Aphid acceptance of Hordeum genotypes is affected by plant volatile exposure and is correlated with aphid growth

Nineteen genotypes of Hordeum vulgare (L.) were screened and characterized as partially resistant or susceptible regarding growth of the bird cherry—oat aphid (Rhopalosiphum padi L.). In a separate test, these same genotypes were treated with volatiles from undamaged plants of barley cultivar Alva. As a result of this treatment, aphid host acceptance (AHA) was significantly affected in seven genotypes, and the magnitude of the effect was positively correlated with aphid growth (AG) in the independent resistance screening test. Changes in AHA induced by volatiles from the same genotype as the volatile receiver were also positively correlated with AG. All the 19 genotypes were also tested as inducers with cultivar Kara as the receiver of volatiles. Five genotypes induced significant reductions in AHA of Kara. The results show that aphids are able to detect changes in responding plants induced by volatiles from another plant. Plant volatile interactions may thus be a component of induced resistance to aphids. These interactions could influence the results of experiments used to select for insect-resistant plants in plant breeding programmes, where normally plant genotypes are mixed at testing.     

The Yd2 gene and enhanced resistance to barley yellow dwarf virus (BYDV) in winter barley

A breeding programme was developed to obtain barley yellow dwarf virus (BYDV)-resistant winter genotypes using the Yd2 gene. The aim was to incorporate the Yd2 allele into the new high-yielding genotypes to release cultivars that allow barley cultivation in areas where BYDV is endemic. The resistant lines were developed using pedigree selection. An ICARDA resistant line (83RCBB130) carrying the Yd2 gene was crossed with three susceptible, high-yielding winter varieties and their F₁ lines were either selfed or backcrossed to the matching susceptible parent. The best lines selected from subsequent selfing generations were evaluated in replicated trials in the presence or absence of BYDV, starting from F₆ and BC₁F₅ to F₈ and BC₁F₇ generations. Four genotypes with superior agronomic traits and BYDV resistance were selected.     

Marker assisted backcross breeding approach to improve blast resistance in Indian rice (Oryza sativa) variety ADT43

Marker assisted backcrossing breeding has become one of the essential tools in transferring novel genes to adapted varieties and was employed to pyramid three blast resistance genes Pi1, Pi2 and Pi33 to a popular susceptible rice variety ADT43. Gene pyramiding process was facilitated by marker aided selection for both foreground as well as background genotype. Previously reported linked molecular markers were deployed to survey resistant and susceptible genotypes. In the BC₃F₁ generation four lines viz, AC-B3-11-7, AC-B3-11-36, AC-B3-11-57, AC-B3-11-83 were identified to be pyramided with three genes and subjected to background analysis and a genome recovery up to 95 % was observed and advanced to further generations. Morphological, yield and grain quality traits were significantly similar to ADT43. The introgressed lines with three gene combinations were highly resistant to the blast pathogen compared to genotypes with single genes and the susceptible checks under blast nursery screening at two epiphytotic locations; Coimbatore and Gudalur. The selected three gene pyramided backcross lines in the desirable background were advanced to obtain an improved ADT 43 with resistance to blast disease.     

Genetic control of resistance to the aphid Brevicoryne brassicae in the wild species Brassica fruticulosa

Initial studies have shown variable resistance in Brassica fruticulosa to the aphid Brevicoryne brassicae The aim of this work was to fix high levels of resistance to B. brassicae in true breeding lines of B. fruticulosa and obtain data on the genetic control of resistance. Plants from initially variable B. fruticulosa accessions were selfed to produce inbred resistant and susceptible lines that were studied in three separate experiments to determine the extent to which resistance to B. brassicae had been fixed. Results from three experiments using successive generations of resistant and susceptible inbred lines showed that continued selection resulted in resistant inbred lines that supported an average of three aphids per plant compared with an average of 96 aphids per plant for susceptible inbred lines. Data collected from an experiment determining the resistant phenotype of lines including the selfed progenies and the F₁ and F₂ progeny of a cross between resistant and susceptible individual plants indicated that the resistance was not controlled by a single gene.     

