Genetic variability of natural populations of cotton leaf curl geminivirus, a single-stranded DNA virus

Reports on the genetic variability and evolution of natural populations of DNA viruses are scarce in comparison with the abundant information on the variability of RNA viruses. Geminiviruses are plant viruses with circular ssDNA genomes that are replicated by the host plant DNA polymerases. Whitefly...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Journal of molecular evolution 1999-11, Vol.49 (5), p.672-681
Hauptverfasser: Sanz, AI, Fraile, A, Gallego, JM, Malpica, JM, Garcia-Arenal, F
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 681
container_issue 5
container_start_page 672
container_title Journal of molecular evolution
container_volume 49
creator Sanz, AI
Fraile, A
Gallego, JM
Malpica, JM
Garcia-Arenal, F
description Reports on the genetic variability and evolution of natural populations of DNA viruses are scarce in comparison with the abundant information on the variability of RNA viruses. Geminiviruses are plant viruses with circular ssDNA genomes that are replicated by the host plant DNA polymerases. Whitefly-transmitted geminiviruses (WTG) are the agents of important diseases of crop plants and best exemplify emerging plant viruses. In this report we have analyzed the genetic diversity of cotton leaf curl geminivirus (CLCuV), a typical emerging WTG. No genetic differentiation was observed between isolates from different host plant species or geographic regions. Thus, the analyzed isolates represented a unique, undifferentiated population. Genetic variability, estimated as nucleotide diversities at synonymous positions in open reading frames (ORFs) for the AC1 (=replication) protein and coat protein (CP = AV1), was very high, exceeding the values reported for different genes in several plant and animal RNA viruses. This was unexpected in a virus that uses the DNA replication machinery of its eukaryotic host. Diversities at nonsynonymous positions, on the other hand, indicated that variability may be constrained in the genome of CLCuV. The ratio of nonsynonymous-to-synonymous substitutions varied for the different ORFs: they were higher for CP than for AC1 and lower still for the AC4 and AV2 ORFs, which overlap AC1 and CP ORFs, respectively. Analysis of nucleotide diversities at synonymous and nonsynonymous positions of the AC4 and AV2 ORFs suggest that their evolution is constrained by AC1 and CP, respectively. Data suggest that AC4 and AV2 are new genes that may have originated by overprinting on the preexistent AC1 and CP genes. Evidence for recombination was found for the AC1 and CP ORFs and for the noncoding intergenic region (IR). Data indicate that the origin of replication is a major recombination point in the IR, but not the only one. Analyses of the IR also suggest that recombinants may be frequent in the population and that recombination may have an important role in the generation of CLCuV variability.
doi_str_mv 10.1007/PL00006588
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_1859312179</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2611701351</sourcerecordid><originalsourceid>FETCH-LOGICAL-c343t-9101df7af6a5b5b96781d1e4c62e760736ddafd26000f7feb86e0f4b87de60c3</originalsourceid><addsrcrecordid>eNp9kU1rGzEQhkVpqF0nl_yAInoIpWQTfexK2mNI8wUmySH3RbsaGRlZciVtwP--6ziQ0kPnMDPMPLww8yJ0SskFJURePi_JFKJR6hOa05qzap8-ozkhjFVM1fUMfc15TQiVTcu_oBklTcNIreZodQcBihvwq05O9867ssPR4qDLmLTH27gdvS4uhrwfD7GUGLAHPfVj8ngFGxfcq0tjPscaZxdWHqpckg4GDP71eIXflsfoyGqf4eS9LtDL7c3L9X21fLp7uL5aVgOvealaSqixUluhm77pWyEVNRTqQTCQgkgujNHWMDEdbKWFXgkgtu6VNCDIwBfox0F2m-LvEXLpNi4P4L0OEMfcUTU9gDIq2wk9-z8qa0pbwibw-z_gOo4pTFd0LVOSc9buoZ8HaEgx5wS22ya30WnXUdLtXeo-XJrgb--KY78B8xd6sIX_AWHVjF0</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>928733292</pqid></control><display><type>article</type><title>Genetic variability of natural populations of cotton leaf curl geminivirus, a single-stranded DNA virus</title><source>SpringerLink Journals - AutoHoldings</source><creator>Sanz, AI ; Fraile, A ; Gallego, JM ; Malpica, JM ; Garcia-Arenal, F</creator><creatorcontrib>Sanz, AI ; Fraile, A ; Gallego, JM ; Malpica, JM ; Garcia-Arenal, F</creatorcontrib><description>Reports on the genetic variability and evolution of natural populations of DNA viruses are scarce in comparison with the abundant information on the variability of RNA viruses. Geminiviruses are plant viruses with circular ssDNA genomes that are replicated by the host plant DNA polymerases. Whitefly-transmitted geminiviruses (WTG) are the agents of