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Wheat stripe mosaic virus (WhSMV) is the causal agent of soilborne wheat mosaic disease (SBWMD) in Brazil, which is a serious threat to wheat production in the southern part of the country. WhSMV also occurs in Paraguay and South Africa. The virus is soilborne, transmitted by Polymyxa graminis, and management strategies are mainly based on genetic resistance. Variation in the reaction (type and severity of symptoms) of cultivars has been reported depending on the region and/or year of cultivation, leading wheat breeding programmes to test their materials in several locations, which increases costs and is time‐consuming. One hypothesis is that this variation in symptoms is a result of the genetic variability of WhSMV. We assessed the genetic variability and population structure of WhSMV infecting wheat in Brazil and South Africa. In field experiments conducted in different locations in southern Brazil, a consistent reproducibility of symptoms was observed in a set of cultivars, and molecular analysis showed a low degree of genetic variability of the Brazilian viral population. The hypothesis that the variation in SBWMD symptoms in Brazil is due to genetic variability of the virus was thus rejected. Comparison of the Brazilian and South African WhSMV isolates indicated that they comprise distinct subpopulations and that the Brazilian subpopulation is more variable than the South African subpopulation. The lower genetic variability of the South African subpopulation suggests genetic stability or a recent emergence of WhSMV in that region. [ABSTRACT FROM AUTHOR]

Fungicides play an important role in wheat blast management in Brazil. To determine whether the reported patterns of fungicide resistance are present in Pyricularia oryzae populations from wheat and signal grass grown in Minas Gerais state, Brazil, we characterized the sensitivity of a contemporary collection (2018 and 2019) of 64 fungal isolates to seven fungicides belonging to DMI (tebuconazole and epoxiconazole), QoI (azoxystrobin and pyraclostrobin) and SDHI (bixafen, fluxapyroxad and benzovindiflupyr) groups. We further assessed if the differential sensitivity of selected isolates affected disease control using commercial doses of the fungicides applied protectively (prior to inoculation) on the heads of potted plants. Despite finding relatively low levels of in vitro sensitivity to some of the fungicides (e.g., azoxystrobin, fluxapyroxad and bixafen), control efficacies (percentage reductions in head blast severity) were significantly higher than the untreated plants and not affected by the sensitivity of the strain to all fungicides but azoxystrobin. The levels of head blast control for some of the fungicides (>70%) in the greenhouse were similar to or higher than previously reported in the field. The molecular data for a set of isolates representing different fungicide sensitivity levels were generally not predictive of the phenotype. The wheat‐infecting isolates were less sensitive than signal grass‐infecting isolates to all fungicides including azoxystrobin. Our study not only confirms previous reports of low sensitivity to some fungicides, but it also suggests options among site‐specific fungicides, most notably tebuconazole and benzovindiflupyr, that can still be used under an antiresistance strategy such as coformulation with multisite fungicides. [ABSTRACT FROM AUTHOR]

Root‐lesion nematodes (RLNs) Pratylenchus thornei and P. neglectus are globally important pathogens of cereal and pulse crops. These RLNs can occur together in farming systems and must be managed concurrently to minimize substantial yield losses in intolerant crop cultivars. Australian wheat cultivars with resistance to P. neglectus, have either the Rlnn1 resistance gene, which provides a high level of resistance but is linked with yellow flour colour that reduces cultivar marketability for bread production, or QRlnn.lrc‐2B, which provides moderate resistance. We evaluated a collection of 91 P. thornei‐resistant Iranian landrace wheats (ILWs) for their resistance to P. neglectus in four glasshouse experiments to (a) identify genotypes with resistance to both RLNs, (b) determine if any genotypes carried Rlnn1 and/or QRlnn.lrc‐2B and (c) develop ILW‐derived advanced breeding lines (ABLs) with resistance to both RLNs. A factor analytic linear mixed model (FA‐1) that explained 70% of the genetic variation, where the genetic correlations between the experiments ranged from 0.54 to 0.77, was used for the combined analysis of all experiments. Seven P. neglectus‐resistant genotypes were identified, with five that had potentially novel resistance. Subsequently, six breeding lines that were resistant to both RLNs were developed by crossing six ILWs with Australian cultivars and selecting for resistance in each generation. Both the ILWs and ABLs will be valuable genetic resources for wheat breeders to develop cultivars with dual resistance, enabling better management of mixed RLN populations with novel P. neglectus resistance that potentially is not linked with yellow flour colour. [ABSTRACT FROM AUTHOR]

The worldwide spread of wheat yellow rust lineage PstS1/S2 adapted to higher temperatures prompted us to investigate how diverse temperature responses of this lineage are in the Middle East, where diversity was previously observed within this lineage for pathotypes and genotypes. Here we highlight the diversity of response to temperature within a PstS1/S2 population. Twenty‐six isolates from eight countries and different altitudes, which were tested under four combinations of cold and warm incubation and postincubation temperature conditions, showed diversity for infection efficiency (IE) and latency period (LP). IE of the various isolates ranged from 5.8% to 13.7% under cold (5°C) and 0.04% to 1% under warm (20°C) incubation temperatures. LP varied from 10.2 days under warm to 4.43 days under cold incubation. LP of isolates from the same country could differ by 2 days. Significant differences in thermal aptitudes of the isolates were observed between and within countries. IE and LP diversity was not related to altitude origin of the isolates on the whole; however, a trade‐off between IE and LP was observed for isolates from low altitude (<400 m) under a warm regime. We showed diversity for thermal aptitude for IE and LP of isolates belonging to the same PstS1/S2 lineage. Understanding Pst temperature aptitude among geographically distant isolates of the same clonal lineage may help to identify the geographic range of pathogens and also to improve forecast models or breeding programmes. [ABSTRACT FROM AUTHOR]