大麦BYDV抗性的印迹杂交分析

大麦抗黄矮病毒 (BYDV)育种面临的主要困难之一 ,就是常规生物学抗性检测技术不能准确地进行抗性检测和抗性基因筛选。本文在前人的基础上 ,以大麦黄矮病毒 PAV株系和 RPV株系基因组中的特异核酸序列为探针 ,应用斑点印迹杂交分析技术 ,建立了一套简单、快速、有效的 BYDV抗性检测方法和抗性基因 (Yd2 )的筛选方法 ;同时也建立了一套适用于大麦 BYDV抗性检测的较为有效的带毒蚜虫饲养和管理方法。选用了 12个已知抗性和基因型的大麦品种 (系 )进行抗性检测 ,结果证实了这一抗性检测技术体系的可靠性与有效性。     

Assessment of genomic diversity of wild and cultivated tomato through Resistance Gene Analogue Polymorphism and I2 homologues

Plant disease resistance gene analogue polymorphism (RGAP) in tomato has been studied on the basis of NBS–LRR (Nucleotide Binding Site–Leucine Rich Repeat) class of genes using degenerated primers. Results revealed variable degree of polymorphism of the Group II compared to the Group I class of R genes. The probable explanation could be further diversification of the Group II class within tomato genotypes compared to the Group I class, which is relatively conserved. Furthermore, investigation of the diversity of the I2 class of genes, responsible for resistance to Fusarium oxysporum f.sp. lycopersici, revealed that genomic PCR mediated identification of functional I2 using the specific primers designed from the conserved domain of LRR region of I2 class of genes, is not possible on the basis of amplified fragment size. On the contrary, PCR amplification of 249 bp fragment from the conserved LRR region of I2 homologue I2C1/C2 gene from all the resistant lines indicated co-segregation of I2C1/C2 to the susceptible background along with the I2 gene during introgression. This may be an indirect PCR-mediated approach for marker-assisted breeding of functional allele of I2.     

Identification of RAPD markers closely linked to the mlo-locus in barley

Developing resistance to powdery mildew, Erysiphe graminis f.sp. hordei, is a major goal of many barley breeding programmes. Several resistance genes have been tagged or mapped with molecular markers. The mlo gene confers durable resistance towards all known isolates of the pathogen. In this study, RAPD markers and bulked segregant analysis were used to determine PCR-based markers linked to the mlo-locus. Sixty doubled haploid lines from a cross between an isogenic line of ‘Ingrid’ carrying the mlo11 allele and a susceptible cv. ‘Pokko’ were used as plant material. Seven linked RAPD markers were found, the closest lying 1.6 cM away from the resistance gene. When eight barley varieties were assayed for the presence of this band, F4-980, it was found in the resistant varieties but not in the susceptible ones. The linked marker bands could be amplified from DNA-samples prepared by using three different methods, including a quick squash technique. PCR-based markers linked to the resistance gene can be used as tools for selection in breeding programmes.     

Field screening of simulated segregating barley populations for resistance to scald

Summary Simulated segregating barley populations were screened for resistance to scald (Rhynchosporium secalis) in the field at commercial seeding rates. A reduction in infection on the susceptible component occurred with increasing proportions of resistant genotypes. Similar trends were seen in space planted experiments but the use of susceptible buffer rows counteracted the effect, enhanced the infection in susceptible plants and greatly improved discrimination between resistant and susceptible. These results have been applied to the routine testing of F₂ populations in the barley breeding programme.     

