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Article

Powdery Mildew Resistance Genes in European Barley Cultivars Registered in the Czech Republic from 2016 to 2020

by
Antonín Dreiseitl
Department of Integrated Plant Protection, Agrotest Fyto Ltd., Havlíčkova 2787, CZ-767 01 Kroměříž, Czech Republic
Genes 2022, 13(7), 1274; https://doi.org/10.3390/genes13071274
Submission received: 23 June 2022 / Revised: 13 July 2022 / Accepted: 16 July 2022 / Published: 18 July 2022
(This article belongs to the Section Plant Genetics and Genomics)
Versions Notes

Abstract

:
Barley is an important crop grown annually on about 55 Mha and intensively cultivated in Europe. In central and north-western Europe, spring and winter barley can be grown in similar environments which creates suitable conditions for the development of barley pathogens, including Blumeria graminis f. sp. hordei, the causal agent of powdery mildew. Apart from pesticide application, it can be controlled by inexpensive and environmentally-friendly genetic resistance. In this contribution, results of the resistance gene identification in 58 barley cultivars to powdery mildew are presented. In 56 of them their resistances were postulated and in two hybrid cultivars a recently developed method of gene identification was used. In total, 18 known resistance genes were found and several unknown genes were detected. In spring barley, a gene of durable resistance mlo is still predominant. MlVe found in winter SU Celly was the only new resistance gene recorded in barley cultivars registered in the Czech Republic in this time span. Since 2001 eight new genes of specific resistance have been identified in cultivars registered in the country and their response under field conditions is discussed, including the corresponding responses of the pathogen population due to directional selection. Different strategies for breeding spring and winter barley are recommended.

1. Introduction

In Europe barley (Hordeum vulgare L.) plays a more important role in crop cultivation than elsewhere in the world. In 2020, 46% of the global area of barley was grown in the subcontinent totaling more than 60% of world production. In the Czech Republic, the crop occupied 332 thousand ha and 1.82 Mt of grain was harvested [1]. In the same year, 124 barley cultivars (68 spring and 56 winter) were registered in the country [2], but the cultivated spring crop was almost at a historical low of only 217 thousand ha [3]. Only 15 cultivars were of domestic origin, but they occupied 50% of the growing area. Winter barley was grown on 115 thousand ha and the only two domestic cultivars comprised 1.2% of the seed propagation area [4].
In the country the ratio of winter to spring barley is almost exactly 1:2. These proportions create good epidemiological conditions for regular infection of cultivars with low resistance to diseases caused by the airborne pathogens [5] including the fungus Blumeria graminis (DC.) Golovin ex Speer f. sp. hordei Em. Marchal (Bgh).
Barley powdery mildew caused by Bgh can be controlled by inexpensive and environmentally-friendly genetic resistance or suitable fungicides [6]. Effective resistance protects cultivars and reduces the production of inoculum that could infect other cultivars including those that are susceptible. Many major resistance genes [7,8] and fungicides have been used to control powdery mildew, but numerous agro-chemical compounds [9] and genes of specific resistance have lost their protective effect due to adaptation of the pathogen [10,11].
Adaptive evolution of Bgh [12] takes place in large populations that permit frequent mutations from avirulence to virulence [13], mixed reproduction—i.e., alternating vegetative and generative cycles—almost unlimited recombination ability, polycyclic infection during the vegetative growth stages with explosive reproduction, and migration through the long-distance dissemination of airborne spores [14].
In Central and Northwestern Europe, these general characteristics of the pathogen are enhanced by a long-term and massive use of diverse cultivar resistances [15], a high concentration of barley forming an almost perfect “green bridge” optimized by mild climatic conditions that enable joint cultivation of spring and winter barley. During a period of cold, Bgh reproduces on its winter host. In the ensuing summer, the vegetation of spring and winter types are linked by a great mass of volunteer plants, which carry the same genes of specific resistance as their parent cultivars, but which often differ between these two forms. All these factors promote directional selection of virulent pathotypes on cultivars with diverse genes of specific resistance and result in a high virulence complexity and pathogen diversity [16]. To obtain sufficient durability of resistance against powdery mildew by breeding cultivars with specific resistances and their combinations is difficult.
The determination of genes of specific resistance against diseases [17,18], later described as ‘postulation’ [19], began to be widely used after the elucidation of the genetic relationships between host-specific resistance and the virulence of a pathogen [20], an interaction subsequently known as the gene-for-gene hypothesis [21], concept [22] or model [23]. The gene postulation of specific resistance against powdery mildew in barley cultivars was carried out mainly in North-western (Denmark, France, the Netherlands, Sweden, United Kingdom) and Central Europe (Austria, Czech Republic, Germany and Poland), and already in 1991 resistance genes of 699 European varieties were collated into a catalogue [15].
The postulation of specific resistances is based on recording the phenotypic responses of a variety after inoculation with pathogen isolates to obtain an infection response array (IRA) also known as the resistance spectrum [24], resistance profile [25] or reaction (response) type array [26,27]. Comparing the IRAs of tested varieties with IRAs of standard genotypes possessing known resistance genes results in the postulation of known or unknown genes and gene combinations.
Resistance to powdery mildew had already been studied in all barley cultivars registered in the country until 2015 [27] and similar studies are extended in this report, which will address the following questions: (i) Do all the tested cultivars contain one or more major resistance genes to powdery mildew? (ii) Are there any new resistances present in the series of cultivars under test? (iii) Does the gene mlo of non-specific resistance still play a key role in the resistance of spring cultivars? (iv) What was the effectiveness of resistance genes newly used in this century? and (v) What kind of resistances can be recommended for breeding spring and winter barley?

2. Materials and Methods

2.1. Plant Material

In the period 2016–2020, a total of 57 commercial barley cultivars were registered and the resistance genes of 55 of them are postulated here. Spring barley Zeppelin registered in 2012 whose resistance was not identified in the previous study [27] was added. Resistance of a hybrid winter cultivar SU Hylona was recorded earlier and another hybrid SY Maliboo was studied here using a new method as described for SU Hylona [28]. For SY Maliboo, 1920 leaf segments were obtained from plants derived from seeds harvested from 40 separate spikes.

