Biological and molecular characterization of Prunus necrotic ringspot virus isolates from sweet and sour cherry

Biological and molecular properties of six Prunus necrotic ringspot virus (PNRSV) isolates originating from sweet and sour cherry trees were studied. Double-antibody sandwich enzyme-linked immunosorbent assay (DAS-ELISA) showed PNRSV infection in leaf samples from the respective source trees. While...

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Main Authors: Ivanka Kamenova, Aneliya Borisova
Format: Article
Language:English
Published: Taylor & Francis Group 2021-01-01
Series:Biotechnology & Biotechnological Equipment
Subjects:
Online Access:http://dx.doi.org/10.1080/13102818.2021.1901608
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spelling doaj-8888b381a201465bad8230706454df1b2021-04-21T16:14:21ZengTaylor & Francis GroupBiotechnology & Biotechnological Equipment1310-28181314-35302021-01-0135156757510.1080/13102818.2021.19016081901608Biological and molecular characterization of Prunus necrotic ringspot virus isolates from sweet and sour cherryIvanka Kamenova0Aneliya Borisova1Biotic Stress Group, Agricultural Academy, AgroBioinstituteDepartment of Agrotechnology, Plant Protection and Economics on Crops, Agricultural Academy, Institute of AgricultureBiological and molecular properties of six Prunus necrotic ringspot virus (PNRSV) isolates originating from sweet and sour cherry trees were studied. Double-antibody sandwich enzyme-linked immunosorbent assay (DAS-ELISA) showed PNRSV infection in leaf samples from the respective source trees. While one of the infected source trees was symptomless, the other five showed symptoms, ranging from chlorotic to necrotic spots on the leaves. The reaction of greenhouse-grown seedlings of 22 herbaceous test plant species was investigated. The woody indicators Prunus serrulata cv. Kwanzan, wild cherry Prunus avium, P. cerasus, P. cerasifera and P. tomentosa were chip-budded. Chenopodium quinoa, Cucumis sativus cv. Amelia, C. sativus cv. Levina and P. tomentosa appeared as the most suitable test plants for the bioassay of the studied PNRSV isolates. The nucleotide sequences corresponding to the full-length coat (CP) and movement (MP) proteins were obtained. The nucleotide sequence identity among the studied isolates both in CP and MP genes was from 94% to 100%. The CP and MP amino acid sequence identities were from 95% to 100% and from 94% to 100%, respectively. Phylogenetic analyses performed with MP and CP nucleotide sequences showed that three isolates belonged to PV32-I and the other three to PV96-II phylogroups. Comparative amino acid analyses of MP and CP genes, together with the symptoms on naturally infected trees showed a higher affiliation of the studied isolates with the mild type than with the rugose types of isolates. The molecular variability correlated with the symptomatology on the naturally infected trees.http://dx.doi.org/10.1080/13102818.2021.1901608pnrsvhost rangecapsid proteinmovement proteinsequencingphylogenetic analyses
collection DOAJ
language English
format Article
sources DOAJ
author Ivanka Kamenova
Aneliya Borisova
spellingShingle Ivanka Kamenova
Aneliya Borisova
Biological and molecular characterization of Prunus necrotic ringspot virus isolates from sweet and sour cherry
Biotechnology & Biotechnological Equipment
pnrsv
host range
capsid protein
movement protein
sequencing
phylogenetic analyses
author_facet Ivanka Kamenova
Aneliya Borisova
author_sort Ivanka Kamenova
title Biological and molecular characterization of Prunus necrotic ringspot virus isolates from sweet and sour cherry
title_short Biological and molecular characterization of Prunus necrotic ringspot virus isolates from sweet and sour cherry
title_full Biological and molecular characterization of Prunus necrotic ringspot virus isolates from sweet and sour cherry
title_fullStr Biological and molecular characterization of Prunus necrotic ringspot virus isolates from sweet and sour cherry
title_full_unstemmed Biological and molecular characterization of Prunus necrotic ringspot virus isolates from sweet and sour cherry
title_sort biological and molecular characterization of prunus necrotic ringspot virus isolates from sweet and sour cherry
publisher Taylor & Francis Group
series Biotechnology & Biotechnological Equipment
issn 1310-2818
1314-3530
publishDate 2021-01-01
description Biological and molecular properties of six Prunus necrotic ringspot virus (PNRSV) isolates originating from sweet and sour cherry trees were studied. Double-antibody sandwich enzyme-linked immunosorbent assay (DAS-ELISA) showed PNRSV infection in leaf samples from the respective source trees. While one of the infected source trees was symptomless, the other five showed symptoms, ranging from chlorotic to necrotic spots on the leaves. The reaction of greenhouse-grown seedlings of 22 herbaceous test plant species was investigated. The woody indicators Prunus serrulata cv. Kwanzan, wild cherry Prunus avium, P. cerasus, P. cerasifera and P. tomentosa were chip-budded. Chenopodium quinoa, Cucumis sativus cv. Amelia, C. sativus cv. Levina and P. tomentosa appeared as the most suitable test plants for the bioassay of the studied PNRSV isolates. The nucleotide sequences corresponding to the full-length coat (CP) and movement (MP) proteins were obtained. The nucleotide sequence identity among the studied isolates both in CP and MP genes was from 94% to 100%. The CP and MP amino acid sequence identities were from 95% to 100% and from 94% to 100%, respectively. Phylogenetic analyses performed with MP and CP nucleotide sequences showed that three isolates belonged to PV32-I and the other three to PV96-II phylogroups. Comparative amino acid analyses of MP and CP genes, together with the symptoms on naturally infected trees showed a higher affiliation of the studied isolates with the mild type than with the rugose types of isolates. The molecular variability correlated with the symptomatology on the naturally infected trees.
topic pnrsv
host range
capsid protein
movement protein
sequencing
phylogenetic analyses
url http://dx.doi.org/10.1080/13102818.2021.1901608
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