Characterization of a strain of murine cytomegalovirus which fails to grow in the salivary glands of mice
Division of Medical Microbiology, University of British Columbia, Faculty of Medicine, 2733 Heather Street, Vancouver, British Columbia V5Z 1M9, Canada Characterization of a tissue culture-adapted strain of murine cytomegalovirus (MCMV), the Vancouver strain, which demonstrated altered tissue tropis...
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Veröffentlicht in: | Journal of general virology 1992-08, Vol.73 (8), p.2021-2029 |
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creator | Boname, J. M Chantler, J. K |
description | Division of Medical Microbiology, University of British Columbia, Faculty of Medicine, 2733 Heather Street, Vancouver, British Columbia V5Z 1M9, Canada
Characterization of a tissue culture-adapted strain of murine cytomegalovirus (MCMV), the Vancouver strain, which demonstrated altered tissue tropism in mice was undertaken to help understand the mechanism of pathogenesis of cytomegaloviruses. The Vancouver strain grew to a limited extent in the spleen but failed to grow in the salivary glands of inoculated mice. This mutation probably arose during multiple in vitro passaging of the parental Smith strain. The Vancouver strain replicated more quickly and produced a greater yield of virus per cycle than the Smith strain in vitro , resulting in a larger plaque size. In addition to these phenotypic differences, the Vancouver strain was found to have a 9.4 kb deletion spanning the Xba I I/L junction of the parental Smith strain (0.960 to 0.995 map units), and a 0.9 kb insertion which mapped to the Eco RI K fragment (0.37 to 0.47 map units). Analysis of virus-induced proteins at various times post-infection identified only one major change in Vancouver strain-infected cells, the absence of a 42K protein found in Smith-infected cells at early and late times.
Present address: Department of Microbiology and Immunology, Stanford University School of Medicine, Stanford, California 95305-5402, U.S.A.
Received 22 January 1992;
accepted 24 April 1992. |
doi_str_mv | 10.1099/0022-1317-73-8-2021 |
format | Article |
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Characterization of a tissue culture-adapted strain of murine cytomegalovirus (MCMV), the Vancouver strain, which demonstrated altered tissue tropism in mice was undertaken to help understand the mechanism of pathogenesis of cytomegaloviruses. The Vancouver strain grew to a limited extent in the spleen but failed to grow in the salivary glands of inoculated mice. This mutation probably arose during multiple in vitro passaging of the parental Smith strain. The Vancouver strain replicated more quickly and produced a greater yield of virus per cycle than the Smith strain in vitro , resulting in a larger plaque size. In addition to these phenotypic differences, the Vancouver strain was found to have a 9.4 kb deletion spanning the Xba I I/L junction of the parental Smith strain (0.960 to 0.995 map units), and a 0.9 kb insertion which mapped to the Eco RI K fragment (0.37 to 0.47 map units). Analysis of virus-induced proteins at various times post-infection identified only one major change in Vancouver strain-infected cells, the absence of a 42K protein found in Smith-infected cells at early and late times.
Present address: Department of Microbiology and Immunology, Stanford University School of Medicine, Stanford, California 95305-5402, U.S.A.
