Grasses are able to harbor the oversummering of urediospores and the overwintering of teliospores of Puccinia striiformis f. sp. tritici in China
Phytopathology Research volume 4, Article number: 24 (2022)
Puccinia striiformis f. sp. tritici (Pst), the cause of wheat stripe rust, is a biotrophic and heteroecious rust fungus with five spore types. Cool and humid climatic conditions are conducive for the development of wheat stripe rust, and in turn, temperatures above 22 °C limit or even cease the disease. The survival of Pst during summer after wheat harvest is responsible for the infection on autumn-sown wheat to maintain disease cycle all the year round. Teliospores formed at late stage of wheat growth are essential for initiating sexual reproduction in spring. Although Chinese native grasses have been experimentally testified as susceptible hosts for Pst and teliospores produced on wheat have been shown to be potential inoculum sources causing infection on alternate hosts (mainly Berberis) in spring, the roles of grass hosts in harboring the survival of urediospores and teliospores of Pst and promoting the emergence of diverse races under field conditions in China have not been known. Herein, Gansu, as a hotspot and an important oversummering region for Pst, was exemplified to demonstrate these roles of grass hosts. As a result, 63 Pst isolates, derived from 2184 uredial samples collected from grass hosts during harvesting period (from mid-June to mid-to-late July) and seeding period (mid to late September) in 2012 and 2013, were identified as 52 diverse phenotypes (82.5%) on the Chinese differential hosts. Subsequently, after inoculation of barberry, 52 Pst isolates with high infection type, 20 known races and 32 new races, were recovered from 1,712 single aecium, which are derived from 35 telial samples of grass hosts. Our experiments showed that Pst urediospores can oversummer on grass species in Gansu or other oversummering regions with similar ecological and climatic conditions. Pst teliospores, which are produced on these grass hosts, are important inoculum source for barberry infection in spring. Therefore, treatment of grasses hosts should be taken into consideration in management of wheat stripe rust.
Wheat stripe rust, caused by Puccinia striiformis Westend. f. sp. tritici Eriks. (Basidiomycota), is one of the most devastating diseases threatening wheat production worldwide. The disease occurs in all wheat-producing regions, particularly in cool and humid areas, and results in a yield loss of 10–30% in epidemic years (Li and Zeng 2002; Wellings 2011), and even a complete harvest failure after severe early infections on highly susceptible wheat cultivars (Chen 2005).
Pst is an obligate, biotrophic and heteroecious cereal rust fungus with a complex life cycle consisting of five different spore stages on two taxonomically different plant species. The urediospore stage is on wheat and grasses (the primary hosts) where the pathogen completes serial asexual transmission; the teliospore stage required for the sexual cycle is on the alternate dicot hosts (HovmØller et al. 2011). Production of teliospores can occur at all wheat growth stages especially when plants reach maturity (Chen et al. 2021). Basidiospores ejected from germinated teliospores infect Berberis and Mahonia species, the alternate (or aecial) hosts on which the pathogen has pycnial and aecial stages, to accomplish sexual reproduction. Aeciospores are spread by wind to the primary hosts where uredia are produced. Therefore, teliospore production is essential for Pst to complete sexual cycle.
It has been proven that grasses can be infected by Pst. Besides wheat, Pst potentially over-summers for surviving on 320 grass species of 50 genera (Hassebrauk 1965; Stubbs 1985). Grasses are demonstrated to have roles in the oversummering survival of Pst in temperate regions of the world, but their roles in initiating stripe rust on wheat varies from one region to another are not clearly known. In the United States, Pst oversummering on grass hosts is regarded as an important inoculum source for wheat stripe rust epidemics in the mountainous regions of the Pacific Northwest and California (Hendrix et al. 1965; Tollenaar and Houston 1967). Whereas, wild grasses were found to have only minor roles in wheat stripe rust epidemics compared with volunteer wheat in Oregon (Shaner and Powelson 1973) and Montana (Sharp and Hehn 1963), and have no role in the Sacramento Valley of California in 1975 (Line 1976). However, in Europe, the survival of the wheat stripe rust on wild grasses has been shown to provide inoculum sources for epidemics in the Harz regions of Germany (Becker and Hart 1939), but not in northwestern Europe (Zadoks 1961). In southeast Kazakstan, Pst survival on wild grasses during the summer was demonstrated to be an important inoculum source for stripe rust infections of wheat (Abiev et al. 1982). In China, although 88 gramineous grass species from 16 genera have been experimentally confirmed as uredial hosts of Pst (Lin and Li 1990; Niu et al. 1991; Li and Zeng 2002), studies have suggested that Pst can not survive on grasses during the summer in Chengdu Plain, Sichuan (Chen et al. 1957). Moreover, it has not been known the role of grass hosts in the survival of Pst for oversummering, and the role of oversummering urediospores as potential inoculum source for infection on autumn-sown wheat (Li and Zeng 2002).
