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Powdery mildew caused by Blumeria graminis f. sp. tritici (Bgt), is one of the serious diseases that attack wheat plants during the growing season. The Bgt virulence was screened against 16 Egyptian wheat cultivars and 21 powdery mildew differential lines carrying different (Pm) resistance genes in two regions (Kafr-Elsheikh and El-Minya) in Egypt 2021–2022. Broad-spectrum virulence and high diversity were observed at both regions. Regional populations of Bgt in Egypt are independent of each other. Genes, Pm2a, Pm3a, Pm1b, Pm3b, Pm21, Pm34, Pm36, Pm37, Pm53, PmNCA6, PmMIAG12, and PmNCAG13 were nationally effective, while Pm4a, Pm4b, Pm6, and Pm8 appeared to be defeated throughout the country affected by broad-spectrum virulence. Field responses showed that only four cultivars, Misr-1, Misr-2, Sakha-95 and Shandweel-1 were resistant in both regions. A strong correlation was recorded between FDS and AUDPC which implies that wheat pathologists and breeders may be able to assess their lines by a single scoring at an appropriate time. Phenotypic and genotypic data proved that ineffective Pm8 was present in four susceptible cultivars, Sakha-93, Sakha-94, Gemmeiza-10, and Gemmeiza-11, while it was present in combination with effective Pm3a in two resistant cultivars, Sakha-95 and Shandweel-1. This suggests that cultivar susceptibility may be attributed to the existence of ineffective gene Pm8 potentially suppressed by effective Pm3a in hexaploid-resistant wheat. Pyramiding effective resistance genes particularly those that have a suppression effect like Pm3a may be a viable option to avoid the risk of broad-spectrum Bgt virulence at a regional scale. [ABSTRACT FROM AUTHOR]

Rye (Secale cereale genome RR), a close relative of common wheat, possesses valuable resistance genes for wheat improvement. Due to the co-evolution of pathogen virulence and host resistance, some resistance genes derived from rye have lost effectiveness. Development and identification of new, effective resistance genes from rye is thus required. In the current study, wheat-rye line WR56 was produced through distant hybridization, embryo rescue culture, chromosome doubling and backcrossing. WR56 was then proved to be a wheat-rye 2RL ditelosomic addition line using GISH (genomic in situ hybridization), mc-FISH (multicolor fluorescence in situ hybridization), ND-FISH (non-denaturing FISH), mc-GISH (multicolor GISH) and rye chromosome arm-specific marker analysis. WR56 exhibited a high level of adult plant resistance to powdery mildew caused by Blumeria graminis f. sp. tritici (Bgt). This resistance was carried by the added 2RL telosomes and presumed to be different from Pm7 which is also located on chromosome arm 2RL but confers resistance at the seedling and adult stages. WR56 will be a promising bridging parent for transfer of the resistance to a more stable wheat breeding line. A newly developed 2RL-specific KASP (kompetitive allele specific PCR) marker should expedite that work.

A recessive gene PmQ conferring powdery mildew resistance was previously localized on the long arm of chromosome 2B in winter wheat landrace Qingxinmai. Breeder-friendly molecular markers are necessary for introgressing this gene into adapted wheat backgrounds for developing disease-resistant wheat cultivars. Three Kompetitive allele-specific PCR (KASP) markers were developed and validated based on SNP variants detected by Bulked segregant analysis-RNA-Seq (BSR-Seq) analysis using a recombinant inbred population derived from cross Qingxinmai × 041133. Two polymorphic SSR markers were also developed from the motifs in the Chinese Spring reference genome sequences of the target genomic region. Those markers were incorporated into a more saturated genetic linkage map for PmQ. The two flanking markers, Xicsq405 and Xicsk18, are 1.1 and 0.9 cM from PmQ, respectively. The KASP marker Xicsk19 produced unique amplification pattern in 158 out of 160 wheat cultivars or breeding lines. This marker with the gene-linked SSR markers Xicsqc, Xicsqd and Xicsq405 provides an efficient means in molecular marker-assisted selection for PmQ in wheat breeding. The corresponding genomic region of PmQ in the Chinese Spring reference genome has a conserved synteny with the genomes of sequenced wheat cultivars and Triticum durum, T. diccocoides, T. uratu, and barley. The annotation of the two genes, TraesCS2B01G517400.1 and TraesCS2B01G517700.1, associated with plant defense against pathogens placed a start for cloning PmQ. [ABSTRACT FROM AUTHOR]

