K. Noorollahi, M. Falahati Rastegar, B. Jafarpour,
Volume 4, Issue 1 (spring 2000)
Abstract
Four hundred isolates of Ascochyta rabiei (Pass.) Lab. collected from different parts of the country, such as Zarivar Marivan Lake in Kordestan Province Shabestar and Khosroshahr in Eastern Azarbaigan Province Serow, Bokan and Shahindeg in Western Azarbaigan Province Mashhad and Ilam were used in this experiment.
These isolates showed little differences in their cultural and morphological characters and pathogenic behaviors. They were categorized into 17 groups on the basis of collection regions and, based on cultural characteristics, were then reduced to 11 groups. Isolate number 16 from Mashhad showed the highest growth rate while isolate number 1 from Kordestan had the lowest growth rate.
One isolate was chosen as a representative for each group. Pathogenicity of representative isolates from each of the 11 groups were tested. Reaction type of all isolates was studied on differential hosts and one local chickpea line Jam was examined, using Reddy and Nene (1979) method. Races No. 4 and 6 were identified as the two physiologic races.
A. Dariaee, M. Falahati Rastegar, B. Jafarpour,
Volume 5, Issue 4 (winter 2002)
Abstract
This study was carried out on the biochemical aspects of chickpea cultivars and the genomic behavior of A. rabiei pathotypes 4 and 6 in four parts: 1) Determining the number of resistant genes in chickpea native cultivars, 2) Comparing the variation of sodium and potassium electrolytes concentrations in noninfected and infected seedling stems of resistant and susceptible cultivars, 3) Studying the effect of potassium deficiency on five differential cultivars by Hoagland nutrient culture, and 4) Using RAPD-PCR method to detect any genomic differences between the two pathotypes used in this study.
Eighteen native chickpea cultivars were chosen for this study. The result of the experiments showed that cultivar 1-60-144 possesses the highest number of resistant genes, while the others were either relatively tolerant or susceptible. The reduction of electrolytes concentration in infected cultivar ILC-1929 in comparison to resistant cultivar ILC-5928 is an indication of compatibility between the host plant and the pathogen. Increasing the level of resistance in differential cultivars and appearance of induced resistance as the result of potassium deficiency is due to the production of putrecine diamine. Eighty percent similarity of pathotypes genomic bands by using CG marker and primer 171 showed insufficient primer numbers and the necessity for using complementary methods.
A. Zeynaddini, B. Jafarpour, M. Flahaty Rastegar,
Volume 9, Issue 2 (summer 2005)
Abstract
The study of dispersion of alfalfa mosaic virus (ALMV) infection based on DAS-ELISA indicated that the fields of Alfalfa, potatoes and tomatoes from Chenaran, Ghochan, Shirvan, Mashhad, Neishaboor and Torbat Heydarieh were infected with the virus. The Statistical analysis indicated that the amount of infection did not differ in the surveyed regions and total mean of infection was 53 percent. The samples collected from the Alfalfa field of Mashhad was propagated in the Nicotiana tabacum L.cv Samsun and then virus was purified. The Mechanical inoculation of this isolate of the alfalfa mosaic virus (ALMV) induced the local lesion in Chenopodium quinoa,C. amaranticolor,Vigna unguiculata, Phaseolus vulgaris cv Redkidney and the systemic vein clearing and mosaic in Nicotiana glutinosa, N. tabacum cv. Samsun, Ocimum basilicum, Cicer arietinum and Lycopersicon esculentum. In the case of the infected Cucumis sativus, no symptoms was observed. ALMV was purified by the method of the kaiser and Robertson(1976). The virus yield was 11/05 mg per 100g of infected tissue on the basis of serological properties. This isolate of ALMV is similar to the American isolation in SDS-PAGE and Western Blot analysis,the molecular weight of the virus coat proteins were estimated at about 24000 daltons.in this regard,this isolation of ALMV is similar to the other isolates of ALMV reported elswhere.
