One is enough: in vivo effective population size is dose-dependent for a plant RNA virus
Effective population size (N(e)) determines the strength of genetic drift and the frequency of co-infection by multiple genotypes, making it a key factor in viral evolution. Experimental estimates of N(e) for different plant viruses have, however, rendered diverging results. The independent action h...
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description | Effective population size (N(e)) determines the strength of genetic drift and the frequency of co-infection by multiple genotypes, making it a key factor in viral evolution. Experimental estimates of N(e) for different plant viruses have, however, rendered diverging results. The independent action hypothesis (IAH) states that each virion has a probability of infection, and that virions act independent of one another during the infection process. A corollary of IAH is that N(e) must be dose dependent. A test of IAH for a plant virus has not been reported yet. Here we perform a test of an IAH infection model using a plant RNA virus, Tobacco etch virus (TEV) variants carrying GFP or mCherry fluorescent markers, in Nicotiana tabacum and Capsicum annuum plants. The number of primary infection foci increased linearly with dose, and was similar to a Poisson distribution. At high doses, primary infection foci containing both genotypes were found at a low frequency ( |
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Experimental estimates of N(e) for different plant viruses have, however, rendered diverging results. The independent action hypothesis (IAH) states that each virion has a probability of infection, and that virions act independent of one another during the infection process. A corollary of IAH is that N(e) must be dose dependent. A test of IAH for a plant virus has not been reported yet. Here we perform a test of an IAH infection model using a plant RNA virus, Tobacco etch virus (TEV) variants carrying GFP or mCherry fluorescent markers, in Nicotiana tabacum and Capsicum annuum plants. The number of primary infection foci increased linearly with dose, and was similar to a Poisson distribution. At high doses, primary infection foci containing both genotypes were found at a low frequency (<2%). The probability that a genotype that infected the inoculated leaf would systemically infect that plant was near 1, although in a few rare cases genotypes could be trapped in the inoculated leaf by being physically surrounded by the other genotype. The frequency of mixed-genotype infection could be predicted from the mean number of primary infection foci using the independent-action model. Independent action appears to hold for TEV, and N(e) is therefore dose-dependent for this plant RNA virus. The mean number of virions causing systemic infection can be very small, and approaches 1 at low doses. Dose-dependency in TEV suggests that comparison of N(e) estimates for different viruses are not very meaningful unless dose effects are taken into consideration.</description><identifier>ISSN: 1553-7374</identifier><identifier>ISSN: 1553-7366</identifier><identifier>EISSN: 1553-7374</identifier><identifier>DOI: 10.1371/journal.ppat.1002122</identifier><identifier>PMID: 21750676</identifier><language>eng</language><publisher>United States: Public Library of Science</publisher><subject>Biology ; Capsicum - virology ; Competition ; Estimates ; Evolution ; Experiments ; Flowers & plants ; Genetic aspects ; Genotype ; Genotype & phenotype ; Health aspects ; Host-Pathogen Interactions - physiology ; Hypotheses ; Infections ; Leaves ; Nicotiana - virology ; Plant Diseases - virology ; Plant viruses ; Plant Viruses - physiology ; Population ; Population Density ; Population genetics ; Potyvirus - genetics ; Potyvirus - growth & development ; Potyvirus - pathogenicity ; RNA, Viral - metabolism ; Studies ; Viral Load - physiology ; Virus diseases of plants ; Virus Replication ; Viruses</subject><ispartof>PLoS pathogens, 2011-07, Vol.7 (7), p.e1002122-e1002122</ispartof><rights>COPYRIGHT 2011 Public Library of Science</rights><rights>2011 Zwart et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited: Zwart MP, Daròs J-A, Elena SF (2011) One Is Enough: In Vivo Effective Population Size Is Dose-Dependent for a Plant RNA Virus. 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Experimental estimates of N(e) for different plant viruses have, however, rendered diverging results. The independent action hypothesis (IAH) states that each virion has a probability of infection, and that virions act independent of one another during the infection process. A corollary of IAH is that N(e) must be dose dependent. A test of IAH for a plant virus has not been reported yet. Here we perform a test of an IAH infection model using a plant RNA virus, Tobacco etch virus (TEV) variants carrying GFP or mCherry fluorescent markers, in Nicotiana tabacum and Capsicum annuum plants. The number of primary infection foci increased linearly with dose, and was similar to a Poisson distribution. At high doses, primary infection foci containing both genotypes were found at a low frequency (<2%). The probability that a genotype that infected the inoculated leaf would systemically infect that plant was near 1, although in a few rare cases genotypes could be trapped in the inoculated leaf by being physically surrounded by the other genotype. The frequency of mixed-genotype infection could be predicted from the mean number of primary infection foci using the independent-action model. Independent action appears to hold for TEV, and N(e) is therefore dose-dependent for this plant RNA virus. The mean number of virions causing systemic infection can be very small, and approaches 1 at low doses. Dose-dependency in TEV suggests that comparison of N(e) estimates for different viruses are not very meaningful unless dose effects are taken into consideration.