Received 22 January 1992;
accepted 24 April 1992.</description><identifier>ISSN: 0022-1317</identifier><identifier>EISSN: 1465-2099</identifier><identifier>DOI: 10.1099/0022-1317-73-8-2021</identifier><identifier>PMID: 1322959</identifier><identifier>CODEN: JGVIAY</identifier><language>eng</language><publisher>Reading: Soc General Microbiol</publisher><subject>3T3 Cells ; Animals ; Biological and medical sciences ; Blotting, Southern ; cytomegalovirus ; Cytomegalovirus - chemistry ; Cytomegalovirus - genetics ; Cytomegalovirus - growth & development ; Female ; Fundamental and applied biological sciences. Psychology ; Genome, Viral ; Mice ; Mice, Inbred Strains ; Microbiology ; Mutation - genetics ; Replicative cycle, interference, host-virus relations, pathogenicity, miscellaneous strains ; Restriction Mapping ; Salivary Glands - microbiology ; Viral Plaque Assay ; Viral Proteins - analysis ; Virology ; Virus Replication</subject><ispartof>Journal of general virology, 1992-08, Vol.73 (8), p.2021-2029</ispartof><rights>1992 INIST-CNRS</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c438t-874cdec54f3aeacfba2e34eedf61f3989bb6af89e48571df0ff7572f2350260c3</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,3746,3747,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=5532151$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/1322959$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Boname, J. M</creatorcontrib><creatorcontrib>Chantler, J. K</creatorcontrib><title>Characterization of a strain of murine cytomegalovirus which fails to grow in the salivary glands of mice</title><title>Journal of general virology</title><addtitle>J Gen Virol</addtitle><description>Division of Medical Microbiology, University of British Columbia, Faculty of Medicine, 2733 Heather Street, Vancouver, British Columbia V5Z 1M9, Canada
Characterization of a tissue culture-adapted strain of murine cytomegalovirus (MCMV), the Vancouver strain, which demonstrated altered tissue tropism in mice was undertaken to help understand the mechanism of pathogenesis of cytomegaloviruses. The Vancouver strain grew to a limited extent in the spleen but failed to grow in the salivary glands of inoculated mice. This mutation probably arose during multiple in vitro passaging of the parental Smith strain. The Vancouver strain replicated more quickly and produced a greater yield of virus per cycle than the Smith strain in vitro , resulting in a larger plaque size. In addition to these phenotypic differences, the Vancouver strain was found to have a 9.4 kb deletion spanning the Xba I I/L junction of the parental Smith strain (0.960 to 0.995 map units), and a 0.9 kb insertion which mapped to the Eco RI K fragment (0.37 to 0.47 map units). Analysis of virus-induced proteins at various times post-infection identified only one major change in Vancouver strain-infected cells, the absence of a 42K protein found in Smith-infected cells at early and late times.
Present address: Department of Microbiology and Immunology, Stanford University School of Medicine, Stanford, California 95305-5402, U.S.A.
Received 22 January 1992;
accepted 24 April 1992.</description><subject>3T3 Cells</subject><subject>Animals</subject><subject>Biological and medical sciences</subject><subject>Blotting, Southern</subject><subject>cytomegalovirus</subject><subject>Cytomegalovirus - chemistry</subject><subject>Cytomegalovirus - genetics</subject><subject>Cytomegalovirus - growth & development</subject><subject>Female</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Genome, Viral</subject><subject>Mice</subject><subject>Mice, Inbred Strains</subject><subject>Microbiology</subject><subject>Mutation - genetics</subject><subject>Replicative cycle, interference, host-virus relations, pathogenicity, miscellaneous strains</subject><subject>Restriction Mapping</subject><subject>Salivary Glands - microbiology</subject><subject>Viral Plaque Assay</subject><subject>Viral Proteins - analysis</subject><subject>Virology</subject><subject>Virus Replication</subject><issn>0022-1317</issn><issn>1465-2099</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1992</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkc1u1DAUhS0EKtPCEyAkLxDqJuCfOImXaEQLUqVuYG3dONeJURIXO-moPH2dzqhdsvKV7neO7XMI-cDZF860_sqYEAWXvC5qWTSFYIK_IjteVirPWr8mu2fiLTlP6Q9jvCxVfUbOuBRCK70jfj9ABLtg9P9g8WGmwVGgaYngn-ZpjX5Gah-WMGEPY7j3cU30MHg7UAd-THQJtI_hQLNgGZAmGP09xAfajzB36cnEW3xH3jgYE74_nRfk99X3X_sfxc3t9c_9t5vClrJZiqYubYdWlU4CgnUtCJQlYucq7qRudNtW4BqNZaNq3jnmXK1q4YRUTFTMygvy-eh7F8PfFdNiJp8sjvkxGNZkasl0pXjzX5BXVZ3BKoPyCNoYUorozF30U_6h4cxsTZgtZ7PlnN1NY7YmsurjyX5tJ-xeNMfo8_7TaQ_JwugizNanZ0wpKbjabC6P2OD74eAjmh7nnGcMrQ8ml_Fy4yOsg6A2</recordid><startdate>19920801</startdate><enddate>19920801</enddate><creator>Boname, J. M</creator><creator>Chantler, J. K</creator><general>Soc