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Construction of an infectious full-length cDNA clone of Chrysanthemum virus B
An infectious full-length cDNA clone of Chrysanthemum virus B (CVB, genus Carlavirus ), was constructed. Four cDNA fragments covering the whole genome of CVB-S were cloned between the Cauliflower mosaic virus 35S promoter and the nopaline synthase (NOS) terminator. Chrysanthemum and garland chrysant...
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Published in: | Journal of general plant pathology : JGPP 2008-12, Vol.74 (6), p.434-437 |
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container_end_page | 437 |
container_issue | 6 |
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container_title | Journal of general plant pathology : JGPP |
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creator | Ohkawa, A.(Utsunomiya Univ. (Japan). Coll. of Agriculture) Ishikawa Suehiro, N Okuda, S Natsuaki, T |
description | An infectious full-length cDNA clone of
Chrysanthemum virus B
(CVB, genus
Carlavirus
), was constructed. Four cDNA fragments covering the whole genome of CVB-S were cloned between the
Cauliflower mosaic virus
35S promoter and the nopaline synthase (NOS) terminator. Chrysanthemum and garland chrysanthemum were inoculated with the constructed plasmid, named pCVB, using a gene gun system. As is the case in wild-type, CVB-infected plants, no visible symptoms were observed on plants inoculated with pCVB; however, western blotting and electron microscopy indicated the presence of the progeny virus of pCVB. pCVB could be a useful tool for analyzing the functions of carlaviral proteins. |
doi_str_mv | 10.1007/s10327-008-0120-6 |
format | article |
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Chrysanthemum virus B
(CVB, genus
Carlavirus
), was constructed. Four cDNA fragments covering the whole genome of CVB-S were cloned between the
Cauliflower mosaic virus
35S promoter and the nopaline synthase (NOS) terminator. Chrysanthemum and garland chrysanthemum were inoculated with the constructed plasmid, named pCVB, using a gene gun system. As is the case in wild-type, CVB-infected plants, no visible symptoms were observed on plants inoculated with pCVB; however, western blotting and electron microscopy indicated the presence of the progeny virus of pCVB. pCVB could be a useful tool for analyzing the functions of carlaviral proteins.</description><identifier>ISSN: 1345-2630</identifier><identifier>EISSN: 1610-739X</identifier><identifier>DOI: 10.1007/s10327-008-0120-6</identifier><identifier>CODEN: JGPPBQ</identifier><language>eng</language><publisher>Japan: Springer Japan</publisher><subject>Agriculture ; Biomedical and Life Sciences ; CARLAVIRUS ; CARLAVIRUSES ; Cauliflower mosaic virus ; CHRYSANTHEME ; Chrysanthemum ; Chrysanthemum virus b ; CHRYSANTHEMUMS ; CLONACION MOLECULAR ; CLONAGE MOLECULAIRE ; CLONE ; CLONES ; Cloning ; CRISANTEMOS ; Deoxyribonucleic acid ; DNA ; FONCTION PHYSIOLOGIQUE ; FUNCION FISIOLOGICA ; Genomics ; INOCULACION ; INOCULATION ; Life Sciences ; Microbiology ; MOLECULAR CLONING ; PHYSIOLOGICAL FUNCTIONS ; Plant Pathology ; Viral and Viroid Diseases ; Viruses</subject><ispartof>Journal of general plant pathology : JGPP, 2008-12, Vol.74 (6), p.434-437</ispartof><rights>The Phytopathological Society of Japan and Springer 2008</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c463t-373f474a119a6b7ab536c253eee2863ecf45ff5a1e837dad9c0293d01d227a173</citedby><cites>FETCH-LOGICAL-c463t-373f474a119a6b7ab536c253eee2863ecf45ff5a1e837dad9c0293d01d227a173</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids></links><search><creatorcontrib>Ohkawa, A.(Utsunomiya Univ. (Japan). Coll. of Agriculture)</creatorcontrib><creatorcontrib>Ishikawa Suehiro, N</creatorcontrib><creatorcontrib>Okuda, S</creatorcontrib><creatorcontrib>Natsuaki, T</creatorcontrib><title>Construction of an infectious full-length cDNA clone of Chrysanthemum virus B</title><title>Journal of general plant pathology : JGPP</title><addtitle>J Gen Plant Pathol</addtitle><description>An infectious full-length cDNA clone of
