Beilong virus, a novel paramyxovirus with the largest genome of non-segmented negative-stranded RNA viruses
During a subtraction study on gene expression in human kidney mesangial cells (HMCs), cDNA clones with sequence homology to paramyxovirus P, M and F genes were isolated. Subsequent investigation revealed that this particular HMC line was infected with a previously unknown paramyxovirus. Here, we rep...
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creator | Li, Zhuo Yu, Meng Zhang, Hong Magoffin, Danielle E. Jack, Philippa J.M. Hyatt, Alex Wang, Hai-Yan Wang, Lin-Fa |
description | During a subtraction study on gene expression in human kidney mesangial cells (HMCs), cDNA clones with sequence homology to paramyxovirus P, M and F genes were isolated. Subsequent investigation revealed that this particular HMC line was infected with a previously unknown paramyxovirus. Here, we report the isolation and genome characterization of this new virus, now named
Beilong virus (BeV). The genome of BeV is 19,212 nucleotides (nt) in length and is the largest among all known members of the order Mononegavirales. The BeV genome contains eight genes in the order 3′-N-P/V/C-M-F-SH-TM-G-L-5′. The SH and TM genes code for a small hydrophobic protein of 76 aa and a transmembrane protein of 254 aa, respectively. The BeV G gene, at 4527 nt, codes for an attachment protein of 734 aa and contains two additional open reading frames (ORFs) in the 3′ half of the gene, coding for putative proteins of 299 and 394 aa in length. Although the exact origin of BeV is presently unknown, we provide evidence indicating that BeV was present in a rat mesangial cell line used in the same laboratory prior to the acquisition of the HMC line, suggesting a potential rodent origin for BeV. |
doi_str_mv | 10.1016/j.virol.2005.10.039 |
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Beilong virus (BeV). The genome of BeV is 19,212 nucleotides (nt) in length and is the largest among all known members of the order Mononegavirales. The BeV genome contains eight genes in the order 3′-N-P/V/C-M-F-SH-TM-G-L-5′. The SH and TM genes code for a small hydrophobic protein of 76 aa and a transmembrane protein of 254 aa, respectively. The BeV G gene, at 4527 nt, codes for an attachment protein of 734 aa and contains two additional open reading frames (ORFs) in the 3′ half of the gene, coding for putative proteins of 299 and 394 aa in length. Although the exact origin of BeV is presently unknown, we provide evidence indicating that BeV was present in a rat mesangial cell line used in the same laboratory prior to the acquisition of the HMC line, suggesting a potential rodent origin for BeV.</description><identifier>ISSN: 0042-6822</identifier><identifier>EISSN: 1096-0341</identifier><identifier>DOI: 10.1016/j.virol.2005.10.039</identifier><identifier>PMID: 16325221</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Amino Acid Sequence ; Animals ; Base Sequence ; Beilong virus ; Cell Line ; Genome, Viral ; Humans ; J-virus ; Mesangial Cells - virology ; Molecular Sequence Data ; Mononegavirales ; Paramyxovirinae - classification ; Paramyxovirinae - genetics ; Paramyxovirinae - isolation & purification ; Paramyxovirus ; Phylogeny ; Rats ; Rats, Sprague-Dawley ; RNA Viruses - classification ; RNA Viruses - genetics ; Rodents ; Viral Proteins - genetics</subject><ispartof>Virology (New York, N.Y.), 2006-03, Vol.346 (1), p.219-228</ispartof><rights>2005 Elsevier Inc.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c388t-bbb64512624e70f9005a655fe7ba61a5fffc7846488c269185d4b4ab92b9d94f3</citedby><cites>FETCH-LOGICAL-c388t-bbb64512624e70f9005a655fe7ba61a5fffc7846488c269185d4b4ab92b9d94f3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0042682205007336$$EHTML$$P50$$Gelsevier$$Hfree_for_read</linktohtml><link.rule.ids>314,776,780,3536,27903,27904,65309</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/16325221$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Li, Zhuo</creatorcontrib><creatorcontrib>Yu, Meng</creatorcontrib><creatorcontrib>Zhang, Hong</creatorcontrib><creatorcontrib>Magoffin, Danielle E.