Rabies virus detection by RT-PCR in decomposed naturally infected brains
The warm climate of Israel and mishandling of the cadavers during transit to the laboratory requires an accurate method for diagnosis of rabies in decomposed tissues. By using the reverse transcriptase polymerase chain reaction (RT-PCR) 10 decomposed brain samples that collected between 1998 and 200...
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Veröffentlicht in: | Veterinary microbiology 2002-06, Vol.87 (2), p.111-118 |
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creator | David, D. Yakobson, B. Rotenberg, D. Dveres, N. Davidson, I. Stram, Y. |
description | The warm climate of Israel and mishandling of the cadavers during transit to the laboratory requires an accurate method for diagnosis of rabies in decomposed tissues. By using the reverse transcriptase polymerase chain reaction (RT-PCR) 10 decomposed brain samples that collected between 1998 and 2000 were diagnosed as negative by direct fluorescent antibody test (FAT), were found positive. Three of the 10 decomposed brains were confirmed as positive by isolation of rabies virus in tissue culture and by mouse inoculation (MIT) while the other seven decomposed samples were found positive only by RT-PCR. Direct sequencing and molecular analysis of a 328
bp fragment of the N gene of all the rabies sequences confirmed their geographical origin. These results demonstrated the importance of the RT-PCR in the detection of rabies virus in decomposed naturally infected brains, especially in cases when the sample is not suitable for other laboratory assays. Thus, the RT-PCR can provide a positive diagnosis; however, when a negative result is obtained due to the nature of the decomposed tissue that can be caused by technical reasons and a false negative might be the case. |
doi_str_mv | 10.1016/S0378-1135(02)00041-X |
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bp fragment of the N gene of all the rabies sequences confirmed their geographical origin. These results demonstrated the importance of the RT-PCR in the detection of rabies virus in decomposed naturally infected brains, especially in cases when the sample is not suitable for other laboratory assays. Thus, the RT-PCR can provide a positive diagnosis; however, when a negative result is obtained due to the nature of the decomposed tissue that can be caused by technical reasons and a false negative might be the case.</description><identifier>ISSN: 0378-1135</identifier><identifier>EISSN: 1873-2542</identifier><identifier>DOI: 10.1016/S0378-1135(02)00041-X</identifier><identifier>PMID: 12034539</identifier><identifier>CODEN: VMICDQ</identifier><language>eng</language><publisher>Amsterdam: Elsevier B.V</publisher><subject>Animal viral diseases ; Animals ; Base Sequence ; Biological and medical sciences ; Brain - virology ; Brain Diseases - veterinary ; Brain Diseases - virology ; Cattle ; Decomposed brains ; Dogs ; Fluorescent Antibody Technique - veterinary ; Infectious diseases ; Medical sciences ; Mice ; Molecular Sequence Data ; Natural infection ; Nucleocapsid Proteins - chemistry ; Nucleocapsid Proteins - genetics ; Rabies - veterinary ; Rabies - virology ; Rabies virus ; Rabies virus - genetics ; Rabies virus - isolation & purification ; Reverse Transcriptase Polymerase Chain Reaction - veterinary ; RNA, Viral - chemistry ; RNA, Viral - genetics ; RT-PCR ; Sequence analysis ; Sequence Analysis, DNA ; Sequence Homology, Nucleic Acid ; Songbirds ; Viral diseases</subject><ispartof>Veterinary microbiology, 2002-06, Vol.87 (2), p.111-118</ispartof><rights>2002 Elsevier Science B.V.</rights><rights>2002 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c422t-527fbc6061a5da15d35d4c8a449aac081c46c82a6e4b9772191525e123d7d0143</citedby><cites>FETCH-LOGICAL-c422t-527fbc6061a5da15d35d4c8a449aac081c46c82a6e4b9772191525e123d7d0143</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/S0378-1135(02)00041-X$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,777,781,3537,27905,27906,45976</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=13697733$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/12034539$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>David, D.</creatorcontrib><creatorcontrib>Yakobson, B.</creatorcontrib><creatorcontrib>Rotenberg, D.</creatorcontrib><creatorcontrib>Dveres, N.