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Crop Breed Genet Genom. 2019;1:e190021. https://doi.org/10.20900/cbgg20190021

Article

Breeding Progress in Seedling Resistance against Various Races of Stripe and Leaf Rust in European Bread Wheat

Holger Zetzsche * , Albrecht Serfling , Frank Ordon

Julius Kuehn-Institute (JKI), Federal Research Centre for Cultivated Plants, Institute for Resistance Research and Stress Tolerance, Erwin-Baur-Strasse 27, 06484 Quedlinburg, Germany

* Correspondence: Holger Zetzsche, Tel.: +49-3946-47-305.

Received: 26 June 2019; Accepted: 11 October 2019; Published: 14 October 2019

This article belongs to the Virtual Special Issue "Genetic Gains in Plant Breeding"

ABSTRACT

Background: Stripe and leaf rust are major constraints of wheat production with substantial impacts on grain yield. Population dynamics of both pathogens and the emergence of new virulent races have resulted in relentless efforts related to wheat breeding to improve resistance during the last decades.

Methods: To evaluate the breeding progress achieved with respect to race-specific resistance, a set of nine isolates of the two rust pathogens have been tested in seedling assays on a panel of 191 elite winter wheat cultivars representing wheat breeding in Europe between 1966 and 2013.

Results: Significant differences in the resistance of wheat cultivars concerning both pathogens have been detected by means of two-way ANOVA. Isolates as well as genotype × isolate interaction had a significant effect for both pathogens. Breeding progress, resulting in an increased seedling resistance, has been achieved against all nine isolates over the past five decades. The slope of progress was steeper for leaf rust than for stripe rust isolates. Progress against the highly common leaf rust isolate “4171” and” the stripe rust isolate “Warrior(-)” was strongest.

Conclusions: The study reveals that a steady increase in seedling resistance was achieved during the past five decades. An additive contribution of these isolate specific R genes after breakdown has been hypothesised.

KEYWORDS: Triticum aestivum; Puccinia striiformis f.sp. tritici; Puccinia triticina; fungal pathogen; rust; isolates; seedling resistance; R genes; breeding progress

INTRODUCTION

Stripe and leaf rust, caused by the fungal pathogens Puccinia striiformis f.sp. tritici (ps) and Puccinia triticina (pt), are major constraints of wheat (Triticum aestivum L.) cultivated under temperate climatic conditions with a substantial impact on grain yield [1–3]. Biological control through the utilisation of resistance genes has been applied in wheat as a cost-effective and ecologically friendly means to avoid yield losses. However, the rise of new virulent races and their dispersal have resulted in considerable intraspecific variation, which have dynamically altered the importance of single pathogen races within years [4,5].

Two types of genes have been distinguished to mediate resistance against rusts in wheat. Seedling resistance (R) genes expressed at all growth stages are regarded as race-specific and qualitative, while adult plant resistance (APR) effective in later growth stages is described as primarily quantitative [6,7]. In general, R genes in plants often encode nucleotide-binding site leucine-rich repeat (NBS-LrR) proteins and recognise specific pathogen effectors, also referred to as avirulence proteins, in a gene-for-gene mode [7]. R genes tend to have greater effects but have been reported to lose their effectiveness mostly after several years [7,8]. APR genes appear to encode different proteins, such as ABC transporter, protein kinase, or hexose transporter [7,9]. Although genes involved in APR may lose their efficacy as well, some are described as slow-rusting APR genes [10]. A high level of durable resistance can be achieved by pyramiding either ARP or R genes or by stacking several APR and R genes [7,11].