</creatorcontrib><creatorcontrib>Jack, Philippa J.M.</creatorcontrib><creatorcontrib>Hyatt, Alex</creatorcontrib><creatorcontrib>Wang, Hai-Yan</creatorcontrib><creatorcontrib>Wang, Lin-Fa</creatorcontrib><title>Beilong virus, a novel paramyxovirus with the largest genome of non-segmented negative-stranded RNA viruses</title><title>Virology (New York, N.Y.)</title><addtitle>Virology</addtitle><description>During a subtraction study on gene expression in human kidney mesangial cells (HMCs), cDNA clones with sequence homology to paramyxovirus P, M and F genes were isolated. Subsequent investigation revealed that this particular HMC line was infected with a previously unknown paramyxovirus. Here, we report the isolation and genome characterization of this new virus, now named
Beilong virus (BeV). The genome of BeV is 19,212 nucleotides (nt) in length and is the largest among all known members of the order Mononegavirales. The BeV genome contains eight genes in the order 3′-N-P/V/C-M-F-SH-TM-G-L-5′. The SH and TM genes code for a small hydrophobic protein of 76 aa and a transmembrane protein of 254 aa, respectively. The BeV G gene, at 4527 nt, codes for an attachment protein of 734 aa and contains two additional open reading frames (ORFs) in the 3′ half of the gene, coding for putative proteins of 299 and 394 aa in length. Although the exact origin of BeV is presently unknown, we provide evidence indicating that BeV was present in a rat mesangial cell line used in the same laboratory prior to the acquisition of the HMC line, suggesting a potential rodent origin for BeV.</description><subject>Amino Acid Sequence</subject><subject>Animals</subject><subject>Base Sequence</subject><subject>Beilong virus</subject><subject>Cell Line</subject><subject>Genome, Viral</subject><subject>Humans</subject><subject>J-virus</subject><subject>Mesangial Cells - virology</subject><subject>Molecular Sequence Data</subject><subject>Mononegavirales</subject><subject>Paramyxovirinae - classification</subject><subject>Paramyxovirinae - genetics</subject><subject>Paramyxovirinae - isolation & purification</subject><subject>Paramyxovirus</subject><subject>Phylogeny</subject><subject>Rats</subject><subject>Rats, Sprague-Dawley</subject><subject>RNA Viruses - classification</subject><subject>RNA Viruses - genetics</subject><subject>Rodents</subject><subject>Viral Proteins - genetics</subject><issn>0042-6822</issn><issn>1096-0341</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2006</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkc1u2zAQhImiQe24fYICBU89VQ5JURR1yMENkjaAkQBBeyYoaSnTkUiHlJ3m7UP_ALk1pwUH384udxD6SsmcEiou1vOdDb6fM0KKpMxJXn1AU0oqkZGc049oSghnmZCMTdB5jGuS3mVJPqEJFTkrGKNT9PgTbO9dh5PXNv7AGju_gx5vdNDDyz9_kPGzHVd4XAHudeggjrgD5wfA3iTcZRG6AdwILXbQ6dHuIItj0K5NysPd4ugN8TM6M7qP8OVUZ-jvzfWfq9_Z8v7X7dVimTW5lGNW17XgBWWCcSiJqdL3tCgKA2WtBdWFMaYpJRdcyoaJisqi5TXXdcXqqq24yWfo-9F3E_zTNq2rBhsb6HvtwG-jEqWQRFD5LkhLSmSe8wTmR7AJPsYARm2CHXR4UZSofRhqrQ5hqH0YezGFkbq-ney39QDtW8_p-gm4PAKQrrGzEFRsLLgGWhugGVXr7X8HvAIMnZ0z</recordid><startdate>20060301</startdate><enddate>20060301</enddate><creator>Li, Zhuo</creator><creator>Yu, Meng</creator><creator>Zhang, Hong</creator><creator>Magoffin, Danielle E.</creator><creator>Jack, Philippa J.M.</creator><creator>Hyatt, Alex</creator><creator>Wang, Hai-Yan</creator><creator>Wang, Lin-Fa</creator><general>Elsevier Inc</general><scope>6I.