Potential use of doubled haploid lines for the screening of resistance to yellow rust (Puccinia striiformis) in hexaploid wheat

Doubled haploid lines derived from anther culture of two Iranian spring wheat genotypes‘Ghods’susceptible and‘9106’resistant to yellow rust in Iranian field conditions, and their F₁ hybrids were used in this study. Seedlings of 36 doubled haploid lines, selected out of 96 according to their agronomic traits and the two parental genotypes were inoculated with eight races of yellow rust. The parental genotypes (‘Ghods’and‘9106’) were segregating for some of the races but their doubled haploid lines were either resistant or susceptible to them.‘Ghods’was susceptible to three of the races studied but three doubled haploid lines derived from it were resistant to them. Five selected doubled haploids from the‘9106’genotype and six from F₁ hybrid plants were resistant to all eight races tested. After further investigations in Iranian field conditions it was found that some of these lines can be used as donor genotypes for resistance to yellow rust in wheat breeding programmes. Use of these genotypes should be possible if the French yellow rust races used for selection also represent the dominant races in Iran. It can be concluded that anther culture provides an efficient method for fixing genes of resistance to yellow rust and desirable doubled haploids from F₁ plants can be derived.     

Effect of the Russian Wheat Aphid on the Composition and Synthesis of Water Soluble Proteins in Resistant and Susceptible Wheat

The effect of Russian wheat aphid ( Diuraphis noxia) infestation on polypeptide composition and protein synthesis in the presence or absence of chloramphenicol and cycloheximide were studied in genetically comparable wheat ( Triticum aestvum) resistant (cv. PI 137739/5* Tugela) and susceptible (cv. Tugela) to the aphid. The aim is to gain information of molecular nature on the resistance phenomenon which may promote future breeding programmes. In the absence of feeding aphids polypeptide profiles of the two wheat lines were similar indicating the absence or presence at low levels of a constitutive resistance factor. Aphid infestation induced enhanced expression of certain genes in the resistant wheat only. A 100 kD nuclear encoded polypeptide is strongly induced in the resistant wheat. It is also evident that the synthesis of a 56 kD organel encoded polypeptide is suppressed by the feeding aphids in the susceptible wheat.     

Molecular markers for the identification of resistance genes and marker-assisted selection in breeding wheat for leaf rust resistance

The resistance genes Lr9, Lr24, Lr25, Lr29, Lr35 and Lr37, which were not previously utilised in Hungary, have been incorporated into four Martonvásár winter wheat cultivars using marker-assisted selection with PCR-based markers. In the course of a backcross programme, the genes were transferred into Martonvásár wheat varieties and various BC generations were produced. Work aimed at pyramiding resistance genes is currently underway in Martonvásár, and plants containing the gene combinations Lr9 + Lr24, Lr9 + Lr25 and Lr9 + Lr29 are now available. From the BC₂F₄ generation of the ‘Mv Emma’*3/’R.L.6010’ combination (‘R.L.6010’ is the donor of the Lr9 gene) 287 lines were tested for leaf rust resistance in an artificially inoculated nursery. A co-dominant primer combination was designed to identify both resistant and susceptible offsprings. The results of resistance tests and molecular marker detection agreed in most cases. Designated leaf rust resistance genes were identified with molecular markers in wheat varieties and breeding lines. The Lr26 and Lr34 resistance genes occur frequently in the Martonvásár gene pool, and the presence of the Lr37 gene has also been detected in a number of Hungarian genotypes.     

油菜抗咪唑啉酮类除草剂基因BnALS1R等位基因特异PCR标记的开发与应用

油菜抗咪唑啉酮类除草剂基因BnALS1R是从抗性突变体M9中克隆获得,抗性基因BnALS1R与野生型基因BnALS1存在1处SNP,即乙酰乳酸合酶第638位丝氨酸残基被天冬酰胺酸替代。为获得油菜抗除草剂基因BnALS1R的分子标记,根据该处点突变,结合获得的BnALS3与BnALS1序列,开发30条等位基因特异PCR (allele-specific PCR,AS-PCR)引物,采用筛选出的3条AS-PCR引物在F₂、BC₁和BC₂群体中进行PCR扩增。结果表明,该标记有效检测出群体中存在的3种基因型,其分离比分别为1∶2∶1、1∶1、1∶1,均遵循单基因遗传规律。应用该标记对获得的抗性恢复系进行PCR扩增,结果发现所有抗性恢复系均能扩增出抗性基因BnALS1R目的条带,表明3条标记引物可应用于抗性基因的检测。AS-PCR标记的获得将促进以抗性基因进行油菜抗除草剂分子标记辅助选择育种。     