important diseases of crop plants and best exemplify emerging plant viruses. In this report we have analyzed the genetic diversity of cotton leaf curl geminivirus (CLCuV), a typical emerging WTG. No genetic differentiation was observed between isolates from different host plant species or geographic regions. Thus, the analyzed isolates represented a unique, undifferentiated population. Genetic variability, estimated as nucleotide diversities at synonymous positions in open reading frames (ORFs) for the AC1 (=replication) protein and coat protein (CP = AV1), was very high, exceeding the values reported for different genes in several plant and animal RNA viruses. This was unexpected in a virus that uses the DNA replication machinery of its eukaryotic host. Diversities at nonsynonymous positions, on the other hand, indicated that variability may be constrained in the genome of CLCuV. The ratio of nonsynonymous-to-synonymous substitutions varied for the different ORFs: they were higher for CP than for AC1 and lower still for the AC4 and AV2 ORFs, which overlap AC1 and CP ORFs, respectively. Analysis of nucleotide diversities at synonymous and nonsynonymous positions of the AC4 and AV2 ORFs suggest that their evolution is constrained by AC1 and CP, respectively. Data suggest that AC4 and AV2 are new genes that may have originated by overprinting on the preexistent AC1 and CP genes. Evidence for recombination was found for the AC1 and CP ORFs and for the noncoding intergenic region (IR). Data indicate that the origin of replication is a major recombination point in the IR, but not the only one. Analyses of the IR also suggest that recombinants may be frequent in the population and that recombination may have an important role in the generation of CLCuV variability.</description><identifier>ISSN: 0022-2844</identifier><identifier>EISSN: 1432-1432</identifier><identifier>DOI: 10.1007/PL00006588</identifier><identifier>PMID: 10552048</identifier><language>eng</language><publisher>Germany: Springer Nature B.V</publisher><subject>AC1 gene ; AC4 gene ; ACP gene ; AV2 gene ; Cotton leaf curl virus ; CP AV1 protein ; Deoxyribonucleic acid ; DNA ; Evolutionary biology ; Geminivirus ; Genetic diversity ; Leaves ; Mutation ; Natural populations ; Plant pathology ; Plant species ; Variability ; Viruses</subject><ispartof>Journal of molecular evolution, 1999-11, Vol.49 (5), p.672-681</ispartof><rights>Springer-Verlag New York Inc. 1999</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c343t-9101df7af6a5b5b96781d1e4c62e760736ddafd26000f7feb86e0f4b87de60c3</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27923,27924</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/10552048$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Sanz, AI</creatorcontrib><creatorcontrib>Fraile, A</creatorcontrib><creatorcontrib>Gallego, JM</creatorcontrib><creatorcontrib>Malpica, JM</creatorcontrib><creatorcontrib>Garcia-Arenal, F</creatorcontrib><title>Genetic variability of natural populations of cotton leaf curl geminivirus, a single-stranded DNA virus</title><title>Journal of molecular evolution</title><addtitle>J Mol Evol</addtitle><description>Reports on the genetic variability and evolution of natural populations of DNA viruses are scarce in comparison with the abundant information on the variability of RNA viruses. Geminiviruses are plant viruses with circular ssDNA genomes that are replicated by the host plant DNA polymerases. Whitefly-transmitted geminiviruses (WTG) are the agents of important diseases of crop plants and best exemplify emerging plant viruses. In this report we have analyzed the genetic diversity of cotton leaf curl geminivirus (CLCuV), a typical emerging WTG. No genetic differentiation was observed between isolates from different host plant species or geographic regions. Thus, the analyzed isolates represented a unique, undifferentiated population. Genetic variability, estimated as nucleotide diversities at synonymous positions in open reading frames (ORFs) for the AC1 (=replication) protein and coat protein (CP = AV1), was very high, exceeding the values reported for different genes in several plant and animal RNA viruses. This was unexpected in a virus that uses the DNA replication machinery of its eukaryotic host. Diversities at nonsynonymous positions, on the other hand, indicated that variability may be constrained in the genome of CLCuV. The ratio of nonsynonymous-to-synonymous substitutions varied for the different ORFs: they were higher for CP than for AC1 and lower still for the AC4 and AV2 