Septoria tritici blotch (STB) is one of the main causes of wheat yield loss in the world. Apart from good agrotechnical practice, disease‐resistant cultivars are required to prevent yield losses. Breeding of such cultivars is time‐consuming and laborious, mainly due to the quantitative character of such resistance, but can be shortened using precise phenotyping. We show that fluorescence parameters, collected in a high‐throughput system, can be used for estimating wheat STB resistance. Using machine learning methods (deep learning network, random forest), we demonstrate that disease resistance based on the percentage of necrotic leaf area can be estimated by alterations in fluorescence parameters 8 days after inoculation, and before disease symptoms become visible. Moreover, we applied a random forest classifier to assess the significance of fluorescence parameters in an informative way (classification accuracy = 64.84%, p value [Accuracy >No information rate] <0.001). Based on this, we observed extensive alterations in parameters of sensitive cultivars, reflecting worse photosynthetic performance. The most highly altered parameters were fluorescence intensity measurements and descriptors of energy flux through photosystem II (PSII) reaction centres towards PSI such as F2, F3 and F4 fluorescence intensities at 0.1, 0.270 and 2 ms; initial to maximal fluorescence ratio (F0/Fm); the time derivative of relative variable fluorescence (dV/dT0); maximum quantum yield of PSII in the dark‐adapted state (Fv/Fm); maximum electron transport flux at PSII (ET0/RC); maximum trapped excitonic energy flux per excited PSII cross section (CS) at time T0 (TR0/CS0); and quantum efficiency of the reduction of end acceptors dR0 [dR0/(1 − dR0)]. [ABSTRACT FROM AUTHOR]

Wheat farmers rely on fungicides to protect fields against several foliar and flowering diseases, including Fusarium head blight (FHB). A range of active ingredients is used in isolation or in dual premixes that include a dimethylation inhibitor (DMI) or a quinone outside inhibitor (QoI) fungicide. Comprehensive information about fungicide resistance in F. graminearum is available for DMIs, while for QoIs the data are scarce. We characterized 225 strains obtained from two states in southern Brazil, Rio Grande do Sul (RS) and Paraná (PR), in relation to their response to two QoIs. The median EC50 (effective concentration leading to 50% inhibition of conidial germination) value for azoxystrobin (n = 25 isolates) was 2.20 μg/ml in the PR population and 4.04 μg/ml in the RS population. For pyraclostrobin (n = 50), the median EC50 was 0.28 μg/ml in the PR population and 0.24 μg/ml in the RS population. Evidence of cross‐resistance could not be detected. Screening using a discriminatory dose (DD) for azoxystrobin in a larger number of isolates from PR (n = 75) and RS (n = 100) states allowed the detection of 50% and 28% sensitive strains, respectively. Using the DD for pyraclostrobin, 33% and 18.8% were classified as less sensitive in the PR and RS isolates, respectively. In RS, the frequency of less‐sensitive isolates increased over time (2007–2011). No point mutation at any of the target spots (F129L, G137R, G143A) was detected. Our results represent an important step towards the establishment of a sensitivity profile for two of the most commonly used QoIs in commercial premixes targeting FHB control. [ABSTRACT FROM AUTHOR]

We conducted a five‐year survey (2011–2015) of barley and wheat fields in Paraná state, Brazil, obtaining 754 Fusarium isolates from spikes with fusarium head blight (FHB)‐symptoms. Multilocus genotyping and TEF‐1α gene sequence analyses confirmed the dominance of the F. graminearum species complex (FGSC, 75.7%), but F. poae (11.5%), as well as F. avenaceum and related members of the F. tricinctum species complex (FTSC, 8.1%) appeared as substantial contributors to FHB. Within the FGSC, F. graminearum of the 15‐ADON genotype was dominant (63%), followed by F. meridionale of the NIV genotype (23.1%), F. cortaderiae of the NIV (7%) or 3‐ADON (2.6%) genotypes, and F. austroamericanum (3.8%) of the 3‐ADON genotype. Substantial variation in pathogen composition was observed across years, with F. poae and F. meridionale frequencies significantly elevated in some years. Most F. poae strains produced DAS, diANIV, and butenolide, but not neosolaniol, T‐2, or HT‐2. All FTSC species produced moniliformin. Enniatin production was widespread among FTSC species, with the single F. acuminatum strain found to be the strongest producer of enniatins. Our findings confirm FGSC as a major contributor to FHB and expand considerably our knowledge of the presence, frequency, and conditions under which other pathogens may emerge, altering the spectrum of toxins that may accumulate in grain. [ABSTRACT FROM AUTHOR]