Identification of dominant and recessive genes for resistance to Fusarium wilt in pigeonpea and their implication in breeding hybrids

Fusarium wilt is an important disease of pigeonpea [Cajanus cajan (L.) Millsp.] and it can cause severe yield losses. Chemical control of this disease is difficult and expensive; therefore, cultivation of resistant varieties/hybrids is the most efficient strategy for enhancing the production. In the present study, by using a wilt susceptible cytoplasmic-nuclear male-sterile line and four wilt resistant fertility restorers, one dominant and one recessive gene with dominant suppressive epistatic effects were found responsible for controlling resistance to Fusarium wilt. Considering the annual losses and wide spread nature of wilt diseases in pigeonpea, it is imperative that all the inbred and hybrid cultivars have high level of resistance to this disease. The presence of dominant gene for resistance will increase the efficiency of breeding wilt resistant cultivars because it will yield greater proportion of resistant genotypes in segregating generations. In hybrid breeding also, the presence of dominant gene for wilt resistance will be an advantage. The transfer of this gene in female hybrid parents will ease the breeding of wilt resistant hybrids because this will allow the use of both wilt resistant as well as susceptible restorers in generating wilt resistant hybrid combinations.     

Resistance to Rhopalosiphum padi (Homoptera: Aphididae) in Hordeum vulgare subsp. spontaneum and in hybrids with H. vulgare subsp. vulgare

Summary Accessions of Hordeum vulgare subsp. spontaneum, the progenitor of cultivated barley, were screened in field and glasshouse trials for resistance to the aphid Rhopalosiphum padi. A few selected lines were furthermore hybridized with a modern barley variety and the resulting populations evaluated. High levels of resistance were found among some of the spontaneum accessions resulting in lower aphid growth rates (maximum reduction 57%). Segregation patterns among siblings in F2 populations were continuous, indicating the presence of several genes with possibly additive effects. The usefulness of H. vulgare subsp. spontaneum for breeding aphid resistant barley is discussed.     

Histological and inheritance studies of partial resistance in the Brassica napus–Albugo candida host-pathogen interaction

Traditional and doubled haploid (DH) genotypes of oilseed Brassica spp. resistant, partially resistant, moderately susceptible, and susceptible to Albugo candida were compared for phenotypic development of host‐pathogen interaction and histology of host‐pathogen interaction. The partially resistant genotype showed pinhead‐size pustules, mainly on the upper surface of cotyledonary leaves. Relatively less mycelium was observed in the partially resistant genotype compared with the susceptible genotype. In resistant B. napus genotypes, there was neither pustule development nor any mycelial growth. In the moderately susceptible genotype, the pustules were similar to those in the partially resistant genotype in being of pinhead‐size and occasionally coalescing. However, ample mycelial growth in the mesophyll tissue in the moderately susceptible genotype was similar to that in the susceptible control B. rapa cv. ‘Torch’. The susceptible genotype B. rapa cv. ‘Torch’ also showed large coalescing pustules. In the non‐host B. juncea cv. ‘Commercial Brown’, no pustules were formed although some mycelial growth was observed beneath the epidermal cell layer and in the mesophyll cell layer of the cotyledonary leaf tissue. For inheritance studies, two partially resistant B. napus genotypes were crossed with a resistant B. napus genotype. Various generations viz., F1, F1(reciprocal), F₂, and DHs produced from the crosses were inoculated with a zoospore suspension of race 7v of A. candida. The partially resistant phenotype appeared to be controlled by a single recessive gene designated as wpr with variable expression. The simple inheritance of partial resistance has implications for disease resistance breeding against white rust, as this type of resistance can be easily incorporated into elite breeding lines through conventional and DH breeding methods.     

