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Wild emmer wheat (Triticum dicoccoides, (DIC)) is an important source of resistance to stripe rust due to presence of Puccinia striiformis in its natural habitats with high humidity and relatively low temperatures that are favorable for stripe rust development. Previously, we showed that DIC accessions from northern Israel were highly resistant to stripe rust. According to the rust responses of three DIC accessions (G25, H52, G303) and mapping of the resistance to relatively close, but different, genetic positions on chromosome 1BS, three different resistance genes were assumed to be present. However, the development of additional critical recombinants and new higher resolution genetic maps for these three genes in subsequent work led us to place YrH52 and YrG303 in the same genetic interval as Yr15, suggesting that the three putative genes are allelic or identical. The recent cloning of Yr15 allowed us to test this hypothesis using an EMS mutagenesis approach. We sequenced the Yr15 locus in five yrH52 and three yrG303 susceptible mutants and identified missense point mutations associated with the susceptible phenotype in each one. Thus, YrH52 and YrG303 may not be new genes. Further work is under way to determine if these genes are allelic or identical.
Stem rust, caused by Puccinia graminis f. sp. tritici (Pgt), is a threat to wheat production worldwide. To manage this important disease, new sources of genetic resistance are needed and common wheat landraces are a potential source of such resistance. Landrace accessions from the USDA-ARS National Small Grains Collection were evaluated for seedling resistance to the Ug99 race group. To identify accessions most likely to carry novel resistance genes, a bulked segregant analysis (BSA) approach was used. Seven resistant accessions were crossed to a susceptible parent line and F3 families were tested against Pgt race TTKSK. The resistant plants were identified and grouped into two bulks per population. The bulks, along with the parents and F1 progeny, were genotyped with the 90K wheat iSelect SNP genotyping platform. Four of the populations appeared to segregate in a 1:1 phenotypic resistant/susceptible ratio, one in a 1:2 ratio, and two in 1:3 ratios. However, chi squared tests indicated the ratios were statistically the best fit for only two of the 1:1 segregating populations and one of the 1:3 segregating populations. Initial BSA results indicate the markers associated with reduced stem rust infection are located on wheat chromosomes 1DL and 2B. These mapping populations are being advanced for further evaluation to ascertain if novel resistance to the Ug99 stem rust race group is present.
Wheat rust diseases are a major cause of yield losses of this crop. Yellow (Puccinia striiformis f. sp. tritici) rust is of the most widespread and dangerous disease of wheat and is the major factor that adversely affects wheat yield and quality. The use of genetic host resistance is the most effective, economical and environmentally safe method of controlling stripe rust that allows elimination of fungicides and minimize crop losses from this disease. Due to the threat of the development of epiphytoties of rust disease it is necessary to identify new donors of resistance to yellow rust and to develop resistant wheat breeding material. In the present study, attention was drawn to the effective yellow rust resistance genes Yr5, Yr10 and Yr15, which were identified in the process of molecular screening of wheat germplasm. Genetic analysis using S23M41 molecular marker linked to Yr5 revealed the presence of this gene in 17 out of 136 promising lines. Thirteen genotypes screened with Xbarc8 generated the DNA fragment associated with Yr15. Three advanced lines with Yr10 were identified using the SCAR marker. Three lines carrying two Yr genes (Yr5 and Yr15) were detected. Combination of Yr5 and Yr10 were found in 15 wheat lines. We identified a number of wheat genotypes highly resistant to stripe rust, which could be further evaluated to release new resistant varieties or to be used in the breeding program.
In recent years, wheat stem rust, caused by Puccinia graminis f.sp. tritici, has been reconsidered in Iran due to its prevalence and the emergence of the dangerous Ug99 race. This study was conducted to understand pathogenic variation in the population of P. graminis f.sp. tritici, detection of effective genes, and identification of resistance in Iranian commercial wheat cultivars or advanced lines, by planting stem rust trap nurseries under natural disease infection in several regions of Iran during the 2016-2017 cropping season. The trap nursery in each location included 48 wheat lines each carrying a single gene of stem rust (Sr) resistance, seven lines each carrying Sr multigenes, eight additional lines to confirm four Sr genes, 149 commercial wheat cultivars or advanced lines from Iran, plus several susceptible checks. The percentage leaf area affected (disease severity) and infection type were recorded at adult plant stage when disease was well developed on flag leaves of susceptible checks. Results showed presence of virulence for several Sr genes in one or more locations. However, the single genes of Sr13, Sr23, Sr24, and two complex genes of Sr7a+Sr6+Sr12 and Sr6+Sr24+Sr36+Sr1RS-Am were still effective against stem rust in all locations. The results of evaluations of commercial wheat cultivars or advanced lines showed that approximately 16% the genotypes tested including wheat cultivars Gonbad, Shiroudi, Chamran-2, Baharan, Dena, Karkheh, and Arya were resistant in all locations.