2.2. Pathogen Isolates

For resistance tests 62 selected reference isolates of Bgh were used (for SY Malibo, 48 isolates), which had been collected in 12 countries in all nonpolar continents over a period of 68 years (1953–2021) and comprised the global virulence/avirulence diversity of the pathogen. Before inoculation all isolates were checked for their purity and their correct pathogenicity phenotypes were verified on standard barley lines [29]. The isolates were multiplied on leaf segments of the susceptible cultivar Stirling.

2.3. Testing Procedure

About 60 seeds of each accession were sown in two pots (80 mm diameter) filled with a gardening peat substrate and placed in a mildew-proof greenhouse under natural daylight. The primary leaves were excised when the second leaves were emerging, and leaf segments 15 mm long were cut from the middle part of healthy fully expanded leaves. Three segments of each accession were placed on the surface of the media (0.8% water agar containing 40 mg−L of benzimidazole—a leaf senescence inhibitor) in a 150 mm Petri dish. Leaf segments were placed adjacent to each other along with four segments of susceptible Stirling oriented diagonally with their adaxial surfaces facing upward.
For inoculation, a cylindrical metal settling tower of 150 mm diameter and 415 mm in height closed at the top was used, and a dish with segments was placed at the bottom of the tower. Conidia of each isolate taken from a leaf segment of the susceptible cultivar with fully-developed pathogen colonies were shaken onto a square piece of black paper (40 × 40 mm) to visually control the amount of inoculum deposited. Then, the paper was rolled to form a blowpipe and conidia of the isolate were blown through a side hole of 13 mm diameter with its center 50 mm from the upper end into the settling tower over the Petri dish at a concentration of ca. 10 conidia mm−2. The dishes with inoculated leaf segments were incubated at 20 ± 1 °C under cool-white fluorescent lamps providing 12 h light at 30 ± 5 μmol m−2 s−1.

2.4. Evaluation

Seven days after inoculation, infection responses (IR = phenotype of accession × isolate interaction) were scored on a scale of 0–4 [30], where 0 = no mycelium and sporulation, and 4 = strong mycelial growth and sporulation. IRs 3, 3–4 and 4 were considered susceptible. Each accession was tested with a minimum of two replications. If there were significant differences in IRs between replicates, additional tests were done. A set of 62 IRs provided an infection response array (IRA) for each accession. Based on the gene-for-gene hypothesis [22], the resistance genes in accessions were postulated by comparing their IRAs with previously determined IRAs of standard barley genotypes possessing known resistance genes. During phenotyping special attention was paid to boundary IRs 2–3 and 3 separating resistance and susceptibility, which pose the greatest risk of error in distinguishing between resistance and susceptibility [31]. Other details of Material and Methods have been recently described [32].

3. Results

In 2016–2020, 57 barley cultivars were registered in the Czech Republic. Resistance of Zeppelin could not be identified in a previous study [27] and was added to this set. Therefore, in this paper, the resistance of 56 cultivars was postulated. Hybrid cultivars SU Hylona and SY Maliboo have been studied using a different method [28], the former within this cited article. Hence, the results of resistance gene determination in 58 barley cultivars to powdery mildew are presented herein.
Nineteen IRAs were recorded among postulated cultivars and indicated 18 known resistance genes. However, only three of these were found singly in the tested cultivars, while 15 genes were combined with other genes. Therefore, the set of IRAs was supplemented by 15 IRAs characterizing the phenotype of these genes. A fully susceptible IRA demonstrating the absence of any major resistance gene was also added. Twelve isolates were sufficient to characterize the 35 IRAs (Table 1).
Among 29 cultivars of spring barley, seven known resistance genes were found. In 21 cultivars, the durable resistance gene mlo with a characteristic phenotype IR0(3) and effective against all isolates used was present. This gene was also detected in one of the two lines of Spitfire, while the other line contained a combination of three Ml genes a1, g and La. The other two cultivars, Adam and Leenke, were also resistant to all the isolates used. However, in both cases in addition to rare IR0(3), IRs of hypersensitive reactions typical for specific resistances were recorded—often IR2 in Adam and less frequently IR1 in Leenke. Therefore, it seems likely that both of these cultivars have an unknown specific resistance, although the presence of mlo cannot be excluded, especially in Leenke. Bente, Clarinet, Pop, Remark and Zeppelin contained MlSI-1 and Pionier MlRo in combination with Mla8.
Tests of six two-rowed winter barleys revealed five resistance genes, none of which was identical to the seven genes recorded here in spring cultivars. Valerie contained Mla7, which is more typically present in spring barleys. In other cultivars, Mlra and Mlh, found almost exclusively in winter barley, and MlCh, known to be in both growth types, were revealed. SU Celly carries MlVe combined with another unidentified resistance.
The greatest genetic diversity of resistance genes was observed in a set of six-rowed winter cultivars, in which there were 11 Ml genes, and six of these (a6, IM9, aLo, aLv, Ru2 and p) were absent in the cultivars of the previous two sets. Combinations of four identical genes (a6, aLo, IM9 and ra) were found in four cultivars. In this set there were also two hybrid cultivars, SU Hylona and SY Maliboo. A full set of IRs that developed on leaf segments of SY Maliboo after inoculation with 48 isolates is shown in Table S1. MlaLo (RT0 after inoculation with Race I and J-462) and an unknown resistance (RT2 after inoculation with pathotypes GH, C-512 and Z-6) were detected in all tested SY Maliboo plants. This result indicates that both these genes were contained in both parents of this cultivar whereas Mlh was present in about half of the tested F2 plants and probably originates from one parent. An unknown resistance was found in eight out of the set of 58 cultivars (Table 2).