Blast disease, caused by the Magnaporthe oryzae Triticum pathotype (MoT), is a major concern for wheat production in tropical and subtropical regions. The most destructive symptoms occur in wheat spikes. Infected spikes become bleached due to partial or total sterility, producing small and wrinkled grains. High disease pressure of the disease results in significant yield losses. This study aimed to identify wheat quantitative trait loci (QTLs) conferring resistance to blast disease at the heading stage. A doubled‐haploid population was developed from the cross between BRS 209 (susceptible) and CBFusarium ENT014 (resistant, carrying the 2NS translocation). A linkage map was constructed containing 5,381 molecular markers and the inclusive composite interval mapping method was employed for QTL detection. Four QTLs were mapped in response to two MoT isolates. The major QTL identified on the 2AS chromosome explained an average of 84.0% of the phenotypic variation for spike bleaching at 9 days postinoculation and reinforces the potency of the 2NS translocation. Recombination between the distal region of chromosome 2AS and the 2NS marker was found. These results could explain why some lines carrying the VENTRIUP/LN2 marker have a variable reaction to the disease. QTLs on 5B and 7B chromosomes were also identified. Two mechanisms of resistance were hypothesized: the hypersensitive response and resistance to colonization of host tissues. The KASP markers thus developed and simple sequence repeats (SSRs) allocated in QTL regions can be used in the future for the development of wheat blast‐resistant cultivars. [ABSTRACT FROM AUTHOR]

Spot blotch (SB), caused by Bipolaris sorokiniana, is a devastating disease of wheat globally, especially in South Asia and South America. Understanding the genetics of resistance to SB is important for developing breeding strategies to improve resistance. A panel of 301 genotypes from Afghanistan was phenotyped over two crop seasons using a mixture of virulent B. sorokiniana isolates and genotyped using DArTSeq to obtain genome‐wide markers. Fifty genotypes (16.6%) showed disease scores less than the resistant control. Principal component analysis using the genotypic data clustered the genotypes into five different groups. Among models used for genome‐wide association mapping, the multilocus mixed model, and fixed and random model circulating probability unification algorithms were most effective in identifying significant marker‐trait associations (MTA). Twenty‐five MTAs at p ≤.001 were identified on chromosomes 1A, 1B, 1D, 2B, 2D, 3A, 3B, 4A, 5A, 5B, 6A, 7A, and 7D, indicating the quantitative nature of resistance to SB. Phenotypic variation explained by these markers ranged from 2.0% to 17.7%, and genomic regions on the chromosomes 1D, 2D, 3A, 3B, 4A, 5A, and 5B coincided with loci identified in previous studies. Three single nucleotide polymorphism (SNP) markers on chromosomes 1B (SNP 1113207) and 5A (SNPs 5411867 and 998276) were significant in both crop seasons as well as in the combined analysis across seasons. Marker 5411867 is close to Vrn‐A1, shown to be associated with SB in previous studies. Furthermore, among known SB resistance genes, Sb2 on chromosome 5B was predicted to be significant in this panel. [ABSTRACT FROM AUTHOR]

Leaf rust, caused by the fungus Puccinia triticina, is one of the most damaging rust diseases of wheat in Russia. Populations of P. triticina were monitored in seven regions of Russia from 2001 to 2018, with a total of 5,191 single urediniospore isolates from bread wheat (Triticum aestivum) being analysed. Populations have changed significantly in all regions since 2012, after 2 years of drought (2010–2011). Regional collections of P. triticina were also significantly different between the two periods 2001–2009 and 2012–2018, with changes along two geographic gradients from West Siberia to the north‐west and south‐west (North Caucasia) of the European part of Russia. All tested isolates were avirulent to resistance gene Lr9 in 2001–2009 but, since 2010, virulence to Lr9 has occurred and annually increased in the Asian part of Russia (Ural and West Siberia) due to deployment of cultivars with the Lr9 gene. Virulence to Lr2a and Lr15 was considerably lower in Dagestan (6%–33%) and all European regions (35%–67%) than in Asian regions (84%–96%). During 2001–2009, virulence on Lr1 was also lower in Dagestan (33%) and the European regions (50%–77%) than in Asia (91%–96%); however, by 2012–2018, nearly all isolates were virulent on Lr1. Remarkable changes were observed in frequencies of P. triticina races defined by their virulence/avirulence to Lr1 and Lr2a genes. We postulate the P. triticina population in Dagestan is specific to that area and pathogen populations in European and Asian parts of Russia are distinct. [ABSTRACT FROM AUTHOR]

Understanding how disease foci arise from single source lesions has not been well studied. Here, single wheat leaves were inoculated with Puccinia striiformis f. sp. tritici urediniospores, and all wheat leaves within two intersecting 0.3 × 3.0 m transects were sampled in eight replicates over 3 years. The lesions observed on each of the top three leaves on plants within 1.5 m from the source lesion were three-dimensionally mapped. The total number of lesions within a 1.5 m radius was estimated by dividing the number of lesions observed within each 0.025 m-wide annulus by the fraction of the annulus sampled. The estimated total number of lesions produced within 1.5 m of a single source lesion ranged from 27 to 776, with a mean of 288 lesions. Eighty percent of the lesions were recorded within 0.69 m of the source infection. The proportion of total lesions observed at a given distance from the source was fitted well by the Lomax and Weibull distributions, reflecting the large proportion of lesions arising close to the source, and when fitted by an inverse power distribution had a slope ( b) of 2.5. There were more lesions produced on leaves higher in the canopy than on lower leaves, with more lesions being detected above than below the point of inoculation. Simultaneous measurement of lesion gradients and spore dispersal in the final year of the study suggests that this pattern is due to greater susceptibility of upper leaves, rather than increased dispersal to upper leaves. [ABSTRACT FROM AUTHOR]