The dynamics of pathogen races virulent against particular resistance genes required continuous efforts in wheat breeding during the past decades. As a result, multiple stripe rust and leaf rust resistance genes (Yr and Lr) of both types of resistance have been introduced into elite wheat cultivars [12]. The following common Yr genes were identified in European cultivars: Yr1, Yr2, Yr6, Yr9, Yr17, and Yr32, [13]. Lr genes, such as Lr1, Lr3, Lr10, Lr13, Lr14a, Lr24, Lr26, and Lr37, were the most common genes against leaf rust [14,15]. Unfortunately, virulent PS races that are able to overcome resistance genes which have been introduced more recently, such as Yr10, Yr24, and Yr27, have already been reported [16–18]. Moreover, resistance genes, such as Yr5 and Yr15, which are still effective to date are rarely or never employed in European elite wheat cultivars [13,19]. Lr genes used in elite cultivars are also mostly race-specific, and most of these have already been overcome [17,20], including resistance gene Lr37 which is carried by many cultivars registered in Germany [21]. Similar to PS races, PT races recently prevalent in Germany carry multiple virulence genes against most of the resistance genes present in elite wheat cultivars [22].

Breeding progress in economically successful European winter wheat was investigated in field trials with respect to production intensity, including the impact of fungal pathogens [23]. Accordingly, a steady decrease in susceptibility to stripe rust and powdery mildew of adult plants was detected in the past five decades. These results confirmed a previous report of a significant improvement of German wheat cultivars relative to several fungal pathogens, including leaf rust, over the same period [24].

The present study aims to investigate the susceptibility and breeding progress in seedling resistance against different isolates of stripe and leaf rust in high-yielding winter wheat cultivars released in Europe in the past 50 years.

MATERIALS AND METHODS

Plant Material

A panel of 191 wheat cultivars was selected for their agronomic importance in wheat production in Western Europe, particularly in Germany, during their release period between 1966 and 2013 [23]. All cultivars aside from the hybrids were replicated by self-pollination under field conditions. Seeds of hybrids (F1 seeds) were provided by the respective breeding companies. The test panel represents long-term plant breeding progress in Western Europe. Details including the year and country of registration are provided in the supplementary information of [23].

Rust Isolates

All isolates of both rust pathogens were initially derived from single pustules on the susceptible genotypes “Akteur” (stripe rust) and “Borenos” (leaf rust). Races of P. striiformis (PS: “Warrior(-)”, “Warrior + Yr27”, “Oakley,v7/Kranich”, “Triticale aggressive”) were determined through virulence analysis by K. Flath (JKI Kleinmachnow) and multiplied according to [25]. Virulences of P. triticina isolates (PT: “4083”, “4171”, “77WxR”, “FI17”, “HkLr13”) were determined according to [22]. Lr12, Lr13, Lr22, Lr35, Lr37, and Lr46 are race-specific APR genes [7,20,26,27] carried by near isogenic lines (NILs) and have been included into the virulence analysis according to [20]. Virulence against all of these Lr genes was observed at the seedling stage (Table 1, marked by bold letters and asterisk). All isolates were increased so that a sufficient number of spores was available for inoculation. After multiplication, PS and PT spores were dried using a desiccator and stored at 5 °C until inoculation within 10 days.

Seedling Tests

Seedling assays were performed in semi-controlled greenhouse conditions between November 2017 and April 2018 (PS) and between September 2018 and May 2019 (PS), respectively. Three seedlings of each cultivar, each with two replicates per isolate, were grown in 7 × 11 potting trays filled with soil substrate Fruhstorfer Typ T (Hawita Gruppe GmbH, Vechta, Germany) and raised at 21 °C until the second leaf was fully expanded. Seedlings were prepared for inoculation by spraying with 0.005% aqueous Tween® 20 (Carl Roth GmhH+Co.KG, Karlsruhe, Germany) to facilitate the even adhesion of spores to the leaves. Inoculation was performed with 50 milligrams of urediniospores of each isolate mixed with clay (1:2) using a powder atomiser. Subsequently, seedling assays were incubated under plastic hoods at 100% humidity for 24 h (PS at 5–8 °C, PT at 16–18 °C). To maximise infection, seedlings were then grown at 10–12 °C for PS and at 18–20 °C for PS at a photoperiod of 14/10 h with supplementary lighting. Seedlings were scored for both infection types (resistant: “0”, “;”, “N;”, “1”; moderately susceptible: “2”; susceptible: “3”, “4”) on a modified scale according to [8] and the percentage of leaf area infected based on [28], which is restricted to visible sporulation. Stripe rust was phenotyped 14 days after inoculation and leaf rust after 10 days, respectively.

