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Isolation, identification, and partial cDNA cloning of genomic RNA of jaagsiekte retrovirus, the etiological agent of sheep pulmonary adenomatosis
The genome of the jaagsiekte (JS) retrovirus (JSRV), the etiological agent of sheep pulmonary adenomatosis (jaagsiekte), has been identified, isolated, and partly cloned. The JSRV genome is ca. 8.7 kb long. EDNA of the genomic RNA was synthesized and cloned. A clone, JS 46.1, was isolated and charac...
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Published in: | Journal of Virology 1991-09, Vol.65 (9), p.5061-5067 |
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creator | York, D.F. (Faculte de Medecine Nord, Marseille, France) Vigne, R Verwoerd, D.W Querat, G |
description | The genome of the jaagsiekte (JS) retrovirus (JSRV), the etiological agent of sheep pulmonary adenomatosis (jaagsiekte), has been identified, isolated, and partly cloned. The JSRV genome is ca. 8.7 kb long. EDNA of the genomic RNA was synthesized and cloned. A clone, JS 46.1, was isolated and characterized. It has an insert of 2.1 kb which hybridizes to the same 8.7-kb RNA in all the JSRV-infected sheep lung washes tested but does not hybridize to maedi-visna virus, a sheep lentivirus often found coinfecting JSRV-infected lungs. Comparison of the amino acid sequence encoded by JS 46.1 with those encoded by other retroviruses revealed that JSRV has homology to the type D and B oncoviruses and to human endogenous retrovirus |
doi_str_mv | 10.1128/jvi.65.9.5061-5067.1991 |
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(Faculte de Medecine Nord, Marseille, France) ; Vigne, R ; Verwoerd, D.W ; Querat, G</creator><creatorcontrib>York, D.F. (Faculte de Medecine Nord, Marseille, France) ; Vigne, R ; Verwoerd, D.W ; Querat, G</creatorcontrib><description>The genome of the jaagsiekte (JS) retrovirus (JSRV), the etiological agent of sheep pulmonary adenomatosis (jaagsiekte), has been identified, isolated, and partly cloned. The JSRV genome is ca. 8.7 kb long. EDNA of the genomic RNA was synthesized and cloned. A clone, JS 46.1, was isolated and characterized. It has an insert of 2.1 kb which hybridizes to the same 8.7-kb RNA in all the JSRV-infected sheep lung washes tested but does not hybridize to maedi-visna virus, a sheep lentivirus often found coinfecting JSRV-infected lungs. Comparison of the amino acid sequence encoded by JS 46.1 with those encoded by other retroviruses revealed that JSRV has homology to the type D and B oncoviruses and to human endogenous retrovirus</description><identifier>ISSN: 0022-538X</identifier><identifier>EISSN: 1098-5514</identifier><identifier>DOI: 10.1128/jvi.65.9.5061-5067.1991</identifier><identifier>PMID: 1651422</identifier><language>eng</language><publisher>Washington, DC: American Society for Microbiology</publisher><subject>ADENOMATOSE PULMONAIRE ; ADENOMATOSIS PULMONAR ; ADN ; AIDS/HIV ; Amino Acid Sequence ; Animals ; ARN ; Biological and medical sciences ; Blotting, Northern ; Centrifugation, Isopycnic ; CLONACION ; CLONAGE ; Cloning, Molecular ; DNA - genetics ; Fundamental and applied biological sciences. Psychology ; Gene Products, env - genetics ; GENETICA ; Genetics ; GENETIQUE ; GENOMAS ; GENOME ; LENTIVIRINAE ; Lentivirus - isolation & purification ; Lung - microbiology ; Microbiology ; Molecular Sequence Data ; NUCLEOTIDE ; NUCLEOTIDOS ; OVIN ; OVINOS ; Pulmonary Adenomatosis, Ovine - microbiology ; RETROVIRIDAE ; Retroviridae - genetics ; Retroviridae - isolation & purification ; RNA, Viral - genetics ; RNA, Viral - isolation & purification ; Sheep ; Virology</subject><ispartof>Journal of Virology, 1991-09, Vol.65 (9), p.5061-5067</ispartof><rights>1993 INIST-CNRS</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4851-94bed975a6cb466903236ea474279615994abe676d05a7e30ba463e8e25cc5143</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC248970/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC248970/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,727,780,784,885,3188,3189,27924,27925,53791,53793</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=4340978$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/1651422$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>York, D.F. (Faculte