</description><subject>Biology</subject><subject>Capsicum - virology</subject><subject>Competition</subject><subject>Estimates</subject><subject>Evolution</subject><subject>Experiments</subject><subject>Flowers & plants</subject><subject>Genetic aspects</subject><subject>Genotype</subject><subject>Genotype & phenotype</subject><subject>Health aspects</subject><subject>Host-Pathogen Interactions - physiology</subject><subject>Hypotheses</subject><subject>Infections</subject><subject>Leaves</subject><subject>Nicotiana - virology</subject><subject>Plant Diseases - virology</subject><subject>Plant viruses</subject><subject>Plant Viruses - physiology</subject><subject>Population</subject><subject>Population Density</subject><subject>Population genetics</subject><subject>Potyvirus - genetics</subject><subject>Potyvirus - growth & development</subject><subject>Potyvirus - pathogenicity</subject><subject>RNA, Viral - metabolism</subject><subject>Studies</subject><subject>Viral Load - physiology</subject><subject>Virus diseases of plants</subject><subject>Virus Replication</subject><subject>Viruses</subject><issn>1553-7374</issn><issn>1553-7366</issn><issn>1553-7374</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2011</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>BENPR</sourceid><sourceid>DOA</sourceid><recordid>eNqVkk1v1DAQhiMEoqXwDxBE4oA4ZPFH_BEOSKuKj5WqViogcbOceLz1KhundrICfj3eblo1qBfkg63xM-_MvJose4nRAlOB32_8GDrdLvpeDwuMEMGEPMqOMWO0EFSUj--9j7JnMW4QKjHF_Gl2RLBgiAt-nP286CB3MYfOj-urD7nr8p3b-RyshWZwO8h734-tHpzv8uj-3MDGRygM9NAZ6Ibc-pDrvG91el-eL5NAGOPz7InVbYQX032S_fj86fvp1-Ls4svqdHlWNILwoQCCJAFpuS2J0QgxWdXSVIhxmhqs6xrjhmipDbesZIzIKk0hOEc1oozWkp5krw-6feujmkyJCu9JwcqKJWJ1IIzXG9UHt9Xht_LaqZuAD2ulw-CaFpTVAJIZAZLzUhIma1sTsNrSypCy1knr41RtrLdgmjR-0O1MdP7TuSu19jtFk_OE0yTwdhII_nqEOKitiw20yTzwY1RScEklY1Ui3_xDPjzcRK116t911qeyzV5TLVM9zioheKIWD1DpGNi6xndgXYrPEt7NEhIzwK9hrccY1erb5X-w53O2PLBN8DEGsHfWYaT2a307pNqvtZrWOqW9um_7XdLtHtO_wz7x5w</recordid><startdate>20110701</startdate><enddate>20110701</enddate><creator>Zwart, Mark P</creator><creator>Daròs, José-Antonio</creator><creator>Elena, Santiago F</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>ISN</scope><scope>ISR</scope><scope>3V.</scope><scope>7QL</scope><scope>7U9</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</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>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>H94</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M7P</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope></search><sort><creationdate>20110701</creationdate><title>One is enough: in vivo effective population size is dose-dependent for a plant RNA virus</title><author>Zwart, Mark P ; 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Experimental estimates of N(e) for different plant viruses have, however, rendered diverging results. The independent action hypothesis (IAH) states that each virion has a probability of infection, and that virions act independent of one another during the infection process. A corollary of IAH is that N(e) must be dose dependent. A test of IAH for a plant virus has not been reported yet. Here we perform a test of an IAH infection model using a plant RNA virus, Tobacco etch virus (TEV) variants carrying GFP or mCherry fluorescent markers, in Nicotiana tabacum and Capsicum annuum plants. The number of primary infection foci increased linearly with dose, and was similar to a Poisson distribution. At high doses, primary infection foci containing both genotypes were found at a low frequency (<2%). The probability that a genotype that infected the inoculated leaf would systemically infect that plant was near 1, although in a few rare cases genotypes could be trapped in the inoculated leaf by being physically surrounded by the other genotype. The frequency of mixed-genotype infection could be predicted from the mean number of primary infection foci using the independent-action model. Independent action appears to hold for TEV, and N(e) is therefore dose-dependent for this plant RNA virus. The mean number of virions causing systemic infection can be very small, and approaches 1 at low doses. Dose-dependency in TEV suggests that comparison of N(e) estimates for different viruses are not very meaningful unless dose effects are taken into consideration.</abstract><cop>United States</cop><pub>Public Library of Science</pub><pmid>21750676</pmid><doi>10.1371/journal.ppat.1002122</doi><oa>free_for_read</oa></addata></record> |
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subjects | Biology Capsicum - virology Competition Estimates Evolution Experiments Flowers & plants Genetic aspects Genotype Genotype & phenotype Health aspects Host-Pathogen Interactions - physiology Hypotheses Infections Leaves Nicotiana - virology Plant Diseases - virology Plant viruses Plant Viruses - physiology Population Population Density Population genetics Potyvirus - genetics Potyvirus - growth & development Potyvirus - pathogenicity RNA, Viral - metabolism Studies Viral Load - physiology Virus diseases of plants Virus Replication Viruses |
title | One is enough: in vivo effective population size is dose-dependent for a plant RNA virus |
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