Statistical Analysis

Descriptive and summary statistics of infection types and the percentage of leaf area infected by both pathogens were calculated using the statistical software JMP 14.0.0 from [29]. Relative susceptibility was calculated based on [30], combining infection type and the percentage of leaf area infected (%LAinf) to receive robust and continuous data to estimate breeding progress for resistance. First, infection type data were transformed into continuous data based on [31]. Pearson’s correlation coefficients between transformed infection type data and the percentage of leaf area infected were calculated using the PROC CORR procedure of SAS 9.4, as implemented in JMP 14.0.0. Transformed infection type (IT) data were then combined with the percentage of leaf area infected (%LAinf), assuming a random distribution of square root values using Equation (1). Both transformed parameters contributed equally to the resulting parameter relative susceptibility.

Two-way ANOVA was computed for relative susceptibility assuming a linear mixed model using the SAS PROC MIXED procedure implemented in JMP14.0.0 [29]. Isolates were considered as fixed effects, and cultivars and replicates were regarded as random. A Tukey–Kramer Honestly Significant Difference (HSD) test was performed at an alpha level of 0.05 to analyse differences between isolate means. To quantify resistance progress, linear regression analyses were performed with the year of cultivar release regarded as a continuous variable and LS-means of relative susceptibility of each pathogen, as well as isolate and cultivar as input data using the PROC MIXED procedure.

RESULTS

Pathogenic Complexity of the Isolates Tested

The virulence patterns and complexity of the rust isolates used in this study are indicated in Table 1. Virulence complexities based on pathogenicity tests on 21 differential lines range from five (“Triticale aggr.”) to 16 (“Warrior + Yr27”) for PS isolates with a mean of 12.3. “Oakley,v7/Kranich” and the Warrior isolates are relatively similar, differing primarily by virulences to Yr4 (only in the Warrior isolates), Yr27 (only moderately in “Warrior + Yr27”), and YrAmb (not in “Warrior(-)”). “Triticale aggr.” differs strongly, as it is virulent to Yr10 and Yr8 while it is avirulent to Yr1, Yr3, Yr4, Yr9, Yr17, Yr25, Yr27, Yr32, YrSd, YrSu, YrSp, YrAvc.S, and YrAmb.

TABLE 1
Table 1. Pathotypes and number of virulence or avirulence genes of Puccinia striiformis f.sp. tritici and Puccinia triticina isolates used in single isolate assays to test seedling resistance of 191 elite winter wheat cultivars. Brackets indicate ambiguous results due to the differing symptom ratings between replications or moderate susceptibility (infection type 2).

Virulence or avirulence complexities of the leaf rust isolates are substantially higher, ranging from virulence complexities of 34 (“4171”) up to 41 (“77WxR”) with a mean of 37.2, based on tests for pathogenicity on differential Thatcher NILs carrying 51 resistance genes. In total, all five PT isolates differ in 17 predicted virulence genes. Precisely, “4171” is virulent to only eight of these 17 Lr genes, “HkLr13” is virulent to nine, and “4083” as well as “77WxR” are virulent to 13 out of these 17 genes, respectively. The PT isolates are relatively similar in terms of virulence against resistance genes frequently used in breeding of European bread wheat against leaf rust, such as Lr1, Lr2a, Lr3a, Lr10, Lr13, Lr14a, Lr17, Lr20, Lr23, Lr26, Lr37, differing in virulence to Lr3a (only “4083”, “77WxR”, “HkLr13”), Lr10 (all, except “4171”), and Lr26 (“77WxR”, “FI17”), only.