SUMMARY: Cultivated wheat is continually exposed to various pathogens. Blumeria graminis f. sp. tritici (Bgt) causes powdery mildew disease and significant yield loss. Pm60 was cloned from Triticum urartu and confers race‐specific powdery mildew resistance in wheat. Pm60a and Pm60b are allelic variants of Pm60 and have two leucine‐rich repeat motifs deletions and insertions, respectively, which were detected in other T. urartu accessions. Through map‐based cloning, virus‐induced gene silencing, and stable transformation assays, we demonstrated that Pm60a and Pm60b conferred Bgt E09 resistance resembling that provided by Pm60. However, the homozygous Pm60a (but not Pm60 or Pm60b) transformants driven by the native promoters lacked race‐specific resistance when they were inoculated with Bgt E18. As all three T. urartu accessions contained the three foregoing alleles, they had high resistance to Bgt E18. Pyramiding Pm60a with either of the allelic genes in F1 plants did not cause mutual allele suppression or interference with Bgt E18 resistance. Deletion (but not insertion) of the two leucine‐rich repeat motifs in Pm60a substantially narrowed the resistance spectrum. In T. urartu accession PI428210, we identified another locus adjacent to Pm60a and resistant to Bgt E18. Characterization of the alleles at the Pm60 locus revealed their diversity and similarity and may facilitate wheat breeding for resistance to powdery mildew disease caused by B. graminis f. sp. tritici. Significance Statement: In the present study, we identified Pm60a and Pm60b, which are allelic variants at the Pm60 locus. The three foregoing alleles confer resistance to Bgt E09, which causes powdery mildew disease in wheat. Bgt E18 resistance was only absent in Pm60a transgenic plants as this allele has two leucine‐rich repeat (LRR) motif deletions. Pyramiding Pm60a with Pm60 or Pm60b did not hinder Bgt E18 resistance in wheat. Assays involving 54 Bgt isolates confirmed that deletion of the two LRR motifs in Pm60a markedly narrows the Bgt resistance spectrum. In contrast, the insertion of additional LRR motifs in Pm60b did not enhance Bgt resistance. The foregoing findings demonstrated diversity and similarity among alleles at the Pm60 locus and may support wheat breeding for powdery mildew disease resistance. [ABSTRACT FROM AUTHOR]

Wheat genotypes resistant to powdery mildew (Blumeria graminis f. sp. tritici , Bgt) provide a sustainable means for disease control. We developed a pair of near-isogenic lines H962R and H962S with contrasting reactions to powdery mildew from a residue heterozygous line. H962R was resistant to 127 out of the 136 Bgt isolates collected from the major wheat-producing regions of China and showed a similar virulence/avirulence pattern as Fuzhuang 30, Xiaobaidong, and Hongquanmang carrying resistance allele of Pm5e , but H962S was resistant to none of them. A dominant gene was responsible for the powdery mildew resistance of H962R as revealed by the genetic analysis using segregating populations derived from a cross between H962R and H962S. Molecular marker analysis detected a resistance locus, designated PmH962 , on a genetic interval of the chromosome arm 7BL where Pm5e resides. This locus was co-segregated with the functional marker of Pm5e. The PCR-based sequence alignment of Pm5e demonstrated that H962R had an identical sequence as Fuzhuang 30 (haplotype HapGA), and H962S possessed the same sequence as the powdery mildew susceptible cultivar Kenong 199. The genomic compositions of lines H962R and H962S were highly comparable as evidenced by only a small percentage of SNP variations detected by the 16K Genotyping by Target Sequencing (GBTS) SNP array and the 90K Illumina iSelect Wheat SNP array. The two lines performed similarly in the yield-related and plant growth traits investigated, except for greater kernel weight in H962R than in H962S. This indicates that Pm5e has no deleterious effect and can be served as an excellent disease resistance gene in wheat breeding. [ABSTRACT FROM AUTHOR]

