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Experimental Infection of Different Tomato Genotypes with Tomato mosaic virus Led to a Low Viral Population Heterogeneity in the Capsid Protein Encoding Region

The complete genome sequence of a Slovak SL-1 isolate of Tomato mosaic virus (ToMV) was determined from the next generation sequencing (NGS) data, further confirming a limited sequence divergence in this tobamovirus species. Tomato genotypes Monalbo, Mobaci and Moperou, respectively carrying the sus...

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Autores principales: Sihelská, Nina, Vozárová, Zuzana, Predajňa, Lukáš, Šoltys, Katarína, Hudcovicová, Martina, Mihálik, Daniel, Kraic, Ján, Mrkvová, Michaela, Kúdela, Otakar, Glasa, Miroslav
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Korean Society of Plant Pathology 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5624493/
https://www.ncbi.nlm.nih.gov/pubmed/29018314
http://dx.doi.org/10.5423/PPJ.NT.04.2017.0082
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author Sihelská, Nina
Vozárová, Zuzana
Predajňa, Lukáš
Šoltys, Katarína
Hudcovicová, Martina
Mihálik, Daniel
Kraic, Ján
Mrkvová, Michaela
Kúdela, Otakar
Glasa, Miroslav
author_facet Sihelská, Nina
Vozárová, Zuzana
Predajňa, Lukáš
Šoltys, Katarína
Hudcovicová, Martina
Mihálik, Daniel
Kraic, Ján
Mrkvová, Michaela
Kúdela, Otakar
Glasa, Miroslav
author_sort Sihelská, Nina
collection PubMed
description The complete genome sequence of a Slovak SL-1 isolate of Tomato mosaic virus (ToMV) was determined from the next generation sequencing (NGS) data, further confirming a limited sequence divergence in this tobamovirus species. Tomato genotypes Monalbo, Mobaci and Moperou, respectively carrying the susceptible tm-2 allele or the Tm-1 and Tm-2 resistant alleles, were tested for their susceptibility to ToMV SL-1. Although the three tomato genotypes accumulated ToMV SL-1 to similar amounts as judged by semi-quantitative DAS-ELISA, they showed variations in the rate of infection and symptomatology. Possible differences in the intra-isolate variability and polymorphism between viral populations propagating in these tomato genotypes were evaluated by analysis of the capsid protein (CP) encoding region. Irrespective of genotype infected, the intra-isolate haplotype structure showed the presence of the same highly dominant CP sequence and the low level of population diversity (0.08–0.19%). Our results suggest that ToMV CP encoding sequence is relatively stable in the viral population during its replication in vivo and provides further demonstration that RNA viruses may show high sequence stability, probably as a result of purifying selection.
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spelling pubmed-56244932017-10-10 Experimental Infection of Different Tomato Genotypes with Tomato mosaic virus Led to a Low Viral Population Heterogeneity in the Capsid Protein Encoding Region Sihelská, Nina Vozárová, Zuzana Predajňa, Lukáš Šoltys, Katarína Hudcovicová, Martina Mihálik, Daniel Kraic, Ján Mrkvová, Michaela Kúdela, Otakar Glasa, Miroslav Plant Pathol J Note The complete genome sequence of a Slovak SL-1 isolate of Tomato mosaic virus (ToMV) was determined from the next generation sequencing (NGS) data, further confirming a limited sequence divergence in this tobamovirus species. Tomato genotypes Monalbo, Mobaci and Moperou, respectively carrying the susceptible tm-2 allele or the Tm-1 and Tm-2 resistant alleles, were tested for their susceptibility to ToMV SL-1. Although the three tomato genotypes accumulated ToMV SL-1 to similar amounts as judged by semi-quantitative DAS-ELISA, they showed variations in the rate of infection and symptomatology. Possible differences in the intra-isolate variability and polymorphism between viral populations propagating in these tomato genotypes were evaluated by analysis of the capsid protein (CP) encoding region. Irrespective of genotype infected, the intra-isolate haplotype structure showed the presence of the same highly dominant CP sequence and the low level of population diversity (0.08–0.19%). Our results suggest that ToMV CP encoding sequence is relatively stable in the viral population during its replication in vivo and provides further demonstration that RNA viruses may show high sequence stability, probably as a result of purifying selection. Korean Society of Plant Pathology 2017-10 2017-10-01 /pmc/articles/PMC5624493/ /pubmed/29018314 http://dx.doi.org/10.5423/PPJ.NT.04.2017.0082 Text en © The Korean Society of Plant Pathology This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0) which permits unrestricted noncommercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Note
Sihelská, Nina
Vozárová, Zuzana
Predajňa, Lukáš
Šoltys, Katarína
Hudcovicová, Martina
Mihálik, Daniel
Kraic, Ján
Mrkvová, Michaela
Kúdela, Otakar
Glasa, Miroslav
Experimental Infection of Different Tomato Genotypes with Tomato mosaic virus Led to a Low Viral Population Heterogeneity in the Capsid Protein Encoding Region
title Experimental Infection of Different Tomato Genotypes with Tomato mosaic virus Led to a Low Viral Population Heterogeneity in the Capsid Protein Encoding Region
title_full Experimental Infection of Different Tomato Genotypes with Tomato mosaic virus Led to a Low Viral Population Heterogeneity in the Capsid Protein Encoding Region
title_fullStr Experimental Infection of Different Tomato Genotypes with Tomato mosaic virus Led to a Low Viral Population Heterogeneity in the Capsid Protein Encoding Region
title_full_unstemmed Experimental Infection of Different Tomato Genotypes with Tomato mosaic virus Led to a Low Viral Population Heterogeneity in the Capsid Protein Encoding Region
title_short Experimental Infection of Different Tomato Genotypes with Tomato mosaic virus Led to a Low Viral Population Heterogeneity in the Capsid Protein Encoding Region
title_sort experimental infection of different tomato genotypes with tomato mosaic virus led to a low viral population heterogeneity in the capsid protein encoding region
topic Note
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5624493/
https://www.ncbi.nlm.nih.gov/pubmed/29018314
http://dx.doi.org/10.5423/PPJ.NT.04.2017.0082
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