Response of Wheat Varieties to Rust Isolates

Results of the analysis of the infection type response using a modified scale developed by [8] at seedling stage and percentage of infected leaf area are summarised in Table 2 and illustrated in Figure 1. “Oakley,v7/Kranich” was the most virulent PS isolate, infecting 86.4% (susceptible + resistant cultivars = 100%) of all cultivars. In contrast, “Triticale aggr.” was the least aggressive PS isolate in the panel, with 49.4% resistant cultivars. In terms of leaf rust, “HkLr13” was the most virulent PT isolate in the panel (65.1%), while the majority of the cultivars (70.7%) were resistant to PT isolate “FI17”.

The analysis of leaf damage measured in terms of percentage of leaf area infected gave comparable results. Susceptibility to all PS isolates (mean 8.6 ± 9.7% leaf area infected) was typically lower than susceptibility against PT isolates (mean 10.2 ± 13.1%). Susceptibility was lowest against the PS isolate “Triticale aggr.” (2.5 ± 4.5%), while “Oakley,v7/Kranich” (14.8 ± 11.0%) caused the strongest damage. For leaf rust, susceptibility to the isolate “4171” (16.6 ± 15.7%) was highest and was rather low to “FI17” (1.6 ± 3.2%). All four PS isolates were significantly different from each other, as revealed by Tukey Kramer’s HSD (p ≤ 0.05) test (Figure 1, letters in boxplot). PT isolates were divided into two separate groups, namely “4083”, “4171”, together with “HkLr13” and “77WxR” with “FI17”.

Transformed infection type values and the percentage of leaf area infected were combined into the relative susceptibility, as the Pearson correlation was highly significant (p < 0.001) with the Pearson coefficient r = 0.79 of stripe rust and r = 0.78 for leaf rust between both parameters, respectively.

ANOVA of relative susceptibility values reveal significant (p ≤ 0.001) genetic variation among cultivars (G) as well as among isolates (I) for both rust pathogens (Table 3). Moreover, virulence of the isolates differed significantly among the cultivars, as indicated by significant G × I interaction.

TABLE 2
Table 2. Summary of infection type response (cf. Supplementary Table S1), leaf area infected (%), and relative susceptibility of 191 winter wheat cultivars assessed with four stripe rust and five leaf rust isolates.
FIGURE 1
Figure 1. Analysis of susceptibility of 191 winter wheat cultivars to different isolates of P. striiformis and P. triticina. Mosaic plots of contingency tables of infection types for isolates of stripe rust (A) and leaf rust (B) and illustration of class frequencies and boxplots of infected leaf area (%) by isolate with letters (a, b, c, d) representing groups of isolates with significant pairwise differences tested by Tukey Kramer HSD.
TABLE 3
Table 3. ANOVA results of relative susceptibility to isolates of P. striiformis and P. triticina, each with levels of significance (*** <0.001, ** <0.01, and * <0.05) of 191 winter wheat cultivars tested in single isolate assays.

Relative susceptibility against both rusts correlated significantly negatively with the year of cultivars’ release (Table 4, Figure 2). The average annual rate of relative susceptibility, estimated based on the slope of linear regression, decreased for both groups of isolates, with −0.015 a−1 against PS and with −0.035 a−1 against PT isolates. Particularly strong improvements have been achieved against PT isolate “4171” with −0.051a−1 and against PS isolate “Warrior(-)” with −0.021 a−1, respectively. Although the cultivar’s mean susceptibilities against “Triticale aggr.”, “Oakley,v7/Kranich”, and “Warrior + Yr27” were rather different, susceptibility against these PS isolates decreased at about the same rate (between −0.012 a−1 and −0.013 a−1). The PS isolate “Oakley,v7/Kranich” caused the strongest stripe rust infestation on older cultivars, but resistance against that isolate did not improve much in modern varieties. In contrast, susceptibility to PT isolate “FI17” decreased further from a relatively low base in older varieties.