Tianshui in Gansu has been considered the most crucial oversummering region for Pst and is therefore an important inoculum source in China. In this region, winter wheat is sown in the autumn from mid-late September to late October and is harvested during the following summer from late June to mid-to-late July (Additional file 1: Figure S1). As an obligate, biotrophic pathogen, Pst depends on living hosts and requires relatively low temperatures (0–22 °C for germination, infection, growth and survival. Once the air temperature exceeds 23 °C Pst can not oversummer (Li and Zeng 2002). Hence, during the period from wheat harvest to the emergence of autumn-sown winter wheat, an average 10-day (called ‘Xun’ in Chinese) temperature below 22 °C is required for Pst survival (Li and Zeng 2002). Tianshui is located in the mountainous region with elevations ranging from 1000 to 3120 m. During the summer, the climate in this region is usually cool and humid, which is favorable for the oversummering survival of Pst. So far, it has been demonstrated that Pst can oversummer on late-maturing wheat or volunteer wheat in the highland areas (> 1600 m) where the average ‘Xun’ temperature during the hottest days in July and August is below 22 °C and suitable for the development of the disease. After oversummering, viable urediospores in high-elevation regions are spread from grasses to seedlings of autumn-sown winter wheat grown in the low-elevation regions in September (Li and Zeng 2002). Based on previous studies in China, considerable attentions have been paid to the susceptibility of grasses to Pst. Although a few Pst isolates have been recovered from some grass species, most of those are known races with low virulence diversity (Ling 1945; Lu et al. 1956; Chen et al. 1957; Peng and Chen 1987; Niu et al. 1991; Yuan et al. 1994). However, it has not been determined whether Pst can oversummer on grass hosts in Tianshui, and thus the role of grass hosts that harbor Pst for oversummering has not been clearly defined in the Gansu region.
It has been suggested that Pst completes its sexual cycle on alternate hosts in the spring in Gansu and other regions of China (Zhao et al. 2013; Wang et al. 2016). This indicates that teliospores can maintain viability and are able to germinate in the spring to form basidiospores, which can infect newly emerging barberry leaves. A recent study in China has demonstrated that valid Pst teliospores potentially provided inoculum for barberry infection by stripe rust-infested wheat plants growing in fields adjacent to barberry bushes and a great deal of diseased wheat straws or debris inside wheat stacks around barberry bushes in Gansu and other wheat-growing regions. In those areas, Pst teliospores, which are produced at all growth stages of wheat and on diseased wheat straw or debris after wheat harvests, can germinate to produce basidiospores to infect barberry shoots emerging in the next spring (Chen et al. 2021). But, in contrast, the sexual stage is not detected in the U. S. Pacific Northwest (Wang and Chen 2015) and other regions of the world. Asexual hosts of Pst, besides wheat, also include grasses (Stubbs 1985). However, little is known about the survival of Pst teliospores on grass hosts in spring.
In recent years, in our field investigations of the Pst oversummering regions in Gansu, we routinely observed stripe rust infections on Agropyron and Elymus plants, and we also found the production of teliospores in these grass species in autumn. However, we did not directly determine whether the teliospores could overwinter on the grasses and germinate to provide inoculum for barberry infections. Therefore, the objectives of the current study were: (1) to determine whether grasses could harbor Pst teliospores for overwintering, and (2) to investigate the potential of teliospores originating from grasses to germinate in the next spring and infect barberry plants under natural conditions.
Characterization of Pst isolates from uredial samples of grasses
In Gansu, during two successive years (2012 and 2013), 2184 uredia from three stripe rust-infected grass species (Agropyron cristatum, Elymus cylindricus and E. excelsus) were collected at 21 sampling sites (Fig. 1a–f; Table 1). Among the samples, 1,905 uredial infections elicited immune or necrotic reactions on seedlings of the susceptible wheat cultivar Mingxian 169 (Fig. 2a) according to the 0-to-4 scale (Hungerford and Owens 1923), and 279 produced uredia derived from 12.8% of the total samples, with different infection types (ITs) ranging from 1 to 4 on the Mingxian 169 seedlings (Fig. 2b–e; Table 2). Among the 279 samples, 63 (22.6%) developed highly pathogenic infection types of 3 or 4, and 216 (77.4%) had relatively low pathogenicity with infection type of 1 and 2 on the cultivar (Table 2).