Chrysanthemum virus B
(CVB, genus
Carlavirus
), was constructed. Four cDNA fragments covering the whole genome of CVB-S were cloned between the
Cauliflower mosaic virus
35S promoter and the nopaline synthase (NOS) terminator. Chrysanthemum and garland chrysanthemum were inoculated with the constructed plasmid, named pCVB, using a gene gun system. As is the case in wild-type, CVB-infected plants, no visible symptoms were observed on plants inoculated with pCVB; however, western blotting and electron microscopy indicated the presence of the progeny virus of pCVB. pCVB could be a useful tool for analyzing the functions of carlaviral proteins.</description><subject>Agriculture</subject><subject>Biomedical and Life Sciences</subject><subject>CARLAVIRUS</subject><subject>CARLAVIRUSES</subject><subject>Cauliflower mosaic virus</subject><subject>CHRYSANTHEME</subject><subject>Chrysanthemum</subject><subject>Chrysanthemum virus b</subject><subject>CHRYSANTHEMUMS</subject><subject>CLONACION MOLECULAR</subject><subject>CLONAGE MOLECULAIRE</subject><subject>CLONE</subject><subject>CLONES</subject><subject>Cloning</subject><subject>CRISANTEMOS</subject><subject>Deoxyribonucleic acid</subject><subject>DNA</subject><subject>FONCTION PHYSIOLOGIQUE</subject><subject>FUNCION FISIOLOGICA</subject><subject>Genomics</subject><subject>INOCULACION</subject><subject>INOCULATION</subject><subject>Life Sciences</subject><subject>Microbiology</subject><subject>MOLECULAR CLONING</subject><subject>PHYSIOLOGICAL FUNCTIONS</subject><subject>Plant Pathology</subject><subject>Viral and Viroid Diseases</subject><subject>Viruses</subject><issn>1345-2630</issn><issn>1610-739X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2008</creationdate><recordtype>article</recordtype><recordid>eNp9kEtLxDAUhYMoOI7-ABdCceEuepO0Sbsc65vxsVBwFzJpMtOhk2rSCvPvTakguHB174XvnHs4CB0TOCcA4iIQYFRggBwDoYD5DpoQTgALVrzvxp2lGaacwT46CGENQAkT2QQ9lq0Lne91V7cuaW2iXFI7a4a7D4ntmwY3xi27VaKvnmaJblpnBq5c-W1QrluZTb9Jvmof6ctDtGdVE8zRz5yit5vr1_IOz59v78vZHOuUsw4zwWwqUkVIofhCqEXGuKYZM8bQnDOjbZpZmyliciYqVRUaaMEqIBWlQhHBpuhs9P3w7WdvQic3ddCmaZQzMbakkAHN468pOv0Drtveu5hNUpLzPIsPIkRGSPs2BG-s_PD1RvmtJCCHduXYroztyqFdORjTURMi65bG_xr_JzoZRVa1Ui19HeTDCwUoIEJ5yr4BGM2Efw</recordid><startdate>20081201</startdate><enddate>20081201</enddate><creator>Ohkawa, A.(Utsunomiya Univ. 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Coll. of Agriculture) ; Ishikawa Suehiro, N ; Okuda, S ; Natsuaki, T</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c463t-373f474a119a6b7ab536c253eee2863ecf45ff5a1e837dad9c0293d01d227a173</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2008</creationdate><topic>Agriculture</topic><topic>Biomedical and Life Sciences</topic><topic>CARLAVIRUS</topic><topic>CARLAVIRUSES</topic><topic>Cauliflower mosaic virus</topic><topic>CHRYSANTHEME</topic><topic>Chrysanthemum</topic><topic>Chrysanthemum virus b</topic><topic>CHRYSANTHEMUMS</topic><topic>CLONACION MOLECULAR</topic><topic>CLONAGE MOLECULAIRE</topic><topic>CLONE</topic><topic>CLONES</topic><topic>Cloning</topic><topic>CRISANTEMOS</topic><topic>Deoxyribonucleic acid</topic><topic>DNA</topic><topic>FONCTION PHYSIOLOGIQUE</topic><topic>FUNCION FISIOLOGICA</topic><topic>Genomics</topic><topic>INOCULACION</topic><topic>INOCULATION</topic><topic>Life Sciences</topic><topic>Microbiology</topic><topic>MOLECULAR CLONING</topic><topic>PHYSIOLOGICAL FUNCTIONS</topic><topic>Plant Pathology</topic><topic>Viral and Viroid Diseases</topic><topic>Viruses</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ohkawa, A.