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1.
C. F. E. Topp G. Hughes I. M. Nevison A. Butler S. J. P. Oxley N. D. Havis 《Plant pathology》2019,68(6):1179-1187
A programme of field trials for the study of the winter barley–Rhynchosporium commune pathosystem is reported. The associated seedborne disease rhynchosporium leaf scald is regarded as having an important impact on barley yields. The analysis in this study relates to the impact of the seed source (commercial or farm-saved seed) on disease incidence and to the spatial pattern of rhynchosporium leaf scald disease incidence. Disease incidence data were calculated from field data recorded as disease severity. Mean disease incidence was higher in the crops grown from farm-saved seed than in those grown from commercial seed, although great agronomic significance cannot be attached to this result. The spatial pattern of rhynchosporium leaf scald disease incidence was characterized in terms of the binary power law (BPL) and was indicative of an aggregated pattern. Programme-wide BPL results were described using a novel phytopathological application of a random coefficients model. These results have application in field sampling for rhynchosporium leaf scald disease. 相似文献
2.
大麦云纹斑病菌对杀菌剂的抗性检测及同工酶谱类型 总被引：2，自引：0，他引：2
1993～1994年大麦云纹斑病菌(Rhynchosporium secalis)对杀菌剂多菌灵、三唑醇的抗药性监测表明,该菌对两种杀菌剂的敏感程度发生了变化,并且首次在田间发现了大麦云纹斑病菌的多抗菌株。这类菌株对多菌灵、乙霉威及三唑醇都具有抗药性,且抗性程度很高。与1990～1991年得到的资料相比,随着杀菌剂选择压力的增加,大田群体中三唑醇高抗菌株比例逐年增加。对该菌同工酶分析结果表明,α—酯酶有7种表现型,磷酸葡萄糖变位酶有2种表现型,过氧化氢酶有3种表现型,无论对去甲基抑制剂类(DMI)表现抗性或敏感菌株,无论调节酶还是非调节酶,其酶谱表现型的变异基本相似。这表明大麦云纹斑病菌对DMI类抗药性突变存在于多个菌系的基因型背景群体中,而不是只起源于单一的广泛分布的菌系。 相似文献
3.
Development of SCAR markers linked to a scald resistance gene derived from wild barley 总被引：1，自引：0，他引：1
The F2 progeny of a third backcross(BC3) line, BC line 240, derived from a Turkish accession of wild barley (Hordeum vulgare ssp. spontaneum),segregated for resistance to scald (Rhynchosporium secalis) in a manner indicating the presence of a single dominant resistance gene. Two SCAR marker slinked to this resistance were
developed from AFLP markers. Screens of disomic and ditelosomic wheat-barley addition lines with the SCAR markers demonstrated
that the scald resistance gene is located in the centromeric region of barley chromosome 3H,a region previously reported to
contain a major scald resistance locus, Rrs1. Markers that flank the Rrs1 locus were used to screen the wild barley-derivedBC3F2 population. These markers also flank the wild barley-derived scald resistance, indicating that it maps to the same locus
as Rrs1; it may beallelic, or a separate gene within a complex locus. However, BC line 240 does not respond to treatment with the
Rhynchosporium secalis avirulence factorNIP1 in the same way as the Rrs1-carrying cultivar Atlas46. This suggests that the scald resistance gene derived from wild barley confers a different specificity
of response to theRrs1 allele in Atlas46.In order to increase the durability of scald resistance in the field, we suggest that at least two scald
resistances should be combined into barley cultivars before release. The scald resistance gene described here will be of value
in the Australian environment, and the several markers linked to it will facilitate pyramiding.
This revised version was published online in July 2006 with corrections to the Cover Date. 相似文献
4.
Haitham Sayed Gunter Backes Hamed Kayyal Amor Yahyaoui Salvatore Ceccarelli Stefania Grando Ahmad Jahoor Michael Baum 《Euphytica》2004,135(2):225-228
A partial genetic linkage map was constructed on 71 doubled-haploid lines derived from a cross between the barley lines Tadmor
and WI2291 with 181 molecular markers. The segregating population was used to detect markers linked to the gene Mlg conferring resistance to powdery mildew (Erysiphe graminis f. sp. hordei) and to genes for quantitative resistance to scald (Rhynchosporium secalis). The gene Mlg on chromosome 4H was flanked by two AFLP markers at a distance of 2.0 and 2.4 cM, respectively. QTLs for resistance to scald
were detected on chromosomes 2H and 3H. This association of molecular markers with qualitative and quantitative disease resistance
loci represents a valuable starting-point for marker-assisted selection.
This revised version was published online in July 2006 with corrections to the Cover Date. 相似文献
5.
The effects of fungicides used to control Rhynchosporium secalis in winter barley were investigated in five field trials in Co. Down, Northern Ireland. Benzimidazole resistance was present in the R. secalis population of each site. Fungicide performance was evaluated in terms of disease control, maintenance of green leaf area, grain yield and grain quality. Samples of R. secalis isolates taken before and after treatment in each field were assessed for sensitivity to carbendazim in the laboratory. Carbendazim contributed little to disease control, the maintenance of green leaf area, grain yield or grain quality. Carbendazim was associated with a significant increase in disease severity in some plots. Treatments containing carbendazim, either alone or in mixture, caused an increase in the proportion of carbendazim-resistant isolates within R. secalis populations. Propiconazole-containing treatments performed well in terms of disease control, maintenance of green leaf area and grain quality. They caused no change in carbendazim resistance frequency. 相似文献
6.
