Helminthosporium leaf blight resistance and agronomic performance of wheat genotypes across warm regions of South Asia

Helminthosporium leaf blight (HLB) is the most important disease constraint to wheat (Triticum aestivum L.) cultivation in the eastern Gangetic Plains of South Asia. A Helminthosporium Monitoring Nursery (HMN) including potential adapted and exotic sources of HLB resistance was developed in Bangladesh, India and Nepal to assess the stability of genetic resistance across locations. The 8th, 9th and 10th HMN assessed the HLB resistance and agronomic traits of 17 wheat genotypes across 20 environments of Bangladesh, India and Nepal in the 1999‐2000, 2000‐2001 and 2001‐2002 cropping seasons, respectively. The area under the disease progress curve (AUDPC) for HLB, grain yield, thousand‐kernel weight (TKW), days to heading, days to maturity, and plant height were examined. The 17 genotypes showed a range of variability for disease and agronomic characters. Disease severity (AUDPC) differed in the 3 years and showed the highest values in 2002. The increase in AUDPC in 2002 caused the lowest grain yield, with an average 18% reduction due to HLB. A few genotypes (SW 89‐5422, Yangmai‐6 and Ning 8201) appeared to have stable HLB resistance across environments. However, most of the higher‐yielding genotypes, except BL 1883, were unstable. The results suggest that careful selection of HLB resistance with acceptable grain yield, TKW and plant height may be possible using the wheat genotypes included in the HMN.     

Inheritance of insensitivity to culture filtrate of Pyrenophora tritici-repentis, race 2, in wheat (Triticum aestivum L.)

Tan spot of wheat is caused by the fungus Pyrenophora tritici‐repentis. On susceptible hosts, P. tritici‐repentis induces two phenotypically distinct symptoms, tan necrosis and chlorosis. This fungus produces several toxins that induce tan necrosis and chlorosis symptoms in susceptible cultivars. The objectives of this study were to determine the inheritance of insensitivity to necrosis‐inducing culture filtrate of P. tritici‐repentis, race 2, and to establish the relationship between the host reaction to culture filtrate and spore inoculation with respect to the necrosis component. The F₁, F₂, and BC₁F₁ plants and F_2:8 lines of five crosses involving resistant wheat genotypes ‘Erik’, ‘Red Chief’, and line 86ISMN 2137 with susceptible cultivars ‘Glenlea’ and ‘Kenyon’ were studied. Plants were spore‐inoculated at the two‐leaf stage. Four days later, the newly emerged uninoculated third leaf was infiltrated with a culture filtrate of isolate Ptr 92–164 (race 2). Reactions to the spore inoculation and the culture filtrate were recorded 8 days after spore inoculation. The segregation observed in the F₂ and BC₁F₁ generations and the F_2:8 lines of all crosses indicated that a single recessive gene controlled insensitivity to necrosis caused by culture filtrate. This gene also controlled resistance to necrosis induced by spore inoculation.     

Evidence of allelism between genes Pm8 and Pm17 and chromosomal location of powdery mildew and leaf rust resistance genes in the common wheat cultivar'Amigo'

TIBL-1RS wheat-rye translocation cultivars utilized in wheat programmes worldwide carry powdery mildew resistance gene Pm8. Cultivar‘Amigo’possesses resistance gene Pm17 on its TIAL-1RS translocated chromosome. To be able to use Pm17efficiently in breeding programmes, this gene was transferred to a TIBL-1RS translocation in line Helami-105, and allelism between Pm8 and Pm17was studied. The progenies of the hybrids in the F₂ generation and F₃ families provided evidence that the two genes are allelic. Genetic studies using monosomic analyses confirmed that in cultivar‘Amigo', Pm17 and leaf rust resistance gene Lr24 are located on a translocated chromosome involving 1 A and 1B, respectively.     

Single-gene resistance to Septoria tritici blotch in the spring wheat cultivar 'Tadinia'