The fungal pathogen Fusarium graminearum is the causal agent of fusarium head blight in wheat and other small grain cereals. This fungus is known to produce high amounts of cell wall-degrading enzymes during infection of wheat spikes. In addition, wheat tissue is particularly rich in xylan, which can be hydrolysed by fungal xylanases. In order to establish the role of F. graminearum xylanase activity in pathogenicity, targeted gene disruption of the F. graminearum xyr1 gene, encoding the major regulator of xylanase gene expression, was performed. When grown on xylan as carbon source, the xylanase activity of the Δ xyr1 mutant was dramatically reduced and fungal growth was significantly reduced compared to the wildtype fungus. When grown on carboxymethylcellulose, the cellulolytic activity of the mutant was also reduced and the mutant did not grow on wheat cell walls. The disruption of the xyr1 gene greatly reduced the expression of xylanase-encoding genes both in vitro and during wheat spike infection, thus confirming the involvement of F. graminearum Xyr1 in the regulation of genes controlling xylan degradation. However, despite the deep impact caused by xyr1 gene disruption on the expression of xylanase genes and on total xylanase activity, the virulence of the Δ xyr1 mutant appeared unaffected on Triticum aestivum and T. durum spikes and on soybean seedlings. In conclusion, although a possible role for residual xylanase activity in the virulence of F. graminearum cannot be conclusively excluded, the results question the importance of xylanase activity during the infection process. [ABSTRACT FROM AUTHOR]

The objective of this study was to determine whether genetically distinct groups of Puccinia triticina are present in four regions of the Russian Federation. Collections of P. triticina were obtained from the Central, North Caucasus, Volga and West Siberia regions from 2006 to 2010. Ninety-nine single uredinial isolates were tested for virulence phenotype with 20 Thatcher near-isogenic lines of wheat. Forty-one virulence phenotypes were found in the four regions, with eight in common between the widely separated Central and West Siberia regions. A total of 72 isolates were tested for molecular genotype with 23 simple sequence repeat ( SSR) primer pairs, and 66 isolates were used for further analysis after clone correction for virulence and molecular genotype. Analysis of variation showed no overall differentiation of SSR genotypes or virulence phenotypes based on region of origin. Linkage disequilibria for SSR genotypes were high across the entire population. The regional populations had higher than expected levels of allelic heterozygosity that indicated clonal reproduction. Based on cluster analysis of SSR genotypes there were two groups of P. triticina isolates that were widely distributed across Russia. The two SSR groups also differed significantly for virulence. Puccinia triticina may be dispersed from a common source of inoculum in the European or Caucasus regions of Russia. The Russian P. triticina populations were highly differentiated for SSR genotype from populations in Tajikistan, Kyrgyzstan, Uzbekistan, Armenia, Georgia and Azerbaijan and more similar to populations from southern Kazakhstan and northern Kazakhstan. [ABSTRACT FROM AUTHOR]

The expression of the resistance phenotypes of QPst.jic-2D and QPst.jic-4B, two quantitative trait loci (QTL) for stripe rust resistance in wheat cv. Alcedo, were assessed relative to plant growth stage, while a histopathology analysis was undertaken to characterize the cellular interaction between Puccinia striiformis f. sp. tritici (the causal agent of stripe rust) and each QTL. QPst.jic-2D expressed a partial resistant phenotype at seedling growth stages, with the level of resistance increasing as the wheat plant matured, conferring a disease-free phenotype at heading. QPst.jic-4B, however, did not express a resistant phenotype until booting (growth stage 41 on the Zadoks scale), displaying its full resistant phenotype at heading. Microscopic examination in flag leaves showed that infection sites formed in all genotypes tested, with full infection-site establishment being observed by 36 h post-inoculation (hpi). In lines carrying both QPst.jic-2D and QPst.jic-4B, as well as the parental cv. Alcedo, no microcolony formation, defined by the appearance of runner hyphae, was observed. Microcolony formation was observed in lines carrying only one, or neither QTL. Cell death associated with infection sites was observed for all genotypes, although the timing of first appearance and the extent of the cell death response varied considerably. In lines carrying both QPst.jic-2D and QPst.jic-4B cell death did not extend beyond one to three cells. In lines carrying only one QTL more extensive cell death was observed and cell death appeared later in lines with QPst.jic-4B than QPst.jic-2D. Cell death was also occasionally observed in lines without either QTL, although only at 264 hpi. [ABSTRACT FROM AUTHOR]

By carefully separating type I and type II resistances, the possible effects of plant height on fusarium head blight (FHB) resistance in wheat were assessed using near-isogenic lines (NILs) for several different reduced-height ( Rht) genes. Tall isolines all gave better type I resistance than their respective dwarf counterparts when assessed at their natural heights. These differences largely disappeared when the dwarf isolines were physically raised so that their spikes were positioned at the same height as those of their respective tall counterparts. The effects of plant height on type II resistance was less clear. For those NIL pairs which showed significant differences, it was the dwarf isolines which gave better resistance. As the Rht genes involved in these NILs locate at different genomic regions, the differences in FHB between the dwarf and tall isolines are unlikely to be the result of linkages between each of the different Rht loci with a beneficial or a deleterious gene affecting type I or type II resistance. Rather, the different FHB resistances are probably caused by direct or indirect effects of height difference per se, and microclimate may have contributed to the better type I resistance of the tall plants. Thus, caution should be exercised when attempting to exploit any of the FHB resistant loci co-located with Rht genes. [ABSTRACT FROM AUTHOR]

