Stem rust of wheat caused by the fungal pathogen Puccinia graminis f. sp. tritici historically caused major yield losses of wheat worldwide. To understand the genetic basis of stem rust resistance in contemporary North American spring wheat, genome-wide association analysis was conducted on 250 elite lines. The lines were evaluated in separate nurseries each inoculated with a different P. graminis f. sp. tritici race for three years (2013, 2015 and 2016) at Rosemount, Minnesota. The lines were also challenged with the same four races at the seedling stage in a greenhouse facility at the USDA-ARS Cereal Disease Laboratory. A total of 22,310 high-quality SNPs obtained from the Infinium 90,000 SNPs chip were used to perform association analysis. Markers strongly associated with resistance to the four races at seedling and field environments were identified. At the seedling stage, the most significant marker-trait associations were detected in the regions of known major genes (Sr6, Sr7a and Sr9b) except for race QFCSC where a strong association was detected on chromosome arm 1AL. Markers presumably linked to Sr6 and Sr7a were associated with both seedling and field resistance to specific races. A field resistance QTL on chromosome arm 2DS was detected for response to races RCRSC and TPMKC. A QTL specific to field resistance was detected for QFCSC and TPMKC on 2BL. The markers that showed strong association signals may be useful to pyramid and track race-specific stem rust resistance genes in wheat breeding programs. We postulated the presence of Sr2, Sr6, Sr7a, Sr8a, Sr9b, Sr11, Sr12, Sr24, Sr25, Sr31, and Sr57 (Lr34) in this germplasm based on phenotypic and marker data. We found that combinations of genes conferring resistance to specific P. graminis f. sp. tritici races accounts for the prevalent stem rust resistance in North American spring wheat.
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Wheat stem rust, caused by Puccinia graminis f. sp. tritici (Pgt), is a significant disease limiting wheat yield in Ethiopia. Wheat varieties such as 'Digalu' with single major-effect stem rust resistance genes have not exhibited durable resistance in Ethiopia. Identifying wheat lines with adult plant resistance (APR) has been proposed as a strategy to select for durable resistance. Our objective was to test the hypothesis that APR to stem rust is non-race-specific. We selected 31 wheat lines (including 10 durum and 21 bread wheat lines) that were susceptible as seedlings to Pgt races TTKSK, TKTTF, and TRTTF. These 31 wheat lines and Digalu were evaluated in 2014 and 2015 at the Kulumsa Agricultural Research Center, Ethiopia. The lines were planted in 1 m rows and replicated twice in separate single-race-inoculated nurseries. The three single-race nurseries inoculated with Pgt races TTKSK, TKTTF, and TRTTF were separated by at least 100 m and included selective spreaders. Plot yield, thousand kernel weight (TKW), and visual disease responses were measured for each plot. We used a least-squared means test to detect differences in coefficient of infection and TKW of each line across paired race comparisons. Lines 'Park', 'CI11469', and 'CI12818' displayed significantly different coefficient of infections between races TTKSK and TRTTF. For CI11469 and CI12818, this difference was validated by significant differences in TKW. Significant differences in TKW were also detected between various race comparisons for 'ETHBW019', 'CI14798', 'CI15159', 'CI14618', and 'CI14094'. Our data demonstrated that APR in the selected germplasm was largely non-race-specific, but there were exceptions where race-specificity of APR was detected. These results have implications for resistance breeding and monitoring: testing of breeding material against prevalent Pgt races in target environments, not relying only on hotspot screening locations, and careful monitoring of deployed APR varieties are all warranted.