4. Discussion

4.1. Spring Barley

The most frequently identified resistance gene was mlo, present in at least 22 spring barley cultivars. The first commercial cultivar with this gene was the Dutch Atem registered in 1979 [33], and the first cultivar registered in the Czech Republic was the domestically-bred Forum, registered in 1993 [34,35]. The recessive gene mlo represents non-specific resistance; virulence against it has not been found and the possibility of its emergence is not expected. Its effectiveness is highly stable even after 43 years of its presence in commercial cultivars, and despite these cultivars having been predominant in Europe at least in the last three decades. The phenotype of cultivars containing this gene is represented by IR0(3), i.e., the presence of a small number (ca. 1% compared to the susceptible control) of less developed colonies. However, almost all cultivars containing mlo carry also one or more specific resistance genes, which, after inoculation with avirulent pathotypes, overlap its characteristic phenotype. Such cultivars are then often characterized by IR0, i.e., a frequent phenotype of new, fully effective but non-durable specific resistances, from which the cultivars based on the durable resistance Mlo are difficult to distinguish. Table 1 shows the wild phenotype (IRA) of this gene.
The presence of mlo cannot be excluded from Adam and Leenke. For Adam, the pedigree, which would have been beneficial, was not provided by the breeding company. Leenke was selected from an identical cross as Forman and has in its pedigree Salome—one of the first cultivars carrying mlo [33]. Unlike Leenke, in Forman there are no doubts about the presence of mlo. Spitfire also contains mlo, although only in one of two lines. Thus, this gene is present in 22 to 24 of the 29 spring cultivars.
In Pionier MlRo was identified, designated accordingly Roxana—the first known commercial cultivar containing this gene and registered in Germany in 2000. MlRo was recorded in Kangoo, the first cultivar with this gene registered in the Czech Republic (2008) and one of whose parents was Roxana. MlRo was also found in Marnie [36], one of the parents of Pionier and many other cultivars with this gene. The first five cultivars containing MlRo were registered in the Czech Republic in 2008–2010. Because of the probable migration from neighboring countries, especially Germany, and the intensive directional selection, the frequency of virulences to this gene in the domestic population of the pathogen increased from 3.5% in 2009 [37] to 81.9% in 2015 [16].
Four cultivars (Bente, Klarinette, Pop and Remark) were postulated with the resistance SI-1. The same resistance was revealed also in the Danish cultivar Zeppelin, the first with SI-1 cultivated in the Czech Republic. However, the resistance of Zeppelin remained unknown for many years [16,27] and has only been identified in this work. The presence of a putative second gene in Zeppelin (Mlg) [27] seems less likely. Zeppelin is a parent of the cultivars containing SI-1 except Pop. The first isolate virulent to MlSI-1 in the Danish spring cultivar Camilla—different from Austrian winter barley Camilla tested here—was found in an airborne population of the pathogen in 2015 [16] and since then the frequency of this virulence has been gradually increasing.

4.2. Winter Barley

In Beckenbauer, two genes, MlIM9 and Mla6, were detected. In the Czech Republic, the first cultivar containing MlIM9 was the German-bred cultivar Carola, registered here in 2001; it also contains Mla6 and Mlra [38]. After the discovery of MlLo in Lomerit and other cultivars [39], this gene was also found in Carola. MlLo was later mapped to the Mla locus or closely linked to it [28]. Carola is in the pedigree of nine cultivars registered in the Czech Republic, five of which contain MlIM9 [27], but none of them is part of this set. All four Ml genes in Carola (IM9, a6, aLo and ra) were subsequently found in several other cultivars including KWS Meridian [26] and its four daughter cultivars Journey, KWS Higgins, Novira and Rumcajs investigated here. However, in 2004, 14.1% of 262 isolates were virulent on Carola [40] and this proportion of isolates virulent to MlIM9 increased rapidly [41].
MlLv was identified in five winter barley cultivars, including the hybrid SU Hylona, which was named as the German cultivar Laverda and registered in the Czech Republic in 2007 [42]. This gene was subsequently located at the Mla locus [28]. The phenotype (IRA) corresponding to the presence of MlaLv was exhibited in Azrah and in three cultivars (Belissa, LG Zoro and SU Lauvira) this gene is present together with MlaLo. However, tests with four selected isolates (Table 3) showed that all five cultivars (four postulated here and the standard Laverda) differed not only in the presence of MlaLo but also other unknown genes. In addition, Mla6 and Mlra, which often occur in six-rowed winter barley cultivars, are likely to be in some of these cultivars. Nevertheless, these two genes cannot be detected in the presence of MlaLv as the pathogen gene bank does not contain any isolate virulent to MlaLv and Mlra but avirulent to Mla6. If Mla6, together with Mla14 closely linked to Mla6, is detected in at least one of these cultivars, it would contain a cluster of four genes located at or near the Mla locus (a6, a14, aLo and aLv). Cultivars carrying MlaLv followed a similar path to the resistance of MlRo when the frequency of virulence to MlaLv increased from 0.0% in 2008 [43] to 50.5% in 2013 [44].
Jakubus and SU Ellen contained Mlp and other genes. The parent of SU Ellen is the German-bred Saturn, which was the first cultivar with this gene registered in the Czech Republic in 2012 and Jakubus is a descendant of SU Ellen. Between 2000 and 2011, more than 800 isolates derived from the domestic airborne pathogen population were tested on Mlp-bearing cultivars and none of them was virulent to this gene. The first virulent isolates were detected in the country in 2009 [44], but their low frequency (around 1%) was stable at least until 2017 [16]. However, in 2019, the virulence frequency to this gene increased to approximately 5%, and in 2021 had already exceeded 50% [45]. This sudden change must have been caused by an influx of inoculum from other European countries [46] where cultivars with Mlp were cultivated in earlier years (at least in Germany and Poland) and supported by directional selection on cultivars grown here.
The two-rowed barley SU Celly is the first cultivar registered in the Czech Republic in which MlVe was found (in addition to an unknown resistance). The gene was designated according to the German naming of Venezia [47], which had been included in the Czech registration trials in 2004. Since 2009, Venezia has been added to the differentiation set for the study of domestic airborne populations and the first virulence was found in 2011 after studying 451 isolates [47]. In contrast to the Czech Republic, cultivars with Ve resistance were grown in Germany, where the pathogen population apparently adapted rapidly to this specific resistance. As a result of spore migration the frequency of a corresponding virulence reached 8.3% in the domestic population in 2017. The registration of SU Celly containing MlVe in 2020 came too late for this gene to have any positive effect on its resistance in the field. In spite of that, MlVe is the only new resistance gene present in barley cultivars registered in the Czech Republic in the given period.
SU Hylona and SY Maliboo are hybrid winter cultivars. The first hybrid registered in the Czech Republic in 2013 was the Swiss cultivar Hobbit. The identification of resistance genes of hybrid cultivars is usually too difficult for gene postulation, not only because hybrid cultivars (F1 generation) are characterized by the higher complexity of resistance genes due to the joint presence of alleles located at the same loci, but also because of the high heterogeneity resulting from multiplication of hybrid seed. Therefore, a method combining gene postulation with classical genetic analysis has been developed [28]. SU Hylona served as one of the six model cultivars for the development of this method. In the current work only one hybrid cultivar—SY Maliboo—was studied. The IRAs of both hybrid cultivars are not listed in Table 1 as they can only be assembled artificially, and as a rule, none of the tested sets of leaf segments derived from plants of F2 generation shows the relevant IRAs. Resistance of winter barley cultivars in the field is generally low and the hybrid cultivars studied so far have not led to progress towards greater or more durable resistance [28].