Wheat genotypes resistant to powdery mildew (Blumeria graminis f. sp. tritici, Bgt) provide a sustainable means for disease control. We developed a pair of near-isogenic lines H962R and H962S with contrasting reactions to powdery mildew from a residue heterozygous line. H962R was resistant to 127 out of the 136 Bgt isolates collected from the major wheat-producing regions of China and showed a similar virulence/avirulence pattern as Fuzhuang 30, Xiaobaidong, and Hongquanmang carrying resistance allele of Pm5e, but H962S was resistant to none of them. A dominant gene was responsible for the powdery mildew resistance of H962R as revealed by the genetic analysis using segregating populations derived from a cross between H962R and H962S. Molecular marker analysis detected a resistance locus, designated PmH962, on a genetic interval of the chromosome arm 7BL where Pm5e resides. This locus was co-segregated with the functional marker of Pm5e. The PCR-based sequence alignment of Pm5e demonstrated that H962R had an identical sequence as Fuzhuang 30 (haplotype HapGA), and H962S possessed the same sequence as the powdery mildew susceptible cultivar Kenong 199. The genomic compositions of lines H962R and H962S were highly comparable as evidenced by only a small percentage of SNP variations detected by the 16K Genotyping by Target Sequencing (GBTS) SNP array and the 90K Illumina iSelect Wheat SNP array. The two lines performed similarly in the yield-related and plant growth traits investigated, except for greater kernel weight in H962R than in H962S. This indicates that Pm5e has no deleterious effect and can be served as an excellent disease resistance gene in wheat breeding.

To incorporate resistance genes of powdery mildew (Pm) and leaf rust (Lr) effectively in breeding programs allelic interaction should be explored. The response and molecular patterns of three Pm genes, Pm3, Pm8, Pm17, and three Lr genes, Lr10, Lr24, and Lr26 were investigated in 15 Egyptian wheat cultivars. Postulation of different Pm and Lr resistance genes in Egyptian wheat cultivars was carried out according to seedling phenotyping data that resulted from inoculation with a set of five pathotypes of Blumeria graminis f. sp. tritici and twelve pathotypes of Puccinia triticina. Responses and molecular patterns revealed the presence of resistance genes Pm3 and Lr10 in the cultivar Misr-1, Pm17, and Lr24 in the cultivar Giza-171, and Pm8 and Lr26 in a further ten cultivars. Molecular markers confirmed the presence of Pm8 and Lr26 in six wheat cultivars, Sakha-94, Sakha-95, Gemmeiza-10, Gemmeiza-11, Sids-13, and Shandweel-1. The presence of Pm17 in Giza-171 was confirmed by the STS marker iag95. A comparison of phenotypic and genotypic data between cultivars Giza-171 and Amigo demonstrated that Pm17 in cv Giza-171 is allelic to Pm8. The existence of Lr24 in Giza-171 was confirmed by using STS marker J09. Based on these results, Pm17 and Lr24 in Giza-171 may be located on translocated chromosomes. In cv Misr-1, the presence of Pm3 and Lr10 on the same region of 1AS chromosome could represent a rare recombination event. Field responses revealed specific resistance of Misr-1 and Giza-171, which may be attributed to the presence of Pm3 and Lr10 in Misr-1 and Pm17 and Lr24+ additional genes in Giza-171. [ABSTRACT FROM AUTHOR]

Resistance to powdery mildew is an important trait of interest in many wheat breeding programs. The information on genes conferring resistance to powdery mildew in wheat cultivars is useful in parental selection. Winter wheat breeding line DH51302 derived from Liangxing 99 and cultivar Shimai 26 derived from Jimai 22 showed identical infection patterns against 13 isolates of Blumeria graminis f. sp. tritici (Bgt) that causes wheat powdery mildew. DH51302 and Shimai 26 were crossed to a powdery mildew susceptible cultivar Zhongzuo 9504 and the F2:3 families were used in molecular localization of the resistance genes. Fourteen polymorphic markers, which were linked to Pm52 from Liangxing 99, were used to establish the genetic linkage maps for the resistance genes PmDH51302 and PmSM26 in DH51302 and Shimai 26, respectively. These genes were placed in the same genetic interval where Pm52 resides. Analysis of gene-linked molecular markers indicated that PmDH51302 and PmSM26 differed from other powdery mildew resistance genes on chromosome arm 2BL, such as Pm6, Pm33, Pm51, MlZec1, MlAB10, and Pm64. Based on the results of reaction patterns to different Bgt isolates and molecular marker localization, together with the pedigree information, DH51302 and Shimai 26 carried the same gene, Pm52, which confers their resistance to powdery mildew.