Evaluation of candidate lines to develop resistant varieties at multiplications in Pakistan is a regular activity which has been successfully done for many years. This approach assists in generation of future resistant cultivars around appropriate genes combinations thereby providing durable resistance outputs for wheat productivity. This year, National Uniform Wheat Yield Trial (NUWYT) comprised of 60 candidate lines. Among these 15 lines were also present in the last years NUWYT. The two years data revealed that there was only one line V-12066 resistant to all three rusts during the two consecutive seasons 2015-16 and 2016-17. Four candidate lines NR-487, V-122557, PR-115 and NRL-1123 were found resistant to yellow and leaf rust during 2015-16 and 2016-17. A candidate line DN-111 was found resistant to leaf and stem rust. There were three lines NW-1-8183-8, NW-5-20-1 and MSH which were found resistant to leaf rust only during two consecutive seasons. Similarly, two candidate lines V-122559 and QS-3 were found resistant to stem rust only, while one line NR-443 was resistant to yellow rust only. The present study provide the screening and evaluation system of Pakistan for promoting and releasing the resistant wheat varieties.
This work was carried out to study the response of five bread and two durum wheat cultivars to stem rust and its effect on grain yield under field conditions at Sids and Beni Sweif stations during the three growing seasons 2011/2012, 2012/2013 and 2013/2014. The loss in grain yield and kernel weight of the different wheat genotypes was variable according to the varietal response. Grain yield and kernel weight of the protected plots (protected by the effective fungicide Sumi-eight 5EC(CE)-1-(2,4-dichlorophenyl)1-4,4-dimethyl1-2-(1,2,4-triazol-y1)Pent -1-en -3-0L) at the rate of 70cm /200litter water per Fadden ) of all wheat genotypes were higher than the infected ones. Significant differences were found between infected and protected wheat genotypes.. Disease severity was recorded weekly to estimate area under disease progress curve (AUDPC). The AUDPC ranged from 85.33 to 405.00 (Sids 1 and Sohag 3) during 2011/2012, from 181.66 to 805.00 (Shandwel 1 and Sohag 3) during 2012/2013, and from 142.33 to 585.00 (Shandwel 1 and Sohag 3) during 2013/2014. Losses in kernel weight ranged from 3.39% to 31.03% (Sids 1 and Misr 1) during 2011/2012, from 9.79% to 44.18% (Sids 1 and Sohag 3) during 2012/2013,and from 5.67% to 26.86% (Sids 1 and Sohag 3) during 2013/2014. Yield losses ranged from 5.70% to 37.52% (Shandwel 1 and Misr 1) during 2011/2012, from 7.75% to 45.78% (Shandwel 1 and Misr 1) during 2012/2013, and from 7.14% to 30.59% (Sids 1 and Sohag 3) during 2013/2014. Yield losses correlated strongly with AUDPC. The results of this study indicate that bread wheat cultivars are (Giza 168,Sakha 93, Sids 1, Misr 1, Misr 2 and Shandwel 1) and Durum wheat are ( Beni Sweif 5 and Sohag 3) more tolerant than durum wheat cultivars. The Egyptian bread wheat cultivars Sids 1 and Shandawel 1 are more tolerant than the other bread wheat cultivars.
Stem rust caused by Puccinia graminis f. sp. tritici (Pgt) is a major production constraint in most wheat growing areas of Ethiopia. The stem rust pathogen is capable of rapidly developing new virulence to resistance genes. The highlands of Ethiopia are considered a hot spot for Pgt diversity. The present study was conducted to investigate the virulence diversity and spatial distribution of races of Pgt in the major wheat growing areas of Ethiopia. The physiologic races of Pgt were determined on seedlings of the standard wheat stem rust differentials following the international system of nomenclature. Stem rust race analyses were carried out both at Ambo Plant Protection Center and the Cereal Disease Laboratory in Minnesota. 426 stem rust samples were collected from major wheat growing of the country in the 2016 cropping season and 185 viable samples were analyzed. Stem rust races TKTTF, TTKSK, TTTTF, JRCQC and RRTTF were identified. Among the identified races, TKTTTF was dominant at a frequency of 78.7% followed by TTKSK (10.6%). Race TTTTF was found for the first time in Ethiopia in 2016. Only one resistance gene in the differential set, Sr24, was effective against all isolates. Stem rust resistance gene Sr31 was found to confer resistance to most of the races prevalent in Ethiopia with the exception of Ug99. Sr24 could be used in combination with other resistance genes in breeding for resistance to stem rust in Ethiopia.