ORFs, which overlap AC1 and CP ORFs, respectively. Analysis of nucleotide diversities at synonymous and nonsynonymous positions of the AC4 and AV2 ORFs suggest that their evolution is constrained by AC1 and CP, respectively. Data suggest that AC4 and AV2 are new genes that may have originated by overprinting on the preexistent AC1 and CP genes. Evidence for recombination was found for the AC1 and CP ORFs and for the noncoding intergenic region (IR). Data indicate that the origin of replication is a major recombination point in the IR, but not the only one. Analyses of the IR also suggest that recombinants may be frequent in the population and that recombination may have an important role in the generation of CLCuV variability.</description><subject>AC1 gene</subject><subject>AC4 gene</subject><subject>ACP gene</subject><subject>AV2 gene</subject><subject>Cotton leaf curl virus</subject><subject>CP AV1 protein</subject><subject>Deoxyribonucleic acid</subject><subject>DNA</subject><subject>Evolutionary biology</subject><subject>Geminivirus</subject><subject>Genetic diversity</subject><subject>Leaves</subject><subject>Mutation</subject><subject>Natural populations</subject><subject>Plant pathology</subject><subject>Plant species</subject><subject>Variability</subject><subject>Viruses</subject><issn>0022-2844</issn><issn>1432-1432</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1999</creationdate><recordtype>article</recordtype><sourceid>8G5</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><sourceid>GUQSH</sourceid><sourceid>M2O</sourceid><recordid>eNp9kU1rGzEQhkVpqF0nl_yAInoIpWQTfexK2mNI8wUmySH3RbsaGRlZciVtwP--6ziQ0kPnMDPMPLww8yJ0SskFJURePi_JFKJR6hOa05qzap8-ozkhjFVM1fUMfc15TQiVTcu_oBklTcNIreZodQcBihvwq05O9867ssPR4qDLmLTH27gdvS4uhrwfD7GUGLAHPfVj8ngFGxfcq0tjPscaZxdWHqpckg4GDP71eIXflsfoyGqf4eS9LtDL7c3L9X21fLp7uL5aVgOvealaSqixUluhm77pWyEVNRTqQTCQgkgujNHWMDEdbKWFXgkgtu6VNCDIwBfox0F2m-LvEXLpNi4P4L0OEMfcUTU9gDIq2wk9-z8qa0pbwibw-z_gOo4pTFd0LVOSc9buoZ8HaEgx5wS22ya30WnXUdLtXeo-XJrgb--KY78B8xd6sIX_AWHVjF0</recordid><startdate>19991101</startdate><enddate>19991101</enddate><creator>Sanz, AI</creator><creator>Fraile, A</creator><creator>Gallego, JM</creator><creator>Malpica, JM</creator><creator>Garcia-Arenal, F</creator><general>Springer Nature B.V</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7QL</scope><scope>7QP</scope><scope>7QR</scope><scope>7T7</scope><scope>7TK</scope><scope>7U9</scope><scope>7X7</scope><scope>7XB</scope><scope>88A</scope><scope>88E</scope><scope>8AO</scope><scope>8FD</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>8G5</scope><scope>ABUWG</scope><scope>AEUYN</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>C1K</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>H94</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M2O</scope><scope>M7N</scope><scope>M7P</scope><scope>MBDVC</scope><scope>P64</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>Q9U</scope><scope>RC3</scope><scope>7X8</scope></search><sort><creationdate>19991101</creationdate><title>Genetic variability of natural populations of cotton leaf curl geminivirus, a single-stranded DNA virus</title><author>Sanz, AI ; Fraile, A ; Gallego, JM ; Malpica, JM ; Garcia-Arenal, F</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c343t-9101df7af6a5b5b96781d1e4c62e760736ddafd26000f7feb86e0f4b87de60c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1999</creationdate><topic>AC1 gene</topic><topic>AC4 gene</topic><topic>ACP gene</topic><topic>AV2 gene</topic><topic>Cotton leaf curl virus</topic><topic>CP AV1 protein</topic><topic>Deoxyribonucleic acid</topic><topic>DNA</topic><topic>Evolutionary biology</topic><topic>Geminivirus</topic><topic>Genetic diversity</topic><topic>Leaves</topic><topic>Mutation</topic><topic>Natural populations</topic><topic>Plant pathology</topic><topic>Plant species</topic><topic>Variability</topic><topic>Viruses</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Sanz, AI</creatorcontrib><creatorcontrib>Fraile, A</creatorcontrib><creatorcontrib>Gallego, JM</creatorcontrib><creatorcontrib>Malpica, JM</creatorcontrib><creatorcontrib>Garcia-Arenal, F</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Calcium &amp; Calcified Tissue Abstracts</collection><collection>Chemoreception Abstracts</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Neurosciences Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Health &amp; Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Biology Database (Alumni Edition)</collection><collection>Medical 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 