Human cytomegalovirus glycoprotein H/glycoprotein L complex modulates fusion-from-without
RS Milne, DA Paterson and JC Booth Department of Medical Microbiology, St George's Hospital Medical School, London, UK. Glycoprotein H/glycoprotein L (gH/gL) complexes of herpesviruses are required for fusion of infecting virions with host cell membranes. In human cytomegalovirus (HCMV), neutra...
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Veröffentlicht in: | Journal of general virology 1998-04, Vol.79 (4), p.855-865 |
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creator | Milne, RS Paterson, DA Booth, JC |
description | RS Milne, DA Paterson and JC Booth
Department of Medical Microbiology, St George's Hospital Medical School, London, UK.
Glycoprotein H/glycoprotein L (gH/gL) complexes of herpesviruses are
required for fusion of infecting virions with host cell membranes. In human
cytomegalovirus (HCMV), neutralizing monoclonal antibodies (MAb) specific
for gH inhibit the transfer of a fluorescent probe to the host cell from
labelled virus particles. In similar fashion, in the present study,
neutralizing gH-specific MAb inhibited HCMV-induced fusion-from- without in
monolayers of both human embryonic fibroblasts and continuous astrocytoma
cells (U373). No fusion was detected in cells co- infected with defective
recombinant adenovirus vectors that elicited high-level expression of gH
and gL, indicating that surface-expressed gH was not intrinsically
fusogenic. However, when such cells were superinfected with HCMV that gave
fusion-from-without, the resulting cell-to-cell fusion was considerably
enhanced. Thus, under our experimental conditions, gH/gL on the cell
surface functioned to increase membrane fusion once this was initiated by
other components in the virus envelope. |
doi_str_mv | 10.1099/0022-1317-79-4-855 |
format | Article |
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Department of Medical Microbiology, St George's Hospital Medical School, London, UK.
Glycoprotein H/glycoprotein L (gH/gL) complexes of herpesviruses are
required for fusion of infecting virions with host cell membranes. In human
cytomegalovirus (HCMV), neutralizing monoclonal antibodies (MAb) specific
for gH inhibit the transfer of a fluorescent probe to the host cell from
labelled virus particles. In similar fashion, in the present study,
neutralizing gH-specific MAb inhibited HCMV-induced fusion-from- without in
monolayers of both human embryonic fibroblasts and continuous astrocytoma
cells (U373). No fusion was detected in cells co- infected with defective
recombinant adenovirus vectors that elicited high-level expression of gH
and gL, indicating that surface-expressed gH was not intrinsically
fusogenic. However, when such cells were superinfected with HCMV that gave
fusion-from-without, the resulting cell-to-cell fusion was considerably
enhanced. Thus, under our experimental conditions, gH/gL on the cell
surface functioned to increase membrane fusion once this was initiated by
other components in the virus envelope.</description><identifier>ISSN: 0022-1317</identifier><identifier>EISSN: 1465-2099</identifier><identifier>DOI: 10.1099/0022-1317-79-4-855</identifier><identifier>PMID: 9568982</identifier><language>eng</language><publisher>England: Soc General Microbiol</publisher><subject>Adenoviridae - genetics ; Antibodies, Monoclonal - pharmacology ; Base Sequence ; Cells, Cultured ; Cytomegalovirus - genetics ; Cytomegalovirus - pathogenicity ; Cytomegalovirus - physiology ; Dactinomycin - pharmacology ; Defective Viruses - genetics ; DNA Primers - genetics ; Humans ; Membrane Fusion - drug effects ; Membrane Fusion - physiology ; Polymerase Chain Reaction ; Recombination, Genetic ; Viral Envelope Proteins - genetics ; Viral Envelope Proteins - immunology ; Viral Envelope Proteins - physiology</subject><ispartof>Journal of general virology, 1998-04, Vol.79 (4), p.855-865</ispartof><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c405t-5a3299da07053408c0a74cd6cfab4d9215ce8b9e302e97558a51a9191e4bbfc33</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,3732,3733,27903,27904</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/9568982$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Milne, RS</creatorcontrib><creatorcontrib>Paterson, DA</creatorcontrib><creatorcontrib>Booth, JC</creatorcontrib><title>Human cytomegalovirus glycoprotein H/glycoprotein L complex modulates fusion-from-without</title><title>Journal of general virology</title><addtitle>J Gen Virol</addtitle><description>RS Milne, DA Paterson and JC Booth
Department of Medical Microbiology, St George's Hospital Medical School, London, UK.