Infection type classification of Pst isolates from telial samples of grasses
Teliospores from leaves of two grass species, A. cristatum and E. cylindricus, were tested for germination in March, 2014 (Fig. 3a–d). Teliospore germination was initiated at 6 h post incubation, increased with prolonged incubation and peaked at 72 h (Fig. 4). The capacity of teliospore germination for E. cylindricus was higher than that for A. cristatum with a germination ratio of 31.4% and 26.4%, respectively.
Both 26 telial samples of A. cristatum and 9 ones of E. cylindricus produced aecia on barberry leaves after inoculation (Fig. 5a, b; Table 3). In total, four ITs 3–4 isolates and four ITs 1–2 ones were recovered from 227 single aecial cups of 60 aecia derived from teliospores on 26 A. cristatum leaf segment samples (Table 3). Likewise, forty-eight ITs 3–4 isolates, and twenty-two ITs 1–2 ones were obtained from 1,485 single aecial cups of 339 aecia derived from teliospores of 9 E. cylindricus leaf segment samples (Table 3). Thus, 78 (4.6%) isolates were pathogenic to the wheat cultivar Mingxian 169. Among these isolates, 52 (66.7%) were highly pathogenic (ITs 3-4) and 26 (33.3%) showed low pathogenicity (ITs 1-2). Most of aecial cups, accounting for 95.4% (1634/1712) of the total, only elicited necrotic flecks that failed to produce uredia on Mingxian 169 (Fig. 5c–g; Table 3).
Characterization of nonpathogenic and pathogenic Pst isolates recovered from grass plants
A total of 63 Pst isolates, with infection types of 3 and 4, were recovered from uredial samples of grass. Phenotyping of the isolates on a set of 19 Chinese differential hosts (genotypes) indicated that the 63 isolates elicited 52 different phenotypes, Ph1–Ph52, which exhibited variation as high as 82.5% in virulence (Table 4), Among the 63 isolates, many had mixed AV or VA phenotypes to some wheat genotypes. These included isolate 3-28-5, which had an AV reaction to the Lutescenes 128 wheat genotype with an unknown resistance gene, and isolate 2-56-1, which had a VA response against the Yr6 locus in the Trigo Eureka wheat genotype. Results as above indicated that these isolates were heterozygous in their abilities to infect plants with both known and unknown resistance loci. The results also demonstrated that grass species could harbor Pst for oversummering survival during the non-wheat growing season and could provide potential inoculum sources for Pst epidemics on autumn-sown winter wheat.
After barberry seedlings were inoculated with basidiospores from germinating telia that had overwintered on grasses, 52 Pst isolates with high infection types of 3 and 4, were obtained. Of these 52 isolates, 48 were recovered from E. cylindricus with 17 being previously reported races and 31 belonging to undescribed races. The remaining 4 A. cristatum samples consisted of 3 known races and 1 unknown race (Table 5). The 20 isolates of known races corresponded to 9 races, including 5 CYR33, 3 CYR32, 1 G22-9, 6 Su11-126, 1 Fo-2, 1 Hy8-1, 1 Hy-92, 1 Ky-3, and 1 ZS-6 types (Fig. 6; Table 5). In addition, the 32 isolates of unknown races were classified as virulent on the wheat genotypes Hybrid 46 (HyG) and Suwon 11 (SuG), and represented previously undescribed races (Fig. 6; Table 5). These results indicate that Pst teliospores formed on grasses in the autumn can successfully survive throughout the winter to germinate the next spring during low temperature and dry weather conditions. Thus, the conclusion is that surviving teliospores can germinate to produce basidiospores that can infect newly emerging barberry leaves and provide new sources for virulence in the spring. Therefore, Pst teliospores on grasses represent important inoculum source of barberry infections that function in the sexual cycle of the wheat stripe rust pathogen.