A recessive gene PmQ conferring powdery mildew resistance was previously localized on the long arm of chromosome 2B in winter wheat landrace Qingxinmai. Breeder-friendly molecular markers are necessary for introgressing this gene into adapted wheat backgrounds for developing disease-resistant wheat cultivars. Three Kompetitive allele-specific PCR (KASP) markers were developed and validated based on SNP variants detected by Bulked segregant analysis-RNA-Seq (BSR-Seq) analysis using a recombinant inbred population derived from cross Qingxinmai × 041133. Two polymorphic SSR markers were also developed from the motifs in the Chinese Spring reference genome sequences of the target genomic region. Those markers were incorporated into a more saturated genetic linkage map for PmQ. The two flanking markers, Xicsq405 and Xicsk18, are 1.1 and 0.9 cM from PmQ, respectively. The KASP marker Xicsk19 produced unique amplification pattern in 158 out of 160 wheat cultivars or breeding lines. This marker with the gene-linked SSR markers Xicsqc, Xicsqd and Xicsq405 provides an efficient means in molecular marker-assisted selection for PmQ in wheat breeding. The corresponding genomic region of PmQ in the Chinese Spring reference genome has a conserved synteny with the genomes of sequenced wheat cultivars and Triticum durum, T. diccocoides, T. uratu, and barley. The annotation of the two genes, TraesCS2B01G517400.1 and TraesCS2B01G517700.1, associated with plant defense against pathogens placed a start for cloning PmQ.

Summary: Plant nucleotide‐binding leucine‐rich repeat receptors (NLRs) act as intracellular sensors for pathogen‐derived effector proteins and trigger an immune response, frequently resulting in the hypersensitive cell death response (HR) of the infected host cell. The wheat (Triticum aestivum) NLR Pm2 confers resistance against the fungal pathogen Blumeria graminis f. sp. tritici (Bgt) if the isolate contains the specific RNase‐like effector AvrPm2. We identified and isolated seven new Pm2 alleles (Pm2e–i) in the wheat D‐genome ancestor Aegilops tauschii and two new natural AvrPm2 haplotypes from Bgt. Upon transient co‐expression in Nicotiana benthamiana, we observed a variant‐specific HR of the Pm2 variants Pm2a and Pm2i towards AvrPm2 or its homolog from the AvrPm2 effector family, BgtE‐5843, respectively. Through the introduction of naturally occurring non‐synonymous single nucleotide polymorphisms and structure‐guided mutations, we identified single amino acids in both the wheat NLR Pm2 and the fungal effector proteins AvrPm2 and BgtE‐5843 responsible for the variant‐specific HR of the Pm2 variants. Exchanging these amino acids led to a modified HR of the Pm2–AvrPm2 interaction and allowed the identification of the effector head epitope, a 20‐amino‐acid long unit of AvrPm2 involved in the HR. Swapping of the AvrPm2 head epitope to the non‐HR‐triggering AvrPm2 family member BgtE‐5846 led to gain of a HR by Pm2a. Our study presents a molecular approach to identify crucial effector surface structures involved in the HR and demonstrates that natural and induced diversity in an immune receptor and its corresponding effectors can provide the basis for understanding and modifying NLR–effector specificity. Significance Statement: We have identified seven new alleles of the wheat nucleotide‐binding leucine‐rich repeat immune receptor (NLR) Pm2 and analyzed the molecular determinants defining the specificity towards the corresponding fungal effector proteins from wheat powdery mildew. Our study presents a molecular approach to identify crucial effector surface structures involved in immune responses and demonstrates that natural and induced diversity in an immune receptor and its corresponding effectors can provide the basis for understanding and modifying NLR–effector specificity. [ABSTRACT FROM AUTHOR]

Summary: Pm1a, the first powdery mildew resistance gene described in wheat, is part of a complex resistance (R) gene cluster located in a distal region of chromosome 7AL that has suppressed genetic recombination.A nucleotide‐binding, leucine‐rich repeat (NLR) immune receptor gene was isolated using mutagenesis and R gene enrichment sequencing (MutRenSeq). Stable transformation confirmed Pm1a identity which induced a strong resistance phenotype in transgenic plants upon challenge with avirulent Blumeria graminis (wheat powdery mildew) pathogens.A high‐density genetic map of a B. graminis family segregating for Pm1a avirulence combined with pathogen genome resequencing and RNA sequencing (RNAseq) identified AvrPm1a effector gene candidates. In planta expression identified an effector, with an N terminal Y/FxC motif, that induced a strong hypersensitive response when co‐expressed with Pm1a in Nicotiana benthamiana.Single chromosome enrichment sequencing (ChromSeq) and assembly of chromosome 7A suggested that suppressed recombination around the Pm1a region was due to a rearrangement involving chromosomes 7A, 7B and 7D. The cloning of Pm1a and its identification in a highly rearranged region of chromosome 7A provides insight into the role of chromosomal rearrangements in the evolution of this complex resistance cluster. [ABSTRACT FROM AUTHOR]

