A. Mujeeb-Kazi

Conservation of the genetic variation of Triticum tauschii (Coss.) Schmalh. (Aegilops squarrosa auct. non L.) in synthetic hexaploid wheats (T. turgidum L. s.lat. x T. tauschii; 2n=6x=42, AABBDD) and its potential utilization for wheat improvement

Triticum tauschii (Coss.) Schmalh. (Aegilops squarrosa auct. non L., 2n=2x=14, DD genome) with its diverse range of accessions and distribution provides a unique opportunity for exploiting novel genetic variability for wheat (T. aestivum L.) improvement associated with biotic/abiotic stress factors. From our working collection of 490 T. tauschii accessions we have so far produced 430 different synthetic hexaploids (2n=6x=42, AABBDD) resulting from the chromosome doubling of Triticum turgidum L. s. lat. x T. tauschii F1 hybrids (each synthetic involving a different T. tauschii accession). We present here our results on hybrid production, plantlet regeneration, cytology, colchicine induced doubling of the 2n=3x=21 chromosome F1 hybrids, seed increase of the doubled progeny and screening for a biotic stress; Cochliobolus sativus Ito and Kuribay (syn. Helminthosporium sativum Pamm. King and Bakke); of 250 of these synthetic hexaploid (2n=6x=42) amphiploids. Application of the direct crossing methodology involving susceptible T. aestivum cultivars with resistant T. tauschii accessions is also alluded to.

Agronomic performance of chromosomes 1B and T1BL.1RS near-isolines in the spring bread wheat Seri M82

The T1BL.1RS wheat (Triticum aestivum L.) - rye (Secale cereale L.) translocations have been of particular interest and are widely used in bread wheat breeding programs. The objective of this study was to determine the effect of the T1BL.1RS chromosome on grain yield and its components using 20 near-isolines of spring bread wheat cultivar ‘Seri M82’ (10 homozygous for chromosome 1B substitution and 10 homozygous for T1BL.1RS). The test lines have been produced by substituting the 1B chromosome in Seri M82 (T1BL.1RS, T1BL.1RS) through backrossing. Two field experiments were evaluated under optimum (five irrigations) and reduced (one irrigation) moisture conditions for two consecutive production cycles at the Mexican National Agricultural Research Institute, Ciudad Obregon, Sonora, Mexico. The presence of T1BL.1RS had a significant effect on grain yield, harvest index, grains/m2, grains/spike, 1000-grain weight, test weight, flowering date and physiological maturity in both moisture conditions. The agronomic advantage of the 1B substitution lines on above-ground biomass yield at maturity, spikes/m2and grain-filling duration was expressed only under the optimum moisture condition. The presence of T1BL.1RS increased grain yield 1.6% and 11.3% for optimum and reduced moisture conditions, respectively. These results encourage further use of T1BL.1RS wheats in improving agronomic traits, especially for reduced irrigation or rainfed environments.

Resistance to stripe rust in Triticum turgidum, T. tauschii and their synthetic hexaploids

Resistance to stripe rust (caused by Puccinia striiformis Westend.) of 34 Triticum turgidum L. var.durum, 278 T. tauschii, and 267 synthetic hexaploid wheats (T. turgidum x T. tauschii) was evaluated at the seedling stage in the greenhouse and at the adult-plant stage at two field locations. Mexican pathotype 14E14 was used in all studies. Seedling resistance, expressed as low infection type, was present in all three species. One hundred and twenty-eight (46%) accessions of T. tauschii, 8 (23%) of T. turgidum and 31 (12%) of synthetic hexaploid wheats were highly resistant as seedlings. In the field tests, resistance was evaluated by estimating area under disease progress curve (AUDPC). Synthetic hexaploid wheats showed a wide range of variability for disease responses in both greenhouse and field tests, indicating the presence of a number of genes for resistance. In general, genotypes with seedling resistance were also found to be resistant as adult plants. Genotypes, which were susceptible or intermediate as seedlings but resistant as adult plants, were present in both T. turgidum and the synthetic hexaploids. Resistances from either T. turgidum or T. tauschii or both were identified in the synthetic hexaploids in this study. These new sources of resistance could be incorporated into cultivated hexaploid wheats to increase the existing gene pool of resistance to stripe rust.

Seed protein and isozyme variations in Triticum tauschii (Aegilops squarrosa).

Sixty Triticum tauschii (Aegilops squarrosa, 2n=2x=14, DD) accessions were evaluated for the variability of high-molecular-weight (HMW) glutenins, gliadins and isozymes of seed esterase, β-amylase and glucose-phosphate isomerase. Wide variability was observed for HMW-glutenins and gliadins. The implications of unique HMW-glutenin alleles for quality parameters are discussed. Isozyme evaluations indicated more variability for the Est-Dt5 locus as compared to the Est-D5 of bread-wheat. The polymorphism for β-Amy-Dt1 was less than that of β-Amy-D1. Similar to the bread-wheat situation, Gpi-Dt1 showed no polymorphism. The variability observed with the traits evaluated can be readily observed in T. turgidum x T. tauschii synthetic hexaploids (2n=6x=42, AABBDD) suggesting that T. tauschii accessions may be a rich source for enhancing the genetic variability of T. aestivum cultivars.