Resistance to Mycosphaerella graminicola causal agent of Septoria tritici blotch, was identified in progenies of crosses with European winter wheat cultivars, Tadorna and Cleo. This resistance was used to develop the resistant spring wheat cultivar Tadinia, selected from ‘Tadorna’/‘Inia 66’ released in 1985. Evaluation of the progeny of intercrosses between ‘Tadorna’, ‘Cleo’, ‘Tadinia’, and two short-statured resistant lines derived from hybrids with ‘Tadinia’ as one parent indicate the resistance was inherited as a single gene showing partial to strong dominance. The gene in ‘Tadinia’ was designated Stb4. Crosses between another resistant cultivar, ‘Bulgaria 88’, and ‘Tadinia’ suggest that ‘Bulgaria 88’ does not have Stb4. Successful introgression of Stb4 into Rht1+Rht2 short-statured lines revealed that plant stature and resistance to M. graminicola segregated independently. The Stb4 gene has been effective since 1975 against M. graminicola extant in California. A high positive correlation between seedling and adult plant disease scores, based on scoring of lesions producing pycnidia, indicated that the Stb4 gene is expressed throughout the life cycle under both field and greenhouse conditions, confirming that disease screening can be carried out on seedling plants. Separate assessment of necrotic lesions with and without pycnidia indicated that leaf necrosis without pycnidia, observed, especially under greenhouse conditions, can confound disease evaluations and lead to inaccurate genotype classification.     

Cytogenetic studies in wheat XIX. Chromosome location and linkage studies of a gene for leaf rust resistance in the Australian cultivar 'Harrier'

Monosomic analysis indicated that a seedling leaf rust resistance gene present in the Australian wheat cultivar ‘Harrier’(tentatively designated LrH) is located on chromosome 2A. LrH segregated independently of the stripe rust resistance gene Yr1 located in the long arm of that chromosome, but failed to recombine with Lr17 located in the short arm. LrH was therefore designated Lr17b and the allele formerly known as Lr17 was redesignated as Lr17a. The genes Lr17b and Lr37 showed close repulsion linkage. Tests of allelism indicated that Lr1 7b is also present in the English wheats ‘Dwarf A’(‘Hobbit Sib’), ‘Maris Fundin’ and ‘Norman’. Virulence for Lr17b occurs in Australia, and pathogenicity studies have also demonstrated virulence in many western European isolates of the leaf rust pathogen. Despite this, it is possible that the gene may be of value in some regions if used in combination with other leaf rust resistance genes.     

Identification of resistance gene analogue markers closely linked to wheat powdery mildew resistance gene Pm31

Specific oligonucleotide primers, designed for the sequences of known plant disease resistance genes, were used to amplify resistance gene analogues (RGAs) from wheat genomic DNA. This method was applied in a bulked segregant analysis to screen for the RGA markers linked to the powdery mildew resistance gene Pm31, introgressed into common wheat from wild emmer. Two RGA markers (RGA200 and RGA390) were found to be closely linked to Pm31 and completely co‐segregating with the marker allele of Xpsp3029 linked to Pm31, with a genetic distance of 0.6 cM. These two RGA markers were then integrated into the formerly established microsatellite map of Pm31 region. The result showed the effectiveness of the RGA approach for developing molecular markers linked to disease resistance genes and demonstrated the efficiency of denaturing polyacrylamide‐gel electrophoresis for detecting polymerase chain reaction polymorphism.     

Chromosome location and microsatellite markers linked to a powdery mildew resistance gene in wheat line 'Lankao 90(6)'

Wheat lines known as 'Lankao 90(6)', derived from the cross 'Mzalenod Beer' (hexaploid triticale)/'Baofeng 7228'//'90 Xuanxi', carry a recessive powdery mildew resistance gene temporarily named PmLK906 . Gene PmLK906 appears to be different from known wheat powdery mildew resistance genes. PmLK906 was tagged using microsatellite markers in a segregating population derived from the cross 'Chinese Spring'/'Lankao 90(6)21-12'. The dominant microsatellite marker Xgwm265-2AL was linked in repulsion with PmLK906 at a genetic distance of 3.72 cM, whereas the co-dominant Xgdm93-2AL was linked to PmLK906 at a genetic distance of 6.15 cM. Both markers were placed on chromosome arm 2AL using 'Chinese Spring' nulli-tetrasomic lines. The recessive PmLK906 has a different specificity to the dominant resistance alleles located at the Pm4 locus and appeared to be located to a locus different from Pm4 .     

Microsatellite marker for yellow rust resistance gene Yr5 in wheat introgressed from spelt wheat

Yellow rust of wheat caused by Puccinia striiformis f sp. tritici has been periodically epidemic and severely damaged wheat production in China and throughout the world. Breeding for resistant cultivars has been proved to be an effective way to resolve the problem. A yellow rust resistance gene, Yr5, derived from Triticum spelta shows immunity or high resistance to the most popular isolates Tiaozhong 30 and 31 in China. Establishment of DNA markers for the Yr5 gene will facilitate marker‐assisted selection and gene pyramiding in the breeding programme. Since the Yr5 gene was cytologically located on the long arm of chromosome 2B, By33, the donor of Yr5, was crossed and backcrossed with the susceptible line 441, and BC₃F₂ and BC₃F₃ segregating populations were screened for polymorphism by using 11 microsatellite primers mapped on chromosome 2B. A marker, Xgwm501‐195 bp/160 bp, was found to be linked to Yr5, with a genetic distance of 10.5‐13.3 cM.     

