ELIMINATION OF APPLE STEM PITTING VIRUS FROM PEAR CULTIVARS BY IN VITRO CHEMOTHERAPY

2011 ◽  
pp. 111-115 ◽  
Author(s):  
J. Sedlak ◽  
F. Paprstein ◽  
L. Talacko
2013 ◽  
Vol 40 (No. 4.) ◽  
pp. 186-190 ◽  
Author(s):  
F. Parštein ◽  
J. Sedlák ◽  
L. Svobodová ◽  
J. Polák ◽  
S. Gadiou

The effect of the chemotherapy with ribavirin on the elimination of the pome fruit viruses from in vitro grown plants of infected apple cv. Fragnance has been investigated. The results of ELISA and RT-PCR testing proved the presence of mixed infection of Apple stem pitting virus (ASPV), Apple chlorotic leaf spot virus (ACLSV) and Apple stem grooving virus (ASGV) in the initial field-grown tree of this apple cultivar. Obtained actively growing in vitro shoots with well-developed leaves and shoot tips were subsequently used for chemotherapy with ribavirin. Attempts to fully eliminate viruses by ribavirin in lower concentration 20 mg/l were not successful. However in vitro plants of one mericlone (FR1R20) sanitated from ASPV and ASGV, which were infected with ACLSV only after the first chemotherapy cycle, were subjected to repeated treatment on medium with higher ribavirin concentration 100 mg/l. The success of chemotherapy with ribavirin at 100 mg/l was 76% for ACLSV elimination after the second round. In the course of both chemotherapy cycles (20 mg/l and 100 mg/l), in vitro plants did not display symptoms of phytotoxicity.


2001 ◽  
Vol 91 (11) ◽  
pp. 1085-1091 ◽  
Author(s):  
M. M. Klerks ◽  
G. Leone ◽  
J. L. Lindner ◽  
C. D. Schoen ◽  
J. F. J. M. van den Heuvel

Currently, detection of Apple stem pitting virus (ASPV; genus Foveavirus) in apple trees for certification purposes occurs by woody indexing. This method requires a minimum of 12 to 24 weeks in greenhouse testing to up to 2 years in field testing. In this paper, the development of a single tube AmpliDet RNA system for the rapid gel-free detection of ASPV in apple tree tissues is described. The system relies on the specific amplification of the viral RNA by nucleic acid sequence-based amplification and the simultaneous fluorescent detection of the amplification product through molecular beacons. A sensitivity of a minimum of 100 molecules of transcript RNA was obtained by the ASPV-specific AmpliDet RNA. All biologically characterized ASPV isolates from a field trial and 12 of 14 isolates from a plant virus collection were readily detected with this AmpliDet RNA system. In addition, the efficiency of this method for detecting ASPV in ‘Golden Delicious’ and ‘Gravenstein’ apple trees was compared throughout the year with mechanical inoculation onto Nicotiana occidentalis 37B, a candidate indicator for ASPV. This revealed that only AmpliDet RNA consistently detected the virus in bark tissue, irrespective of the season. Season-specific tissues such as buds, petals, and fruits, but not leaves, also were reliable sources for detection of ASPV by the AmpliDet RNA system.


2018 ◽  
Vol 46 (5) ◽  
pp. 705-713 ◽  
Author(s):  
Sajad Un Nabi ◽  
Javid Iqbal Mir ◽  
Om Chand Sharma ◽  
Desh Beer Singh ◽  
Shafia Zaffer ◽  
...  

2012 ◽  
Vol 38 (No. 1) ◽  
pp. 13-17 ◽  
Author(s):  
J.K. Kundu

The reverse transcription polymerace chain reaction (RT-PCR) assay was successfully used for the detection of Apple stem pitting virus (ASPV) and Apple stem grooving virus (ASGV) in four apple cultivars of a 25 years old orchard. These two main pome fruit viruses were detected frequently in all tested apple cultivars. ASGV and ASPV occurred in as many as 16 trees (in the cultivar Spartan) and 13 trees (in the cultivar Idared) out of 20 tested trees, respectively. Mixed infection by ASGV and ASPV was found in all tested cultivars (as many as 9 out of 20 tested trees of the cultivar Spartan).


2011 ◽  
Vol 158 (1-2) ◽  
pp. 263-267 ◽  
Author(s):  
Beata Komorowska ◽  
Paweł Siedlecki ◽  
Szymon Kaczanowski ◽  
Beata Hasiów-Jaroszewska ◽  
Tadeusz Malinowski

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