An effective partnership between CIMMYT, KALRO, EIAR and Delivering Genetic Gains in Wheat (DGGW) project on global stem rust phenotyping has made a significant progress and impact on the Global wheat community in addressing the threat of Ug99 race group and other important stem rust races in the region. International stem rust phenotyping networks play a key role in evaluating global wheat germplasm from many countries and institutions: identifying new sources of resistance, pre-breeding, CIMMYT-Kenya shuttle breeding, pathogen survey and surveillance, varietal release and genomic selection. About 600,000 lines have been screened against Pgt race Ug99 and derivatives since 2005, and the screening capacity at KALRO has increased to 50,000 lines each year from over 20-25 countries and research institutions each year. The results from international nurseries show a shift to higher frequencies of lines with resistance to race Ug99 since the screening activities were initiated in 2008.
KALRO and EIAR and several national programs have a dynamic and successful breeding programs that benefit from collaboration, testing, and release of materials coming out of the CIMMYT breeding program. The release of over 15 varieties in Kenya as well as in Ethiopia and more than 90 varieties released in several countries globally over the years is a testament to the success of the program. with spillover effects of varieties released in Burundi, Rwanda, and Uganda.
CIMMYT-Kenya shuttle breeding has resulted in rapid recycling of over 2000 breeding populations each year between Mexico and Kenya to evaluate and select lines in early generations against virulent stem rust races in Kenya to ensure lines have adequate levels of resistance are advanced not only in early generations of breeding cycle but also materials in the yield trails (10,000 annually) that are later constituted as international nurseries and distributed to National programs and partners.
Wheat cultivar McNair 701 carries resistance gene SrMcN and is used as a differential line to identify Pgt races using the international letter code nomenclature. The inheritance and location of the resistance gene has not been characterized. We developed a doubled haploid (DH) population from cross LMPG/McNair 701 to study the genetics and chromosomal location of SrMcN. A DH population inoculated with race QCCJB segregated 100 resistant : 94 susceptible, a 1:1 ratio (?2=0.186, P=0.666, NS) indicative of segregation at a single locus. This gene was mapped to chromosome 2DL using the Infinium 90k platform. The map position of SrMcN was similar to that of Sr54, one of two genes previously found in Norin 40. Comparison of stem rust seedling reactions using 12 diverse Pgt races indicated that McNair 701 and an Sr54 line derived from Norin 40 had an identical pattern of responses and similar low infection types (IT=12-) to races LCBNB and QCCJB. Based on the chromosomal location on 2DL and identical seedling responses to Sr54, it is likely that the resistance gene in McNair 701 formerly known as SrMcN is Sr54. This finding will be confirmed by a test of allelism.
Rusts (Puccinia spp.) are the most significant disease affecting wheat yield and quality in Turkey. Knowing the resistance status of wheat genotypes in crossing program is an important issue for breeding programs. The aim of the study was to determine of the resistance of the 106 wheat genotypes consisting of Crossing Block Spring Wheat (CBSW) nursery developed by the International Winter Wheat Improved Project (IWWIP). For this purpose, adult plant and seedling test were conducted for yellow rust while only seedling test were conducted for leaf and stem rust. Evaluations were carried out at the research facilities of CRIFC at İkizce and Yenimahalle in Ankara in the 2014 season. For adult plant reactions; the genotypes were inoculated with local Pst populations (virulent on Yr2,6,7,8,9,25,27,Sd,Su,Avs). Stripe rust development on each entry were scored using the modified Cobb scale when the susceptible check Little Club had reached 80S infection severity in June, 2014. Coefficients of infections were calculated and values below 20 were considered to be resistant. For seedling test; the seedling was inoculated with local Pgt (avirulent on Sr24, Sr26, Sr27, and Sr31), Pt (avirulent on Lr9, Lr19, Lr24, and Lr28) and Pst populations. Stripe, leaf and stem rust development on each entry were scored after 14 days with 0-4 and 0-9 scale for leaf-stem rust and yellow rust, respectively. In seedling stage, thirty nine (37%), 47 (44%), and 20 (19%) genotypes were resistant to local Pgt, Pt, and Pst populations, respectively. In adult plant test, 46 (43%) genotypes were resistant to Pst. The resistance genotypes to stem, leaf, and stripe rust were determined with this research.