Novel gene for adult plant resistance to Puccinia recondita in the wheat cultivar'Arjun'

Inheritance of resistance in the wheat cultivar‘Arjun’(HD 2009) against leaf rust pathotype 77–1 revealed that its durable resistance is attributable to a novel dominant adult plant resistance (APR) gene. Lr13, another gene reported in the cultivar played no role. This new gene is established as different from Lr34, the only effective APR gene from Triticum aestivum known for durability.     

Genetics of leaf rust resistance in three Americano landrace-derived wheat cultivars from Uruguay

A genetic analysis of the landrace‐derived wheat accessions Americano 25e, Americano 26n, and Americano 44d, from Uruguay was conducted to identify the leaf rust resistance genes present in these early wheat cultivars. The three cultivars were crossed with the leaf rust susceptible cultivar ‘Thatcher’ and approximately 80 backcross (BC1) F₂ families were derived for each cross. The BC1F₂ families and selected BC1F₄ lines were tested for seedling and adult plant leaf rust resistance with selected isolates of leaf rust, Puccinia triticina. The segregation and infection type data indicated that Americano 25e had seedling resistance genes Lr3, Lr16, an additional unidentified seedling gene, and one adult plant resistance gene that was neither Lr12 nor Lr13, and did not phenotypically resemble Lr34. Americano 26n was postulated to have genes Lr11, Lr12, Lr13, and Lr14a. Americano 44d appeared to have two possibly unique adult plant leaf rust resistance genes.     

大穗小麦多小穗基因的染色体定位

采用中国春单体系列对大穗普通小麦品系“88F2185”的多小穗性状进行了基因定位研究。结果表明，“88F2185”决定多小穗的基因位于其1B、3D和5A染色体上，其中3D染色体的效应最强。“88F2185”1B和3D染色体上的基因表现显性，而5A染色体上的基因表现隐性。此外，“88F2185”4D染色体上还存在减少小穗数目的隐性基因。据前人研究及本试验结果分析认为，“88F2185”5”的1B及4D染色体上具控制小穗数目的新基因。     

Identification of powdery-mildew-resistance genes in common wheat (Triticum aestivum L. em. Thell.). V. Old German cultivars and cultivars released in the former GDR

A total of 59 old wheat cultivars grown in Germany prior to 1960 were tested for mildew response using a collection of 12 differential isolates of Erysiphe graminis DC f. sp. tritici Marchal (Blumeria graminis (DC) Speer f. sp. tritici). Nineteen cultivars did not possess any major resistance gene and 25 were characterized by susceptible or intermediate responses. Fifteen cultivars revealed isolate-specific response patterns that could not be attributed to known major resistance genes or gene combinations. Many of the old German cultivars inherited a mildew-resistance gene from the Canadian cultivar ‘Garnet’ which is tentatively designated M1-Ga. Cultivars ‘Bretonischer Bartweizen’ (designated M1-Br) and ‘Adlungs Alemannen’ (designated M1-Ad) appeared to carry unknown resistance genes. Among 18 winter wheat cultivars released in the former GDR. eight showed susceptibility to all isolates used. Cv. “Borenos” carries resistance gene Pm3c. Five cultivars possess gene Pm4b. two cultivars gene pm5 and one cultivar a combination of genes Pm2 and Pm4b. Cultivar ‘Zentos’ was resistant to almost all isolates used. Its resistance might be conditioned by different unknown major resistance genes.     

Effectiveness and environmental stability of quantitative powdery mildew (Blumeria graminis) resistance among winter wheat cultivars

