount>136</abstractWordCount><abstractCharCount>856</abstractCharCount><keywordCount>0</keywordCount><score>8.235</score><pdfWordCount>4603</pdfWordCount><pdfCharCount>27925</pdfCharCount><pdfVersion>1.3</pdfVersion><pdfPageCount>8</pdfPageCount><pdfPageSize>612 x 792 pts (letter)</pdfPageSize></qualityIndicators><title>Superinfection exclusion of vaccinia virus in virus-infected cell cultures</title><pmid><json:string>2294646</json:string></pmid><pii><json:string>0042-6822(90)90051-R</json:string></pii><genre><json:string>research-article</json:string></genre><serie><title>Methods in Enzymology</title><language><json:string>unknown</json:string></language><volume>Vol. 100</volume><pages><first>255</first><last>266</last></pages><editor><json:item><name>R. Wu</name></json:item><json:item><name>L. Grossman</name></json:item><json:item><name>K. Moldave</name></json:item></editor></serie><host><title>Virology</title><language><json:string>unknown</json:string></language><publicationDate>1990</publicationDate><issn><json:string>0042-6822</json:string></issn><pii><json:string>S0042-6822(00)X0363-7</json:string></pii><volume>174</volume><issue>1</issue><pages><first>35</first><last>42</last></pages><genre><json:string>journal</json:string></genre></host><namedEntities><unitex><date><json:string>35S</json:string><json:string>1990</json:string></date><geogName></geogName><orgName><json:string>Press, Inc</json:string><json:string>National Science Foundation PCM</json:string></orgName><orgName_funder><json:string>National Science Foundation PCM</json:string></orgName_funder><orgName_provider></orgName_provider><persName><json:string>B. 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The extent of superinfecting virus propagation depends on the time of superinfection; there is 90% exclusion by 4 hr after the initial infection, and more than 99% by 6 hr. When superinfection is attempted at 6 hr after infection, the superinfecting virus is incapable of carrying out DNA replication or early gene transcription, demonstrating that an early event in the virus life cycle is inhibited. The rate of adsorption of the superinfecting virus is unaltered which shows that exclusion is affected at a point between adsorption and early gene transcription. In order to exclude superinfection, the primary infecting virus does not require replication of its DNA or expression of its late genes but it must express one or more early genes.</p></abstract></profileDesc><revisionDesc><change when="1990">Published</change></revisionDesc></teiHeader></istex:fulltextTEI><json:item><extension>txt</extension><original>false</original><mimetype>text/plain</mimetype><uri>https://api.istex.fr/ark:/67375/6H6-ZHH760W7-V/fulltext.txt</uri></json:item></fulltext><metadata><istex:metadataXml wicri:clean="Elsevier, elements deleted: tail"><istex:xmlDeclaration>version="1.0" encoding="utf-8"</istex:xmlDeclaration><istex:docType PUBLIC="-//ES//DTD journal article DTD version 4.5.2//EN//XML" URI="art452.dtd" name="istex:docType"></istex:docType><istex:document><converted-article version="4.5.2" docsubtype="fla"><item-info><jid>YVIRO</jid><aid>9090051R</aid><ce:pii>0042-6822(90)90051-R</ce:pii><ce:doi>10.1016/0042-6822(90)90051-R</ce:doi><ce:copyright type="unknown" year="1990"></ce:copyright></item-info><head><ce:title>Superinfection exclusion of vaccinia virus in virus-infected cell cultures</ce:title><ce:author-group><ce:author><ce:given-name>Linda</ce:given-name><ce:surname>Christen</ce:surname></ce:author><ce:author><ce:given-name>Janny</ce:given-name><ce:surname>Seto</ce:surname></ce:author><ce:author><ce:given-name>Edward G.</ce:given-name><ce:surname>Niles</ce:surname><ce:cross-ref refid="COR1"><ce:sup>1</ce:sup></ce:cross-ref></ce:author><ce:affiliation><ce:textfn>Department of Biochemistry, State University of New York, Buffalo, New York 14214, USA</ce:textfn></ce:affiliation><ce:correspondence id="COR1"><ce:label>1</ce:label><ce:text>To whom requests for reprints should be addressed.</ce:text></ce:correspondence></ce:author-group><ce:date-received day="14" month="6" year="1989"></ce:date-received><ce:date-accepted day="22" month="8" year="1989"></ce:date-accepted><ce:abstract><ce:section-title>Abstract</ce:section-title><ce:abstract-sec><ce:simple-para>Vaccinia virus-infected BSC 40 cells do not permit the replication of superinfecting vaccinia virus. The extent of superinfecting virus propagation depends on the time of superinfection; there is 90% exclusion by 4 hr after the initial infection, and more than 99% by 6 hr. When superinfection is attempted at 6 hr after infection, the superinfecting virus is incapable of carrying out DNA replication or early gene transcription, demonstrating that an early event in the virus life cycle is inhibited. The rate of adsorption of the superinfecting virus is unaltered which shows that exclusion is affected at a point between adsorption and early gene transcription. In order to exclude superinfection, the primary infecting virus does not require replication of its DNA or expression of its late genes but it must express one or more early genes.</ce:simple-para></ce:abstract-sec></ce:abstract></head></converted-article></istex:document></istex:metadataXml><mods version="3.6"><titleInfo><title>Superinfection exclusion of vaccinia virus in virus-infected cell cultures</title></titleInfo><titleInfo type="alternative" contentType="CDATA"><title>Superinfection exclusion of vaccinia virus in virus-infected cell cultures</title></titleInfo><name type="personal"><namePart type="given">Linda</namePart><namePart type="family">Christen</namePart><affiliation>Department of Biochemistry, State University of New York, Buffalo, New York 14214, USA</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">Janny</namePart><namePart type="family">Seto</namePart><affiliation>Department of Biochemistry, State University of New York, Buffalo, New York 14214, USA</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">Edward G.</namePart><namePart type="family">Niles</namePart><affiliation>Department of Biochemistry, State University of New York, Buffalo, New York 14214, USA</affiliation><description>To whom requests for reprints should be addressed.</description><role><roleTerm type="text">author</roleTerm></role></name><typeOfResource>text</typeOfResource><genre type="research-article" displayLabel="Full-length article" authority="ISTEX" authorityURI="https://content-type.data.istex.fr" valueURI="https://content-type.data.istex.fr/ark:/67375/XTP-1JC4F85T-7">research-article</genre><originInfo><publisher>ELSEVIER</publisher><dateIssued encoding="w3cdtf">1990</dateIssued><copyrightDate encoding="w3cdtf">1990</copyrightDate></originInfo><language><languageTerm type="code" authority="iso639-2b">eng</languageTerm><languageTerm type="code" authority="rfc3066">en</languageTerm></language><abstract lang="en">Abstract: Vaccinia virus-infected BSC 40 cells do not permit the replication of superinfecting vaccinia virus. The extent of superinfecting virus propagation depends on the time of superinfection; there is 90% exclusion by 4 hr after the initial infection, and more than 99% by 6 hr. When superinfection is attempted at 6 hr after infection, the superinfecting virus is incapable of carrying out DNA replication or early gene transcription, demonstrating that an early event in the virus life cycle is inhibited. The rate of adsorption of the superinfecting virus is unaltered which shows that exclusion is affected at a point between adsorption and early gene transcription. 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