scholarly journals Screening of Exotic Potato Germplasm against Potato Virus PVX, PVY and PLRV through Biological and Serological Test (ELISA)

2020 ◽  
Vol 36 (3) ◽  
Author(s):  
Arifa Khan ◽  
Danish Anwar ◽  
Shazia Erum ◽  
Naveeda Riaz ◽  
Shahid Riaz ◽  
...  
2016 ◽  
Vol 3 (3) ◽  
pp. 600-605
Author(s):  
Ata-ul- Haq ◽  
◽  
Yasir Iftikhar ◽  
Muhammad Irfan Ullah ◽  
Mustansar Mubeen ◽  
...  

2016 ◽  
Vol 96 (5) ◽  
pp. 737-742 ◽  
Author(s):  
Xianzhou Nie ◽  
Fayruza Lalany ◽  
Virginia Dickison ◽  
Donna Wilson ◽  
Mathuresh Singh ◽  
...  

Molecular markers reported to be linked to extreme resistance (ER) against Potato virus Y (PVY) were evaluated in potato germplasm. YES3-3A and YES3-3B, markers linked to Rysto, were detected in ‘Barbara’ and its three descendants that exhibit ER to PVY; RYSC3, a marker linked to Ryadg, was detected in breeding clones NY121 and NY123. Assessment of RYSC3 as a marker for selection for Ryadg-mediated ER validated its efficacy in identification of selections with ER to PVY.


1987 ◽  
Vol 59 (3) ◽  
pp. 169-178 ◽  
Author(s):  
Aarne Kurppa ◽  
Matti Vuento

A simple kit for rapid detection of potato virus Y by latex serological test was developed. The test is carried out on a white cardboard sheet and the results can be read by naked eye in two minutes. A test card of 10 x 6 cm holds latex sensitized antibodies, buffers and other necessary ingredients as dry blue colored formulate on the ringed areas of the card. A test card includes space for six tests and positive and negative controls. The kit also includes disposable plastic sticks for mixing the samples with test reagents and a hand press with disposable plastic tips. For testing, dried reagents are dissolved in drops of sample and mixed. After gentle rotation, samples containing virus appear clearly granulated while samples from healthy plants remain unagglutinated. The testing of undiluted extracts of evenly developed tuber sprouts resulted in over 91 % identity with the results obtained with ELISA that was used as a control method. Testing of diluted leaf extracts reached the same reliability but undiluted leaf extracts from glasshouse grown potatoes were not well suitable as test samples because of their dark green color. No such problems occurred with field grown material and a complete identity with the ELISA readings was true when the samples included secondarily infected potato plants. No reaction to other potato viruses than PVY was obtained by the test kit.


2010 ◽  
Vol 22 (1) ◽  
pp. 253
Author(s):  
C. Ponsart ◽  
J. Gatien ◽  
N. Pozzi ◽  
P. Humblot ◽  
B. Guérin

Infection by Bluetongue virus (BTV) may affect reproductive performance but little is known about its real impact on fertility and occurrence of abortions. The aim of this study was to describe the effects of BTV infection on fetal mortality in 53 herds located in the east of France that were infected by the virus between August and November 2007. In 2008, 2 visits were performed 50 days apart by local veterinary surgeons and pregnancy was checked by ultrasonography. The first visit aimed to record data on pregnancy and infection status and to register clinical signs. A total of 1939 cows were classified within 3 groups: nonpregnant (n = 262), early pregnant (<3 months, n = 1041), and late pregnant (>3 months, n = 636). For each cow, a blood sample was collected approximately 8 days after the first visit and BTV status was determined by ELISA. The rates of clinical symptoms and fetal losses were compared in seronegative and seropositive cows using chi-square tests. Bluetongue status was found positive in 69.5% of the cows (80% of beef v. 67% of dairy cows). Prevalence was highly variable between herds: 19% of herds had 100% of cows with positive serological results and 10 herds presented at least 70% of seronegative results. Clinical signs were reported by farmers in 40% (457/1141) of seropositive cows compared to 20% (90/460) of seronegative cows (P < 0.001). As a consequence, clinical signs should not be considered as a reliable tool for diagnosing BTV infection with enough accuracy. At first visit, ultrasonography was performed in cows that were supposed to be pregnant. At second visit, a positive pregnancy status was confirmed in 78% of the cows, but this proportion was higher in seronegative cows when compared with seropositive cows (81 v. 76%; P < 0.02). This proportion was associated with the presence of clinical signs. Out of 1311 pregnant cows at first visit, only 37 presented a fetal mortality at second pregnancy check (2.8%).The rate of fetal mortality was related to the BTV-seropositive status of cows as well as stage of pregnancy (P < 0.05; Table 1). Calving interval did not differ between seropositive and seronegative females (411 ± 77 days v. 405 ± 82 days; P > 0.10); however, number of AI per conception was significantly higher in seropositive than in seronegative females (2.0 ± 1.2 v. 1.8 ± 1.1; P < 0.001). These results show that a seropositive BTV status assessed by serological test (ELISA) is associated with an increased frequency of fetal mortality in beef and dairy cattle, and with an increased number of AI per conception. Table 1.Rate of fetal mortality observed between 2 pregnancy diagnosis 50 days apart (negative pregnancy check during the 2nd visit in cows which were pregnant at first visit) The authors thank the farmers and veterinarians who participated to this trial, as well as the GDS (Groupements de Defense Sanitaire) organization from Moselle and Meuse departments for collecting the data.


1973 ◽  
Vol 51 (9) ◽  
pp. 1699-1702 ◽  
Author(s):  
C. Hlruki ◽  
P. Shukla

The presence of potato virus S (PVS) in the local lesions of Chenopodium quinoa was shown by bioassay, a serological test, and electron microscopy of negatively stained preparations of the infected tissues. Amorphous aggregates of particles believed to be PVS were found with the electron microscope in ultra-thin sections of both necrotic and nearby chlorotic cells of lesions sampled 8 days after inoculation of C. quinoa. The virus masses were confined to the cytoplasm and found in close proximity to the nucleus, chloroplasts, and tonoplasts. No other cellular inclusions were found in these cells.


2015 ◽  
Vol 3 (2) ◽  
pp. 21-24
Author(s):  
Misbah Iqbal Qamar ◽  
Yasir Iftikhar ◽  
Zafar Iqbal ◽  
Mustansar Mubeen ◽  
Ata-ul Haq

1999 ◽  
Vol 20 (3) ◽  
pp. 357-362 ◽  
Author(s):  
Susan M. Angell ◽  
David C. Baulcombe

Sign in / Sign up

Export Citation Format

Share Document