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Molecular characterization and In Vitro synthesis of infectious RNA of a Turnip vein-clearing virus isolated from Alliaria petiolata in Hungary
A tobamovirus was isolated from leaves of Alliaria petiolata plants, showing vein-clearing, interveinal chlorosis, and moderate deformation. Host range experiments revealed a high similarity of isolate ApH both to ribgrass mosaic viruses and turnip vein-clearing viruses. The complete nucleotide sequ...
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Published in: | PloS one 2019-10, Vol.14 (10), p.e0224398 |
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description | A tobamovirus was isolated from leaves of Alliaria petiolata plants, showing vein-clearing, interveinal chlorosis, and moderate deformation. Host range experiments revealed a high similarity of isolate ApH both to ribgrass mosaic viruses and turnip vein-clearing viruses. The complete nucleotide sequence of the viral genome was determined. The genomic RNA is composed of 6312 nucleotides and contains four open reading frames (ORF). ORF1 is 3324 nt-long and encodes a polypeptide of about 125.3 kDa. The ORF1 encoded putative replication protein contains an Alphavirus-like methyltransferase domain. ORF2 is 4806 nt-long and encodes a polypeptide of about 182 kDa. The ORF2 encoded putative replication protein contains an RNA-dependent RNA polymerase, catalytic domain. ORF3 encodes the putative cell-to-cell movement protein with a molecular weight of 30.1 kDa. ORF4 overlaps with ORF3 and encodes the coat protein with a size of 17.5 kDa. Sequence comparisons revealed that the ApH isolate has the highest similarity to turnip vein-clearing viruses and should be considered an isolate of Turnip vein-clearing virus (TVCV). This is the first report on the occurrence of TVCV in Hungary. In vitro transcripts prepared from the full-length cDNA clone of TVCV-ApH were highly infectious and induced typical symptoms characteristic to the original isolate of the virus. Since infectious clones of TVCV-ApH and crTMV (another isolate of TVCV) markedly differed in respect to recovery phenotype in Arabidopsis thaliana, it is feasible to carry out gene exchange or mutational studies to determine viral factors responsible for the symptom recovery phenotype. |
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Host range experiments revealed a high similarity of isolate ApH both to ribgrass mosaic viruses and turnip vein-clearing viruses. The complete nucleotide sequence of the viral genome was determined. The genomic RNA is composed of 6312 nucleotides and contains four open reading frames (ORF). ORF1 is 3324 nt-long and encodes a polypeptide of about 125.3 kDa. The ORF1 encoded putative replication protein contains an Alphavirus-like methyltransferase domain. ORF2 is 4806 nt-long and encodes a polypeptide of about 182 kDa. The ORF2 encoded putative replication protein contains an RNA-dependent RNA polymerase, catalytic domain. ORF3 encodes the putative cell-to-cell movement protein with a molecular weight of 30.1 kDa. ORF4 overlaps with ORF3 and encodes the coat protein with a size of 17.5 kDa. Sequence comparisons revealed that the ApH isolate has the highest similarity to turnip vein-clearing viruses and should be considered an isolate of Turnip vein-clearing virus (TVCV). This is the first report on the occurrence of TVCV in Hungary. In vitro transcripts prepared from the full-length cDNA clone of TVCV-ApH were highly infectious and induced typical symptoms characteristic to the original isolate of the virus. Since infectious clones of TVCV-ApH and crTMV (another isolate of TVCV) markedly differed in respect to recovery phenotype in Arabidopsis thaliana, it is feasible to carry out gene exchange or mutational studies to determine viral factors responsible for the symptom recovery phenotype.