Suppression/expression of resistance to stripe rust in synthetic hexaploid wheat (Triticum turgidum×T. tauschii)

Seventy-four hexaploid wheats, synthesized by either crossing resistantTriticum turgidum L. var.durum with susceptible/intermediateT. tauschii or susceptible/intermediateT. turgidum with resistantT. tauschii, and their parents were evaluated as seedlings in the greenhouse and as adult-plants at two field locations in Mexico for resistance to pathotype 14E14 of stripe (or yellow) rust (caused byPuccinia striiformis Westend). The seedlings of different synthetic hexaploids showed high phenotypic diversity for resistance. However, the resistance level of only 15 of the 74 synthetic hexaploid wheats were similar to the low infection types of the respective donor parents. The remaining synthetic wheats displayed either intermediate or high infection types. A similar result was also obtained in field tests, where only 18 synthetic hexaploids were resistant as adult-plants. In general, genotypes with seedling resistance were also resistant as adult-plants. A few synthetic hexaploids, which displayed intermediate or susceptible infection types as seedlings were resistant as adult-plants, indicating that additional genes for adult-plant resistance were also present. The fact that resistance of some donor parents was not expressed, or only partially expressed, in a synthetic hexaploid background suggests the presence of suppressor genes in the both the A or B, and D genomes ofT. turgidum andT. tauschii, respectively. The resistance of a donor parent was expressed in a synthetic hexaploid only if the corresponding suppressor was absent in the second parent. Moreover, the suppressors appeared to be resistance gene specific.

Characterisation of high- and low-molecular weight glutenin subunits associated to the D genome of Aegilops tauschii in a collection of synthetic hexaploid wheats

Abstract Synthetic hexaploid wheats (2n=6x=42, AABBDD) involving genomes from Triticum turgidum (2n= 4x=28, AABB) and Aegilops tauschii (2n=2x=14, DD) have been produced as a means for introducing desirable characteristics into bread wheat. In the present work we describe the genetic variability present at the Glu-Dt1 and Glu-Dt3 loci, encoding high- (HMW) and low-molecular-weight (LMW) glutenin subunits respectively, derived from Ae. tauschii, using electrophoretic and chromatographic methods, in a collection of synthetic hexaploid wheats. A wide variation both in mobility and surface hydrophobicity of HMW glutenin subunits was observed between different accessions of Ae. tauschii used in the production of the synthetic hexaploids. A combination of electrophoretic and chromatographic methods improves the identification of HMW glutenin subunits; in fact subunits with identical apparent mobility were revealed to have a different surface hydrophobicity by reversed-phase high performance liquid chromatography. None of the Dx5t subunits present in Ae. tauschii showed the presence of the extra cysteine residue found in the HMW glutenin subunit Dx5 of Triticum aestivum, as revealed by selective amplification with polymerase chain reaction (PCR). The wide variability and the high number of subunits encoded by the Glu-Dt3 locus suggests that Ae. tauschii may be a rich source for enhancing the genetic variability of glutenin subunits in bread wheat and improving bread-making properties.

A diagnostic molecular marker allowing the study of Th. intermedium-derived resistance to BYDV in bread wheat segregating populations

Abstract Barley yellow dwarf (BYD) is the most important viral disease of small cereal grains. True resistance to the disease is not found in wheat (Triticum aestivum L.), but it has been introgressed from Thinopyrum intermedium (Ti) on chromosome 7DL of recombinant wheat lines designated TC. The objectives of our study were to identify a high through-put scoring tool for the presence of the translocated Th. intermedium fragment and to assess its suitability for evaluating resistance to BYDV in segregating populations. Segregation of the Ti fragment was followed in the F2 population of an Anza (bread wheat) by TC14/2*Spear (TC14) cross. Resistance to BYDV isolates PAV-Mex and MAV-Mex in F3, F4, and F5 populations was evaluated under field and/or greenhouse conditions by measuring the virus titers of infected plants using ELISA, and the number of infected plants per plot. The SSR marker gwm37 was polymorphic for the translocation. In F4 lines it was associated with the physical presence of an intact translocation on chromosome 7DL and with low virus titers of BYDV-PAV. Reductions in virus titer of 27% and 55% in the F3 and 18% and 45% in the F5 populations were observed when the fragment was present in the heterozygous and homozygous states, respectively, confirming a dosage effect of the resistance allele. A lower proportion of infected individuals in the field was associated with the presence of the fragment, indicating a mechanism that may interfere with aphid feeding or virus translocation within infected plants. Despite significant differences between groups with and without the fragment, the OD values of infected lines overlapped, and it was not possible to definitively detect the fragment based solely on ELISA. We conclude that gwm37 is a reliable marker for the Ti translocation that will allow efficient detection of the translocation in breeding populations and greatly assist in selecting BYDV-resistant wheats in the absence of the disease.