General Microbiol</general><general>Society for General Microbiology</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>19920801</creationdate><title>Characterization of a strain of murine cytomegalovirus which fails to grow in the salivary glands of mice</title><author>Boname, J. M ; Chantler, J. K</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c438t-874cdec54f3aeacfba2e34eedf61f3989bb6af89e48571df0ff7572f2350260c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1992</creationdate><topic>3T3 Cells</topic><topic>Animals</topic><topic>Biological and medical sciences</topic><topic>Blotting, Southern</topic><topic>cytomegalovirus</topic><topic>Cytomegalovirus - chemistry</topic><topic>Cytomegalovirus - genetics</topic><topic>Cytomegalovirus - growth & development</topic><topic>Female</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Genome, Viral</topic><topic>Mice</topic><topic>Mice, Inbred Strains</topic><topic>Microbiology</topic><topic>Mutation - genetics</topic><topic>Replicative cycle, interference, host-virus relations, pathogenicity, miscellaneous strains</topic><topic>Restriction Mapping</topic><topic>Salivary Glands - microbiology</topic><topic>Viral Plaque Assay</topic><topic>Viral Proteins - analysis</topic><topic>Virology</topic><topic>Virus Replication</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Boname, J. M</creatorcontrib><creatorcontrib>Chantler, J. K</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>Journal of general virology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Boname, J. M</au><au>Chantler, J. K</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Characterization of a strain of murine cytomegalovirus which fails to grow in the salivary glands of mice</atitle><jtitle>Journal of general virology</jtitle><addtitle>J Gen Virol</addtitle><date>1992-08-01</date><risdate>1992</risdate><volume>73</volume><issue>8</issue><spage>2021</spage><epage>2029</epage><pages>2021-2029</pages><issn>0022-1317</issn><eissn>1465-2099</eissn><coden>JGVIAY</coden><abstract>Division of Medical Microbiology, University of British Columbia, Faculty of Medicine, 2733 Heather Street, Vancouver, British Columbia V5Z 1M9, Canada
Characterization of a tissue culture-adapted strain of murine cytomegalovirus (MCMV), the Vancouver strain, which demonstrated altered tissue tropism in mice was undertaken to help understand the mechanism of pathogenesis of cytomegaloviruses. The Vancouver strain grew to a limited extent in the spleen but failed to grow in the salivary glands of inoculated mice. This mutation probably arose during multiple in vitro passaging of the parental Smith strain. The Vancouver strain replicated more quickly and produced a greater yield of virus per cycle than the Smith strain in vitro , resulting in a larger plaque size. In addition to these phenotypic differences, the Vancouver strain was found to have a 9.4 kb deletion spanning the Xba I I/L junction of the parental Smith strain (0.960 to 0.995 map units), and a 0.9 kb insertion which mapped to the Eco RI K fragment (0.37 to 0.47 map units). Analysis of virus-induced proteins at various times post-infection identified only one major change in Vancouver strain-infected cells, the absence of a 42K protein found in Smith-infected cells at early and late times.
Present address: Department of Microbiology and Immunology, Stanford University School of Medicine, Stanford, California 95305-5402, U.S.A.
Received 22 January 1992;
accepted 24 April 1992.</abstract><cop>Reading</cop><pub>Soc General Microbiol</pub><pmid>1322959</pmid><doi>10.1099/0022-1317-73-8-2021</doi><tpages>9</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 | 3T3 Cells Animals Biological and medical sciences Blotting, Southern cytomegalovirus Cytomegalovirus - chemistry Cytomegalovirus - genetics Cytomegalovirus - growth & development Female Fundamental and applied biological sciences. Psychology Genome, Viral Mice Mice, Inbred Strains Microbiology Mutation - genetics Replicative cycle, interference, host-virus relations, pathogenicity, miscellaneous strains Restriction Mapping Salivary Glands - microbiology Viral Plaque Assay Viral Proteins - analysis Virology Virus Replication |
title | Characterization of a strain of murine cytomegalovirus which fails to grow in the salivary glands of mice |
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