</description><identifier>ISSN: 1932-6203</identifier><identifier>EISSN: 1932-6203</identifier><identifier>DOI: 10.1371/journal.pone.0224398</identifier><identifier>PMID: 31648277</identifier><language>eng</language><publisher>United States: Public Library of Science</publisher><subject>Agricultural biotechnology ; Agricultural research ; Alliaria petiolata ; Arabidopsis ; Arabidopsis thaliana ; Base sequence ; Biology and Life Sciences ; Brassicaceae - virology ; Chemical synthesis ; Chlorosis ; Clearing ; Cloning ; Coat protein ; Computer and Information Sciences ; Deoxyribonucleic acid ; DNA ; DNA polymerase ; DNA, Complementary - genetics ; DNA-directed RNA polymerase ; Engineering and Technology ; Genes ; Genomes ; Genomics ; Host range ; Hungary ; Leaves ; Methyltransferase ; Molecular weight ; Movement protein ; Nucleotide sequence ; Nucleotides ; Open reading frames ; Phenotypes ; Phosphatase ; Phylogenetics ; Plant viruses ; Proteins ; Recovery ; Replication ; Research and Analysis Methods ; Ribonucleic acid ; RNA ; RNA, Viral - biosynthesis ; RNA-directed RNA polymerase ; Sequence Analysis ; Similarity ; Tobamovirus ; Tobamovirus - genetics ; Tobamovirus - isolation & purification ; Tobamovirus - metabolism ; Transcription ; Transcription, Genetic ; Transferases ; Turnips ; Veins (plant anatomy) ; Viroids ; Virus replication ; Viruses</subject><ispartof>PloS one, 2019-10, Vol.14 (10), p.e0224398</ispartof><rights>COPYRIGHT 2019 Public Library of Science</rights><rights>2019 Tóth et al. This is an open access article distributed under the terms of the Creative Commons Attribution License: http://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. 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Host range experiments revealed a high similarity of isolate ApH both to ribgrass mosaic viruses and turnip vein-clearing viruses. The complete nucleotide sequence of the viral genome was determined. The genomic RNA is composed of 6312 nucleotides and contains four open reading frames (ORF). ORF1 is 3324 nt-long and encodes a polypeptide of about 125.3 kDa. The ORF1 encoded putative replication protein contains an Alphavirus-like methyltransferase domain. ORF2 is 4806 nt-long and encodes a polypeptide of about 182 kDa. The ORF2 encoded putative replication protein contains an RNA-dependent RNA polymerase, catalytic domain. ORF3 encodes the putative cell-to-cell movement protein with a molecular weight of 30.1 kDa. ORF4 overlaps with ORF3 and encodes the coat protein with a size of 17.5 kDa. Sequence comparisons revealed that the ApH isolate has the highest similarity to turnip vein-clearing viruses and should be considered an isolate of Turnip vein-clearing virus (TVCV). This is the first report on the occurrence of TVCV in Hungary. In vitro transcripts prepared from the full-length cDNA clone of TVCV-ApH were highly infectious and induced typical symptoms characteristic to the original isolate of the virus. Since infectious clones of TVCV-ApH and crTMV (another isolate of TVCV) markedly differed in respect to recovery phenotype in Arabidopsis thaliana, it is feasible to carry out gene exchange or mutational studies to determine viral factors responsible for the symptom recovery phenotype.</description><subject>Agricultural biotechnology</subject><subject>Agricultural research</subject><subject>Alliaria petiolata</subject><subject>Arabidopsis</subject><subject>Arabidopsis thaliana</subject><subject>Base sequence</subject><subject>Biology and Life Sciences</subject><subject>Brassicaceae - virology</subject><subject>Chemical synthesis</subject><subject>Chlorosis</subject><subject>Clearing</subject><subject>Cloning</subject><subject>Coat protein</subject><subject>Computer and Information Sciences</subject><subject>Deoxyribonucleic acid</subject><subject>DNA</subject><subject>DNA polymerase</subject><subject>DNA, Complementary - genetics</subject><subject>DNA-directed RNA polymerase</subject><subject>Engineering and Technology</subject><subject>Genes</subject><subject>Genomes</subject><subject>Genomics</subject><subject>Host range</subject><subject>Hungary</subject><subject>Leaves</subject><subject>Methyltransferase</subject><subject>Molecular weight</subject><subject>Movement protein</subject><subject>Nucleotide