Grass hosts harbor the survival of Pst for oversummering and Pst isolates from grass hosts exhibit high-level phenotypic variation
Over the past decades, a few studies of Pst infection on grasses in China have been carried out, which have mainly concentrated on grass species susceptible to Pst to serve as uredial hosts (Ling 1945; Lu et al. 1956; Chen et al. 1957; Peng and Chen 1987; Lin and Li 1990; Niu et al. 1991; Yuan et al. 1994). Previous studies in China described recovery of 20 Pst isolates from 17 grass species, including Aegilops binucialis, A. columnaris, A. crassa, A. cylindrica, A. squarrosa, A. tauschii, Agropyron spp. (two), Elymus chinense, E. sibiricus, Elytrigia dasystachys, El. spicata, Glyceria sp., Psathyrostachys haushanica, Puccinellia distans, Roegneria ciliaris and Thinopyrum podperae. Most of these 20 Pst isolates belonged to 7 races (CYR17, CYR18, CYR22, CYR24, CYR25, CYR26 and CYR29), the prevalent races at that time (Lu et al. 1956; Peng and Chen 1987; Lin and Li 1990; Yuan et al. 1994). In comparison, there was a low frequency of new races. Totally, only five isolates, Y1 from E. chinense (Lu et al. 1956), Y9 and Y10 from two Agropyron spp. (Lu et al. 1956), one unnamed isolate from E. sibiricus (Lu et al. 1956) as well as W8403 from a Glyceria sp. (Peng and Chen 1987), were classified as new races. However, those previous studies as above have not determined the roles of grass hosts in harboring the survival of Pst for oversummering and in generating diverse pathogenic races in China. Our study extends these results because uredia derived from several Pst grass isolates failed to correspond to any known races. Furthermore, we found that telia-derived Pst isolates from grass hosts included not only known races but also new races. Each of the Pst populations from either uredial or telial samples had high levels of phenotypic variation, and mixed reactions of races (with avirulent and virulent reactions) on wheat differential hosts were detected in both populations. Similar mixtures of newly emerged phenotypic races in wheat have subsequently developed into prevalent races due to widespread cultivation of susceptible wheat cultivars (Wan et al. 2002). In the present study, we determined that grass hosts are important for the oversummering survival of Pst in Gansu and other oversummering regions with similar environmental conditions in China. Moreover, Pst isolates derived from these grasses exhibited highly diversified phenotypes. Likewise, in the United States Cheng et al. (2016) found that grasses harbor more diverse phenotypic and genotypic stripe rust isolates than those on cereal plants. Additionally, the results of annual race surveillances conducted during 2013–2018 in Gansu (Jia et al. 2018, 2021) showed that, besides a large number of known races, there was a proportion (an average of approximately 10%) of new races among Pst isolates, which were unclassified into any known races. It is speculated that grasses probably play a role in generating new races through somatic recombination between formae speciales of P. striiformis (Little and Manners 1969). On the other hand, it has been demonstrated that in recent years sexual reproduction of Pst on its susceptible alternate host, barberry plants, promotes the emergence of new races distinguished from the parent isolates. However, the main wheat cultivars grown in this region carry resistance genes against wheat stripe rust, which may reduce the occurrence of new races from grasses or barberry. Therefore, based on the identification of new races and known races recovered from uredial and telial samples of grass hosts, we suggest that grass hosts not only harbor Pst for oversummering to potentially provide inoculum sources to autumn-sown winter wheat in Gansu and other wheat-growing regions to cause stripe rust infection, but also play an important role in developing race diversity of Pst in China.
Grass hosts harbor viable Pst teliospores as potential inoculum sources for barberry infection and can be managed for the control of wheat stripe rust
Pst teliospores have very short or no dormancy. Eriksson and Henning (1896) first reported that Pst teliospores can germinate and generate basidiospores in both the fall and spring seasons. Raeder and Bever (1931) also found that some Pst teliospores can germinate immediately after maturation without a dormant period, and that the remainder could not germinate until the next spring. Both studies hinted that a part of Pst teliospores can maintain the germination capacity for a long time till next spring. Therefore, teliospore germination may have two phases, each of which can be affected by environmental conditions (Wellings 2011; Wang and Chen 2015; Chen et al. 2021).
The duration of teliospore viability is affected by various environmental conditions, including sunlight, humidity and temperature. Anikster (1986) found that Pst teliospores failed to germinate when kept outdoors for a year and then exposed to sunlight or shade. Wang and Chen (2015) also determined that teliospores preserved their viability for less than one year (from July until May in the following year) under uncontrolled outdoor conditions in the US Pacific Northwest. On the other hand, teliospores could keep the ability to germinate for up to 3 years under low temperature and dry conditions, or for as long as 14 years in airtight, partial vacuum and dry conditions (Anikster 1986).
Under natural conditions, the survival of Pst teliospores varies from one region to another worldwide. In China, in Gansu and other regions similar to Gansu, ecological and climatic conditions as well as cropping system (i.e. traditional agricultural model in some regions of northwestern China) are suitable for maintaining the validity of Pst teliospores until next spring. However, teliospore viability does not always overlap with the growth stage of the alternate host barberry, as is the case in the U. S. Pacific Northwest where teliospores usually degrade to inactivation prior to the appearance of new barberry shoots (Wang and Chen 2015). Additionally, another similar case was provided in Sweden where some Puccinia spp., including P. graminis f. sp. avenae, P. graminis f. sp. tritici/secalis and P. graminis f. sp. arrhenatheri, rather than Pst was detected in aecial samples from barberry species, (Berlin et al. 2013). The failure for Pst to complete sexual cycle in Sweden is most likely due to the unavailability of vigorous teliospores. Even if viable teliospores are presented, unfavorable climatic conditions for teliospore germination and barberry infection may not trigger initiation of sexual reproduction.