Rebirth of synthetic hexaploids with global implications for wheat improvement

Aegilops tauschii (syn.Triticum tauschii (Coss.) Schmalh., syn. Ae. squarrosa auct. Non L., 2n = 2x = 14, DD genome), with its numerous accessions and wide distribution, provides unparallelled genetic diversity for addressing global wheat production constraints through genetic improvement. From our working collection of ~750 Ae. tauschii accessions, hybridisation efforts produced 1014 synthetic hexaploid combinations (2n = 6x = 42, AABBDD), resulting from chromosome doubling of the F1 hybrids between elite Triticum turgidum L. s. lat. cultivars and Ae. tauschii accessions. The extensive production of synthetic hexaploids represents a step-wise progression over 2 decades in the generation of a valuable resource of user-friendly genetic diversity. The synthetic germplasm has been validated, maintained, screened, formed into targetted stress-related subsets for focused utilisation, and been allowed global distribution for use in pre-breeding/breeding with advent into molecular technologies. Abundant synthetic hexaploids with different Ae. tauschii accessions have been identified from their screening for yield per se, and various biotic/abiotic stresses. Encouraging diversity data have been obtained for key abiotic constraints such as drought, salinity, heat, and water-logging. A similar response was prevalent for the salient biotic stresses such as fusarium head scab, spot blotch, septoria leaf blotch, and karnal bunt. Global distribution of the selected synthetics has further added valuable information for several other stress constraints and led to utilisation of the synthetic diversity for molecular investigations. The superiority of the primary synthetics has been transferred with ease via pre-breeding/breeding to conventional bread wheat cultivars and varietal releases have started globally. The success and status of the D genome diversity are the focus of this paper and we are optimistic that researchers will devise additional strategies to harness other genomes as efficiently by adding on new technologies that ensure wheat production security in the decades ahead.

Yield loss to spot blotch in spring bread wheat in warm nontraditional wheat production areas

Twenty-five spring bread wheat (Triticum aestivum L.) cultivars were evaluated for 2 years at Poza Rica, Mexico, for grain yield, aboveground biomass at maturity, harvest index, yield components, and test weight under a natural epidemic of spot blotch (caused by Cochliobolus sativus) with and without fungicide protection. Diseased plot yields were 43.2% lower than fungicide-protected plot yields. Aboveground biomass yield at maturity and harvest index were reduced by 18 and 31.3%, respectively, on blotched plots. The average percent reduction on primary yield components due to the disease was highest for number of grains per m 2 (32.8%), followed by 1,000-grain weight (30.5%), number of grains per spike (24.6%), and number of spikes per m 2 (12%). Test weight was reduced 8.4%. Resistance to Cochliobolus sativus present in cultivars with resistance from Thinopyrum curvifolium or materials derived from Chinese germ plasm increased grain yield. This germ plasm may be a valuable source of genes for spot blotch resistance in T. aestivum.

Production and cytogenetics of Triticum aestivum L. hybrids with some rhizomatous Agropyron species.

SummaryIntergeneric hybrids between Triticum aestivum L. and conventional rhizomatous Agropyron species were produced in variable frequencies. They were recovered in high percentage frequencies for T. aestivum cultivars with A. acutum (14.6%), A. intermedium (48.0%), A. pulcherrimum (53.3%), and A. trichophorum (46.6%). The crossability percentages with the highly crossable cultivar ‘Chinese Spring’ for these Agropyron species accessions were 33.12%, 65.0%, 53.3%, and 65.4%, respectively. Autosyndetic associations of two of their three genomes gave mean meiotic chromosome association data of 17.0 I (univalents) +1.53 II (ring bivalents) + 7.04 II (rod bivalents) +1.43 III (trivalents) +0.05 IV (quadrivalents) +0.01 IV (pentavalents) for A. acutum and of 21.8 I + 1.56 II (rings) +7.22 II (rods) +0.84 III + 0.04 IV for A. intermedium. Chromosome pairing at metaphase I was comparatively lower for A. pulcherrimum (34.4 I + 0.2 II (rings) +3.4 II (rods) +0.14 III) and A. trichophorum (36.7 I + 0.35 II (rings) +2.26 II (rods) + 0.04 III) hybrids with T. aestivum. Hybrids of wheat with A. campestre and A. repens were obtained in low frequency. Direct crossing did not permit T. aestivum/ A. desertorum hybridization. However, by utilizing the 2n=10x=70 A. repens/A. desertorum amphiploid as the pollen source, hybridization with T. aestivum did indeed occur. Aneuploidy was prevalent in this hybrid combination while all other hybrid combinations were apparently normal.