Plant Virus Epidemiology and Control

A special issue of Viruses (ISSN 1999-4915). This special issue belongs to the section "Viruses of Plants, Fungi and Protozoa".

Deadline for manuscript submissions: closed (31 December 2019) | Viewed by 16982

Special Issue Editors


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Guest Editor
Department of Plant Pathology, Division of Agriculture, University of Arkansas System, Little Rock, AR, USA
Interests: plant virus epidemiology; virus-vector interactions

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Guest Editor
USDA-ARS, Horticultural Crops Research Unit, Corvallis, OR, USA
Interests: characterize viruses of small fruit crops, viruses diagnostics, viruses epidemiology, develop resistance to viruses of small fruit crops

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Guest Editor
Department of Plant Virology, Institute of Plant Molecular Biology, Biology Centre of the Czech Academy of Sciences, v.v.i., 370 05 České Budějovice, Czech Republic
Interests: plant virus; virus vector interactions; viral quasi-species; plant viromes
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Special Issue Information

Dear Colleagues,

The single most important step in managing plant diseases is through the use of clean stock and seed programs. Once established, the knowledge of pathogen epidemiology is used in the development of control strategies to keep plantings healthy for as long as possible.  This is particularly important for plant viruses, where exclusion is often the only available option, and thus disease forecasting and management are matters of utmost importance. In this Issue, we aim to highlight the importance of virus epidemiology and how information is used in developing and implementing control strategies. This includes virus traditional and molecular ecology tools (distribution, host range, transmission, population structures, and virus–vector–host interactions) and control strategies from RNA interference; to CRISPR; to holistic, systems-based approaches that aim to avoid or control epidemics.

Prof. Dr. Ioannis E. Tzanetakis
Dr. Robert R. Martin
Dr. Igor Koloniuk
Guest Editors

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Keywords

  • ecology
  • epidemiology
  • control

Published Papers (5 papers)

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Editorial

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2 pages, 166 KiB  
Editorial
Special Issue “Plant Virus Epidemiology and Control”
by Ioannis E. Tzanetakis, Robert Martin and Igor Koloniuk
Viruses 2020, 12(3), 309; https://doi.org/10.3390/v12030309 - 12 Mar 2020
Viewed by 1775
Abstract
We recently completed the Special Issue on ‘Plant Virus Epidemiology and Control’ [...] Full article
(This article belongs to the Special Issue Plant Virus Epidemiology and Control)