Summary: Powdery mildew poses severe threats to wheat production. The most sustainable way to control this disease is through planting resistant cultivars.We report the map‐based cloning of the powdery mildew resistance allele Pm5e from a Chinese wheat landrace. We applied a two‐step bulked segregant RNA sequencing (BSR‐Seq) approach in developing tightly linked or co‐segregating markers to Pm5e. The first BSR‐Seq used phenotypically contrasting bulks of recombinant inbred lines (RILs) to identify Pm5e‐linked markers. The second BSR‐Seq utilized bulks of genetic recombinants screened from a fine‐mapping population to precisely quantify the associated genomic variation in the mapping interval, and identified the Pm5e candidate genes.The function of Pm5e was validated by transgenic assay, loss‐of‐function mutants and haplotype association analysis. Pm5e encodes a nucleotide‐binding domain leucine‐rich‐repeat‐containing (NLR) protein. A rare nonsynonymous single nucleotide variant (SNV) within the C‐terminal leucine rich repeat (LRR) domain is responsible for the gain of powdery mildew resistance function of Pm5e, an allele endemic to wheat landraces of Shaanxi province of China.Results from this study demonstrate the value of landraces in discovering useful genes for modern wheat breeding. The key SNV associated with powdery mildew resistance will be useful for marker‐assisted selection of Pm5e in wheat breeding programs. [ABSTRACT FROM AUTHOR]

The increasing severity and prevalence of powdery mildew aided by extensive use of semi-dwarf cultivars and high levels of nitrogenous fertilizers are causing significant yield losses in wheat. Resistant cultivars are the most cost-effective and environmentally friendly approach to manage the disease. The objective of this study was to identify quantitative trait loci (QTL) for powdery mildew resistance in a doubled haploid (DH) population from a cross between leading Chinese cultivars, Yangmai 16 and Zhongmai 895. A high-density genetic map comprising of 14,480 non-redundant markers (equal to 148,179 SNPs) in 21 wheat chromosomes was constructed by genotyping the population with the Wheat 660 K SNP array. The DH population was phenotyped for powdery mildew resistance at the adult plant stage in multiple field trials, including four environments in the 2016–2017 cropping season and two environments in 2017–2018. Composite interval mapping detected six stable QTL explaining 3.8–23.6% of the phenotypic variance across environments. QPmyz.caas-5DS, QPmyz.caas-6BL and QPmyz.caas-7BS, are probably new QTL for powdery mildew resistance. One SNP marker closely linked to QPmyz.caas-6BL, the most stable QTL, was converted into a Kompetitive Allele-Specific PCR marker (K_AX-94973433) and validated on 103 commercial wheat cultivars. Significantly lower maximum disease severities of cultivars with the resistance-associated allele than those with the susceptibility-associated allele at QPmyz.caas-6BL in some environments indicated partial effectiveness of the marker. The novel QTL and their closely linked markers identified in the present study should facilitate development of cultivars with improved powdery mildew resistance. [ABSTRACT FROM AUTHOR]

Main conclusion : A novel broad-spectrum powdery mildew resistance gene PmPB74 was identified in wheat- Agropyron cristatum introgression line Pubing 74. Development of wheat cultivars with broad-spectrum, durable resistance to powdery mildew has been restricted by lack of superior genetic resources. In this study, a wheat- A. cristatum introgression line Pubing 74, originally selected from a wide cross between the common wheat cultivar Fukuhokomugi (Fukuho) and Agropyron cristatum (L.) Gaertn (2 n = 4 x = 28; genome PPPP), displayed resistance to powdery mildew at both the seedling and adult stages. The putative alien chromosomal fragment in Pubing 74 was below the detection limit of genomic in situ hybridization (GISH), but evidence for other non-GISH-detectable introgressions was provided by the presence of three STS markers specific to A. cristatum. Genetic analysis indicated that Pubing 74 carried a single dominant gene for powdery mildew resistance, temporarily designated PmPB74. Molecular mapping showed that PmPB74 was located on wheat chromosome arm 5DS, and flanked by markers Xcfd81 and HRM02 at genetic distances of 2.5 and 1.7 cM, respectively. Compared with other lines with powdery mildew resistance gene(s) on wheat chromosome arm 5DS, Pubing 74 was resistant to all 28 Blumeria graminis f. sp tritici ( Bgt) isolates from different wheat-producing regions of northern China. Allelism tests indicated that PmPB74 was not allelic to PmPB3558 or Pm2. Our work showed that PmPB74 is a novel gene with broad resistance to powdery mildew, and hence will be helpful in broadening the genetic basis of powdery mildew resistance in wheat. [ABSTRACT FROM AUTHOR]