Inheritance of resistance to Fusarium wilt in Indian lentil germplasm (Lens culinaris Medik.)

Summary Three lentil genotypes resistant to Fusarium oxysporum f.sp. lentis viz. Pant L 234, JL 446 and LP 286 were crossed with two susceptible ones. The hybrid plants were all resistant in the eight crosses evaluated. Segregation pattern for wilt reaction in F₂, BC(P₁), BC(P₂) and F₃ generations in field and glasshouse conditions indicated that resistance to Fusarium wilt is under the control of two dominant duplicate genes in Pant L 234 and two independent dominant genes with complementary effects in JL 446 and LP 286. A third dominant gene complementary to the dominant genes in JL 446 and LP 286 is present in two susceptible lines. Allelic tests suggest the presence of five independently segregating genes for resistance. Duplicate dominant genes in Pant L 234 are non-allelic to two dominant genes with complementary effects in LP 286 and JL 446 and the third gene complementary to the two genes in JL 446 and LP 286 in susceptible lines JL 641 and L 9–12. Gene symbols among parental genotypes have been designated.     

Characterization of resistance genes against scald (Rhynchosporium secalis (Oudem.) J.J. Davis) in barley (Hordeum vulgare L.) lines from central Norway, by means of genetic markers and pathotype tests

Rhynchosporium secalis is a serious pathogen of barley (Hordeum vulgare L.) in central Norway. A breeding effort was initiated in 1977 to introduce resistance from different sources into adapted genotypes, and the first cultivar from the program was recently released. However, little is known about the resistance genes introgressed in this cultivar or in advanced breeding lines. An effort was made to address this issue through a set of isolates and available molecular markers. Fourteen breeding lines and their resistance donors were investigated by evaluating their reactions to 11 R. secalis isolates. Bulked segregant analysis was used to identify molecular markers linked to resistance genes in 12 of the breeding lines. The isolates were found to be of less discriminating value than the markers. Useful information has been obtained as to the nature of several of the resistance genes introgressed. Eight of the 12 breeding lines contained introgressed genes that were located at the `complex Rh' locus on chromosome 3H and hence may not easily be pyramided into the same genotype. Previous information about the nature of the resistance in `Jet' is questioned. Neither of the resistance genes Rh or Rh2 seems to have been incorporated into Norwegian breeding material.     

Sources of Resistance to Powdery Mildew in Barley Lines Derived from Hordeum spontaneum Collected in Israel

Fourty two barley lines direved from the F₇ of crosses between barley cultivars and different accessions of Hordeum spontaneum collected in Israel and 30 lines or varieties with known genes for resistance to powdery mildew were included m this study. Eleven European and three Israeli powdery mildew cultures, possessing virulence genes corresponding to known resistance genes, were used to make comparisons between the varieties with known resistance genes and H. spontaneum derived lines. The reaction pattern of 39 H. spontaneum derived lines was clearly different from the reaction pattern o; any of the known genes for mildew resistance included in this study. Only two cases were observed in which the reaction pattern of H. spontaneum derived lines agreed with reaction patterns of known genes for mildew resistance viz. Ml-a9 and Ml-p. Trie Mildew resistance of one line apparently traces back to uncontrolled outcrossing with a Ml-a.6+Ml-g resistant cultivar. Since the majority of the 42 host genotypes tested showed distinctive variation in resistant reaction types against different mildew cultures, this study docs not support the assumption that differences in resistant infection types against distinct mildew cultures are sufficient to indicate the presence of supplementary genes for resistance in a given genotype of the host. The results justify the conclusion that the natural population of H. spontaneum in Israel forms a large gene pool for mildew resistance which is not yet used m cultivated barley.