Glycoprotein H/glycoprotein L (gH/gL) complexes of herpesviruses are
required for fusion of infecting virions with host cell membranes. In human
cytomegalovirus (HCMV), neutralizing monoclonal antibodies (MAb) specific
for gH inhibit the transfer of a fluorescent probe to the host cell from
labelled virus particles. In similar fashion, in the present study,
neutralizing gH-specific MAb inhibited HCMV-induced fusion-from- without in
monolayers of both human embryonic fibroblasts and continuous astrocytoma
cells (U373). No fusion was detected in cells co- infected with defective
recombinant adenovirus vectors that elicited high-level expression of gH
and gL, indicating that surface-expressed gH was not intrinsically
fusogenic. However, when such cells were superinfected with HCMV that gave
fusion-from-without, the resulting cell-to-cell fusion was considerably
enhanced. Thus, under our experimental conditions, gH/gL on the cell
surface functioned to increase membrane fusion once this was initiated by
other components in the virus envelope.</description><subject>Adenoviridae - genetics</subject><subject>Antibodies, Monoclonal - pharmacology</subject><subject>Base Sequence</subject><subject>Cells, Cultured</subject><subject>Cytomegalovirus - genetics</subject><subject>Cytomegalovirus - pathogenicity</subject><subject>Cytomegalovirus - physiology</subject><subject>Dactinomycin - pharmacology</subject><subject>Defective Viruses - genetics</subject><subject>DNA Primers - genetics</subject><subject>Humans</subject><subject>Membrane Fusion - drug effects</subject><subject>Membrane Fusion - physiology</subject><subject>Polymerase Chain Reaction</subject><subject>Recombination, Genetic</subject><subject>Viral Envelope Proteins - genetics</subject><subject>Viral Envelope Proteins - immunology</subject><subject>Viral Envelope Proteins - physiology</subject><issn>0022-1317</issn><issn>1465-2099</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1998</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkE9LwzAYh4Moc06_gCD0pKe4_G2bowx1wsCLHjyFNE27SNPMpnXu25uyMfDkKYTf733y5gHgGqN7jISYI0QIxBRnMBOQwZzzEzDFLOWQxPgUTI-Fc3ARwidCmDGeTcBE8DQXOZmCj-XgVJvoXe-dqVXjv203hKRudtpvOt8b2ybL-Z_rKtHebRrzkzhfDo3qTUiqIVjfwqrzDm5tv_ZDfwnOKtUEc3U4Z-D96fFtsYSr1-eXxcMKaoZ4D7miRIhSoQxxylCukcqYLlNdqYKVgmCuTV4IQxExIuM8VxwrgQU2rCgqTekM3O65cb-vwYReOhu0aRrVGj8EmcV_cpzif4s4ZTindCSSfVF3PoTOVHLTWae6ncRIjuLl6FWOXiNdMhnFx6GbA30onCmPIwfTMb_b52tbr7e2M7I2rbPxicJ6Ga0fSb8olY24</recordid><startdate>19980401</startdate><enddate>19980401</enddate><creator>Milne, RS</creator><creator>Paterson, DA</creator><creator>Booth, JC</creator><general>Soc General Microbiol</general><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>19980401</creationdate><title>Human cytomegalovirus glycoprotein H/glycoprotein L complex modulates fusion-from-without</title><author>Milne, RS ; Paterson, DA ; Booth, JC</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c405t-5a3299da07053408c0a74cd6cfab4d9215ce8b9e302e97558a51a9191e4bbfc33</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1998</creationdate><topic>Adenoviridae - genetics</topic><topic>Antibodies, Monoclonal - pharmacology</topic><topic>Base Sequence</topic><topic>Cells, Cultured</topic><topic>Cytomegalovirus - genetics</topic><topic>Cytomegalovirus - pathogenicity</topic><topic>Cytomegalovirus - physiology</topic><topic>Dactinomycin - pharmacology</topic><topic>Defective Viruses - genetics</topic><topic>DNA Primers - genetics</topic><topic>Humans</topic><topic>Membrane Fusion - drug effects</topic><topic>Membrane Fusion - physiology</topic><topic>Polymerase Chain Reaction</topic><topic>Recombination, Genetic</topic><topic>Viral Envelope Proteins - genetics</topic><topic>Viral Envelope Proteins - immunology</topic><topic>Viral Envelope Proteins - physiology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Milne, RS</creatorcontrib><creatorcontrib>Paterson, DA</creatorcontrib><creatorcontrib>Booth, JC</creatorcontrib><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>Journal of general virology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Milne, RS</au><au>Paterson, DA</au><au>Booth, JC</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Human cytomegalovirus glycoprotein H/glycoprotein L complex modulates fusion-from-without</atitle><jtitle>Journal of general virology</jtitle><addtitle>J Gen Virol</addtitle><date>1998-04-01</date><risdate>1998</risdate><volume>79</volume><issue>4</issue><spage>855</spage><epage>865</epage><pages>855-865</pages><issn>0022-1317</issn><eissn>1465-2099</eissn><abstract>RS Milne, DA Paterson and JC Booth
Department of Medical Microbiology, St George's Hospital Medical School, London, UK.
Glycoprotein H/glycoprotein L (gH/gL) complexes of herpesviruses are
required for fusion of infecting virions with host cell membranes. In human
cytomegalovirus (HCMV), neutralizing monoclonal antibodies (MAb) specific
for gH inhibit the transfer of a fluorescent probe to the host cell from
labelled virus particles. In similar fashion, in the present study,
neutralizing gH-specific MAb inhibited HCMV-induced fusion-from- without in
monolayers of both human embryonic fibroblasts and continuous astrocytoma
cells (U373). No fusion was detected in cells co- infected with defective
recombinant adenovirus vectors that elicited high-level expression of gH
and gL, indicating that surface-expressed gH was not intrinsically
fusogenic. However, when such cells were superinfected with HCMV that gave
fusion-from-without, the resulting cell-to-cell fusion was considerably
enhanced. Thus, under our experimental conditions, gH/gL on the cell
surface functioned to increase membrane fusion once this was initiated by
other components in the virus envelope.</abstract><cop>England</cop><pub>Soc General Microbiol</pub><pmid>9568982</pmid><doi>10.1099/0022-1317-79-4-855</doi><tpages>11</tpages><oa>free_for_read</oa></addata></record> |
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source | MEDLINE; Microbiology Society; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; Alma/SFX Local Collection |
subjects | Adenoviridae - genetics Antibodies, Monoclonal - pharmacology Base Sequence Cells, Cultured Cytomegalovirus - genetics Cytomegalovirus - pathogenicity Cytomegalovirus - physiology Dactinomycin - pharmacology Defective Viruses - genetics DNA Primers - genetics Humans Membrane Fusion - drug effects Membrane Fusion - physiology Polymerase Chain Reaction Recombination, Genetic Viral Envelope Proteins - genetics Viral Envelope Proteins - immunology Viral Envelope Proteins - physiology |
title | Human cytomegalovirus glycoprotein H/glycoprotein L complex modulates fusion-from-without |
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