(Utsunomiya Univ. 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Coll. of Agriculture)</creatorcontrib><creatorcontrib>Ishikawa Suehiro, N</creatorcontrib><creatorcontrib>Okuda, S</creatorcontrib><creatorcontrib>Natsuaki, T</creatorcontrib><collection>AGRIS</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Virology and AIDS Abstracts</collection><collection>Agricultural Science Collection</collection><collection>ProQuest_Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Biology Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Research Library (Alumni Edition)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>Agricultural & Environmental Science Collection</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>AUTh Library subscriptions: ProQuest Central</collection><collection>ProQuest Natural Science Collection</collection><collection>Earth, Atmospheric & Aquatic Science Collection</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</collection><collection>Engineering Research Database</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>Research Library Prep</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Agriculture Science Database</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>ProQuest research library</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biological Science Database</collection><collection>Research Library (Corporate)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Earth, Atmospheric & Aquatic Science Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central Basic</collection><collection>Nucleic Acids Abstracts</collection><jtitle>Journal of general plant pathology : JGPP</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ohkawa, A.(Utsunomiya Univ. (Japan). Coll. of Agriculture)</au><au>Ishikawa Suehiro, N</au><au>Okuda, S</au><au>Natsuaki, T</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Construction of an infectious full-length cDNA clone of Chrysanthemum virus B</atitle><jtitle>Journal of general plant pathology : JGPP</jtitle><stitle>J Gen Plant Pathol</stitle><date>2008-12-01</date><risdate>2008</risdate><volume>74</volume><issue>6</issue><spage>434</spage><epage>437</epage><pages>434-437</pages><issn>1345-2630</issn><eissn>1610-739X</eissn><coden>JGPPBQ</coden><abstract>An infectious full-length cDNA clone of
Chrysanthemum virus B
(CVB, genus
Carlavirus
), was constructed. Four cDNA fragments covering the whole genome of CVB-S were cloned between the
Cauliflower mosaic virus
35S promoter and the nopaline synthase (NOS) terminator. Chrysanthemum and garland chrysanthemum were inoculated with the constructed plasmid, named pCVB, using a gene gun system. As is the case in wild-type, CVB-infected plants, no visible symptoms were observed on plants inoculated with pCVB; however, western blotting and electron microscopy indicated the presence of the progeny virus of pCVB. pCVB could be a useful tool for analyzing the functions of carlaviral proteins.</abstract><cop>Japan</cop><pub>Springer Japan</pub><doi>10.1007/s10327-008-0120-6</doi><tpages>4</tpages></addata></record> |
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source | Springer Nature |
subjects | Agriculture Biomedical and Life Sciences CARLAVIRUS CARLAVIRUSES Cauliflower mosaic virus CHRYSANTHEME Chrysanthemum Chrysanthemum virus b CHRYSANTHEMUMS CLONACION MOLECULAR CLONAGE MOLECULAIRE CLONE CLONES Cloning CRISANTEMOS Deoxyribonucleic acid DNA FONCTION PHYSIOLOGIQUE FUNCION FISIOLOGICA Genomics INOCULACION INOCULATION Life Sciences Microbiology MOLECULAR CLONING PHYSIOLOGICAL FUNCTIONS Plant Pathology Viral and Viroid Diseases Viruses |
title | Construction of an infectious full-length cDNA clone of Chrysanthemum virus B |
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