4.3. Other Remarks

In Table 2, country of origin of the studied cultivars is included. However, this information is of limited importance in the current conditions of breeding concentration. An example is the historically most successful domestic breeding station in Hrubčice, where three studied cultivars (LG Aurus, LG Ester and LG Monus) were bred. However, their country of origin is France, the country of their owner (Limagrain). Also the “national roots” (the initial germplasm of the cultivars) are weakening as a result of the internationalization of breeding. While 10 cultivars from Hrubčice registered in 1976–1985 were bred from 39 parent components, of which 23 (57.5%) were domestic [35], for 10 cultivars bred in 2005–2021 [27,48] including LG Stamgast, the share of domestic parent components was only 35% (7 out of 20).
The number of genes of specific resistance present in cultivars is increasing; in European cultivars registered in the Czech Republic this has risen by eight since 2001 (including MlaLo and MlLu—the last was not detected here). Thus, pathogen gene banks cannot keep such a diverse range of isolates for postulation studies to determine the main resistances as well as all possible gene combinations. This is particularly the case for genes for which there are fewer virulent isolates available. The abundance (frequency) of the pathotypes in the field and atmosphere then depends on the suitability of the conditions for allowing evolutionary forces to operate, especially regarding directional selection and migration [12]. The examples discussed in the previous paragraphs comprise the main resistance genes and their impact on a population. As the number of isolates required for more detailed postulation increases, it is possible to focus on the identification of more complex gene combinations as in the case of Saturn [46], or cultivars carrying MlaLv (Table 3). Sets of isolates can also be selected and after obtaining the required information can be discarded.
Responses of the pathogen population on cultivars containing six specific resistance genes were described above. One of the most successful adaptations of Bgh to a specific resistance due to directional selection and migration was the virulence to Mla13 [49] and its subsequent breakdown [50]. This feature could be summarized as “from a single mildew colony to European barley epidemics” [8]. It illustrates the ‘bust’ part of the ‘boom and bust cycle’ of specific resistances [12] on a continental scale.
Charles Darwin discussed the role of natural selection in evolution. Directional selection of virulent pathotypes on cultivars with specific resistances is a part of this process which can operate rapidly especially in populations of microorganisms. This corresponds to Bgh adapting to specific resistance genes through increased virulence frequencies and results in quickly overcoming the resistances as shown in several examples.

5. Conclusions

The monitored set of cultivars confirms the increasing differences in the resistance of spring and winter barley. The resistance of spring cultivars is based primarily on the durable non-specific resistance Mlo. The proportion of newly registered cultivars with this gene increased from 62.9% in 2006–2010 to 75.7% in 2011–2015 [27] and reached 75.9–82.8% during 2016–2020. This is a high proportion for one resistance, but there are no known reasons why the predominant use of this effective resistance should change. In contrast, all winter barley cultivars studied here are characterized by a wide range of specific resistances often with three or more genes, which, however, have only a slight positive effect on their resistance in the field. The longer growing season of winter barley, especially in the mild winters that have prevailed in recent decades, allows the pathogen to adapt faster to non-durable resistances. It is therefore necessary to move away from the use of major genes of specific resistance when breeding new, especially winter, cultivars.
As already stated [8], pyramiding of quantitative genes of nonspecific resistance [51,52] for reducing powdery mildew infection in the field [53,54,55] or using introgressions derived from bulbous barley grass (Hordeum bulbosum) [56,57] are promising ways for breeding future winter barleys. The utilization of a wide spectrum of resistances derived from more distant species [58], formerly known as non-host [59], can also be adopted once practical methods have been developed.

Supplementary Materials

The following supporting information can be downloaded at: https://www.mdpi.com/article/10.3390/genes13071274/s1, Table S1. Infection responses (IRs) developed on leaf segments excised from plants of F2 generation grown from seed of 40 individually harvested ears of hybrid winter barley cultivar SY Malibo after inoculation with 48 Blumeria graminis f. sp. hordei isolates.

Funding

The study was funded by the Ministry of Agriculture of the Czech Republic, institutional support no. MZE-RO1118.

Institutional Review Board Statement

Not applicable.

Informed Consent Statement

Not applicable.