Powdery mildew in wheat (Blumeria graminis f. sp. tritici) is a major disease in Northern and Central Europe. The aim of the study was to analyse the effectiveness and environmental stability of quantitative powdery mildew resistance under high epidemic pressure in the field across years in the absence/presence of ineffective race‐specific resistances. Cultivars with and without Pm (major) genes were inoculated in three experiments with a genetically broad mildew population with all matching virulences. Resistance was measured three times by assessing the percentage of leaf area covered by powdery mildew on a plot basis (0–100%). Mean powdery mildew severity of the highly susceptible cv. ‘Kanzler’ varied across 10 years from 24% to 66% (Exp. 1). Means of three cultivars without Pm genes, ‘Ramiro’, ‘Miras’ and ‘Zentos’, and several cultivars with ineffective Pm genes varied quantitatively from 4% to 13%. Environmental stability of the quantitative resistances was on average higher than that of susceptible genotypes, as revealed by a regression approach. In the second experiment, all groups of cultivars with ineffective Pm gene(s) contained a large proportion of entries with a similar low mildew rating as the quantitatively resistant standard ‘Miras’. Mildew severity of pairs of cultivars with the same Pm gene(s) was significantly different across 6 years (Exp. 3) indicating the presence of additional quantitative resistances in some of these cultivars. In the analysis of variance, genotypic variance had a high impact (P < 0.01) with low importance of genotype × environment interaction. Consequently, heritabilites were high (0.95–0.97). In conclusion, breeders have already accumulated effective minor genes for powdery mildew resistance in many of the released German winter wheat cultivars. These quantitative resistances are long lasting, environmentally stable and provide a high level of protection to powdery mildew.     

Chromosomal location of a gene (Rkn-mnl) for resistance to the root-knot nematode transferred into wheat from Aegilops variabilis

Root-knot nematode is a significant root-parasite of common wheat. A dominant gene Rkn-mnl for resistance was transferred into wheat from Acgilops variabilis. This gene was shown to be on chromosome 3B. Further analysis indicated that it is on the long arm of this chromosome and independent of the centromere.     

Resistance to leaf rust in cultivars of bread wheat and durum wheat grown in Spain

A set of bread wheat and durum wheat cultivars adapted to Spanish conditions was tested for resistance against leaf rust caused by different pathotypes of Puccinia triticina in field trials and in growth chamber studies. Lower levels of resistance were found in durum wheat than in bread wheat. The most frequent Lr genes found in bread wheat were Lr1, Lr10, Lr13, Lr20, Lr26 and Lr28. In durum wheat, additional resistance genes that differed from the known Lr genes were identified. The level of partial resistance to leaf rust was in general low, although significant levels were identified in some bread wheat and durum wheat cultivars.     

Identification of powdery-mildew-resistance genes in common wheat (Triticum aestivum L.). VI. Wheat cultivars grown in China

A total of 26 common wheat cultivars and advanced breeding lines grown in China were tested with a set of 11 differential powdery-mildew isolates. Seven cultivars were susceptible. Another seven cultivars showed the response pattern of resistance gene Pm2, either individually or in combination with genes Pm3d or Pm4a. Five cultivars expressed the resistance of gene Pm4b singly or in combination with Pm6. Another four cultivars exhibited the response patterns of genes Pm5, Pm6 and Pm8, respectively. Three cultivars, which included one breeding line with a pair of substituted chromosomes from Haynaldia villosa, presumably carrying the resistance gene Pm21, showed resistance-response patterns to all the isolates tested.     

Breeding wheat for resistance to Heterodera avenae in Southeastern Australia

Breeding wheat for resistance to Heterodera avenae in southern Australia has been in progress for nearly 30 years and recently a number of resistant varieties have been released. Early breeding work was hampered by three factors: • a lack of appreciation of the role and extent of the problem, • inaccurate, slow screening methods, ultimately being replaced by the 'tube' test and soon by linked molecular markers, • inappropriate breeding strategies, so that varietal releases have taken place only when the breeding has been fully integrated into the main programs. The experiences in southern Australia will be relevant to many other areas in the world where H. avenae is the major pest. This revised version was published online in August 2006 with corrections to the Cover Date.     

Chromosomal location of powdery mildew resistance gene Pm16 in wheat using SSR marker analysis

The use of resistant cultivars is a most economical way to control powdery mildew (Blumeria graminis f.sp. tritici) in wheat (Triticum aestivum L.). Identification of molecular markers closely linked to resistance genes can greatly increase the efficiency of pyramiding resistance genes in wheat cultivars. The objective of this study was to identify molecular markers closely linked lo the powdery mildew resistance gene Pm16. An F₂ population with 156 progeny was produced from the cross‘Chancellor’(susceptible) ב70281’ (resistant), A total of 45 SSR markers on chromosomes 4A and 5B of wheat and 15 SSRs on chromosome 3 of rice was used lo lest the parents, as well as the resistant and susceptible bulks: the resulting polymorphic markers were used to genotype the F₂ progeny. Results indicated that the SSR marker Xgwm159, located on the short arm of chromosome 5B, is closely linked to Pm16 (genetic distance: 5.3 CM). The cytogenetical data presented in an original report, in combination with this molecular analysis, suggests that Pm16 may he located on a translocated 4A.5BS chromosome.