TABLE 4
Table 4. Bivariate analysis between rust isolates with the year of cultivar’s release based on LS-means of relative susceptibility assuming a linear model. Additionally, phenotypic variance explained (R²), significance levels of p values of each model tested (*** <0.001, ** <0.01, and * <0.05), and equations of linear fit to estimate breeding progress from year of release (YoR) are indicated.
FIGURE 2
Figure 2. Breeding progress against different isolates of P. striiformis and P. triticina. Linear trend lines (each shaded with 95% confidence interval) of relative susceptibility against different isolates of stripe rust (A) and leaf rust (B) based on the relative susceptibility values of 191 winter wheat cultivars in relation to the year of cultivar release.

Breeding success is also indicated by the healthiest cultivars and their respective years of release. The best cultivars, based on mean relative susceptibility against all PS isolates in the panel are “SY Ferry” (released 2012), “Zappa” (2009), “Kredo” (2009), “Potential” (2006), and “Tobak” (2011). Most susceptible were the older cultivars “Flair” (1996) and “Paroli” (2004). The cultivars Rumor (2013), “Rebell” (2013), “Kurt” (2013), “Xanthippe” (2011), and “Rebell” (2013) showed the lowest mean in relative susceptibility against all PT isolates. Conversely, “Nimbus” (1975) and “Vuka” (1975) were the most susceptible.

Seedling resistance as a response to a combination of isolates was further inferred based on infection type scores (cf. Supplementary Table S1). This might be of great interest to breeders, as it maximises the number of virulences which a cultivar might face under natural conditions. 13 out of the 191 cultivars, all released after 2005, were resistant against all PS isolates. Forty-eight cultivars were resistant to all five PT isolates, of which most but not all were released after 2005. A total of eight cultivars exhibited seedling resistance to all isolates of both pathogens, namely “Zappa” (2009), “Kredo” (2009), “Tabasco” (2008), “Tobak” (2011), “SY Ferry” (2012), “Xanthippe” (2011), and “Muskat” (2010). In contrast, 23 mainly older cultivars are susceptible to all rust isolates tested in this analysis.

DISCUSSION

This study focuses on the analysis of the isolate-specific resistance of wheat seedlings to stripe and leaf rust in relation to the time of cultivar release. Evidence of a steady increase in seedling resistance of European winter wheat released in Germany between 1966 and 2013 was found.

Resistance against Single Rust Isolates

Virulence complexity has increased in stripe rust in general and particularly with the occurrence of the Warrior races [18,33], which is also reflected in our selection of PS isolates. However, this might be an effect of the strong selection of the latest wave of immigrated PS races in relation to the increased complexity of resistance genes in winter wheat, as argued by [34].

“Triticale aggr.”, the oldest stripe rust isolate in the assay, infects mainly triticale. It has been detected in Europe since 2006 [5] on triticale but could infect some wheat genotypes in our study at the seedling stage (cf. the means of “infected leaf area” between isolates in Table 1). Its relatively low pathogenicity can beexplained by its low complexity of virulence and, more importantly, that it is not virulent against R genes commonly used in recent European wheat cultivars, such as Yr1, Yr3, Yr9, and Yr32, cf. [13]. In contrast to other stripe rust isolates “Triticale aggr.” is virulent to Yr10 but that resistance gene has been rarely utilized in the German cultivars [35]. The Warrior races became prevalent in Europe beginning in 2011 [5]. Isolates of these races produce telia in much higher quantities even on seedlings [36]. Accordingly, susceptibility to the latter races considerably exceeds infestation by “Triticale aggr.” in terms of both infection type and percentage of leaf area infected. Susceptibility to “Warrior(-)” is higher than to “Warrior + Yr27”, which cannot be explained by Yr27. This suggests that Yr27 is carried rarely by the genotypes in this study. Furthermore, the virulence of “Warrior(-)” in relation to the relatively frequent R genes YrSd (Yr Strubes Dickopf) and YrSu (Suwon 92/Omar) might explain the higher infection level. Against these, only partial virulence is present in “Warrior + Yr27”. Resistance against the “Oakley,v7/Kranich” isolate did not decrease much in comparison to the Warrior races. This might be attributable to the fact that “Oakley,v7/Kranich” is virulent to YrAmb and moderately virulent to YrSd and YrSu in modern cultivars, while each of the Warrior races is not or only moderately virulent to these Yr genes. However, minimal or no information about cultivars carrying these resistances is available. Furthermore, the differential set used in this study did not comprise all of the 80 Yr genes which have been identified for stripe rust [37]. A possible recombination between “Oakley,v7/Kranich” and the Warrior races could result in an increased level of stripe rust infections due to a high number of virulences. However, that would require a long-distance transport of uredospores of such races, as recombination most likely will not occur in Europe [38].

