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
Hauptverfasser: Boname, J. M, Chantler, J. K
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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.
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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. 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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. 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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. 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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. 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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. 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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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