Leaf rust resistance genes Lr9 and Lr19 were previously highly effective against the most predominant races of Puccinia triticina in Egypt. In 2015/2016 growing season, susceptible field reaction was recorded on these two genes where rust severity reached about 40S for Lr9 and 5S for Lr19 under Egyptian field conditions at four locations i.e. El-Behira, El-Minufiya, El-Qalubiya and El-Fayom governorates. Eight leaf rust field samples were collected from these governorates (four from each of Lr9 and Lr19). Forty single isolates were derived from the collected samples of Lr9 and Lr19 (each with 20 isolates). Eight pathotypes were identified from Lr9 and only two pathotypes were identified from Lr19. The most frequent pathotypes virulent to Lr9 were KTSPT (30%) followed by TTTMS (25%). Moreover, the other pathotypes ranged from 5 to 10%. Whereas, the most frequent pathotype virulent to Lr19 was CTTTT (85%) and the lowest PKTST was 15%. Pathotypes i.e. PRSTT, NTKTS and TTTMS identified from Lr9 were more aggressive on most of the tested leaf rust monogenic lines, as they were virulent to 36, 35 and 35 lines, respectively from a total of 39 lines. The two pathotypes; PKTST and CTTTT identified from Lr19 were virulent to 36 and 35 lines, respectively. Moreover, leaf rust pathotypes i.e. NPTNK and PRSTT from Lr9 and PKTST from Lr19 were the most aggressive on the tested wheat cultivars at seedling stage. The Lr2a was the most effective leaf rust resistance genes against the tested pathotypes at adult plant stage. Wheat cultivars Misr 1, Misr 2 and Nubariya 1 were the most resistant cultivars against the tested pathotypes at adult plant stage.
The wild relatives of wheat represent a vast resource of potentially useful genes for agriculture. The genus Aegilops has provided several rust resistance genes used in commercial cultivars. Here we report progress on mapping of potentially new stem and leaf rust resistance from Ae. caudata, Ae. searsii and Ae. mutica (Amblyopyrum muticum). Addition lines derived from the amphiploids Alcedo/ Ae. caudata, TA3368, CS/ Ae. mutica, TA8024 (both from Wheat Genetics Resource Center, Kansas State University, USA) and CS/ Ae. searsii TE10 (kindly provided by Dr Moshe Feldman, Weizmann Institute, Rehovot, Israel) were produced after backcrossing the amphiploids with Australian cv. Angas or Westonia. Backcrossed generations were screened for stem rust and leaf rust responses and both resistant and susceptible plants were sampled for DNA marker analysis. Stem rust resistant plants derived from the Ae. caudata amphiploid and leaf rust resistant plants derived from the Ae. searsii amphiploid showed the presence of non-wheat marker bands after hybridizing restricted genomic DNA with the Triticeae group 5 RFLP probe PSR128, and after PCR using EST-based primers specific for Triticeae group 5. Susceptible plants did not show those non-wheat molecular markers. Hence, stem rust resistance from Ae. caudata was allocated to chromosome 5C, and the resistance gene is temporarily named SrAec1t. Leaf rust resistance from Ae. searsii was allocated in a similar manner to chromosome 5Ss, and is temporarily named LrAesr1t. Leaf rust resistance transferred from Ae. mutica was traced to a 6T chromosome after associating resistance with the presence of Triticeae group 6 RFLP probes (including BCD001, BCD269, BCD276, BCD1426, CDO772, CDO1380, WG933) and that gene is temporarily named LrAmm1t. The addition lines involving the 5C, 5Ss and 6T chromosomes were crossed with Sears’ ph1b mutant to induce homoeologous recombination with related wheat chromosomes.