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Sequence diversity on four ORFs of citrus tristeza virus correlates with pathogenicity

The molecular characterization of isolates of citrus tristeza virus (CTV) from eight locations in Mexico was undertaken by analyzing five regions located at the opposite ends of the virus genome. Two regions have been previously used to study CTV variability (coat protein and p23), while the other t...

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Autores principales: Herrera-Isidrón, Lisset, Ochoa-Sánchez, Juan Carlos, Rivera-Bustamante, Rafael, Martínez-Soriano, Juan Pablo
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2731079/
https://www.ncbi.nlm.nih.gov/pubmed/19642988
http://dx.doi.org/10.1186/1743-422X-6-116
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author Herrera-Isidrón, Lisset
Ochoa-Sánchez, Juan Carlos
Rivera-Bustamante, Rafael
Martínez-Soriano, Juan Pablo
author_facet Herrera-Isidrón, Lisset
Ochoa-Sánchez, Juan Carlos
Rivera-Bustamante, Rafael
Martínez-Soriano, Juan Pablo
author_sort Herrera-Isidrón, Lisset
collection PubMed
description The molecular characterization of isolates of citrus tristeza virus (CTV) from eight locations in Mexico was undertaken by analyzing five regions located at the opposite ends of the virus genome. Two regions have been previously used to study CTV variability (coat protein and p23), while the other three correspond to other genomic segments (p349-B, p349-C and p13). Our comparative nucleotide analyses included CTV sequences from different geographical origins already deposited in the GenBank databases. The largest nucleotide differences were located in two fragments located at the 5' end of the genome (p349-B and p349-C). Phylogenetic analyses on those five regions showed that the degree of nucleotide divergence among strains tended to correlate with their pathogenicity. Two main groups were defined: mild, with almost no noticeable effects on the indicator plants and severe, with drastic symptoms. Mild isolates clustered together in every analyzed ORF sharing a genetic distance below 0.022, in contrast with the severe isolates, which showed a more disperse distribution and a genetic distance of 0.276. Analyses of the p349-B and p349-C regions evidenced two lineages within the severe group: severe common subgroup (most of severe isolates) and severe divergent subgroup (T36-like isolates). This study represents the first attempt to analyze the genetic variability of CTV in Mexico by constructing phylogenetic trees based on new genomic regions that use group-specific nucleotide and amino acid sequences. These results may be useful to implement specific assays for strain discrimination. Moreover, it would be an excellent reference for the CTV situation in México to face the recent arrival of brown citrus aphid.
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spelling pubmed-27310792009-08-24 Sequence diversity on four ORFs of citrus tristeza virus correlates with pathogenicity Herrera-Isidrón, Lisset Ochoa-Sánchez, Juan Carlos Rivera-Bustamante, Rafael Martínez-Soriano, Juan Pablo Virol J Research The molecular characterization of isolates of citrus tristeza virus (CTV) from eight locations in Mexico was undertaken by analyzing five regions located at the opposite ends of the virus genome. Two regions have been previously used to study CTV variability (coat protein and p23), while the other three correspond to other genomic segments (p349-B, p349-C and p13). Our comparative nucleotide analyses included CTV sequences from different geographical origins already deposited in the GenBank databases. The largest nucleotide differences were located in two fragments located at the 5' end of the genome (p349-B and p349-C). Phylogenetic analyses on those five regions showed that the degree of nucleotide divergence among strains tended to correlate with their pathogenicity. Two main groups were defined: mild, with almost no noticeable effects on the indicator plants and severe, with drastic symptoms. Mild isolates clustered together in every analyzed ORF sharing a genetic distance below 0.022, in contrast with the severe isolates, which showed a more disperse distribution and a genetic distance of 0.276. Analyses of the p349-B and p349-C regions evidenced two lineages within the severe group: severe common subgroup (most of severe isolates) and severe divergent subgroup (T36-like isolates). This study represents the first attempt to analyze the genetic variability of CTV in Mexico by constructing phylogenetic trees based on new genomic regions that use group-specific nucleotide and amino acid sequences. These results may be useful to implement specific assays for strain discrimination. Moreover, it would be an excellent reference for the CTV situation in México to face the recent arrival of brown citrus aphid. BioMed Central 2009-07-30 /pmc/articles/PMC2731079/ /pubmed/19642988 http://dx.doi.org/10.1186/1743-422X-6-116 Text en Copyright © 2009 Herrera-Isidrón et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Herrera-Isidrón, Lisset
Ochoa-Sánchez, Juan Carlos
Rivera-Bustamante, Rafael
Martínez-Soriano, Juan Pablo
Sequence diversity on four ORFs of citrus tristeza virus correlates with pathogenicity
title Sequence diversity on four ORFs of citrus tristeza virus correlates with pathogenicity
title_full Sequence diversity on four ORFs of citrus tristeza virus correlates with pathogenicity
title_fullStr Sequence diversity on four ORFs of citrus tristeza virus correlates with pathogenicity
title_full_unstemmed Sequence diversity on four ORFs of citrus tristeza virus correlates with pathogenicity
title_short Sequence diversity on four ORFs of citrus tristeza virus correlates with pathogenicity
title_sort sequence diversity on four orfs of citrus tristeza virus correlates with pathogenicity
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2731079/
https://www.ncbi.nlm.nih.gov/pubmed/19642988
http://dx.doi.org/10.1186/1743-422X-6-116
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