</creatorcontrib><creatorcontrib>Davidson, I.</creatorcontrib><creatorcontrib>Stram, Y.</creatorcontrib><title>Rabies virus detection by RT-PCR in decomposed naturally infected brains</title><title>Veterinary microbiology</title><addtitle>Vet Microbiol</addtitle><description>The warm climate of Israel and mishandling of the cadavers during transit to the laboratory requires an accurate method for diagnosis of rabies in decomposed tissues. By using the reverse transcriptase polymerase chain reaction (RT-PCR) 10 decomposed brain samples that collected between 1998 and 2000 were diagnosed as negative by direct fluorescent antibody test (FAT), were found positive. Three of the 10 decomposed brains were confirmed as positive by isolation of rabies virus in tissue culture and by mouse inoculation (MIT) while the other seven decomposed samples were found positive only by RT-PCR. Direct sequencing and molecular analysis of a 328
bp fragment of the N gene of all the rabies sequences confirmed their geographical origin. These results demonstrated the importance of the RT-PCR in the detection of rabies virus in decomposed naturally infected brains, especially in cases when the sample is not suitable for other laboratory assays. Thus, the RT-PCR can provide a positive diagnosis; however, when a negative result is obtained due to the nature of the decomposed tissue that can be caused by technical reasons and a false negative might be the case.</description><subject>Animal viral diseases</subject><subject>Animals</subject><subject>Base Sequence</subject><subject>Biological and medical sciences</subject><subject>Brain - virology</subject><subject>Brain Diseases - veterinary</subject><subject>Brain Diseases - virology</subject><subject>Cattle</subject><subject>Decomposed brains</subject><subject>Dogs</subject><subject>Fluorescent Antibody Technique - veterinary</subject><subject>Infectious diseases</subject><subject>Medical sciences</subject><subject>Mice</subject><subject>Molecular Sequence Data</subject><subject>Natural infection</subject><subject>Nucleocapsid Proteins - chemistry</subject><subject>Nucleocapsid Proteins - genetics</subject><subject>Rabies - veterinary</subject><subject>Rabies - virology</subject><subject>Rabies virus</subject><subject>Rabies virus - genetics</subject><subject>Rabies virus - isolation & purification</subject><subject>Reverse Transcriptase Polymerase Chain Reaction - veterinary</subject><subject>RNA, Viral - chemistry</subject><subject>RNA, Viral - genetics</subject><subject>RT-PCR</subject><subject>Sequence analysis</subject><subject>Sequence Analysis, DNA</subject><subject>Sequence Homology, Nucleic Acid</subject><subject>Songbirds</subject><subject>Viral diseases</subject><issn>0378-1135</issn><issn>1873-2542</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2002</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqF0ElLxDAYgOEgio7LT1B6UfRQzZe1PYkMbjCgjAreQpqkEOm0Y9IOzL83s6BHT4GPJ9uL0Cnga8Agbt4wlUUOQPklJlcYYwb55w4aQSFpTjgju2j0Sw7QYYxfK1QKvI8OgGDKOC1H6GmqK-9itvBhiJl1vTO979qsWmbT9_x1PM18m8amm8276GzW6n4IummWaV4nm0ZV0L6Nx2iv1k10J9v1CH083L-Pn_LJy-Pz-G6SG0ZIn3Mi68oILEBzq4Fbyi0zhWas1NrgAgwTpiBaOFaVUhIogRPugFArLQZGj9DF5tx56L4HF3s189G4ptGt64aoJEjGQeJ_IRSMEiFkgnwDTehiDK5W8-BnOiwVYLVqrdat1SqkwkStW6vPtO9se8FQzZz927WNm8D5FuhodFMH3Rof_xwV6YeUJne7cS51W3gXVDTetcZZH1JiZTv_z1N-APlwmYA</recordid><startdate>20020620</startdate><enddate>20020620</enddate><creator>David, D.</creator><creator>Yakobson, B.</creator><creator>Rotenberg, D.</creator><creator>Dveres, N.</creator><creator>Davidson, I.</creator><creator>Stram, Y.</creator><general>Elsevier B.V</general><general>Elsevier Science</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>7T7</scope><scope>7U9</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>H94</scope><scope>P64</scope><scope>7X8</scope></search><sort><creationdate>20020620</creationdate><title>Rabies virus detection by RT-PCR in decomposed naturally infected brains</title><author>David, D. ; Yakobson, B. ; Rotenberg, D. ; Dveres, N. ; Davidson, I. ; Stram, Y.