Abstract:Hydroponic systems and intensive irrigation are used widely in horticulture and thus have the potential for rapid spread of water-transmissible plant pathogens. Numerous plant viruses have been reported to occur in aqueous environments, although information on their survival and transmission is minimal, due mainly to the lack of effective detection methods and to the complexity of the required transmission experiments. We have assessed the role of water as a source of plant infection using three mechanically t… Show more
“…In contrast, transmission following tomato fruit handling was considered unlikely unless the fruit has been squashed to release its sap (46). However, recent findings by Mehle et al (24) suggested that PSTVd transmission via roots through water-mediated movement is of concern in hydroponic and intensive irrigation systems, with PSTVd infectivity surviving in water for up to 7 weeks. However, recent findings by Mehle et al (24) suggested that PSTVd transmission via roots through water-mediated movement is of concern in hydroponic and intensive irrigation systems, with PSTVd infectivity surviving in water for up to 7 weeks.…”
Mackie, A. E., Coutts, B. A., Barbetti, M. J., Rodoni, B. C., McKirdy, S. J., and Jones, R. A. C. 2015. Potato spindle tuber viroid: stability on common surfaces and inactivation with disinfectants. Plant Dis. XX:X-X.
“…In contrast, transmission following tomato fruit handling was considered unlikely unless the fruit has been squashed to release its sap (46). However, recent findings by Mehle et al (24) suggested that PSTVd transmission via roots through water-mediated movement is of concern in hydroponic and intensive irrigation systems, with PSTVd infectivity surviving in water for up to 7 weeks. However, recent findings by Mehle et al (24) suggested that PSTVd transmission via roots through water-mediated movement is of concern in hydroponic and intensive irrigation systems, with PSTVd infectivity surviving in water for up to 7 weeks.…”
Mackie, A. E., Coutts, B. A., Barbetti, M. J., Rodoni, B. C., McKirdy, S. J., and Jones, R. A. C. 2015. Potato spindle tuber viroid: stability on common surfaces and inactivation with disinfectants. Plant Dis. XX:X-X.
“…() (Table ) were used for PSTVd and PepMV detection, respectively, as described by Mehle et al . (). For detection of CLVd, the one‐step RT‐qPCR of Monger et al .…”
Section: Methodsmentioning
confidence: 97%
“…Just one infected plant grown from a single infected tomato seed has the potential to rapidly spread the infection mechanically to neighbouring plants, resulting in a larger outbreak. Recently, it has also been shown that irrigation water can be a path for PepMV and PSTVd transmission between plants (Mehle et al, 2014). Therefore, it is essential to monitor for these pathogens through all of the critical points in tomato production and pathogen transmission pathways.…”
Section: Introductionmentioning
confidence: 99%
“…() was used and performed as described by Mehle et al . (). A cytochrome oxidase ( COX ) gene‐specific real‐time RT‐PCR assay was used as the endogenous control (Weller et al ., ).…”
Waterborne and seedborne Pepino mosaic virus (PepMV) and Potato spindle tuber viroid (PSTVd) pose serious threats to tomato production due to seed transmission and mechanical transmission, coupled with their long-term stability outside the host plant. Therefore, rapid and sensitive diagnostic procedures are needed to prevent the spread of these quarantine pathogens. In particular, water and seed contamination are difficult to detect and confirm without efficient concentration methods. This study presents procedures that improve detection of PSTVd from tomato seeds and leaf tissue, and PepMV from water and tomato leaf tissue. For efficient concentration of PepMV from water samples, a procedure was optimized using convective interaction media monolithic chromatography columns, which provides concentration by three orders of magnitude. For concentration of PSTVd from seed extracts, an easy-to-use and efficient method was developed based on RNA binding to positively charged anion-exchange resin beads that provides up to 100-fold more sensitive detection in comparison with procedures without a concentration step. This thus allows confirmation of RT-qPCR results with sequencing of RT-PCR products in samples with low viroid levels. In addition, reverse-transcription loop-mediated isothermal amplification assays for detection of PSTVd and PepMV were optimized and adapted to both laboratory and on-site testing requirements. This allows rapid detection of these pathogens in crude leaf homogenates, in under 30 min. These procedures of concentration and detection are shown to be efficient and to fill the gaps in diagnostics of PepMV and PSTVd, especially when these pathogens are present at low levels in difficult matrices such as water and seeds.
“…There is evidence that bumble bees (Shipp et al 2008), the soil-borne fungus Olpidium virulentus (AlfaroFernández et al 2009) and whiteflies (Noël et al 2014) can function as vectors for PepMV. Seed transmission is likely to play a role in long distance spread (Córdoba-Sellés et al 2007;Hanssen et al 2010), and water was confirmed to be the source of PepMV infection (Schwarz et al 2010;Mehle et al 2014).…”
Pepino mosaic virus (PepMV) has caused great concern in the greenhouse tomato industry after it was found causing a new disease in tomato in 1999. The objective of this paper is to investigate alternative hosts and compare important biological characteristics of the three PepMV strains occurring in Europe when tested under different environmental conditions. To this end we compared the infectivity and symptom development of three, well characterized isolates belonging to three different PepMV strains, EU-tom, Ch2 and US1, by inoculating them on tomato, possible alternative host plants in the family Solanaceae and selected test plants.The inoculation experiments were done in 10 countries from south to north in Europe. The importance of alternative hosts among the solanaceous crops and the usefulness of test plants in the biological characterization of PepMV isolates are discussed. Our data for the three strains tested at 10 different European locations with both international and local cultivars showed that eggplant is an alternative host of PepMV. Sweet pepper is not an important host of PepMV, but potato can be infected when the right isolate is matched with a specific cultivar. Nicotiana occidentalis 37B is a useful indicator plant for PepMV studies, since it reacts with a different symptomatology to each one of the PepMV strains.
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