A slow trend towards higher virulence complexity in European leaf rust (e.g., Lr1, Lr2a, Lr24, Lr25, Lr28 and Lr29) was reported by [39], although virulence towards some Lr genes appears stable (e.g., Lr2b, Lr3a, Lr17) or fluctuating (e.g., Lr30). An increasing trend to higher virulences is not mirrored in our PT isolates, as we included old as well as recent isolates each with above- or below-average complexity. “77WxR” (isolated 1967) is the oldest, and “FI17” (isolated 2017) is the most recent leaf rust isolate in the test. However, both have a high virulence complexity (see above), but the respective mean susceptibility to them is low. “HkLr13”, “4083”, and “4171”, with intermediate age and virulence complexity, cause higher susceptibility on the panel of wheat cultivars analysed. Although PT isolates share 25 virulences and 9 avirulences, the virulence pattern is highly complex, as illustrated in Table 1. PT isolates differ in a few virulences towards resistance genes often deployed in European elite wheat (e.g., Lr3a, Lr10, Lr26) but also in additional virulences (e.g., Lr27, Lr28, Lr33, Lr40, Lr41), as well as in the aggressiveness of many virulences of which the utilisation of the respective resistance genes is not well known.

Breeding for resistances to stripe and leaf rust was lengthy in comparison to the successful control of stem rust beginning in 1915 in most parts of the world by a pyramidisation of R genes [7,40]. However, stem rust resistance in cultivars is based only on several genes, so that the occurrence and spread of Sr31-virulent races in the Ug99 race group caused epidemics in East Africa. Other virulent races resulted in local outbreaks in Ethiopia, Europe, and Central Asia [41].

Breeding Progress in Seedling Resistance

Breeding development against single isolates was estimated based on the year of cultivar release, as each isolate with its constant virulence pattern was tested on all cultivars. Susceptiblity trends differ among isolates, but improvement over time (breeding progress) can be observed against all isolates tested for both rust pathogens. Our results support and specify reports of breeding progress in adult plant resistanceto leaf rust in German winter wheat [24] and to stripe rust in Western European wheat [23] in the past five decades. Breeding progress in seedling resistance was achieved regardless of the complexity of the isolate (relatively low “Triticale aggr.”, “4171”, or high e.g., “Warrior + Yr27”, “77WxR”, “FI17”). It was neither relevant if the isolate was old (“77WxR'), relatively old (“Triticale aggr.”), or new (“FI17”, “Warrior + Yr27”). Thus, breeding progress was achieved despite the rapid changes in population dynamics in stripe rust, where isolates and races with an increasing number of virulence genes have spread in the past decades [18].

