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K. Gürcan, S. Teber, K. Çağlayan (2018)
Further investigation of a genetically divergent group of plum pox virus-M strain in TurkeyJournal of Plant Pathology, 101
K. Gürcan, S. Teber, Thierry Candresse (2020)
Genetic analysis suggests a long and largely isolated evolutionary history of plum pox virus strain D in TurkeyPlant Pathology
Sudhir Kumar, G. Stecher, K. Tamura (2016)
MEGA7: Molecular Evolutionary Genetics Analysis Version 7.0 for Bigger Datasets.Molecular biology and evolution, 33 7
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Adaptation of plum pox virus to a herbaceous host (Pisum sativum) following serial passages.The Journal of general virology, 88 Pt 10
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Detection and identification of Plum pox virus on Prunus species in CrimeaAgriculture and Forestry, 61
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Simultaneous detection and typing of plum pox potyvirus (PPV) isolates by heminested-PCR and PCR-ELISA.Journal of virological methods, 68 2
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Production and characterization of a monoclonal antibody specific to the M serotype of plum pox potyvirusEuropean Journal of Plant Pathology, 103
J. García, M. Glasa, M. Cambra, T. Candresse (2014)
Plum pox virus and sharka: a model potyvirus and a major disease.Molecular plant pathology, 15 3
S. Matić, M. Al-Rwahnih, A. Myrta (2006)
Diversity of Plum pox virus isolates in Bosnia and HerzegovinaPlant Pathology, 55
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Serological and molecular characterization of isolates of Plum pox virus strain El Amar to better understand its diversity, evolution, and unique geographic distribution
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Analysis of the epitope structure of Plum pox virus coat protein.Phytopathology, 101 5
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A simplified RT-PCR-based detection of recombinant Plum pox virus isolates.Acta virologica, 48 3
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I. Mitrofanova, O. Mitrofanova, N. Lesnikova-Sedoshenko, P. Ivanov, A. Sheveleva, S. Chirkov (2017)
Three highly divergent groups of Plum pox virus strain D isolates coexist in stone-fruit plantings of Nikita Botanical Gardens, Crimea, 1163
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Sharka epidemiology and worldwide management strategies: learning lessons to optimize disease control in perennial plants.Annual review of phytopathology, 53
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Plum pox virus and the estimated costs associated with sharka diseaseEppo Bulletin, 36
Screening methods for detecting a complex of Plum pox virus ( PPV ) strains
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Occurrence and characterization of plum pox virus strain D isolates from European Russia and CrimeaArchives of Virology, 161
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(1992)
A highly sensitive immunocap - ture polymerase chain reaction method for Plum pox virus detection
Molecular analysis of new isolates of the plum pox virus (PPV) found in the gene pool collections of peach, apricot, and plum from the Nikitsky Botanical Garden (National Science Center, Russian Academy of Sciences), as well as on wild cherry plum trees in the surrounding area, has been carried out. Using the enzyme-linked immunosorbent assay and reverse transcription polymerase chain reaction, 19 new PPV isolates have been detected. Most of them belonged to the strain D; single isolates of the strains Rec and M were also found. The 3'-terminal sequences of genome of the new isolates were sequenced, including the coat protein (CP) gene and adjacent sequences of the NIb gene and the 3'-nontranslated region. Phylogenetic analysis of these sequences revealed the distribution of PPV-D isolates into several clusters or clades. An average divergence rate between sequences of Crimean PPV-D isolates was 2.0%. A relatively high level of genetic variation indicates a long-standing introduction of the ancestors of the current PPV-D isolates to Nikitsky Botanical Garden (NBG). Isolate H23, identified in the apricot collection, belonged to strain M. This is the first detection of PPV-M in Crimea. Isolate AL-Ch (strain Rec) was found on wild cherry plum. In the CP of isolate K87 (strain D), the K59T mutation was detected, which prevents its recognition by PPV-D-specific 4DG5 monoclonal antibodies. In CP of AL-Ch and previously characterized isolates K28 and Kisl-1pl (strain Rec), amino acid substitutions were detected at position 68, which did not affect the recognition of these isolates by AL monoclonal antibodies. Apparently, position 68 is outside the PPV-M/Rec-specific epitope. The results of the work show that PPV most likely entered the NBG with contaminated drupaceous fruit material as a result of several independent introductions from different regions of the world and spread over plantations by aphids.
Moscow University Biological Sciences Bulletin – Springer Journals
Published: Apr 15, 2020
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