Reversion of a polymerase-defective integrated HIV-1 genome
The 8E5 clonal cell line, derived from HIV-1-infected CEM cells, carries a single, reverse transcriptase (RT)-defective copy of an integrated HIV genome. The absence of RT production is a consequence of a frame shift in the pol gene, due to the addition of a single base at position 3241. We report h...
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Veröffentlicht in: | AIDS research and human retroviruses 1993-10, Vol.9 (10), p.1031-1037 |
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description | The 8E5 clonal cell line, derived from HIV-1-infected CEM cells, carries a single, reverse transcriptase (RT)-defective copy of an integrated HIV genome. The absence of RT production is a consequence of a frame shift in the pol gene, due to the addition of a single base at position 3241. We report here that 8E5 cells produce an infectious virus that can be serially passaged on CD4+ lymphoid cells. This virus (8E5R) is RT positive, but displays a slow replication profile, together with a reduced cytopathic effect. The nucleotide sequence of a segment of the pol region produced by PCR amplification of DNA from 8E5R-infected cells shows that the single nucleotide insertion characteristic of the 8E5 genome had been corrected. The same reversion event was also found to occur in most single-cell clones derived from the 8E5 cell line. Because this cell line is used in many laboratories, notably as a standard for PCR quantitation, and is generally considered as unable to produce infectious virus, our findings should prompt investigators to use particular care in the handling of these cells. |
doi_str_mv | 10.1089/aid.1993.9.1031 |
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The absence of RT production is a consequence of a frame shift in the pol gene, due to the addition of a single base at position 3241. We report here that 8E5 cells produce an infectious virus that can be serially passaged on CD4+ lymphoid cells. This virus (8E5R) is RT positive, but displays a slow replication profile, together with a reduced cytopathic effect. The nucleotide sequence of a segment of the pol region produced by PCR amplification of DNA from 8E5R-infected cells shows that the single nucleotide insertion characteristic of the 8E5 genome had been corrected. The same reversion event was also found to occur in most single-cell clones derived from the 8E5 cell line. Because this cell line is used in many laboratories, notably as a standard for PCR quantitation, and is generally considered as unable to produce infectious virus, our findings should prompt investigators to use particular care in the handling of these cells.</description><identifier>ISSN: 0889-2229</identifier><identifier>EISSN: 1931-8405</identifier><identifier>DOI: 10.1089/aid.1993.9.1031</identifier><identifier>PMID: 7506552</identifier><identifier>CODEN: ARHRE7</identifier><language>eng</language><publisher>Larchmont, NY: Liebert</publisher><subject>AIDS/HIV ; Base Sequence ; Biological and medical sciences ; Cell Line ; Defective Viruses - genetics ; Fundamental and applied biological sciences. Psychology ; Genetics ; Genome, Viral ; HIV Reverse Transcriptase ; HIV-1 - enzymology ; HIV-1 - genetics ; HIV-1 - growth & development ; HIV-1 - ultrastructure ; human immunodeficiency virus 1 ; Humans ; Microbiology ; Molecular Sequence Data ; Mutation ; Polymerase Chain Reaction ; RNA-Directed DNA Polymerase - genetics ; Sequence Analysis, DNA ; Sequence Homology, Nucleic Acid ; Viral Proteins - analysis ; Virology ; Virus Integration ; Virus Replication</subject><ispartof>AIDS research and human retroviruses, 1993-10, Vol.9 (10), p.1031-1037</ispartof><rights>1994 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c352t-6ca12d40766699eee0220219b88e899abcbf1ec1c5245e5f41ea3f6588d52df33</citedby><cites>FETCH-LOGICAL-c352t-6ca12d40766699eee0220219b88e899abcbf1ec1c5245e5f41ea3f6588d52df33</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,3033,27915,27916</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=4124361$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/7506552$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>QUILLENT, C</creatorcontrib><creatorcontrib>DUMEY, N</creatorcontrib><creatorcontrib>DAUGUET, C</creatorcontrib><creatorcontrib>CLAVEL, F</creatorcontrib><title>Reversion of a polymerase-defective integrated HIV-1 genome</title><title>AIDS research and human retroviruses</title><addtitle>AIDS Res Hum Retroviruses</addtitle><description>The 8E5 clonal cell line, derived from HIV-1-infected CEM cells, carries a single, reverse transcriptase (RT)-defective copy of an integrated HIV genome. The absence of RT production is a consequence of a frame shift in the pol gene, due to the addition of a single base at position 3241. We report here that 8E5 cells produce an infectious virus that can be serially passaged on CD4+ lymphoid cells. This virus (8E5R) is RT positive, but displays a slow replication profile, together with a reduced cytopathic effect. The nucleotide sequence of a segment of the pol region produced by PCR amplification of DNA from 8E5R-infected cells shows that the single nucleotide insertion characteristic of the 8E5 genome had been corrected. The same reversion event was also found to occur in most single-cell clones derived from the 8E5 cell line. Because this cell line is used in many laboratories, notably as a standard for PCR quantitation, and is generally considered as unable to produce infectious virus, our findings should prompt investigators to use particular care in the handling of these cells.