Powdery mildew caused by Blumeria graminis f.sp. tritici , an obligate aerial biotrophic fungus, would be one of the most damaging wheat ( Triticum aestivum ) diseases without the extensive use of conventional fungicides. In our study, the expression levels of some basal defence-related genes were investigated during a compatible interaction in order to evaluate wheat reactions to infection, along with the different stages of the infectious process in planta. As fungal conidia initiated their germination and developed appressorial germ tube (AGT), early defence reactions involved the expression of a lipoxygenase (LOX)- and an oxalate oxidase (OXO)-encoding genes, followed by activations of corresponding LOX (EC 1.13.11.12) and OXO (EC 1.2.3.4) activities, respectively. When penetration of AGT took place, up-regulation of chitinases (CHI) and PR1-encoding genes expression occurred along with an increase of CHI (EC 3.2.1.14) activity. Meanwhile, expression of a phenylalanine ammonia-lyase-encoding gene also took place. Up-regulation of a phospholipase C- and lipid transfer proteins-encoding genes expression occurred during the latest stages of infection. Neither the phi glutathione S-transferase (GST)-encoding gene expression nor the GST (EC 2.5.1.13) activity was modified upon wheat infection by powdery mildew. Whether these defence reactions during such a compatible interaction are markers of immunity or susceptibility, and whether they have the ability to contribute to protection upon modulation of their timing and their intensity by resistance inducers are discussed. [ABSTRACT FROM AUTHOR]

The development of high-yielding varieties with broad-spectrum durable disease resistance is the ultimate goal of crop breeding. In plants, immune receptors of the nucleotide-binding-leucine-rich repeat (NB-LRR) class mediate race-specific resistance against pathogen attack. When employed in agriculture this type of resistance is often rapidly overcome by newly adapted pathogen races. The stacking of different resistance genes or alleles in F1 hybrids or in pyramided lines is a promising strategy for achieving more durable resistance. Here, we identify a molecular mechanism which can negatively interfere with the allele-pyramiding approach. We show that pairwise combinations of different alleles of the powdery mildew resistance gene Pm3 in F1 hybrids and stacked transgenic wheat lines can result in suppression of Pm3-based resistance. This effect is independent of the genetic background and solely dependent on the Pm3 alleles. Suppression occurs at the post-translational level, as levels of RNA and protein in the suppressed alleles are unaffected. Using a transient expression system in Nicotiana benthamiana, the LRR domain was identified as the domain conferring suppression. The results of this study suggest that the expression of closely related NB-LRR resistance genes or alleles in the same genotype can lead to dominant-negative interactions. These findings provide a molecular explanation for the frequently observed ineffectiveness of resistance genes introduced from the secondary gene pool into polyploid crop species and mark an important step in overcoming this limitation. [ABSTRACT FROM AUTHOR]

Wheat powdery mildew is controlled mainly by race-specific resistance. To be effective, breeding wheat for resistance to powdery mildew requires knowledge of virulence diversity in local populations of the pathogen. Isolates of Blumeria graminis, collected in 2009 and 2010 from three areas of Iranian production, were analysed for virulence using a host differential series comprised of 16 known genes conferring resistance to powdery mildew. The results showed that high-virulence frequencies to genes Pm1, Pm2, Pm4a, Pm5, Pm6, Pm7, Pm8 and Pm9 were found over both years and across all three areas. Virulence frequencies for Pm3a and Pm3b were intermediate, while virulence frequencies for Pm3a, Pm3c, Pm4a and Pm2, 6 were low. Genes Pm1, 2, 9 and Pm2, 4b, 8 were highly resistant in all regions. Virulence to Pm8 increased to high levels, while virulence to Pm4a decreased across the area surveyed from 2009 to 2010. [ABSTRACT FROM PUBLISHER]