sequence</subject><subject>Nucleotides</subject><subject>Open reading frames</subject><subject>Phenotypes</subject><subject>Phosphatase</subject><subject>Phylogenetics</subject><subject>Plant viruses</subject><subject>Proteins</subject><subject>Recovery</subject><subject>Replication</subject><subject>Research and Analysis Methods</subject><subject>Ribonucleic acid</subject><subject>RNA</subject><subject>RNA, Viral - biosynthesis</subject><subject>RNA-directed RNA polymerase</subject><subject>Sequence Analysis</subject><subject>Similarity</subject><subject>Tobamovirus</subject><subject>Tobamovirus - genetics</subject><subject>Tobamovirus - isolation & purification</subject><subject>Tobamovirus - metabolism</subject><subject>Transcription</subject><subject>Transcription, Genetic</subject><subject>Transferases</subject><subject>Turnips</subject><subject>Veins (plant anatomy)</subject><subject>Viroids</subject><subject>Virus replication</subject><subject>Viruses</subject><issn>1932-6203</issn><issn>1932-6203</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNqNk81uEzEQx1cIREvhDRBYQkJwSPDHxuu9IEUV0EiFSqX0anm9duLIsVN7N6K8BK_MLEmrBPWA9uCV5zf_Gc9HUbwkeExYRT4sY5-C8uN1DGaMKS1ZLR4Vx6RmdMQpZo_3_o-KZzkvMZ4wwfnT4ogRXgpaVcfF76_RG917lZBeqKR0Z5L7pToXA1KhRbOArl2XIsq3oVuY7DKKFrlgjQamz-jy23S4UegK0nFrtDEujLQ3KrkwRxuXgHE5etWZFtkUV2jqvQOrQmsDEmBQoIfO-jBX6fZ58cQqn82L3XlS_Pj86er0bHR-8WV2Oj0faU5pN6qxMRy3EyywFpWuFKFlbdtSNS1mjSbCalWSStua6IZZ2gJISN20XDeccM5Oitdb3bWPWe5qmSVlWPCalpgBMdsSbVRLuU5uBenJqJz8exHTXKrUOXiqFJOqZJBIaS2FqFzgyirR8JYSwbQwoPVxF61vVqbVJnRJ-QPRQ0twCzmPG8kFoYISEHi3E0jxpje5kyuXtfFeBQNdGPKuJ7ikbMj7zT_ow6_bUXMFD4B-RoirB1E55ZhVuKpYBdT4AQq-1qychsGzDu4PHN4fOADTmZ_dXPU5y9n3y_9nL64P2bd77MIo3y1gqPphTvMhWG5BnWLOydj7IhMsh725q4Yc9kbu9gbcXu036N7pblHYH3lVFDo</recordid><startdate>20191024</startdate><enddate>20191024</enddate><creator>Tóth, Tamás</creator><creator>Gyula, Péter</creator><creator>Salamon, Pál</creator><creator>Kis, Szilvia</creator><creator>Sós-Hegedűs, Anita</creator><creator>Szittya, György</creator><general>Public Library of Science</general><general>Public Library of Science (PLoS)</general><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>IOV</scope><scope>ISR</scope><scope>3V.</scope><scope>7QG</scope><scope>7QL</scope><scope>7QO</scope><scope>7RV</scope><scope>7SN</scope><scope>7SS</scope><scope>7T5</scope><scope>7TG</scope><scope>7TM</scope><scope>7U9</scope><scope>7X2</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8C1</scope><scope>8FD</scope><scope>8FE</scope><scope>8FG</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABJCF</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>ARAPS</scope><scope>ATCPS</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BGLVJ</scope><scope>BHPHI</scope><scope>C1K</scope><scope>CCPQU</scope><scope>D1I</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>H94</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>KB.</scope><scope>KB0</scope><scope>KL.</scope><scope>L6V</scope><scope>LK8</scope><scope>M0K</scope><scope>M0S</scope><scope>M1P</scope><scope>M7N</scope><scope>M7P</scope><scope>M7S</scope><scope>NAPCQ</scope><scope>P5Z</scope><scope>P62</scope><scope>P64</scope><scope>PATMY</scope><scope>PDBOC</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>PTHSS</scope><scope>PYCSY</scope><scope>RC3</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope><orcidid>https://orcid.org/0000-0003-0526-8383</orcidid><orcidid>https://orcid.org/0000-0002-3574-2827</orcidid></search><sort><creationdate>20191024</creationdate><title>Molecular characterization and In Vitro synthesis of infectious RNA of a Turnip vein-clearing virus isolated from Alliaria petiolata in Hungary</title><author>Tóth, Tamás ; Gyula, Péter ; Salamon, Pál ; Kis, Szilvia ; Sós-Hegedűs, Anita ; Szittya, György</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c622t-90ee60d5080c87c7a1249fd4abd03bc18fca417cf91cb3f2d080119bd6cb61663</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>Agricultural biotechnology</topic><topic>Agricultural research</topic><topic>Alliaria petiolata</topic><topic>Arabidopsis</topic><topic>Arabidopsis thaliana</topic><topic>Base