Data Availability Statement

All relevant data are presented in the article and Supplementary Table S1.

Acknowledgments

The excellent technical assistance of Dagmar Krejčířová for conducting the resistance tests is highly appreciated.

Conflicts of Interest

The author declares no conflict of interest.

References

  1. FAOSTAT. Available online: https://www.fao.org/worldfoodsituation/csdb/en/ (accessed on 24 May 2022).
  2. Státní Odrůdová Kniha 2020. Available online: https://eagri.cz/public/web/file/654573/_32020.pdf (accessed on 1 June 2022).
  3. Situační a výhledová zpráva. Obiloviny. Available online: https://eagri.cz/public/web/file/702121/SVZ_Obiloviny_12_2021.pdf (accessed on 1 June 2022).
  4. UKZUZ Obilniny 2020. Available online: https://eagri.cz/public/web/file/650948/Obilniny_2020.pdf (accessed on 1 June 2022).
  5. Oguz, A.C.; Karakaya, A. Genetic diversity of barley foliar fungal pathogens. Agronomy 2021, 11, 434. [Google Scholar] [CrossRef]
  6. Hysing, S.C.; Rosenqvist, H.; Wiik, L. Agronomic and economic effect of host resistance vs. fungicide control of barley powdery mildew in southern Sweden. Crop Protect. 2012, 41, 122–127. [Google Scholar] [CrossRef]
  7. Jørgensen, J.H. Genetics of powdery mildew resistance in barley. Crit. Rev. Plant Sci. 1994, 13, 97–119. [Google Scholar] [CrossRef]
  8. Dreiseitl, A. Specific resistance of barley to powdery mildew, its use and beyond. A concise critical review. Genes 2020, 11, 971. [Google Scholar] [CrossRef] [PubMed]
  9. Hollomon, D.W. Resistance of barley powdery mildew to fungicides. ADAS Quart. Rev. 1980, 39, 226–233. [Google Scholar]
  10. Hobbelen, P.H.F.; Paveley, N.D.; van den Bosch, F. The emergence of resistance to fungicides. PLoS ONE 2014, 9, e91910. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  11. Hollomon, D.W. Fungicide resistance: Facing the challenge. Plant Protect. Sci. 2015, 51, 170–176. [Google Scholar] [CrossRef]
  12. McDonald, B.A.; Linde, C. Pathogen population genetics, evolutionary potential, and durable resistance. Annu. Rev. Phytopathol. 2002, 40, 349–379. [Google Scholar] [CrossRef] [Green Version]
  13. Hollomon, D.W.; Brent, K.J. Combating plant diseases—The Darwin connection. Pest Managem. Sci. 2009, 65, 1156–1163. [Google Scholar] [CrossRef]
  14. Brown, J.K.M.; Hovmøller, M.S. Epidemiology—Aerial dispersal of pathogens on the global and continental scales and its impact on plant disease. Science 2002, 297, 537–541. [Google Scholar] [CrossRef] [Green Version]
  15. Brown, J.K.M.; Jørgensen, J.H. A catalogue of mildew resistance genes in European barley varieties. In Integrated Control of Cereal Mildews: Virulence and Their Change, Proceedings of the Second European Workshop on Integrated Control of Cereal Mildews, Risø National Laboratory, Roskilde, Denmark, 23–25 January 1990; Jørgensen, J.H., Ed.; Risø National Laboratory: Roskilde, Denmark, 1991; pp. 263–286. [Google Scholar]
  16. Dreiseitl, A. Great pathotype diversity and reduced virulence complexity in a Central European population of Blumeria graminis f. sp. hordei in 2015–2017. Eur. J. Plant Pathol. 2019, 53, 801–811. [Google Scholar] [CrossRef]
  17. Brückner, F. Powdery mildew (Erysiphe graminis DC.) on barley. V. The resistance of barley varieties to physiological races of Erysiphe graminis DC. detected in Czechoslovakia and the possibility to use it in breeding for resistance. Rostl. Vyrob. 1964, 10, 395–408. [Google Scholar]
  18. Dinoor, A.; Peleg, N. Employing gene-for-gene hypothesis to estimate number of resistance genes in host and virulence in pathogen, and to determine their identity. Israel J. Agricult. Res. 1971, 21, 147. [Google Scholar]
  19. McVey, D.V.; Roelfs, A.P. Postulation of genes for stem rust resistance in entries of 4th International winter-wheat performance nursery. Crop Sci. 1975, 15, 335–337. [Google Scholar] [CrossRef]
  20. Flor, H.H. Host-parasite interaction in flax rust—its genetics and other implications. Phytopathology 1955, 45, 680–685. [Google Scholar]
  21. Metzger, R.J.; Trione, E.J. Application of gene-for-gene relationship hypothesis to Triticum tilletia system. Phytopathology 1962, 52, 363. [Google Scholar]
  22. Flor, H.H. Current status of the gene-for-gene concept. Annu. Rev. Phytopathol. 1971, 9, 275–296. [Google Scholar] [CrossRef]
  23. Browder, L.E.; Eversmeyer, M.G. Sorting of Puccinia-recondita, Triticum infection-type data sets towards the gene-for-gene model. Phytopathology 1980, 70, 666–670. [Google Scholar] [CrossRef]
  24. Jensen, H.P.; Christensen, E.; Jørgensen, J.H. Powdery mildew resistance genes in 127 northwest European spring barley varieties. Plant Breed. 1992, 108, 210–228. [Google Scholar] [CrossRef]