To provide insight into the genetic structure of Mycosphaerella graminicola populations in Iran, a total of 221 isolates were collected from naturally infected wheat fields of five major wheat-growing provinces and analysed using AFLP markers and mating-type loci. All populations showed intermediate to high genotypic diversity. In the Golestan and Ardabil populations two mating types were found at near-equal frequencies, whilst all populations were in gametic disequilibrium. Moreover, clonal haplotypes were identified in different sampling sites within a field in both the Khuzestan and Fars provinces, demonstrating that pycnidia are probably the primary source of inoculum. All five populations had low levels of gene diversity and had private bands. Low levels of gene flow and high genetic differentiation were observed among populations and different clustering methods revealed five genetically distinct groups in accordance with the sampling areas. The Golestan and East Azarbaijan populations were more genetically differentiated than the others. Random genetic drift, selection and geographic barriers may account for the differentiation of the populations. The results of this study indicate a population structure of M. graminicola in Iran contrasting to that of most other countries studied. [ABSTRACT FROM AUTHOR]

The spatial pattern of Fusarium-infected kernels and their mycotoxin contamination was studied in four wheat fields in Germany using geo-referenced sampling grids (12–15 × 20–30 m, 28–30 samples per field) at harvest. For each sample, frequency of Fusarium-infected kernels and spectrum of species were assessed microbiologically; mycotoxin contents were determined by HPLC-MS/MS analysis. Spatial variability of pathogens and mycotoxins was analysed using various parameters including Spatial Analysis by Distance IndicEs (sadie® ). Microdochium majus, the most frequent head blight pathogen in 1998, was less frequent in 1999 and could not be detected in kernels from two fields in 2004. Fusarium avenaceum, F. graminearum and F. poae were the most frequent Fusarium species, with 7–8 species per field. The frequency of Fusarium-infected kernels was 3–15% and the incidence of species showed considerable within-field variability. Spatial patterns varied among Fusarium species as well as from field to field. Although pathogens and mycotoxin were often distributed randomly in the field, F. avenaceum, F. graminearum, F. poae, F. sporotrichioides, F. tricinctum and the mycotoxin moniliformin had an aggregated pattern in at least one field. Patterns are discussed in relation to spread of Fusarium species depending on inoculum sources, spore type, kind of dispersal, availability of susceptible host tissue and micro-climate. Sampling of wheat fields for representative assessment of mycotoxins is complicated by random patterns of Fusarium-infected kernels, especially where the frequency of infection is small. [ABSTRACT FROM AUTHOR]

The association of the cell wall degrading enzyme endo-beta-1,4-xylanase (EC 3.2.1.8) with pathogenicity of Mycosphaerella graminicola was examined in planta. The enzyme production of two M. graminicola isolates (T0372 and T0491), as well as their ability to infect seedlings of susceptible wheat cv. Scorpion, was first compared. No significant difference was found between the two isolates regarding spore germination rates, mycelial growth on the leaf surface or direct and stomatal penetrations. However, restricted hyphal growth was observed inside leaves inoculated with T0372, whereas successful mesophyll colonization with a strong intercellular fungal growth was found in leaves infected with T0491. Likewise, T0372 was unable to induce lesions bearing pycnidia and to produce endo-beta-1,4-xylanase activity until 22 days post-inoculation (d.p.i.). On the other hand, significant high increases of both diseased leaf area bearing pycnidia and endo-beta-1,4-xylanase activity were observed between 16 and 22 d.p.i. for T0491 ( r = 0·98). The investigation of 24 additional isolates, including the IPO323 and IPO94269 reference isolates, highlighted a strong correlation between endo-beta-1,4-xylanase activity and disease development levels ( r = 0·94). This study demonstrates that differences in pathogenicity in M. graminicola are not linked to events on the leaf surface or to frequency of leaf penetration, but to the ability of the fungus to colonize the mesophyll and to produce the cell wall degrading enzyme endo-1,4-beta-xylanase during the necrotrophic phase. [ABSTRACT FROM AUTHOR]

The accumulation of H2O2 (oxidative burst) and the progress of pathogen development were studied in compatible and incompatible wheat-brown rust interactions. The accumulation of H2O2 was detected in 98·7% of guard cells with appressoria 8 h post inoculation (hpi). The reaction in both susceptible and resistant plants declined 2–3 days post inoculation (dpi). The second phase of the oxidative burst was observed in the mesophyll and/or epidermis. In susceptible plants it began 4–5 dpi and was detected only in the epidermis. In resistant plants the response was observed in the mesophyll. In moderately resistant plants it was induced 1–3 dpi, and the percentage of infection units reached 80–90% 8 dpi. This corresponded with severe necrotic symptoms. In highly resistant plants, the oxidative burst was short and transient. The percentage of infection units with H2O2 accumulation reached its highest level (60–70%) 2 dpi, and decreased thereafter. Four days later, the low percentage and weak DAB staining indicated very low H2O2 accumulation. The localization and the time-course changes of the oxidative burst correlated with the profiles of the micronecrotic response, haustorium mother cell formation and pathogen development termination. An early and localized induction of oxidative burst followed by its rapid quenching correlated with high resistance and almost no disease symptoms. The possible correlation of the oxidative burst and pathogen development patterns with the level and durability of resistance conferred by Lr genes are discussed. [ABSTRACT FROM AUTHOR]