</scope><scope>AAFTH</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>7TM</scope><scope>7U9</scope><scope>8FD</scope><scope>FR3</scope><scope>H94</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope></search><sort><creationdate>20060301</creationdate><title>Beilong virus, a novel paramyxovirus with the largest genome of non-segmented negative-stranded RNA viruses</title><author>Li, Zhuo ; Yu, Meng ; Zhang, Hong ; Magoffin, Danielle E. ; Jack, Philippa J.M. ; Hyatt, Alex ; Wang, Hai-Yan ; Wang, Lin-Fa</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c388t-bbb64512624e70f9005a655fe7ba61a5fffc7846488c269185d4b4ab92b9d94f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2006</creationdate><topic>Amino Acid Sequence</topic><topic>Animals</topic><topic>Base Sequence</topic><topic>Beilong virus</topic><topic>Cell Line</topic><topic>Genome, Viral</topic><topic>Humans</topic><topic>J-virus</topic><topic>Mesangial Cells - virology</topic><topic>Molecular Sequence Data</topic><topic>Mononegavirales</topic><topic>Paramyxovirinae - classification</topic><topic>Paramyxovirinae - genetics</topic><topic>Paramyxovirinae - isolation & purification</topic><topic>Paramyxovirus</topic><topic>Phylogeny</topic><topic>Rats</topic><topic>Rats, Sprague-Dawley</topic><topic>RNA Viruses - classification</topic><topic>RNA Viruses - genetics</topic><topic>Rodents</topic><topic>Viral Proteins - genetics</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Li, Zhuo</creatorcontrib><creatorcontrib>Yu, Meng</creatorcontrib><creatorcontrib>Zhang, Hong</creatorcontrib><creatorcontrib>Magoffin, Danielle E.</creatorcontrib><creatorcontrib>Jack, Philippa J.M.</creatorcontrib><creatorcontrib>Hyatt, Alex</creatorcontrib><creatorcontrib>Wang, Hai-Yan</creatorcontrib><creatorcontrib>Wang, Lin-Fa</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Nucleic Acids Abstracts</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><jtitle>Virology (New York, N.Y.)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Li, Zhuo</au><au>Yu, Meng</au><au>Zhang, Hong</au><au>Magoffin, Danielle E.</au><au>Jack, Philippa J.M.</au><au>Hyatt, Alex</au><au>Wang, Hai-Yan</au><au>Wang, Lin-Fa</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Beilong virus, a novel paramyxovirus with the largest genome of non-segmented negative-stranded RNA viruses</atitle><jtitle>Virology (New York, N.Y.)</jtitle><addtitle>Virology</addtitle><date>2006-03-01</date><risdate>2006</risdate><volume>346</volume><issue>1</issue><spage>219</spage><epage>228</epage><pages>219-228</pages><issn>0042-6822</issn><eissn>1096-0341</eissn><abstract>During a subtraction study on gene expression in human kidney mesangial cells (HMCs), cDNA clones with sequence homology to paramyxovirus P, M and F genes were isolated. Subsequent investigation revealed that this particular HMC line was infected with a previously unknown paramyxovirus. Here, we report the isolation and genome characterization of this new virus, now named
Beilong virus (BeV). The genome of BeV is 19,212 nucleotides (nt) in length and is the largest among all known members of the order Mononegavirales. The BeV genome contains eight genes in the order 3′-N-P/V/C-M-F-SH-TM-G-L-5′. The SH and TM genes code for a small hydrophobic protein of 76 aa and a transmembrane protein of 254 aa, respectively. The BeV G gene, at 4527 nt, codes for an attachment protein of 734 aa and contains two additional open reading frames (ORFs) in the 3′ half of the gene, coding for putative proteins of 299 and 394 aa in length. Although the exact origin of BeV is presently unknown, we provide evidence indicating that BeV was present in a rat mesangial cell line used in the same laboratory prior to the acquisition of the HMC line, suggesting a potential rodent origin for BeV.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>16325221</pmid><doi>10.1016/j.virol.2005.10.039</doi><tpages>10</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Amino Acid Sequence Animals Base Sequence Beilong virus Cell Line Genome, Viral Humans J-virus Mesangial Cells - virology Molecular Sequence Data Mononegavirales Paramyxovirinae - classification Paramyxovirinae - genetics Paramyxovirinae - isolation & purification Paramyxovirus Phylogeny Rats Rats, Sprague-Dawley RNA Viruses - classification RNA Viruses - genetics Rodents Viral Proteins - genetics |
title | Beilong virus, a novel paramyxovirus with the largest genome of non-segmented negative-stranded RNA viruses |
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