  25. Andrivon, D.; de Vallavieille-Pope, C. Race-specific resistance genes against Erysiphe graminis f. sp. hordei in old and recent French barley accessions. Plant Breed. 1992, 108, 40–52. [Google Scholar] [CrossRef]
  26. Dreiseitl, A. Genes for resistance to powdery mildew in European winter barley cultivars registered in the Czech Republic and Slovakia to 2010. Plant Breed. 2013, 132, 558–562. [Google Scholar] [CrossRef]
  27. Dreiseitl, A. Genes for resistance to powdery mildew in European barley cultivars registered in the Czech Republic from 2011 to 2015. Plant Breed. 2017, 136, 351–356. [Google Scholar] [CrossRef]
  28. Dreiseitl, A. A novel way to identify specific powdery mildew resistance genes in hybrid barley cultivars. Sci. Rep. 2020, 10, 18930. [Google Scholar] [CrossRef]
  29. Kølster, P.; Munk, L.; Stølen, O.; Løhde, J. Near-isogenic barley lines with genes for resistance to powdery mildew. Crop Sci. 1986, 26, 903–907. [Google Scholar] [CrossRef]
  30. Torp, J.; Jensen, H.P.; Jørgensen, J.H. Powdery Mildew Resistance Genes in 106 Northwest European Spring Barley Cultivars; Year-Book; Royal Veterinary and Agricultural University: Copenhagen, Denmark, 1978; pp. 75–102. [Google Scholar]
  31. Kosman, E.; Chen, X.; Dreiseitl, A.; McCallum, B.; Lebeda, A.; Ben-Yehuda, P.; Gultyaeva, E.; Manisterski, J. Functional variation of plant-pathogen interactions: New concept and methods for virulence data analyses. Phytopathology 2019, 109, 1324–1330. [Google Scholar] [CrossRef]
  32. Dreiseitl, A. Postulation of specific disease resistance genes in cereals: A widely used method and its detailed description. Pathogens 2022, 11, 284. [Google Scholar] [CrossRef]
  33. Jørgensen, J.H. Discovery, characterisation and exploitation of Mlo powdery mildew resistance in barley. Euphytica 1992, 63, 141–152. [Google Scholar] [CrossRef]
  34. Brückner, F. The breeding of the malting barley cultivar of new morphotype Forum. Genet. Šlecht. 1993, 29, 199–203. [Google Scholar]
  35. Dreiseitl, A.; Jørgensen, J.H. Powdery mildew resistance in Czech and Slovak barley cultivars. Plant Breed. 2000, 119, 203–209. [Google Scholar] [CrossRef]
  36. Dreiseitl, A. Resistance of ‘Roxana’ to powdery mildew and its presence in some European spring barley cultivars. Plant Breed. 2011, 130, 419–422. [Google Scholar] [CrossRef]
  37. Dreiseitl, A. Changes in the population of Blumeria graminis f.sp. hordei in the Czech Republic from 2009 to 2010. Plant Protect. Sci. 2011, 47, 43–51. [Google Scholar] [CrossRef] [Green Version]
  38. Dreiseitl, A. Powdery mildew resistance in winter barley cultivars. Plant Breed. 2007, 126, 268–273. [Google Scholar] [CrossRef]
  39. Dreiseitl, A. Dissimilarity of barley powdery mildew resistances Heils Hanna and Lomerit. Czech J. Genet. Plant Breed. 2011, 47, 95–100. [Google Scholar] [CrossRef] [Green Version]
  40. Dreiseitl, A. Virulence frequencies to powdery mildew resistance genes of winter barley cultivars. Plant Protect. Sci. 2004, 40, 135–140. [Google Scholar] [CrossRef] [Green Version]
  41. Dreiseitl, A. Virulence frequency to powdery mildew resistances in winter barley cultivars. Czech J. Genet. Plant Breed. 2008, 44, 160–166. [Google Scholar] [CrossRef] [Green Version]
  42. Dreiseitl, A. Resistance of ‘Laverda’ to powdery mildew and its presence in some winter barley cultivars. Cereal Res. Commun. 2011, 39, 569–576. [Google Scholar] [CrossRef]
  43. Dreiseitl, A. Changes in virulence frequencies and higher fitness of simple pathotypes in the Czech population of Blumeria graminis f. sp. hordei. Plant Protect. Sci. 2015, 51, 67–73. [Google Scholar] [CrossRef] [Green Version]
  44. Dreiseitl, A. Rare virulences of barley powdery mildew found in aerial populations in the Czech Republic from 2009 to 2014. Czech J. Genet. Plant Breed. 2015, 51, 1–8. [Google Scholar] [CrossRef] [Green Version]
  45. Dreiseitl, A. (Department of Integrated Plant Protection, Agrotest Fyto Ltd., Havlíčkova 2787, CZ-767 01 Kroměříž, Czech Republic). Study of the Czech airborne population of Blumeria graminis f. sp. hordei. 2022; Unpublished work. [Google Scholar]
  46. Dreiseitl, A. Emerging Blumeria graminis f. sp. hordei pathotypes reveal ‘Psaknon’ resistance in European barley varieties. J. Agric. Sci. 2016, 154, 1082–1089. [Google Scholar] [CrossRef]
  47. Dreiseitl, A. Resistance of barley variety ‘Venezia’ and its reflection in Blumeria graminis f. sp. hordei population. Euphytica 2018, 214, 40. [Google Scholar] [CrossRef]
  48. Dreiseitl, A. Postulation of genes for resistance to powdery mildew in spring barley cultivars registered in the Czech Republic from 1996 to 2010. Euphytica 2013, 191, 183–189. [Google Scholar] [CrossRef]