１９９７～１９９８年选用１１种坪用禾草品种在自然条件下做了对禾草云斑病的抗性鉴定。结果表明,结缕草、细叶结缕草及狗牙根不发病,表现免疫;高羊茅抗病;草地早熟禾、紫羊茅、黑麦草及匍茎剪股颖发病较重,表现感病。 相似文献
7.
Homozygous mlo -barley plants are resistant to barley powdery mildew but hypersusceptible to the rice blast fungus Magnaporthe oryzae . A mutational analysis was performed in the barley back-cross line BCIngrid mlo5 which led to the identification of two mutants with enhanced capacity to resist infections by M. oryzae , referred to as enhanced M. oryzae resistance mutants emr1 and emr2 . Here, we report on the characterization of emr2 mutant plants which not only show an almost complete reduction in disease severity after inoculation with M. oryzae but are also resistant to the necrotrophic fungi Drechslera teres and Rhynchosporium secalis . Histological analysis revealed that resistance to M. oryzae was based mainly on the formation of papillae at sites of attempted penetration into epidermal cells. There was no progression of fungal growth into the mesophyll. Additionally, because of the presence of the mlo -allele, emr2 -plants retained resistance to powdery mildew. The emr2 -conditioned broad spectrum resistance was inherited as in a recessive manner. Monitoring of PR -gene expression and enzymatic activity of peroxidases revealed a constitutively activated defence in emr2 . 相似文献
8.
The scald susceptible barley cultivar ‘Clipper’ and a third‐backcross (BC3) line homozygous for the Rrs14 scald resistance gene that originally came from Hordeum vulgare ssp. spontaneum were grown in replicated field trials. The level of resistance that Rrs14 confers against field populations of the pathogen Rhynchosporium secalis, the causal agent of scald disease, was evaluated. The Rrs14 BC3 line exhibited 80% and 88% less leaf damage than ‘Clipper’ in 1995 and 1996, respectively. Given this effectiveness of Rrs14, research was undertaken to identify a linked marker locus suitable for indirect selection of Rrs14. Based on linkage to a set of previously mapped loci, Rrs14 was positioned to barley chromosome 1H between the seed storage protein (hordein) loci Hor1 and Hor2, approximately 1.8 cM from the latter locus. The Hor2 locus is thus an ideal codominant molecular marker for Rrs14. The tight linkage between Rrs14 and Hor2 and the availability of alternative biochemical and molecular techniques for scoring Hor2 genotypes, permits simple indirect selection of Rrs14 in barley scald resistance breeding programmes. 相似文献
9.
The potential of the competitive polymerase chain reaction (PCR) assay for quantification of seedborne infection by Rhynchosporium secalis in barley was examined using a primer set (RS1 and RS3) derived from the internal transcribed spacer (ITS) regions of ribosomal RNA genes of this pathogen. Introduction of a heterologous internal control, which competes for the same primer set in the conventional PCR assay, allowed for detection and quantification of R. secalis fungal biomass. In order to generate a standard calibration curve, DNA prepared from infected seeds with different levels of R. secalis infection was subjected to competitive PCR assay. The resulting PCR product ratio for each PCR reaction ( R. secalis -amplified DNA/internal control template-amplified DNA) increased proportionally with increasing levels of infected seed DNA in the reaction mixture. Naturally infected seed lots collected from 1995 to 1999 were used to demonstrate the potential of the competitive PCR assay as an alternative seed health testing method. The results from this competitive PCR assay were compared with those from conventional visual disease assessment and an agar plate assay. Although relatively good correlation between visual disease assessment and the competitive PCR was found in the case of artificially mixed seed samples, there was poor correlation in the experiments using naturally infected seed samples. 相似文献
10.
J. C. Makepeace S. J. P. Oxley N. D. Havis R. Hackett J. I. Burke J. K. M. Brown 《Plant pathology》2007,56(6):934-942
The hypothesis that the increased use of the powdery mildew-resistance gene mlo has caused the increase in spotting diseases of barley over the past 20 years was tested in field trials. Near-isogenic lines with alleles of the Mlo gene for susceptibility or resistance to mildew in two parental backgrounds were trialled at four sites in Scotland and two in Ireland that were prone to spotting diseases, over 3 consecutive years. Mildew was controlled by sprays with quinoxyfen. Disease levels were low in the trials, the two most important diseases being scald caused by Rhynchosporium secalis and ramularia leaf spot caused by Ramularia collo-cygni . There were high levels of abiotic spotting. Lines with mutant mlo alleles consistently developed less Rh. secalis and Ra. collo-cygni , but more abiotic spots. This study indicates that the mlo mildew-resistance gene has not alone been responsible for the rise in spotting diseases over the past 20 years. Possible reasons for the rise are discussed, including the interaction of the mlo gene with the environment. 相似文献