This study reports the discovery of a gene for resistance to septoria tritici blotch (STB) in two spring wheat cultivars, Courtot and Tonic. The gene, named Stb9, confers resistance to Mycosphaerella graminicola isolate IPO89011. It was mapped by quantitative trait loci (QTL) analysis using an existing map of Courtot × Chinese Spring and was located between markers Xfbb226 (3·6 cM) and XksuF1b (9 cM) on the long arm of chromosome 2B. Markers linked to Stb9 in Courtot were then shown to be linked to resistance to IPO89011 in F3 families of Tonic × Longbow. Allelism tests in which Tonic was crossed with Courtot confirmed that Tonic has a gene for resistance to IPO89011 at or very close to the Stb9 locus. SSR markers flanking Stb9 may be used in marker-assisted selection to introgress this gene into winter cultivars or in spring wheat breeding programmes outside Europe. [ABSTRACT FROM AUTHOR]

The size and shape of field plots can impact on both the cost and outcome of epidemiological experiments. In previous studies, epidemic velocity of yellow rust (caused by Puccinia striiformis f.sp. tritici) on wheat ( Triticum aestivum) has been examined in long, narrow plots (6·1 m by 73–171 m). The present study compares spread in square, 61 × 61 m plots versus narrow, 6·1 × 61 m plots at two locations. The objective was to test whether plot shape has a substantial impact on spatiotemporal spread of yellow rust. Velocity increased curvilinearly with time for both plot shapes and at both locations. Curves of epidemic velocity versus time were nearly identical in square versus narrow plots in both the upwind and downwind directions. Contrary to expectation based on simulations, the results did not indicate faster disease spread in square plots, though the plot sizes studied may be beyond that at which there is a rapid change of disease increase with increasing plot area. Velocity also increased curvilinearly in all eight compass directions of the square plots. Results indicate that narrow plots, which are substantially less costly than equidimensional plots, may be justified for studying the spatiotemporal spread of wheat yellow rust and other diseases with similar epidemiological characteristics. [ABSTRACT FROM AUTHOR]

Wheat stem rust samples were collected in 2006 and 2007 in the Arsi, Bale, Shewa and northwest regions of Ethiopia to determine virulence diversity and race distribution in Puccinia graminis f.sp. tritici populations. Stem rust incidence was high in Arsi, Bale and east Shewa. In northwest Ethiopia, and north and west Shewa, stem rust was prevalent at low levels. A total of 152 isolates was analysed and 22 races were identified. Races TTKSR (Ug99), TTHSR and RRTTR were predominant, with frequencies of 26·6, 17·7 and 11·1%, respectively. These races were also detected in all regions. The highly virulent race designated Ug99 was present throughout the country and dominated in all regions except northwest Ethiopia. A variant of Ug99 virulent against the stem rust resistance gene Sr24 was not detected in this study. Four stem rust resistance genes ( Sr13, Sr30, Sr36 and SrTmp) were found to confer resistance to most of the races prevalent in Ethiopia. With the exception of Sr30, which is not effective against Ug99, these genes could be used in breeding for resistance to stem rust in Ethiopia. [ABSTRACT FROM AUTHOR]

Measuring disease resistance accurately and reproducibly is a key requirement for the introgression of partial resistance genes into breeding lines. Here, a qPCR protocol is used to measure fungal biomass, using the wheat- Stagonospora nodorum pathosystem as a model. Seven cultivars of differing reported resistance levels were used. Fungal biomass taken at 220°C thermal days after inoculation accurately predicts the final grain weight loss. It is concluded that a test based on qPCR methods is specific, quantitative, rapid and objective. Such tests could provide useful and economic tools in the development of robustly resistant crop cultivars. [ABSTRACT FROM AUTHOR]

As part of developing a European Pest Risk Analysis (PRA) for Tilletia indica, the causal agent of Karnal bunt of wheat, teliospore survival studies were done outside under quarantine containment at three European sites (Norway, UK, Italy). At each site, experiments were set up in three consecutive years (Experiments 1, 2 & 3) to determine teliospore survival over time (1–3 years) at 5, 10 and 20 cm depths. Experiments were sampled annually and survival assessed in relation to teliospore recovery and to germination at recovery (T0) and 3 months after recovery in case of burial-induced dormancy ( T3). Teliospores survived at all three sites at all depths over all the time periods studied. At each site, there was no evidence of a marked decline in teliospore recovery between sampling years, except in one set of years in one Norwegian experiment. There was no consistent effect of depth on recovery. In general there was little evidence for a marked decline in teliospore germination between sampling years. There was some evidence of a decrease in germination with increasing depth in the UK, and for some time-depth interactions. After 3 years’ incubation (Experiment 1), mean teliospore recovery and mean germination were: UK: 61% recovery and 31% ( 33%) germination for T0 (and T3); Italy: 30% recovery and 36% ( 29%) germination; and Norway: 12% recovery and 19% ( 49%) germination. Germination for laboratory controls ranged from 20–59% (UK), 18–41% (Italy) and 28–59% (Norway). There was no evidence for burial-induced dormancy except in Norway. Teliospores of T. indica can survive for at least three years in European soils. This prolonged period of survival could support establishment of the pathogen if it were introduced into areas of European cereal production. [ABSTRACT FROM AUTHOR]