  49. Brückner, F. The finding of powdery mildew (Erysiphe graminis DC. var. hordei Marchal) race on barley: A race virulent to resistance genes Mla9 and Mla14. Ochr. Rostl. 1982, 18, 101–105. [Google Scholar]
  50. Wolfe, M.S.; Brändle, U.; Koller, B.; Limpert, E.; McDermott, J.M.; Müller, K.; Schaffner, D. Barley mildew in Europe: Population biology and host resistance. Euphytica 1992, 63, 125–139. [Google Scholar] [CrossRef]
  51. Brown, J.K. Durable Resistance of Crops to Disease: A Darwinian Perspective. Annu. Rev. Phytopathol. 2015, 53, 513–539. [Google Scholar] [CrossRef]
  52. Niks, R.E.; Qi, X.; Marcel, T.C. Quantitative Resistance to Biotrophic Filamentous Plant Pathogens: Concepts, Misconceptions, and Mechanisms. Annu. Rev. Phytopathol. 2015, 53, 445–470. [Google Scholar] [CrossRef] [Green Version]
  53. Cowger, C.; Brown, J.K. Durability of Quantitative Resistance in Crops: Greater Than We Know? Annu. Rev. Phytopathol. 2019, 57, 253–277. [Google Scholar] [CrossRef]
  54. Miedaner, T.; Boeven, A.L.G.-C.; Gaikpa, D.S.; Kistner, M.B.; Grote, C.P. Genomics-Assisted Breeding for Quantitative Disease Resistances in Small-Grain Cereals and Maize. Int. J. Mol. Sci. 2020, 21, 9717. [Google Scholar] [CrossRef]
  55. Czembor, J.H.; Czembor, E.; Suchecki, R.; Watson-Haigh, N.S. Genome-wide association study for powdery mildew and rusts adult plant resistance in European spring barley from Polish gene bank. Agronomy 2022, 12, 7. [Google Scholar] [CrossRef]
  56. Xu, J.; Kasha, K.J. Transfer of a dominant gene for powdery mildew resistance and DNA from Hordeum bulbosum into cultivated barley (Hordeum vulgare). Theor. Appl. Genet. 1992, 84, 771–777. [Google Scholar] [CrossRef]
  57. Pickering, R.A.; Hill, A.M.; Michel, M.; Timmerman-Vaughan, G.M. The transfer of a powdery mildew resistance gene from Hordeum bulbosum L. to barley (H. vulgare L.) chromosome 2 (2I). Theor. Appl. Genet. 1995, 91, 1288–1292. [Google Scholar] [CrossRef]
  58. Panstruga, R.; Moscou, M.J. What is the molecular basis of nonhost resistance? Molecul. Plant-Microbe Interact. 2020, 33, 1253–1264. [Google Scholar] [CrossRef]
  59. Niks, R.E. Nonhost plant-species as donors for resistance to pathogens with narrow host range. 2. Concepts and evidence on the genetic-basis of nonhost resistance. Euphytica 1988, 37, 89–99. [Google Scholar] [CrossRef]
Table
Table 1. Infection response arrays (IRAs) produced by 12 Blumeria graminis f. sp. hordei isolates on 35 barley genotypes carrying known Ml resistance genes.
Table 1. Infection response arrays (IRAs) produced by 12 Blumeria graminis f. sp. hordei isolates on 35 barley genotypes carrying known Ml resistance genes.
Ml Resistance Isolate
Gene(s)JAP 1ISRISRDKCZCZCZCZCZCZCZCZ
R-1J-462Y-69EA30I-162I-20X-30Y-4O-11M-8X-1X-8
1953 219791979198620092011201220132016201720212021
none4 344444444444
a14444040444044
a1, g, La0440402–344044
a6044404444444
a6, aLo, IM9, ra004004242444
a6, aLo, p, ra004002422244
a6, aLo, ra004004444444
a6, aLo, ra, Ru2004004442–3444
a6, IM9024204242444
a6, ra044004444444
a70001–244444444
a8044444444444
a8, h04441–24444444
a8, h, Ru214441–24442–3444
aLo004444444444
aLo, Lv004111141141
aLo, ra004044444444
Ch244444444444
Ch, h, ra24401–24444444
Ch, ra244044444444
g044040444444
h44441–24444444
h, ra44401–24444444
IM9224224242444
La4442–3442–344444
Lv11–24111141141
mlo50(3)0(3)0(3)0(3)0(3)0(3)0(3)0(3)0(3)0(3)0(3)0(3)
p244222422244
ra444044444444
Ro440–100–140–10–14400–1
Ro, a8040–100–140–10–14400–1
Ru2444444442–3444
SI-1011000000004
Ve004000400040
Ve, u6004000000040
1 Country of isolate origin: JAP—Japan, ISR—Israel, DK—Denmark, CZ—Czech. 2 Year of isolate collection. 3 According to Torp et al. [30], IR4 represents susceptibility. 4 Highlighted IRAs were found only in standard lines. 5 Wild phenotype. 6 u = Unknown.
Table
Table 2. Powdery mildew resistance genes in 57 European barley cultivars registered in the Czech Republic from 2016 to 2020 and Zeppelin.
Table 2. Powdery mildew resistance genes in 57 European barley cultivars registered in the Czech Republic from 2016 to 2020 and Zeppelin.
CultivarOriginalPedigreeCountryYear ofMl Gene(s)
Designation of OriginRegistration
Spring, Two-Rowed
AccordineAC 10/734/33(Sunshine × SY Firkin) × SY FirkinGermany2018mlo
AdamNORD 15/1107NAGermany2020u
AligatorSTRG 774/11Gundel × S99G153 (Braemar × Roxanna)Germany2016mlo
AvusSTRG 687/15Explorer × ShuffleGermany2020mlo
BenteNORD 13/1114(Vendela × Zeppelin) × GraceGermany2018SI-1
CosmopolitanSJ 152037(KWS Irina × Evergreen) × (Sanette × Paustian)Denmark2019mlo
FandagaNORD 14/2404Ginger × BritneyGermany2020mlo