de Medecine Nord, Marseille, France)</creatorcontrib><creatorcontrib>Vigne, R</creatorcontrib><creatorcontrib>Verwoerd, D.W</creatorcontrib><creatorcontrib>Querat, G</creatorcontrib><title>Isolation, identification, and partial cDNA cloning of genomic RNA of jaagsiekte retrovirus, the etiological agent of sheep pulmonary adenomatosis</title><title>Journal of Virology</title><addtitle>J Virol</addtitle><description>The genome of the jaagsiekte (JS) retrovirus (JSRV), the etiological agent of sheep pulmonary adenomatosis (jaagsiekte), has been identified, isolated, and partly cloned. The JSRV genome is ca. 8.7 kb long. EDNA of the genomic RNA was synthesized and cloned. A clone, JS 46.1, was isolated and characterized. It has an insert of 2.1 kb which hybridizes to the same 8.7-kb RNA in all the JSRV-infected sheep lung washes tested but does not hybridize to maedi-visna virus, a sheep lentivirus often found coinfecting JSRV-infected lungs. Comparison of the amino acid sequence encoded by JS 46.1 with those encoded by other retroviruses revealed that JSRV has homology to the type D and B oncoviruses and to human endogenous retrovirus</description><subject>ADENOMATOSE PULMONAIRE</subject><subject>ADENOMATOSIS PULMONAR</subject><subject>ADN</subject><subject>AIDS/HIV</subject><subject>Amino Acid Sequence</subject><subject>Animals</subject><subject>ARN</subject><subject>Biological and medical sciences</subject><subject>Blotting, Northern</subject><subject>Centrifugation, Isopycnic</subject><subject>CLONACION</subject><subject>CLONAGE</subject><subject>Cloning, Molecular</subject><subject>DNA - genetics</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Gene Products, env - genetics</subject><subject>GENETICA</subject><subject>Genetics</subject><subject>GENETIQUE</subject><subject>GENOMAS</subject><subject>GENOME</subject><subject>LENTIVIRINAE</subject><subject>Lentivirus - isolation & purification</subject><subject>Lung - microbiology</subject><subject>Microbiology</subject><subject>Molecular Sequence Data</subject><subject>NUCLEOTIDE</subject><subject>NUCLEOTIDOS</subject><subject>OVIN</subject><subject>OVINOS</subject><subject>Pulmonary Adenomatosis, Ovine - microbiology</subject><subject>RETROVIRIDAE</subject><subject>Retroviridae - genetics</subject><subject>Retroviridae - isolation & purification</subject><subject>RNA, Viral - genetics</subject><subject>RNA, Viral - isolation & purification</subject><subject>Sheep</subject><subject>Virology</subject><issn>0022-538X</issn><issn>1098-5514</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1991</creationdate><recordtype>article</recordtype><recordid>eNqFks1u1DAUhSMEKkPhBZAQRkKsmmAn_okXLKryV6kCCajEzrrj3GQ8JHFqZwbxGjwxjmZU6IqNLft-5_heHWfZc0YLxsr69XbvCikKXQgqWZ4WVTCt2b1sxaiucyEYv5-tKC3LXFT194fZoxi3lDLOJT_JTphMQFmust-X0fcwOz-eEdfgOLvW2eMZxoZMEGYHPbFvP50T2_vRjR3xLelw9IOz5Eu6TsctQBcd_piRBJyD37uwi2dk3iDBZNb7Lrn2BJJsXvi4QZzItOsHP0L4RaBZ_GD20cXH2YMW-ohPjvtpdv3-3beLj_nV5w-XF-dXueW1YLnma2y0EiDtmkupaVVWEoErXiotmdCawxqlkg0VoLCia-CywhpLYW2avjrN3hx8p916wMam1gL0ZgpuSC0ZD87crYxuYzq_NyWvtaJJ_-qoD_5mh3E2g4sW-x5G9LtoVEmrWmr2X5DJRFJRJ1AdQBt8jAHb22YYNUvsJsVupDDaLLEvizJL7En57N9Z_uoOOaf6y2MdYgqiDTBaF28xXnGq1dLAiwO2cd3mpwtoIA53H03M0wPTgjfQhWRz_VWnj6VqVv0BaUvM2Q</recordid><startdate>19910901</startdate><enddate>19910901</enddate><creator>York, D.F. (Faculte de Medecine Nord, Marseille, France)</creator><creator>Vigne, R</creator><creator>Verwoerd, D.W</creator><creator>Querat, G</creator><general>American Society for Microbiology</general><scope>FBQ</scope><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>8FD</scope><scope>FR3</scope><scope>H94</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>19910901</creationdate><title>Isolation, identification, and partial cDNA cloning of genomic RNA of jaagsiekte retrovirus, the etiological agent of sheep pulmonary adenomatosis</title><author>York, D.F. (Faculte de Medecine Nord, Marseille, France) ; Vigne, R ; Verwoerd, D.W ; Querat, G</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4851-94bed975a6cb466903236ea474279615994abe676d05a7e30ba463e8e25cc5143</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1991</creationdate><topic>ADENOMATOSE