Fusarium head blight (FHB) resistance of 50 cultivars from the National List of winter wheat cultivars approved for sale (or were undergoing trails for approval in 2003) in the UK was compared with 21 reference cultivars from continental Europe which had previously been characterized for resistance. Only three UK National List cultivars (Soissons, Spark and Vector) had stable resistance over trial sites that was significantly greater than that of the FHB susceptible cultivar Wizard. In addition, under moderate disease pressure, 21 of the National List cultivars had levels of the trichothecene mycotoxin deoxynivalenol (DON) above the proposed European Union limit of 1·25 ppm in grain. Surveys show that levels of FHB and DON in the UK crop are currently very low, however, should disease pressure increase for any reason, then an improvement in the overall levels of FHB resistance of UK winter wheat germplasm will be required. In order to infer the origin of resistance and to identify potentially novel resistance, allele sizes of microsatellite (simple sequence repeat, SSR) markers linked to quantitative trait loci (QTL) for FHB resistance were compared between the test cultivars and known, characterized resistance sources. The major FHB resistance QTL from the Chinese cv. Sumai-3 (3BS, 5A and 6B), the Romanian cv. Fundulea F201R (1B and 5A) and the French cv. Renan (5AL) were screened with 17 SSRs. No National List cultivar had haplotypes similar to any of these QTL. However, the highly resistant German reference cultivar Petrus had an identical haplotype to cv. Fundulea F201R on 1B indicating that this cultivar has an allelic FHB resistance QTL at that location. [ABSTRACT FROM AUTHOR]

Point pattern analysis (fitting of the beta-binomial distribution and binary form of power law) was used to describe the spatial pattern of natural take-all epidemics (caused by Gaeumannomyces graminis var. tritici) on a second consecutive crop of winter wheat in plots under different cropping practices that could have an impact on the quantity and spatial distribution of primary inoculum, and on the spread of the disease. The spatial pattern of take-all was aggregated in 48% of the datasets when disease incidence was assessed at the plant level and in 83% when it was assessed at the root level. Clusters of diseased roots were in general less than 1 m in diameter for crown roots and 1–1·5 m for seminal roots; when present, clusters of diseased plants were 2–2·5 m in diameter. Anisotropy of the spatial pattern was detected and could be linked to soil cultivation. Clusters did not increase in size over the cropping season, but increased spatial heterogeneity of the disease level was observed, corresponding to local disease amplification within clusters. The relative influences of autonomous spread and inoculum dispersal on the size and shape of clusters are discussed. [ABSTRACT FROM AUTHOR]

Wangshuibai is a Chinese landrace wheat with a high level of resistance to fusarium head blight (FHB) and deoxynivalenol (DON) accumulation. Using an F7 population of recombinant inbred lines (RILs) derived from the cross between Wangshuibai and Annong 8455 for molecular mapping of quantitative trait loci (QTL) for FHB resistance, the proportion of scabbed spikelets (PSS) and DON content were assessed under field conditions. Composite interval mapping revealed that two and three QTL were significantly associated with low PSS and low DON content, respectively, over 2 years. QTL on chromosomes 3B and 2A explained 17 and 11·5%, respectively, of the phenotypic variance for low PSS, whereas QTL on chromosomes 5A, 2A and 3B explained 12·4, 8·5 and 6·2%, respectively, of the phenotypic variance for low DON content. The 3B QTL appeared to be associated mainly with low PSS, and the 5A QTL primarily with low DON content in Wangshuibai. The 2A QTL had minor effects on both low PSS and DON content. Microsatellite and AFLP markers linked to these QTL should be useful for marker-assisted selection of QTL for low PSS and low DNA content from Wangshuibai. [ABSTRACT FROM AUTHOR]

The pathogenicity of Alternaria spp. isolated from wheat leaves collected in regions where alternaria leaf blight has been reported was compared with that of IMI reference isolates of A. triticina and A. alternata using two durum and two bread wheat genotypes. To identify isolates putatively corresponding to A. triticina, morphological and DNA sequence analyses based on ribosomal DNA from the internal transcribed spacer (ITS) region (ITS1, 5·8S rRNA gene, ITS2) and toxicity bioassays of culture filtrate were combined. Glasshouse inoculations provided reliable information to assess the pathogenicity of A. triticina isolates on wheat. Alternaria leaf blight symptoms were produced by the A. triticina isolates only on durum wheat cv. Bansi, while A. alternata, A. tenuissima and A. arborescens isolates were found to be nonpathogenic on the wheat cultivars tested. Alternaria triticina isolates were distinguished from other Alternaria species by Simmons and Roberts’ sporulation pattern 6 and two to three conidia per sporulation unit associated with primary conidia bearing long (> 7  µm) apical secondary conidiophores. Phylogenetic analysis also proved effective at discriminating wheat-pathogenic A. triticina from other nonpathogenic Alternaria species. Alternaria triticina isolates yielded longer ITS sequences than A. alternata, A. tenuissima and A. arborescens isolates, leading to clear-cut differences as visualized with agarose gel electrophoresis. Additionally, only culture filtrates of A. triticina isolates caused nonspecific necrotic lesions on leaves of 3-week-old wheat plants. [ABSTRACT FROM AUTHOR]