FormanNORD 12/2444(Salome × Livia) × PropinoGermany2017mlo
IsmenaNORD 14/2403NAGermany2019mlo
KlarinettSC 101-12AZeppelin × GraceFrance2019SI-1
KWS FantexKWS 13/207Sunshine × KWS IrinaGermany2018mlo
LaureateSY 412-328Sanette × ConcertoGermany2019mlo
LeenkeNORD 12/2531(Salome × Livia) × PropinoGermany2017u
LG AurusLGBHE3427APetrus × ZhanaFrance2019mlo
LG EsterLGBHE3254BScrabble × SignumFrance2020mlo
LG MonusHE-2645HE 204 × GladysFrance2017mlo
LG NabucoLGBN1315Cropton × LN0925France2018mlo
LG ToscaLGBN14223-2RGT Planet × LGBN1469France2020mlo
LibušeNORD 11/2411NFC 403-135 × GraceGermany2016mlo
MantaAC 07/547/417(Claire × Quench) × LillyGermany2016mlo
OvationLGB12-8317-ANSL 07-8113-B × TeslaFrance2017mlo
PiloteSY 413357Saporis × MeliusSwitzerland2018mlo
PionierSC 65/03 NZ 7CMarnie × BeatrixFrance2016a8, Ro
PopSC 44801 N2Calcul × SY FirkinFrance2017SI-1
RemarkAC 09/547/43Zeppelin × ColumbusGermany2017SI-1
RunnerNORD 14/2534NAGermany2019mlo
SoulmateNOS 16111-55Barabas × KeopsDenmark2017mlo
SpitfireSG-S 212STRG 01/410/41 × WestminsterCzech2018a1, g, La + mlo
TangoLN1147Jazz × ClaireFrance2016mlo
Zeppelin 1SJ 071085(Scandium × Isabella) × SJ 050623Denmark2012SI-1
Winter, Two-Rowed
KWS DonauKW 2-430(KWS Liga × KWS Stella) × KW 2-936Germany2017Ch, ra
NeptunSJ 128045Sandra × MatrosDenmark2019Ra
SobellSJ 128113Augusta × KWS Cassia × MatrosDenmark2019ra, u
SU CellyNORD 13109/14(NORD 2930 × Valentina) × CaliforniaGermany2020Ve, u
TorpedoAC 08/290/26KWS Cassia × AugustaGermany2016Ch, h, ra, u
ValerieBr 11500r6207-589 × SandraGermany2020a7
Winter, Six-Rowed
AzrahSTRG 432/09Laverda × (Cornelia × Carola)Germany2018aLv
BeckenbauerBE 2008024004DKathleen × BE 2718Germany2019a6, IM9
BelissaAC 09/275/22KWS Meridian × AntonellaGermany2017aLo, aLv, u
CamillaSZD 2213ASemper × KathleenAustria2019h, ra
FalbalaLEU 53120(ST 2475 × Fridericus) × AmelieGermany2020a6, ra
ImpalaLEU 43408St. 2474 × Federicus × MeridianGermany2018a6, aLo, ra, Ru2
JakubusNORD 12119/102Bella × SU EllenGermany2020a6, aLo, p, ra
JourneyKW 6-451KWS Meridian × KWS TonicGermany2018a6, aLo, IM9, ra
KWS HigginsKW 6-331KW 6-855 × KWS MeridianGermany2017a6, aLo, IM9, ra
KWS WallaceKW 6-1541KWS Tonic × KW 6-148Germany2019a8, h
LaurinNORD 11002/8Tenor × 08076/86 (Kathleen × Saturn)Germany2018aLo, ra, u
LG TriumphLGBN13W125-43Souleyka × KWS MeridianFrance2017a6, aLo, ra
LG ZoroLGBB15W003KWS Meridian × RafaelaFrance2019aLo, aLv
NoviraAC 09/278/6AC 07/142/36 × KWS MeridianGermany2017a6, aLo, IM9, ra
PegasosLEU 63112(Ramata × ST2426) × ST2427Germany2020aLo, ra
RumcajsSTRG 568/15Kathleen × KWS MeridianCzech2020a6, aLo, IM9, ra
SU EllenNORD 08076/133Kathleen × SaturnGermany2017a6, aLo, p, ra
SU Hylona 2,3DEH 13/1807CMS04LM183L001 × 10HR170D002Germany2018al, aLv
SU JuleBE 2008108012Semper × BE 27090Germany2018a7
SU LauviraNORD 13078/8NORD 11118/64 × ((BYDW 55 × Kathleen) ×Germany2020aLo, aLv, u
(Tenor × Loreley))
SY Maliboo 2SY 216489(F1F180 × RE35) × MT0767Switzerland2020aLo, h, u
WilliamKW 6-437(LP 6-854 × KWS Meridian) × KWS TonicGermany2020Ch, h, Ru2
1 Resistance of Zeppelin could not be postulated previously [27]. 2 Hybrid cultivar. 3 Resistance was published in a set of hybrid cultivars [28]. u = unknown resistance gene. + indicates presence of different genotypes.
Table
Table 3. Infection response arrays produced by four Blumeria graminis f. sp. hordei isolates on five winter barley cultivars carrying MlaLv resistance gene.
Table 3. Infection response arrays produced by four Blumeria graminis f. sp. hordei isolates on five winter barley cultivars carrying MlaLv resistance gene.
CultivarMlISR 1CZCZCZ
ResistanceJ-462Y-4M-4A-1
Gene(s)1979 2201320152015
AzrahaLv4 3444
LG ZoroaLv, aLo0444
SU LauviraaLv, aLo, u0244
BelissaaLv, aLo, u040–14
LaverdaaLv, u1–241–24
1 Country of isolate origin: ISR—Israel, CZ—Czech. 2 Year of isolate collection. 3 According to Torp et al. [30], IR4 represents susceptibility.
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Dreiseitl, A. Powdery Mildew Resistance Genes in European Barley Cultivars Registered in the Czech Republic from 2016 to 2020. Genes 2022, 13, 1274. https://doi.org/10.3390/genes13071274

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Dreiseitl A. Powdery Mildew Resistance Genes in European Barley Cultivars Registered in the Czech Republic from 2016 to 2020. Genes. 2022; 13(7):1274. https://doi.org/10.3390/genes13071274

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Dreiseitl, A. (2022). Powdery Mildew Resistance Genes in European Barley Cultivars Registered in the Czech Republic from 2016 to 2020. Genes, 13(7), 1274. https://doi.org/10.3390/genes13071274

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