Edition)</collection><collection>ProQuest One Sustainability</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</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 &amp; Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health &amp; Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>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>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>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of molecular evolution</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Sanz, AI</au><au>Fraile, A</au><au>Gallego, JM</au><au>Malpica, JM</au><au>Garcia-Arenal, F</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Genetic variability of natural populations of cotton leaf curl geminivirus, a single-stranded DNA virus</atitle><jtitle>Journal of molecular evolution</jtitle><addtitle>J Mol Evol</addtitle><date>1999-11-01</date><risdate>1999</risdate><volume>49</volume><issue>5</issue><spage>672</spage><epage>681</epage><pages>672-681</pages><issn>0022-2844</issn><eissn>1432-1432</eissn><abstract>Reports on the genetic variability and evolution of natural populations of DNA viruses are scarce in comparison with the abundant information on the variability of RNA viruses. Geminiviruses are plant viruses with circular ssDNA genomes that are replicated by the host plant DNA polymerases. Whitefly-transmitted geminiviruses (WTG) are the agents of important diseases of crop plants and best exemplify emerging plant viruses. In this report we have analyzed the genetic diversity of cotton leaf curl geminivirus (CLCuV), a typical emerging WTG. No genetic differentiation was observed between isolates from different host plant species or geographic regions. Thus, the analyzed isolates represented a unique, undifferentiated population. Genetic variability, estimated as nucleotide diversities at synonymous positions in open reading frames (ORFs) for the AC1 (=replication) protein and coat protein (CP = AV1), was very high, exceeding the values reported for different genes in several plant and animal RNA viruses. This was unexpected in a virus that uses the DNA replication machinery of its eukaryotic host. Diversities at nonsynonymous positions, on the other hand, indicated that variability may be constrained in the genome of CLCuV. The ratio of nonsynonymous-to-synonymous substitutions varied for the different ORFs: they were higher for CP than for AC1 and lower still for the AC4 and AV2 ORFs, which overlap AC1 and CP ORFs, respectively. Analysis of nucleotide diversities at synonymous and nonsynonymous positions of the AC4 and AV2 ORFs suggest that their evolution is constrained by AC1 and CP, respectively. Data suggest that AC4 and AV2 are new genes that may have originated by overprinting on the preexistent AC1 and CP genes. Evidence for recombination was found for the AC1 and CP ORFs and for the noncoding intergenic region (IR). Data indicate that the origin of replication is a major recombination point in the IR, but not the only one. Analyses of the IR also suggest that recombinants may be frequent in the population and that recombination may have an important role in the generation of CLCuV variability.</abstract><cop>Germany</cop><pub>Springer Nature B.V</pub><pmid>10552048</pmid><doi>10.1007/PL00006588</doi><tpages>10</tpages></addata></record>
fulltext fulltext
identifier ISSN: 0022-2844
ispartof Journal of molecular evolution, 1999-11, Vol.49 (5), p.672-681
issn 0022-2844
1432-1432
language eng
recordid cdi_proquest_miscellaneous_1859312179
source SpringerLink Journals - AutoHoldings
subjects AC1 gene
AC4 gene
ACP gene
AV2 gene
Cotton leaf curl virus
CP AV1 protein
Deoxyribonucleic acid
DNA
Evolutionary biology
Geminivirus
Genetic diversity
Leaves
Mutation
Natural populations
Plant pathology
Plant species
Variability
Viruses
title Genetic variability of natural populations of cotton leaf curl geminivirus, a single-stranded DNA virus
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-12T12%3A46%3A19IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Genetic%20variability%20of%20natural%20populations%20of%20cotton%20leaf%20curl%20geminivirus,%20a%20single-stranded%20DNA%20virus&rft.jtitle=Journal%20of%20molecular%20evolution&rft.au=Sanz,%20AI&rft.date=1999-11-01&rft.volume=49&rft.issue=5&rft.spage=672&rft.epage=681&rft.pages=672-681&rft.issn=0022-2844&rft.eissn=1432-1432&rft_id=info:doi/10.1007/PL00006588&rft_dat=%3Cproquest_cross%3E2611701351%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=928733292&rft_id=info:pmid/10552048&rfr_iscdi=true