A series of experiments was conducted with wheat stripe rust to analyse competition between simple and complex pathotypes in host mixtures. Two different pathotype combinations were tested, with different host components. Each combination included a complex (able to infect two host components) and two simple pathotypes. For one of the combinations, induced resistance was tested in a separate experiment as a possible interaction among pathotypes. Disease severity and pathotype frequencies were measured three times during the epidemic, on each host component grown in pure stands and in mixtures. In one of the experiments, pathotype frequencies were also measured within secondary foci. One of the complex pathotypes appeared to have a low fitness on one of the host components and did not significantly increase in frequency in host mixtures relative to pure stands. The average frequency of the other complex pathotype increased during the first epidemic cycles, but remained stable afterwards, below expected values. The results suggest that the development of complex pathotypes in host mixtures may be influenced by differential aggressiveness on the host components, by induced resistance and by random effects resulting from the formation of disease foci, and depends on pathogen autoinfection rate and dispersal mechanisms. [ABSTRACT FROM AUTHOR]

Experiments were performed in controlled conditions to compare several aggressiveness components of an isolate ofPuccinia triticinaon different wheat (Triticum aestivum) genotypes. Latency period, urediniospore production per lesion and per unit of sporulating surface, lesion size, and nitrogen and carbon content of the spores were measured on four host genotypes. Three of the host cultivars (Soissons, Altria and Isengrain) were susceptible and the fourth (Trémie) was resistant to the isolate used in the experiments, producing a mesothetic infection type. In all the analyses, lesion density was used as a covariable. The latent period was identical on the susceptible host cultivars, and there were no marked differences in the urediniospore production capacity when related to the sporulating surface area. In cv. Isengrain, differences in lesion size relative to the other susceptible cultivars resulted in lower urediniospore production per lesion. Urediniospore production per lesion and lesion size were density dependent and decreased exponentially with increasing lesion density. Urediniospore production per unit of sporulating surface was either independent of lesion density or marginally dependent (decreased linearly with a limited rate). On the resistant cultivar, Trémie, the latent period was longer and of a much greater variance compared with the susceptible cultivars. Urediniospore production per lesion was considerably reduced, but this reduction was fully accounted for by a reduction in lesion size, the urediniospore production capacity of the diseased tissue remaining equivalent to that observed in the susceptible cultivars. In all cultivars the C and N contents of the urediniospores were considered unchanged, even if minor differences were detected. [ABSTRACT FROM AUTHOR]

Several wheat genotypes, including eight with known field responses, were evaluated for their reaction to Soil-borne cereal mosaic virus (SBCMV, genus Furovirus) by growing in naturally infested soil under controlled environment conditions. Virus antigen titres in the foliage 8–9 weeks after sowing mostly reflected the field responses, showing that growth chamber-based tests can be used to improve the speed and reliability of germplasm screening. Such tests were used to determine the mode of inheritance of the SBCMV resistance in cv. Cadenza, commonly used in UK wheat-breeding programmes. One hundred and eleven doubled haploid (DH) lines derived from an F1 of a cross between cvs Cadenza (resistant) and Avalon (susceptible) were evaluated. This DH population segregated for the reaction to SBCMV in a ratio of 1 : 1 (resistant : susceptible). This suggests that the SBCMV resistance is controlled by a single gene locus. As a first step towards identification of new sources of improved SBCMV resistance (e.g. immunity) as well as sources of the resistance to the virus vector, Polymyxa graminis, a set of 26 Triticum monococcum lines of diverse geographical origin was also screened. Most lines were susceptible to SBCMV, but one line of Bulgarian origin was resistant to the virus and possibly partially resistant to the virus vector. [ABSTRACT FROM AUTHOR]

The effects of the highly aggressive isolate KB-2 of the Karnal bunt pathogen (Neovossia indica) on phenol metabolism, peroxidase (POX) and its isoenzymes were studied in wheat. Two resistant genotypes, HD 29 of bread wheat (Triticum aestivum) and DWL 5023 of durum wheat (T. durum), and one susceptible bread wheat, WL 711, were used. In the bread wheats, total phenols reached a maximum 2 days after inoculation (d.a.i.). In the resistant durum line, total phenols did not change significantly for 6 d.a.i., but declined significantly at 10 d.a.i. Three phenolic compounds, caffeic acid, l-tyrosine and hydroquinone, were detected using thin-layer chromatography. The first two were detected at all times at and after inoculation, but hydroquinone was detected only in the resistant wheats at 6 d.a.i. The activity of POX was highest at 2 d.a.i. in the two resistant wheats, but increased more slowly to a peak at 6 d.a.i. in the susceptible wheat. The number of isoenzymes of POX detected by polyacrylamide gel electrophoresis (PAGE) changed after inoculation with KB-2. The maximum number of isoenzymes occurred at 2 d.a.i. in the two resistant wheats and at 6 d.a.i. in the susceptible wheat. Although the isoenzymes detected in seedlings were not identical to those detected in seeds, the PAGE banding patterns of seeds and seedlings were the same for the two resistant wheats. The potential use of the additional band at a relative mobility of 0·42 in seeds and 0·28 in seedlings as markers for Karnal bunt resistance is discussed. [ABSTRACT FROM AUTHOR]