In 2016 the bread wheat (BW) and durum wheat (DW) landrace accessions were evaluated against PstS2 and in 2017 against a mixture of PstS2 and warrior race in field inoculations at Izmir precision stripe rust phenotyping platform. Inoculation was carried out three times during seedling, tillering and booting stages using mixture of fresh spore and talcum powder. Adult-plant responses of tested accessions were recorded according to 0-9 scale once the flag leaf of the susceptible cultivar became fully susceptible. During 2016, out of 3319 BW accessions, 1135 (36%), 871 (28%) and 1133 (36%) were found resistant (1-3 scale), moderately resistant (4-6), and susceptible (7-9) to PstS2, respectively. Amongst the resistant accessions in 2016, 1043 (33%) remained resistant while 786 (25%) showed moderate resistant and 1310 (42%) became susceptible. In 2017, 43% of moderately resistant accessions showed susceptibility to warrior race and 57% remained resistant to moderately resistant. Within the susceptible accessions to PstS2 race in 2016, 22% showed resistance to the warrior race and the remaining were susceptible. In case of DW in 2016, 76% (553) of the accessions were resistant to PstS2, 23% (163) were moderately resistant and only 1% (7) were found susceptible. In 2017, 329 (46%) of the resistant accessions were found resistant, whereas 289 (40%) and 105 (15%) showed moderately resistance and susceptible reaction to Warrior race, respectively. The present data indicated that BW landraces were generally more susceptible to stripe rust than DWs. Susceptibility of both BW and DW accessions to Warrior race indicated that most likely some of the uncharacterized resistance genes which conferred resistance to PstS2 were ineffective against the warrior race. Sources of resistance to both races were identified in both BW and DW. Genetic architecture of identified sources of resistance in present study requires further investigations.
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Asia and North Africa (CWANA). The total acreage in CWANA is approximately 53 million hectares. Wheat stripe (yellow) rust caused by Puccinia striiformis f. sp. tritici (Pst) continuously poses a serious threat to wheat production in CWANA. Several factors have contributed to the current severe epidemics of stripe rust, including; the rapid shift of virulence in the pathogen population, genetic uniformitity of mega-cultivars, favorability of environmental conditions, and an overlapping/ continuous crop calendar. During 1985-1997 the widespread appearance of Yr9 virulent pathotypes in CWANA, and eventually in the Indian sub-continent, resulted in several epidemics that caused a series of severe crop losses in popular cultivars known to be protected by the Yr9 resistance gene. Following the Yr9 virulence epidemics, susceptible cultivars were extensively replaced with CIMMYT-derived germplasm such as Kauz, Atilla, Opata, Nacozari, Bucbuc and Crow. The resistance of many of the replacement cultivars, including the mega-cultivars in India (PBW343), Pakistan (Inquilab-91, Bakhtwar), Iran (Chamran, Shiroudi), Ethiopia (Kubsa), and Syria (Cham 8) was based on Yr27. Breakdown of Yr27 resistance in PBW343, Inquilab 91 and Chamran, in India, Pakistan, and Iran, respectively, was reported between 2002-2004. Although occasional stripe rust outbreaks appeared in some areas, unfavorable environmental conditions presumably restricted the increase of the Yr27 Pst population until 2009, when conducive environmental conditions resulted in severe epidemics in several CWANA countries e.g., Morocco, Algeria, Uzbekistan, Turkey, Iran, Azerbaijan, Georgia, and Afghanistan. Environmental conditions favouring rust development continued into 2010, with mild winters and adequate rainfall in several CWANA countries resulting in early outbreaks of stripe rust. The 2010 stripe rust outbreaks occurred throughout the major wheat growing areas in the CWANA and Caucasus countries, causing severe yield losses particularly in Syria where Cham 8 (with Yr27) occupied more than 70% of the wheat areas. Inspite of favorable environmental conditions in many areas in CWANA in 2011, similar severe stripe rust epidemics have not been reported to date. Climate change now appears to be playing a major role in Pst population dynamics in CWANA. Direct, multiple affects of climatic changes on epidemiology of rust pathogens are expected, including the survival of primary inoculum, the rate of disease development, duration of rust epidemics, and development and distribution of rust populations. Emergence of stripe rust in non-traditional areas, changes in the frequency of new race evolution, early infection of stripe rust, shifts in predicted pathways of rust migrations, and finally wide spread epidemics of stripe rust in warmer areas as a potential indicator of adaptation to high temperatures are considered as possible consequences of climatic changes. Regional pathogen surveys indicated the widespread distribution of aggressive Pst pathoype (s) with adaptation to higher temperature. In the absence of resistant varieties, fungicide application remains the only practical measure to control stripe rust. Effective disease surveillance and monitoring systems, coupled to timely application of fungicides has effectively controlled stripe rust epidemics in Iran, Turkey, and Syria during 2010-11. Regional monitoring of pathogen variability and disease development must be undertaken as a matter of high priority, and timely chemical control measures will continue to play a major role for control of stripe rust in CWANA in the short-term. In the medium to long-term, existing resistant varieties and advanced breeding lines need to be promoted and susceptible varieties have to be urgently replaced.