With 4 tables Powdery mildew, caused by Blumeria graminis f. sp. tritici, is an important bread wheat ( Triticum aestivum L.) disease that is favoured by the temperate Scandinavian climate. A total of 38 lines, comprising the current spring and winter wheat cultivars in Norway, various breeding lines and introduced sources of partial resistance were evaluated for race-specific resistance at the seedling stage. Various resistance genes were postulated from the reaction patterns of lines with known genes tested against 20 differential isolates in detached leaf assays. Detection of the Pm8 gene and alleles at the Pm3 locus were further aided by specific PCR primers. The most frequently present resistance genes were Pm8, followed by Pm5a, Pm3d, Pm3f, Pm3b and Pm2. Several lines were susceptible to all isolates at the seedling stage, but were known to possess high levels of partial resistance in the field; these included the German spring wheats ‘Naxos’ and ‘Paros’ and the Swedish winter wheats ‘Folke’ and ‘Mjølner’. These lines represent highly valuable sources of partial and potentially durable resistance to powdery mildew. [ABSTRACT FROM AUTHOR]

Powdery mildew ( Blumeria graminis f. sp. tritici) is one of the major diseases of wheat ( Triticum aestivum). Adult plant resistance (APR) to powdery mildew is considered more durable than resistance conferred by major race-specific resistance genes. The objective of the present study was a better understanding of the genetic basis of APR in RE714 by means of QTL analysis of several resistance scores along the growing season. A population of 160 recombinant inbred lines obtained from the cross between RE714 and Hardi (susceptible) was assessed for APR under natural infection conditions during 3 years and a genetic map with whole genome coverage was developed with microsatellite and AFLP markers in this population. Two major QTL on chromosomes 5D and 6A were detected each year, and 6 minor QTL were detected only in 1 or 2 years. The QTL on chromosome 5D was detected during all the growing season each year and its R2 value varied between 8.5 and 56.3%, whereas the QTL on chromosome 6A was detected at 1–4 scoring dates in the 3 years, and its R2 value varied between 6.1 and 20.5%. The two QTL explained between 24.4 and 52.1% of the phenotypic variance for AUDPC, depending on the year. The models including QTL and cofactors in the composite interval mapping explained between 29 and 72% of the variance. The molecular markers linked to the two major QTL could be used in marker-assisted selection for adult plant resistance to powdery mildew. [ABSTRACT FROM AUTHOR]

Little is known about the population structure of wheat powdery mildew in the eastern United States, and the most recent report on virulence in this population involved isolates collected in 1993-94. In the present study, wheat leaves naturally infected with powdery mildew were collected from 10 locations in the southeastern United States in 2003 and 2005 and a collection of 207 isolates was derived from single ascospores. Frequencies of virulence to 16 mildew resistance (Pm) genes were determined by inoculating the isolates individually on replicated plates of detached leaves of differential wheat lines. These virulence frequencies were used to infer local effectiveness of Pm genes, estimate virulence complexity, detect significant associations between pairs of pathogen avirulence loci, and assess whether phenotypic differences between pathogen subpopulations increased with geographic distance. In both years, virulence to Pm3a, Pm3c, Pm5a, and Pm7 was present in more than 90% of sampled isolates and virulence to Pmla, Pm16, Pm17, and Pm25 was present in fewer than 10% of isolates. In each year, 71 to 88% of all sampled isolates possessed one of a few multilocus virulence phenotypes, although there were significant differences among locations in frequencies of virulence to individual Pm genes: Several significant associations were detected between alleles for avirulence to pairs of Pm genes. Genetic (phenotypic) distance between isolate subpopulations increased significantly (R² = 0.40, P < 0.001) with increasing geographic separation; possible explanations include different commercial deployment of Pm genes and restricted gene flow in the pathogen population. [ABSTRACT FROM AUTHOR]