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c422t-527fbc6061a5da15d35d4c8a449aac081c46c82a6e4b9772191525e123d7d0143</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2002</creationdate><topic>Animal viral diseases</topic><topic>Animals</topic><topic>Base Sequence</topic><topic>Biological and medical sciences</topic><topic>Brain - virology</topic><topic>Brain Diseases - veterinary</topic><topic>Brain Diseases - virology</topic><topic>Cattle</topic><topic>Decomposed brains</topic><topic>Dogs</topic><topic>Fluorescent Antibody Technique - veterinary</topic><topic>Infectious diseases</topic><topic>Medical sciences</topic><topic>Mice</topic><topic>Molecular Sequence Data</topic><topic>Natural infection</topic><topic>Nucleocapsid Proteins - chemistry</topic><topic>Nucleocapsid Proteins - genetics</topic><topic>Rabies - veterinary</topic><topic>Rabies - virology</topic><topic>Rabies virus</topic><topic>Rabies virus - genetics</topic><topic>Rabies virus - isolation & purification</topic><topic>Reverse Transcriptase Polymerase Chain Reaction - veterinary</topic><topic>RNA, Viral - chemistry</topic><topic>RNA, Viral - genetics</topic><topic>RT-PCR</topic><topic>Sequence analysis</topic><topic>Sequence Analysis, DNA</topic><topic>Sequence Homology, Nucleic Acid</topic><topic>Songbirds</topic><topic>Viral diseases</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>David, D.</creatorcontrib><creatorcontrib>Yakobson, B.</creatorcontrib><creatorcontrib>Rotenberg, D.</creatorcontrib><creatorcontrib>Dveres, N.</creatorcontrib><creatorcontrib>Davidson, I.</creatorcontrib><creatorcontrib>Stram, Y.</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>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Virology and AIDS Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Veterinary microbiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>David, D.</au><au>Yakobson, B.</au><au>Rotenberg, D.</au><au>Dveres, N.</au><au>Davidson, I.</au><au>Stram, Y.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Rabies virus detection by RT-PCR in decomposed naturally infected brains</atitle><jtitle>Veterinary microbiology</jtitle><addtitle>Vet Microbiol</addtitle><date>2002-06-20</date><risdate>2002</risdate><volume>87</volume><issue>2</issue><spage>111</spage><epage>118</epage><pages>111-118</pages><issn>0378-1135</issn><eissn>1873-2542</eissn><coden>VMICDQ</coden><abstract>The warm climate of Israel and mishandling of the cadavers during transit to the laboratory requires an accurate method for diagnosis of rabies in decomposed tissues. By using the reverse transcriptase polymerase chain reaction (RT-PCR) 10 decomposed brain samples that collected between 1998 and 2000 were diagnosed as negative by direct fluorescent antibody test (FAT), were found positive. Three of the 10 decomposed brains were confirmed as positive by isolation of rabies virus in tissue culture and by mouse inoculation (MIT) while the other seven decomposed samples were found positive only by RT-PCR. Direct sequencing and molecular analysis of a 328
bp fragment of the N gene of all the rabies sequences confirmed their geographical origin. These results demonstrated the importance of the RT-PCR in the detection of rabies virus in decomposed naturally infected brains, especially in cases when the sample is not suitable for other laboratory assays. Thus, the RT-PCR can provide a positive diagnosis; however, when a negative result is obtained due to the nature of the decomposed tissue that can be caused by technical reasons and a false negative might be the case.</abstract><cop>Amsterdam</cop><pub>Elsevier B.V</pub><pmid>12034539</pmid><doi>10.1016/S0378-1135(02)00041-X</doi><tpages>8</tpages></addata></record> |
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subjects | Animal viral diseases Animals Base Sequence Biological and medical sciences Brain - virology Brain Diseases - veterinary Brain Diseases - virology Cattle Decomposed brains Dogs Fluorescent Antibody Technique - veterinary Infectious diseases Medical sciences Mice Molecular Sequence Data Natural infection Nucleocapsid Proteins - chemistry Nucleocapsid Proteins - genetics Rabies - veterinary Rabies - virology Rabies virus Rabies virus - genetics Rabies virus - isolation & purification Reverse Transcriptase Polymerase Chain Reaction - veterinary RNA, Viral - chemistry RNA, Viral - genetics RT-PCR Sequence analysis Sequence Analysis, DNA Sequence Homology, Nucleic Acid Songbirds Viral diseases |
title | Rabies virus detection by RT-PCR in decomposed naturally infected brains |
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