P. Dedic et J. Ptacek, IMMUNOENZYMATIC DIAGNOSIS OF POTATO-VIRUS -Y (PVY) IN PROGENY OF PRIMARILY INFECTED POTATO PLANTS, Rostlinna vyroba, 41(4), 1995, pp. 157-161
The effects of the date of the ELISA diagnosis (in autumn and in sprin
g) and its technological procedures (diagnosis of greenhouse-grown pot
atoe plants after break of dormancy of tubers by gibberellic acid and
diagnosis on tuber sprouts after rindite treatment) on reliability of
the detection of PW in the progeny of primarily infected plants from f
ield provocative conditions were assessed. Seven potato cultivars with
different maturity and resistance to PVY were evaluated in four years
with different level of infection pressure. After natural termination
of vegetation period, two to three tubers from each plant were taken.
The both diagnoses were in each date performed on the same tubers. EL
ISA was conducted as described by Clark, Adams (1977) with minor modif
ications (Dedic, 1985). Diagnostic kit purchased from Bioreba (Switzer
land) was used throughout the experiments. Absorbance (A(405)) values
were determined by a Dynatech spectrofotometer (MR 700) and reactions
were rated as positive if they exceeded a threshold value equal to the
mean absorbance of the healthy control plus three times its standard
deviation, and were higher than 0.1 optical unit. In the year with low
infection pressure (1987) only five tubers of all 476 tested cultivar
s were infected, and this very low rate of infection was unsuitable fo
r evaluation. In the years with severe infection pressure (1988, 1989)
, the two diagnostic procedures were compared in the both dates and th
e results are presented in Tabs I and II. In autumn period the overall
accordance attained 83 to 85%, considering individual cultivars it wa
s 70 to 96%. In spring period the overall accordance ranged from 82 to
87%, and the individual cultivars reached 62 to 97%. Significant and
highly significant differences between the both procedures of sample p
reparation and subsequent diagnosis were observed due to uneven transl
ocation and localization of virus. These differences were consistent f
or all the cultivars tested (statistically insignificant for cultivars
Radka and Nora, which belong to more resistant ones). After artificia
l break of dormancy by means of rindite treatment 1.8 to 2.3 times mor
e infected tubers were detected. Uneven translocation of PVY into part
icular tubers of potato plant after natural infection in field conditi
ons was noted both in cultivars with higher resistance rating and in m
ore susceptible ones. On average of all the cultivars tested, the over
all accordance of diagnosis in parallel (sister) tubers attained 72 to
77% and ranged from 61 to 88% depending on the cultivars (Tab. III).
The results are discussed with regard to the reliability of laboratory
diagnosis of the PVY in the progeny of primarily infected potato plan
ts.