sequence</topic><topic>Biology and Life Sciences</topic><topic>Brassicaceae - 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Host range experiments revealed a high similarity of isolate ApH both to ribgrass mosaic viruses and turnip vein-clearing viruses. The complete nucleotide sequence of the viral genome was determined. The genomic RNA is composed of 6312 nucleotides and contains four open reading frames (ORF). ORF1 is 3324 nt-long and encodes a polypeptide of about 125.3 kDa. The ORF1 encoded putative replication protein contains an Alphavirus-like methyltransferase domain. ORF2 is 4806 nt-long and encodes a polypeptide of about 182 kDa. The ORF2 encoded putative replication protein contains an RNA-dependent RNA polymerase, catalytic domain. ORF3 encodes the putative cell-to-cell movement protein with a molecular weight of 30.1 kDa. ORF4 overlaps with ORF3 and encodes the coat protein with a size of 17.5 kDa. Sequence comparisons revealed that the ApH isolate has the highest similarity to turnip vein-clearing viruses and should be considered an isolate of Turnip vein-clearing virus (TVCV). This is the first report on the occurrence of TVCV in Hungary. In vitro transcripts prepared from the full-length cDNA clone of TVCV-ApH were highly infectious and induced typical symptoms characteristic to the original isolate of the virus. Since infectious clones of TVCV-ApH and crTMV (another isolate of TVCV) markedly differed in respect to recovery phenotype in Arabidopsis thaliana, it is feasible to carry out gene exchange or mutational studies to determine viral factors responsible for the symptom recovery phenotype.</abstract><cop>United States</cop><pub>Public Library of Science</pub><pmid>31648277</pmid><doi>10.1371/journal.pone.0224398</doi><tpages>e0224398</tpages><orcidid>https://orcid.org/0000-0003-0526-8383</orcidid><orcidid>https://orcid.org/0000-0002-3574-2827</orcidid><oa>free_for_read</oa></addata></record> |
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source | PubMed Central Free; Publicly Available Content (ProQuest) |
subjects | Agricultural biotechnology Agricultural research Alliaria petiolata Arabidopsis Arabidopsis thaliana Base sequence Biology and Life Sciences Brassicaceae - virology Chemical synthesis Chlorosis Clearing Cloning Coat protein Computer and Information Sciences Deoxyribonucleic acid DNA DNA polymerase DNA, Complementary - genetics DNA-directed RNA polymerase Engineering and Technology Genes Genomes Genomics Host range Hungary Leaves Methyltransferase Molecular weight Movement protein Nucleotide sequence Nucleotides Open reading frames Phenotypes Phosphatase Phylogenetics Plant viruses Proteins Recovery Replication Research and Analysis Methods Ribonucleic acid RNA RNA, Viral - biosynthesis RNA-directed RNA polymerase Sequence Analysis Similarity Tobamovirus Tobamovirus - genetics Tobamovirus - isolation & purification Tobamovirus - metabolism Transcription Transcription, Genetic Transferases Turnips Veins (plant anatomy) Viroids Virus replication Viruses |
title | Molecular characterization and In Vitro synthesis of infectious RNA of a Turnip vein-clearing virus isolated from Alliaria petiolata in Hungary |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-19T09%3A48%3A39IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-gale_plos_&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Molecular%20characterization%20and%20In%20Vitro%20synthesis%20of%20infectious%20RNA%20of%20a%20Turnip%20vein-clearing%20virus%20isolated%20from%20Alliaria%20petiolata%20in%20Hungary&rft.jtitle=PloS%20one&rft.au=T%C3%B3th,%20Tam%C3%A1s&rft.date=2019-10-24&rft.volume=14&rft.issue=10&rft.spage=e0224398&rft.pages=e0224398-&rft.issn=1932-6203&rft.eissn=1932-6203&rft_id=info:doi/10.1371/journal.pone.0224398&rft_dat=%3Cgale_plos_%3EA603707737%3C/gale_plos_%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c622t-90ee60d5080c87c7a1249fd4abd03bc18fca417cf91cb3f2d080119bd6cb61663%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=2308692403&rft_id=info:pmid/31648277&rft_galeid=A603707737&rfr_iscdi=true |