Powdery mildew, caused by Blumeria graminis f. sp. tritici (syn. Erysiphe graminis f. sp. tritici), is one of the most important diseases of common wheat (Triticum aestivum L.) worldwide. Molecular mapping and cloning of genes for resistance to powdery mildew in hexaploid wheat will facilitate the study of molecular mechanisms underlying resistance to powdery mildew diseases and help understand the structure and function of powdery mildew resistance genes, and permit marker-assisted selection in breeding programs. So far, 48 genes/alleles for resistance to powdery mildew at 32 loci have been identified and located on 16 different chromosomes, of which 21 resistance genes/alleles have been tagged by restriction fragment length polymorphisms (RFLPs), random-amplified polymorphic DNAs (RAPDs), amplified fragment length polymorphisms (AFLPs), sequence characterized amplified regions (SCARs), sequence-tagged sites (STS) or simple sequence repeats (SSRs). Several quantitative trait loci (QTLs) for adult plant resistance (APR) to powdery mildew have been associated with molecular markers. The detailed information on chromosomal location and molecular mapping of these genes has been reviewed. Isolation of powdery mildew resistance genes and development of valid molecular markers for pyramiding resistance genes in breeding programs is also discussed. [ABSTRACT FROM AUTHOR]

Despite the large impact of powdery mildew in wheat cultivated areas, little has been done to study powdery mildew resistance by QTL analysis up to now. The objective of the present paper is to present how the genetic basis of powdery mildew resistance in the resistant wheat line RE714 have been studied by QTL analysis at the adult plant stage over the course of 3 years, and at the vernalized seedling plant stage, and a comparison between the results obtained. Two segregating populations (DH and F2:3) were derived from the cross between the resistant line (RE714), and a susceptible line (Hardi); these were analysed for powdery mildew resistance at the adult plant stage in the field under natural infection conditions in 1996, 1997 and 1998. The DH population was also tested for powdery mildew resistance at the vernalized seedling stage with four different isolates of powdery mildew. At the adult plant stage, a total of three QTLs (on chromosomes 5D, 4A and 6A) and five QTLs (on chromosomes 5D, 6A, 7A and 7B) were found for the DH and F2:3 populations, respectively. The genetic control of resistance was found to be polygenic but involved a major QTL (on chromosome 5D), which was detected each year and which explained a high proportion of the variability observed (28.1%–37.9%). At the vernalized seedling stage, two QTLs were found (on chromosomes 5D and 7B) and the QTL detected on chromosome 5D was common to the four isolates tested. The comparison between the two development stages showed that the QTL on chromosome 5D was detected in all the different environments tested and again explained a high proportion of the variability. Different molecular interpretations of this QTL have also been discussed. [ABSTRACT FROM AUTHOR]

Field trials in two cropping seasons and two locations in central China were conducted on 60 Chinese autumn-sown wheat varieties to assess their partial resistance to powdery mildew. Mean levels of disease severity ranged from close to 0 to more than 90%. The method of inoculation and the location in which trials were conducted affected the relative performance of the varieties, but these effects were much smaller than the main effect of variety. The area under the disease progress curve was highly correlated with final disease severity, but both were poorly correlated with apparent infection rate. Disease severity was regressed against frequencies of virulence in the Blumeria graminis (syn. Erysiphe graminis) f. sp. tritici populations in the trial plots. A vertical distance (D) from the mean mildew severity to the fitted line was calculated for each variety and was used to quantify partial resistance. Five of the 60 varieties, ‘Hx8541’, ‘E28547’, ‘Chuan1066’, ‘Zhe88pin6’ and ‘Lin5064’, consistently expressed relatively low levels of disease despite high frequencies of virulence in the pathogen and had consistently high D-values. They may therefore have good levels of partial resistance. [ABSTRACT FROM AUTHOR]

Powdery mildew (Blumeria graminis f. sp. tritici) is one of the most damaging diseases of wheat (Triticum aestivum). The objective of this study was to locate and map a recently identified powdery mildew resistance gene, MlRE, carried by the resistant line RE714 using microsatellites uniformly distributed among the whole genome together with a bulked segregant analysis (BSA). The bulks consisted of individuals with an extreme phenotype taken from a population of 140 F3 families issued from the cross between RE714 (resistant) and Hardi (susceptible). The population had been tested with three powdery mildew isolates at the seedling stage. Qualitative interpretation of the resistance tests located the MlRE gene on the distal part of the long arm of chromosome 6A. A subsequent quantitative interpretation of the resistance permitted us to detect another resistance factor on a linkage group assigned to chromosome 5D, which was constructed with microsatellites for which a polymorphism of intensity between bulks was observed. This quantitative trait locus (QTL) explained 16.8– 25.34% of the total variation. An interaction between both the resistant factor (MlRE and the QTL) was found for only one of the isolates tested. This study shows the advantage of making a quantitative interpretation of resistant tests and that the use of microsatellites combined with BSA is a powerful strategy to locate resistance genes in wheat. [ABSTRACT FROM AUTHOR]