</description><subject>AIDS/HIV</subject><subject>Base Sequence</subject><subject>Biological and medical sciences</subject><subject>Cell Line</subject><subject>Defective Viruses - genetics</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Genetics</subject><subject>Genome, Viral</subject><subject>HIV Reverse Transcriptase</subject><subject>HIV-1 - enzymology</subject><subject>HIV-1 - genetics</subject><subject>HIV-1 - growth & development</subject><subject>HIV-1 - ultrastructure</subject><subject>human immunodeficiency virus 1</subject><subject>Humans</subject><subject>Microbiology</subject><subject>Molecular Sequence Data</subject><subject>Mutation</subject><subject>Polymerase Chain Reaction</subject><subject>RNA-Directed DNA Polymerase - genetics</subject><subject>Sequence Analysis, DNA</subject><subject>Sequence Homology, Nucleic Acid</subject><subject>Viral Proteins - analysis</subject><subject>Virology</subject><subject>Virus Integration</subject><subject>Virus Replication</subject><issn>0889-2229</issn><issn>1931-8405</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1993</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkE1LAzEURYMotVbXroRZiLtp85JJJsGVFLWFgiDqNqSZlzIyHzWZFvrvncHSravH4557F4eQW6BToErPbFlMQWs-1f3P4YyMQXNIVUbFORlTpXTKGNOX5CrGb0qpZkyMyCgXVArBxuTxHfcYYtk2SesTm2zb6lBjsBHTAj26rtxjUjYdboLtsEgWy68Ukg02bY3X5MLbKuLN8U7I58vzx3yRrt5el_OnVeq4YF0qnQVWZDSXUmqNiJQxykCvlUKltV27tQd04ATLBAqfAVrupVCqEKzwnE_Iw9_uNrQ_O4ydqcvosKpsg-0umlxCzpiCf0GQElTOB3D2B7rQxhjQm20oaxsOBqgZvJreqxm8Gm0Gr33j7ji9W9dYnPijyD6_P-Y2Olv5YBtXxhOWAcu4BP4LLZB-3A</recordid><startdate>19931001</startdate><enddate>19931001</enddate><creator>QUILLENT, C</creator><creator>DUMEY, N</creator><creator>DAUGUET, C</creator><creator>CLAVEL, F</creator><general>Liebert</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>7U9</scope><scope>H94</scope><scope>7X8</scope></search><sort><creationdate>19931001</creationdate><title>Reversion of a polymerase-defective integrated HIV-1 genome</title><author>QUILLENT, C ; DUMEY, N ; DAUGUET, C ; CLAVEL, F</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c352t-6ca12d40766699eee0220219b88e899abcbf1ec1c5245e5f41ea3f6588d52df33</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1993</creationdate><topic>AIDS/HIV</topic><topic>Base Sequence</topic><topic>Biological and medical sciences</topic><topic>Cell Line</topic><topic>Defective Viruses - genetics</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Genetics</topic><topic>Genome, Viral</topic><topic>HIV Reverse Transcriptase</topic><topic>HIV-1 - enzymology</topic><topic>HIV-1 - genetics</topic><topic>HIV-1 - growth & development</topic><topic>HIV-1 - ultrastructure</topic><topic>human immunodeficiency virus 1</topic><topic>Humans</topic><topic>Microbiology</topic><topic>Molecular Sequence Data</topic><topic>Mutation</topic><topic>Polymerase Chain Reaction</topic><topic>RNA-Directed DNA Polymerase - genetics</topic><topic>Sequence Analysis, DNA</topic><topic>Sequence Homology, Nucleic Acid</topic><topic>Viral Proteins - analysis</topic><topic>Virology</topic><topic>Virus Integration</topic><topic>Virus Replication</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>QUILLENT, C</creatorcontrib><creatorcontrib>DUMEY, N</creatorcontrib><creatorcontrib>DAUGUET, C</creatorcontrib><creatorcontrib>CLAVEL, F</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>Virology and AIDS Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>AIDS research and human retroviruses</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>QUILLENT, C</au><au>DUMEY, N</au><au>DAUGUET, C</au><au>CLAVEL, F</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Reversion of a polymerase-defective integrated HIV-1 genome</atitle><jtitle>AIDS research and human retroviruses</jtitle><addtitle>AIDS Res Hum Retroviruses</addtitle><date>1993-10-01</date><risdate>1993</risdate><volume>9</volume><issue>10</issue><spage>1031</spage><epage>1037</epage><pages>1031-1037</pages><issn>0889-2229</issn><eissn>1931-8405</eissn><coden>ARHRE7</coden><abstract>The 8E5 clonal cell line, derived from HIV-1-infected CEM cells, carries a single, reverse transcriptase (RT)-defective copy of an integrated HIV genome. The absence of RT production is a consequence of a frame shift in the pol gene, due to the addition of a single base at position 3241. We report here that 8E5 cells produce an infectious virus that can be serially passaged on CD4+ lymphoid cells. This virus (8E5R) is RT positive, but displays a slow replication profile, together with a reduced cytopathic effect. The nucleotide sequence of a segment of the pol region produced by PCR amplification of DNA from 8E5R-infected cells shows that the single nucleotide insertion characteristic of the 8E5 genome had been corrected. The same reversion event was also found to occur in most single-cell clones derived from the 8E5 cell line. Because this cell line is used in many laboratories, notably as a standard for PCR quantitation, and is generally considered as unable to produce infectious virus, our findings should prompt investigators to use particular care in the handling of these cells.</abstract><cop>Larchmont, NY</cop><pub>Liebert</pub><pmid>7506552</pmid><doi>10.1089/aid.1993.9.1031</doi><tpages>7</tpages></addata></record> |
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subjects | AIDS/HIV Base Sequence Biological and medical sciences Cell Line Defective Viruses - genetics Fundamental and applied biological sciences. Psychology Genetics Genome, Viral HIV Reverse Transcriptase HIV-1 - enzymology HIV-1 - genetics HIV-1 - growth & development HIV-1 - ultrastructure human immunodeficiency virus 1 Humans Microbiology Molecular Sequence Data Mutation Polymerase Chain Reaction RNA-Directed DNA Polymerase - genetics Sequence Analysis, DNA Sequence Homology, Nucleic Acid Viral Proteins - analysis Virology Virus Integration Virus Replication |
title | Reversion of a polymerase-defective integrated HIV-1 genome |
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