Puccinia graminis f. sp. tritici (Pgt) is one of the most destructive pathogens of wheat. Fungal secreted proteins termed effectors play an important role in modulating the host cellular environment and suppressing the plant defense response to enable fungal growth. They also become targets of plant resistance (R) proteins. We have taken a genomics approach to initially identify candidate effectors. We have built a draft genome for a founder Australian Pgt isolate of pathotype (pt.) 21-0 (collected in 1954) by next generation DNA sequencing. A combination of reference-based assembly using the genome of the previously sequenced North American Pgt isolate CDL 75-36-700-3 (p7a) and de novo assembly resulted in a 92 Mbp reference genome for Pgt isolate 21-0. This draft genome was subsequently used to build a pan-genome based on five Australian Pgt isolates. Transcriptomes from germinated urediniospores and haustoria were separately assembled for pt. 21-0 and comparison of gene expression profiles showed differential expression in ~10% of the genes in germinated urediniospores as well as haustoria. A total of 1,924 secreted proteins were predicted from the 21-0 transcriptome, of which 586 were classified as haustorial secreted proteins (HSPs). We are currently exploring effector gene expression during infection of wheat to reduce this candidate list based on a common expression profile identified for Avr genes in the flax rust fungus. Comparison of 21-0 with two presumed clonal field derivatives (collected in 1982 and 1984) that had evolved virulence on four additional resistance genes (Sr5, Sr11, Sr27, SrSatu) identified mutations in 13 HSP effector candidates. These candidate effectors are being assessed for recognition in wheat accessions with the corresponding R genes using a bacterial type three secretion delivery system based on an engineered Pseudomonas fluorescence strain (Upadhyaya NM et al. Mol Plant Microbe Interact 27:255-264).
Stem rust is a potentially destructive fungal disease of wheat worldwide. In 1998 Pgt pathotype TTKSK virulent to Sr31 was detected in Uganda. The same pathotype was confirmed in Lorestan and Hamedan provinces of Iran in 2007. We used a derivative of race TTKSK to phenotype 62 Iranian wheat landraces (resistant to stripe rust in a previous study) at the seedling stage to this new pathotype (TTSSK). Twenty eight accessions were evaluated for the presence of resistance genes Sr2, Sr22, Sr24, Sr25, Sr26, Sr35, Sr36 and Srweb using SSR markers. None carried Sr2, Sr24 or Sr26, but the presence of Sr22, Sr25, Sr35 and Sr36 was indicated. Some susceptible landraces predicted to carry Sr2 by marker analysis require further investigation. To evaluate defense gene expression in compatible and incompatible stem rust interactions we sampled resistant and susceptible cultivars at 0, 12, 18, 24, 72 hours post-inoculation (hpi). ?-1,3 glucanase expression was studied using qGLU-S and qGLUU-AS primers and a real-time PCR step-one ABI machine, with ?-tubulin and EF1-? genes used as internal controls. In incompatible interactions defense gene expression was increased at 24 hpi, but in compatible interactions the highest level of expression occurred at 12 hpi and was significantly decreased at 18 hpi. The results revealed that expression of defense genes such as ?-1,3 glucanase was earlier in compatible than in incompatible interactions but the expression level was less in incompatible interactions. On the other hand, in susceptible genotypes the expression of defense genes increased immediately after inoculation and declined sharply after infection. In contrast defense gene expression in resistant genotypes began to increase after establishment of the pathogen.