Research

Jump to: Editorial

20 pages, 297 KiB  
Article
Updating the Quarantine Status of Prunus Infecting Viruses in Australia
by Wycliff M. Kinoti, Narelle Nancarrow, Alison Dann, Brendan C. Rodoni and Fiona E. Constable
Viruses 2020, 12(2), 246; https://doi.org/10.3390/v12020246 - 23 Feb 2020
Cited by 19 | Viewed by 3749
Abstract
One hundred Prunus trees, including almond (P. dulcis), apricot (P. armeniaca), nectarine (P. persica var. nucipersica), peach (P. persica), plum (P. domestica), purple leaf plum (P. cerasifera) and sweet cherry ( [...] Read more.
One hundred Prunus trees, including almond (P. dulcis), apricot (P. armeniaca), nectarine (P. persica var. nucipersica), peach (P. persica), plum (P. domestica), purple leaf plum (P. cerasifera) and sweet cherry (P. avium), were selected from growing regions Australia-wide and tested for the presence of 34 viruses and three viroids using species-specific reverse transcription-polymerase chain reaction (RT-PCR) or polymerase chain reaction (PCR) tests. In addition, the samples were tested using some virus family or genus-based RT-PCR tests. The following viruses were detected: Apple chlorotic leaf spot virus (ACLSV) (13/100), Apple mosaic virus (ApMV) (1/100), Cherry green ring mottle virus (CGRMV) (4/100), Cherry necrotic rusty mottle virus (CNRMV) (2/100), Cherry virus A (CVA) (14/100), Little cherry virus 2 (LChV2) (3/100), Plum bark necrosis stem pitting associated virus (PBNSPaV) (4/100), Prune dwarf virus (PDV) (3/100), Prunus necrotic ringspot virus (PNRSV) (52/100), Hop stunt viroid (HSVd) (9/100) and Peach latent mosaic viroid (PLMVd) (6/100). The results showed that PNRSV is widespread in Prunus trees in Australia. Metagenomic high-throughput sequencing (HTS) and bioinformatics analysis were used to characterise the genomes of some viruses that were detected by RT-PCR tests and Apricot latent virus (ApLV), Apricot vein clearing associated virus (AVCaV), Asian Prunus Virus 2 (APV2) and Nectarine stem pitting-associated virus (NSPaV) were also detected. This is the first report of ApLV, APV2, CGRMV, CNRNV, LChV1, LChV2, NSPaV and PBNSPaV occurring in Australia. It is also the first report of ASGV infecting Prunus species in Australia, although it is known to infect other plant species including pome fruit and citrus. Full article
(This article belongs to the Special Issue Plant Virus Epidemiology and Control)
7 pages, 683 KiB  
Communication
Prevalences of Pospiviroid Contamination in Large Seed Lots of Tomato and Capsicum, and Related Seed Testing Considerations
by David Dall, Lindsay Penrose, Andrew Daly, Fiona Constable and Mark Gibbs
Viruses 2019, 11(11), 1034; https://doi.org/10.3390/v11111034 - 6 Nov 2019
Cited by 8 | Viewed by 2481
Abstract
Analyses of pospiviroids in commercial seed lots of tomato and capsicum, determined by testing of 12,000 to 40,000 seeds per lot, have enabled the development of empirically-derived distribution curves for the observed prevalences of viroids in those commodities. Those distribution curves can be [...] Read more.
Analyses of pospiviroids in commercial seed lots of tomato and capsicum, determined by testing of 12,000 to 40,000 seeds per lot, have enabled the development of empirically-derived distribution curves for the observed prevalences of viroids in those commodities. Those distribution curves can be considered in conjunction with statistically-based estimates of detection that would be achieved using other sample sizes. Statistical calculations using binomial distributions show that sample sizes of 3000 and 9400 seeds allow detection of viroid prevalences as low as 0.1% and 0.032%, respectively, with 95% confidence. Applying those calculations to observed viroid prevalences in contaminated tomato seed lots, it is estimated that the use of sample sizes of 3000 and 9400 seeds would detect 15% and 42%, respectively, of the contaminated seed lots identified using the larger sample sizes of approximately 20,000 seeds reported in this study. It is concluded that the higher costs associated with testing of larger sample sizes represent a worthwhile investment in agricultural biosecurity. Full article
(This article belongs to the Special Issue Plant Virus Epidemiology and Control)
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14 pages, 2592 KiB  
Article
An Avirulent Strain of Soybean Mosaic Virus Reverses the Defensive Effect of Abscisic Acid in a Susceptible Soybean Cultivar
by Mazen Alazem, Kristin Widyasari and Kook-Hyung Kim
Viruses 2019, 11(9), 879; https://doi.org/10.3390/v11090879 - 19 Sep 2019
Cited by 8 | Viewed by 3824
Abstract
In soybean cultivar L29, the Rsv3 gene is responsible for extreme resistance (ER) against the soybean mosaic virus avirulent strain G5H, but is ineffective against the virulent strain G7H. Part of this ER is attributed to the rapid increase in abscisic acid (ABA) [...] Read more.
In soybean cultivar L29, the Rsv3 gene is responsible for extreme resistance (ER) against the soybean mosaic virus avirulent strain G5H, but is ineffective against the virulent strain G7H. Part of this ER is attributed to the rapid increase in abscisic acid (ABA) and callose, and to the rapid induction of several genes in the RNA-silencing pathway. Whether these two defense mechanisms are correlated or separated in the ER is unknown. Here, we found that ABA treatment of L29 plants increased the expression of several antiviral RNA-silencing genes as well as the PP2C3a gene, which was previously shown to increase callose accumulation; as a consequence, ABA increased the resistance of L29 plants to G7H. The effect of ABA treatment on these genes was weaker in the rsv3-null cultivar (Somyungkong) than in L29. Besides, G5H-infection of Somyungkong plants subverted the effect of ABA leading to reduced callose accumulation and decreased expression of several RNA-silencing genes, which resulted in increased susceptibility to G5H infection. ABA treatment, however, still induced some resistance to G7H in Somyungkong, but only AGO7b was significantly induced. Our data suggest that Rsv3 modulates the effect of ABA on these two resistance mechanisms, i.e., callose accumulation and the antiviral RNA-silencing pathway, and that in the absence of Rsv3, some strains can reverse the effect of ABA and thereby facilitate their replication and spread. Full article
(This article belongs to the Special Issue Plant Virus Epidemiology and Control)
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11 pages, 1848 KiB  
Communication
High-Throughput Sequencing Assists Studies in Genomic Variability and Epidemiology of Little Cherry Virus 1 and 2 infecting Prunus spp. in Belgium
by Rachid Tahzima, Yoika Foucart, Gertie Peusens, Tim Beliën, Sébastien Massart and Kris De Jonghe
Viruses 2019, 11(7), 592; https://doi.org/10.3390/v11070592 - 29 Jun 2019
Cited by 17 | Viewed by 4349
Abstract
Little cherry disease, caused by little cherry virus 1 (LChV-1) and little cherry virus 2 (LChV-2), which are both members of the family Closteroviridae, severely affects sweet (Prunus avium L.) and sour cherry (P. cerasus L.) orchards lifelong production worldwide. [...] Read more.
Little cherry disease, caused by little cherry virus 1 (LChV-1) and little cherry virus 2 (LChV-2), which are both members of the family Closteroviridae, severely affects sweet (Prunus avium L.) and sour cherry (P. cerasus L.) orchards lifelong production worldwide. An intensive survey was conducted across different geographic regions of Belgium to study the disease presence on these perennial woody plants and related species. Symptomatic as well as non-symptomatic Prunus spp. trees tested positive via RT-PCR for LChV-1 and -2 in single or mixed infections, with a slightly higher incidence for LChV-1. Both viruses were widespread and highly prevalent in nearly all Prunus production areas as well as in private gardens and urban lane trees. The genetic diversity of Belgian LChV-1 and -2 isolates was assessed by Sanger sequencing of partial genomic regions. A total RNA High-Throughput Sequencing (HTS) approach confirmed the presence of both viruses, and revealed the occurrence of other Prunus-associated viruses, namely cherry virus A (CVA), prune dwarf virus (PDV) and prunus virus F (PrVF). The phylogenetic inference from full-length genomes revealed well-defined evolutionary phylogroups with high genetic variability and diversity for LChV-1 and LChV-2 Belgian isolates, yet with little or no correlation with planting area or cultivated varieties. The global diversity and the prevalence in horticultural areas of LChV-1 and -2 variants, in association with other recently described fruit tree viruses, are of particular concern. Future epidemiological implications as well as new investigation avenues are exhaustively discussed. Full article
(This article belongs to the Special Issue Plant Virus Epidemiology and Control)
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