Detection of potato spindle tuber viroid by nucleic acid spot hybridization: Evaluation with tuber sprouts and true potato seed

1983 ◽  
Vol 60 (8) ◽  
pp. 587-597 ◽  
Author(s):  
L. F. Salazar ◽  
Robert A. Owens ◽  
D. R. Smith ◽  
T. O. Diener
1986 ◽  
Vol 64 (2) ◽  
pp. 336-340 ◽  
Author(s):  
M. E. Grasmick ◽  
S. A. Slack

The effect of potato spindle tuber viroid infection on pollen viability, fruit-set, botanical seed set, seed weight, and seed germination in potatoes was determined. Pollen collected from the infected cultivar 'Monona' was less viable than pollen collected from healthy plants. Pollen collected from infected plants reduced seed set significantly but did not reduce fruit development or seed set in all cultivars tested. For some cultivars, infected maternal plants increased the frequency of fruit development and seed weight compared with healthy controls. True potato seed from viroid-infected 'Katahdin' × 'Superior' crosses germinated at a higher rate than did seed from comparable uninfected parents. Progeny from viroid-infected parents that exhibited potato spindle tuber viroidlike symptoms did not always test positive for potato spindle tuber viroid by bioassay or polyacrylamide gel electrophoresis tests. Efficiency of potato spindle tuber viroid detection by bioassay was highest for seedlings 2 weeks after imbibition. Potato spindle tuber viroid was detected in 100% of the progeny tested after true potato seed was stored at 4 °C for 12 years. Tests on selfed true potato seed from the viroid-infected cultivar 'Monona' demonstrated a transmission rate of 100% after subinoculation of initial bioassay plants.


2009 ◽  
Vol 64 (9-10) ◽  
pp. 711-716 ◽  
Author(s):  
Kuraba Gopal ◽  
Sundeep Sudarsan ◽  
Venati Gopi ◽  
Latchireddy Naram Naidu ◽  
Maniyaram Ramaiah ◽  
...  

Polymerase chain reaction (PCR) amplification with primers specific to the rDNA region successfully amplified the 1160-bp DNA fragment from a Huanglongbing (HLB)-infected sweet orange sample with mottling symptoms leaves, but not from healthy sweet orange plants. The PCR product of 1160-bp was used as probe labeled with biotin for detection of the HLB pathogen in the nucleic acid spot hybridization (NASH) test. It was found that the HLB pathogen could be detected up to 1:100 dilution in HLB-infected tissue. Total DNA extracted from HLB-infected tissue was diluted 2-fold as 900 ng in TE buffer and spotted on a nitrocellulose membrane. Strong signals were observed up to 225 ng of DNA dilution, whereas a moderate signal was recorded at 112 ng. No hybridization signal was observed in the healthy samples, while strong signals were observed in the positive control


1985 ◽  
Vol 12 (1-2) ◽  
pp. 169-177 ◽  
Author(s):  
Thedi Ziegler ◽  
Veijo Hukkanen ◽  
Pertti Arstila ◽  
Petri Auvinen ◽  
Annika Jalava ◽  
...  

1985 ◽  
Vol 16 (3) ◽  
pp. 213-218 ◽  
Author(s):  
Per Stålhandske ◽  
Timo Hyypiä ◽  
Annika Allard ◽  
Pekka Halonen ◽  
Ulf Pettersson

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