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Characterization of Two Aggressive PepMV Isolates Useful in Breeding Programs

Pepino mosaic virus (PepMV) causes significant economic losses in tomato crops worldwide. Since its first detection infecting tomato in 1999, aggressive PepMV variants have emerged. This study aimed to characterize two aggressive PepMV isolates, PepMV-H30 and PepMV-KLP2. Both isolates were identifie...

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Autores principales: Alcaide, Cristina, Méndez-López, Eduardo, Úbeda, Jesús R., Gómez, Pedro, Aranda, Miguel A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10674935/
https://www.ncbi.nlm.nih.gov/pubmed/38005907
http://dx.doi.org/10.3390/v15112230
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author Alcaide, Cristina
Méndez-López, Eduardo
Úbeda, Jesús R.
Gómez, Pedro
Aranda, Miguel A.
author_facet Alcaide, Cristina
Méndez-López, Eduardo
Úbeda, Jesús R.
Gómez, Pedro
Aranda, Miguel A.
author_sort Alcaide, Cristina
collection PubMed
description Pepino mosaic virus (PepMV) causes significant economic losses in tomato crops worldwide. Since its first detection infecting tomato in 1999, aggressive PepMV variants have emerged. This study aimed to characterize two aggressive PepMV isolates, PepMV-H30 and PepMV-KLP2. Both isolates were identified in South-Eastern Spain infecting tomato plants, which showed severe symptoms, including bright yellow mosaics. Full-length infectious clones were generated, and phylogenetic relationships were inferred using their nucleotide sequences and another 35 full-length sequences from isolates representing the five known PepMV strains. Our analysis revealed that PepMV-H30 and PepMV-KLP2 belong to the EU and CH2 strains, respectively. Amino acid sequence comparisons between these and mild isolates identified 8 and 15 amino acid substitutions for PepMV-H30 and PepMV-KLP2, respectively, potentially involved in severe symptom induction. None of the substitutions identified in PepMV-H30 have previously been described as symptom determinants. The E236K substitution, originally present in the PepMV-H30 CP, was introduced into a mild PepMV-EU isolate, resulting in a virus that causes symptoms similar to those induced by the parental PepMV-H30 in Nicotiana benthamiana plants. In silico analyses revealed that this residue is located at the C-terminus of the CP and is solvent-accessible, suggesting its potential involvement in CP–host protein interactions. We also examined the subcellular localization of PepGFPm2(E236K) in comparison to that of PepGFPm2, focusing on chloroplast affection, but no differences were observed in the GFP subcellular distribution between the two viruses in epidermal cells of N. benthamiana plants. Due to the easily visible symptoms that PepMV-H30 and PepMV-KLP2 induce, these isolates represent valuable tools in programs designed to breed resistance to PepMV in tomato.
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spelling pubmed-106749352023-11-08 Characterization of Two Aggressive PepMV Isolates Useful in Breeding Programs Alcaide, Cristina Méndez-López, Eduardo Úbeda, Jesús R. Gómez, Pedro Aranda, Miguel A. Viruses Article Pepino mosaic virus (PepMV) causes significant economic losses in tomato crops worldwide. Since its first detection infecting tomato in 1999, aggressive PepMV variants have emerged. This study aimed to characterize two aggressive PepMV isolates, PepMV-H30 and PepMV-KLP2. Both isolates were identified in South-Eastern Spain infecting tomato plants, which showed severe symptoms, including bright yellow mosaics. Full-length infectious clones were generated, and phylogenetic relationships were inferred using their nucleotide sequences and another 35 full-length sequences from isolates representing the five known PepMV strains. Our analysis revealed that PepMV-H30 and PepMV-KLP2 belong to the EU and CH2 strains, respectively. Amino acid sequence comparisons between these and mild isolates identified 8 and 15 amino acid substitutions for PepMV-H30 and PepMV-KLP2, respectively, potentially involved in severe symptom induction. None of the substitutions identified in PepMV-H30 have previously been described as symptom determinants. The E236K substitution, originally present in the PepMV-H30 CP, was introduced into a mild PepMV-EU isolate, resulting in a virus that causes symptoms similar to those induced by the parental PepMV-H30 in Nicotiana benthamiana plants. In silico analyses revealed that this residue is located at the C-terminus of the CP and is solvent-accessible, suggesting its potential involvement in CP–host protein interactions. We also examined the subcellular localization of PepGFPm2(E236K) in comparison to that of PepGFPm2, focusing on chloroplast affection, but no differences were observed in the GFP subcellular distribution between the two viruses in epidermal cells of N. benthamiana plants. Due to the easily visible symptoms that PepMV-H30 and PepMV-KLP2 induce, these isolates represent valuable tools in programs designed to breed resistance to PepMV in tomato. MDPI 2023-11-08 /pmc/articles/PMC10674935/ /pubmed/38005907 http://dx.doi.org/10.3390/v15112230 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Alcaide, Cristina
Méndez-López, Eduardo
Úbeda, Jesús R.
Gómez, Pedro
Aranda, Miguel A.
Characterization of Two Aggressive PepMV Isolates Useful in Breeding Programs
title Characterization of Two Aggressive PepMV Isolates Useful in Breeding Programs
title_full Characterization of Two Aggressive PepMV Isolates Useful in Breeding Programs
title_fullStr Characterization of Two Aggressive PepMV Isolates Useful in Breeding Programs
title_full_unstemmed Characterization of Two Aggressive PepMV Isolates Useful in Breeding Programs
title_short Characterization of Two Aggressive PepMV Isolates Useful in Breeding Programs
title_sort characterization of two aggressive pepmv isolates useful in breeding programs
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10674935/
https://www.ncbi.nlm.nih.gov/pubmed/38005907
http://dx.doi.org/10.3390/v15112230
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