PULMONAIRE</topic><topic>ADENOMATOSIS PULMONAR</topic><topic>ADN</topic><topic>AIDS/HIV</topic><topic>Amino Acid Sequence</topic><topic>Animals</topic><topic>ARN</topic><topic>Biological and medical sciences</topic><topic>Blotting, Northern</topic><topic>Centrifugation, Isopycnic</topic><topic>CLONACION</topic><topic>CLONAGE</topic><topic>Cloning, Molecular</topic><topic>DNA - genetics</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Gene Products, env - genetics</topic><topic>GENETICA</topic><topic>Genetics</topic><topic>GENETIQUE</topic><topic>GENOMAS</topic><topic>GENOME</topic><topic>LENTIVIRINAE</topic><topic>Lentivirus - isolation & purification</topic><topic>Lung - microbiology</topic><topic>Microbiology</topic><topic>Molecular Sequence Data</topic><topic>NUCLEOTIDE</topic><topic>NUCLEOTIDOS</topic><topic>OVIN</topic><topic>OVINOS</topic><topic>Pulmonary Adenomatosis, Ovine - microbiology</topic><topic>RETROVIRIDAE</topic><topic>Retroviridae - genetics</topic><topic>Retroviridae - isolation & purification</topic><topic>RNA, Viral - genetics</topic><topic>RNA, Viral - isolation & purification</topic><topic>Sheep</topic><topic>Virology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>York, D.F. (Faculte de Medecine Nord, Marseille, France)</creatorcontrib><creatorcontrib>Vigne, R</creatorcontrib><creatorcontrib>Verwoerd, D.W</creatorcontrib><creatorcontrib>Querat, G</creatorcontrib><collection>AGRIS</collection><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>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Journal of Virology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>York, D.F. (Faculte de Medecine Nord, Marseille, France)</au><au>Vigne, R</au><au>Verwoerd, D.W</au><au>Querat, G</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Isolation, identification, and partial cDNA cloning of genomic RNA of jaagsiekte retrovirus, the etiological agent of sheep pulmonary adenomatosis</atitle><jtitle>Journal of Virology</jtitle><addtitle>J Virol</addtitle><date>1991-09-01</date><risdate>1991</risdate><volume>65</volume><issue>9</issue><spage>5061</spage><epage>5067</epage><pages>5061-5067</pages><issn>0022-538X</issn><eissn>1098-5514</eissn><abstract>The genome of the jaagsiekte (JS) retrovirus (JSRV), the etiological agent of sheep pulmonary adenomatosis (jaagsiekte), has been identified, isolated, and partly cloned. The JSRV genome is ca. 8.7 kb long. EDNA of the genomic RNA was synthesized and cloned. A clone, JS 46.1, was isolated and characterized. It has an insert of 2.1 kb which hybridizes to the same 8.7-kb RNA in all the JSRV-infected sheep lung washes tested but does not hybridize to maedi-visna virus, a sheep lentivirus often found coinfecting JSRV-infected lungs. Comparison of the amino acid sequence encoded by JS 46.1 with those encoded by other retroviruses revealed that JSRV has homology to the type D and B oncoviruses and to human endogenous retrovirus</abstract><cop>Washington, DC</cop><pub>American Society for Microbiology</pub><pmid>1651422</pmid><doi>10.1128/jvi.65.9.5061-5067.1991</doi><tpages>7</tpages><oa>free_for_read</oa></addata></record> |
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subjects | ADENOMATOSE PULMONAIRE ADENOMATOSIS PULMONAR ADN AIDS/HIV Amino Acid Sequence Animals ARN Biological and medical sciences Blotting, Northern Centrifugation, Isopycnic CLONACION CLONAGE Cloning, Molecular DNA - genetics Fundamental and applied biological sciences. Psychology Gene Products, env - genetics GENETICA Genetics GENETIQUE GENOMAS GENOME LENTIVIRINAE Lentivirus - isolation & purification Lung - microbiology Microbiology Molecular Sequence Data NUCLEOTIDE NUCLEOTIDOS OVIN OVINOS Pulmonary Adenomatosis, Ovine - microbiology RETROVIRIDAE Retroviridae - genetics Retroviridae - isolation & purification RNA, Viral - genetics RNA, Viral - isolation & purification Sheep Virology |
title | Isolation, identification, and partial cDNA cloning of genomic RNA of jaagsiekte retrovirus, the etiological agent of sheep pulmonary adenomatosis |
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