Progress has also been achieved in leaf rust, where the isolates have mostly a higher complexity and a recombinant population structure of virulence genes today [21]. Accordingly, R genes have not only been introduced into the European wheat cultivars of the panel but must have also been pyramidised. Otherwise, seedlings of modern cultivars would be more susceptible to at least some races within the rust population. Moreover, seedlings of modern cultivars are also more frequently resistant to a combination of isolates, while seedlings of older cultivars are among the most susceptible. Seedlings of old cultivars are also the most susceptible to low complexity and older isolates. The best explanation of these findings is that R genes contribute to quantitative seedling resistance of cultivars after they have been “overcome” by some isolates, such as Yr1, Yr6, Yr9, and Yr32 by “Oakley,v7/Kranich” and the Warrior isolates as well as Yr27 by “Warrior + Yr27”; Lr1, Lr2a, Lr3a, Lr10, Lr14a, Lr17, Lr20, Lr23, Lr26 by “77WxR”). This conclusion supports hypothesis #5 compiled by [42] that quantitative disease can result from R genes which have been broken down by virulent races. Specifically, the level of disease can be reduced in the presense of a “defeated” R gene relative to the suceptibility in the absense of the respective R gene. That effect of “residual resistance” has been described for different pathosystems, such as wheat-powdery mildew [43], wheat-stem rust [44], and rice-Xanthomonas oryzae [45].

There is no indication that older cultivars in the panel are more resistant to older isolates and that modern cultivars are only adapted to more recent pathogen races. For example, PS isolate “Triticale aggr.” and PT isolate “77WxR” are the oldest isolates tested of each pathogen on the panel. Although in both cases, older cultivars are less susceptible in comparison to other isolates, modern cultivars are even more resistant. That effect is similar to the response to the highly recent and aggressive PS Warrior isolates, with the difference that the relative susceptibility is already higher in older cultivars. Therefore, the thesis that modern European elite wheat cultivars are poorly endowed against probable stressors of the future, as speculated in a recent article [46] and rejected by [47,48], is not supported by our data.

CONCLUSIONS

This study represents the first attempt to assess progress in fungal seedling resistance in a large panel of European elite winter wheat cultivars responding to single isolates of stripe and leaf rust common in Europe. The results prove that a steady increase in seedling resistance was accomplished in five decades of the continuous breeding of winter wheat. An additive contribution of overcome R genes to seedling resistance is hypothesised.

Rust resistance breeding in European winter wheat was effective, as resistance against various isolates and races has been introduced into elite cultivars faster than resistance was lost by the emergence of pathogen races with new virulences. Thus, we conclude that the implemented breeding strategies for both higher yield potential and improved resistance was in summary highly successful.

Breeding progress in seedling resistance of European winter wheat could not be attributed to single R genes in this study because of the multitude of pathogen virulences and R genes which influence the susceptibility of a single cultivar. However, a list of cultivars with seedling resistance to a combination of the isolates tested is provided. The combined dataset of relative susceptibility will be further used in genome-wide association studies (GWAS) to infer isolate specific loci of seedling resistance. Moreover, rigorous data comparison and filtering with quantitative data of susceptibility of adult plants acquired on the same panel and subsequent GWAS might allow one to infer candidate loci of further APR genes.

SUPPLEMENTARY MATERIALS

Supplementary File (XLSX, 22 KB)

DATA AVAILABILITY

The dataset of the study is available from the authors upon reasonable request.

AUTHOR CONTRIBUTIONS

HZ, AS, and FO designed the study. HZ performed the seedling experiments. AS conducted the virulence tests. HZ and AS analysed the data. HZ, AS, and FO wrote the paper with input from all authors.

CONFLICTS OF INTEREST

The authors declare that the study was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

FUNDING

Funding for the study was provided by the German Federal Ministry of Education and Research (BMBF, 031A354F) through Projektträger Jülich (ptJ) within the project Breeding Innovations in Wheat for Efficient Cropping Systems (BRIWECS).

ACKNOWLEDGMENTS

The authors gratefully acknowledge Jana Heinze for technical assistance, Nico Pastor-Käppner and Frauke Gerken for multiplication of the rust pathogen isolates. We thank two anonymous reviewers for critically reading the manuscript and suggesting substantial improvements as well as Janine Ceschia and Stephanie Leguichard for proofreading the article.

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How to Cite This Article

Zetzsche H, Serfling A, Ordon F. Breeding Progress in Seedling Resistance against Various Races of Stripe and Leaf Rust in European Bread Wheat. 2019;1:e190021. https://doi.org/10.20900/cbgg20190021

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