Viable teliospores are essential for initiating Pst sexual cycle. Because sexual stage of Pst has not been found until recently (Jin et al. 2010), teliospores as inoculum sources commencing sexual reproduction under field conditions has not been investigated prior to this finding. Over the past decade, we have demonstrated that Pst sexual cycle on barberry regularly occurs in oversummering regions under field conditions in China (Zhao et al. 2013; Li et al. 2016; Wang et al. 2016). This fact hinted that in spring viable Pst teliospores could act as inoculum for barberry infection. Our previous study testified that in China teliospore sources, which are responsible for sexual reproduction of the rust, originate from growing wheat plants, diseased wheat straws or debris (Chen et al. 2021). In that study, it mentioned that Pst teliospores are produced during all stages of wheat growth in the field in China, and possess the capacity of germination from August to May of the next year. In addition, Pst teliospores inside wheat straw stacks after harvesting can survive until the next spring or later (Chen et al. 2021), which enables teliospores to potentially infect barberry young leaves and sometime other young tissues (petiole, thorn and berry). Our study of teliospores now shows that native grasses provide important sources for Pst sexual reproduction in spring in Gansu region of China. These results can be used to develop an integrated wheat stripe rust management strategy by combining grass and barberry control to reduce stripe rust genetic variability in the Gansu region, or even other oversummering regions of China.
Our study demonstrates that native grass species can contribute to the survival of Pst for oversummering and also provide potential teliospore inoculum for triggering sexual reproduction under natural conditions in China. Determination of production and viability of Pst teliospores is vital for understanding teliospore inoculum sources that cause occurrence of Pst sexual reproduction and preventing from this process of the rust to decrease the emergence of new Pst races that may be able to overcome resistance in established wheat varieties and recently released wheat lines. Therefore, the control of grass hosts and barberry bushes around wheat fields to reduce sexual recombination should be considered for integrated management of wheat stripe rust in China.
Based on previous studies in China, Agropyron and Elymus are more susceptible to Pst than other genera of gramineous grasses and were suggested as potential inoculum sources for stripe rust epidemics on autumn-sown winter wheat (Lu et al. 1956; Lin and Li 1990; Niu et al. 1991). During field investigations, we found that these two grass genera are widely distributed in the oversummering regions of Gansu and were commonly infected by stripe rust fungi. Thus, we concentrated our efforts on sampling and isolation of the pathogen from these two genera, and collected 864 stripe rust-infected leaf samples (with uredia) at 7 different sampling sites in Tianshui from September to October in 2012, and obtained 1320 stripe rust-infected leaf samples (with uredia) at 14 sites in Pingnan and Tianshui, Gansu from August to October in 2013. Thirty-five leaf samples with telia were collected from A. cristatum and E. cylindricus in March 2014 at uredial sampling sites labelled in the autumn 2013. Leaf samples were individually put into paper bags, which were dried in air at room temperature and kept in a silica gel desiccator, and then maintained under low temperature (4–5 °C) in a freezer until use.
Barberry (B. shensiana Ahrendt) seeds collected from Xinjie, Baoji, Shaanxi Province were planted and grown as described by Zhao et al. (2013). The Wheat cultivar, Mingxian 169, which is highly susceptible to all known Chinese Pst races, and a set of wheat differential hosts consisting of 19 wheat genotypes used to identify Pst races were grown in plastic pots in a rust-free growth chamber under the same conditions used to cultivate barberry seedlings.
Inoculation of wheat seedlings with uredial samples from grasses
Individual grass leaves with stripe rust uredia were placed on clean glass slides in a petri dish containing 2–3 layers of wetted filter paper for 1–2 h. A single uredium was then transferred to seedling leaf surfaces of the Mingxian 169 wheat cultivar. The inoculated plants were misted with sterile deionized water, covered with a transparent plastic cylinder and incubated in a dew chamber (E-36L2, Percival, IA, USA) at 10 °C for 24 h in the dark. After incubation, the plants were placed in a controlled growth chamber with a photoperiod of 16 h light at 16℃ and 8 h dark at 13 °C. Infection types (ITs) were recorded 18–20 days post-inoculation based on a scale of 0–4 (Hungerford and Owens 1923). This scale is: ITs 0 = healthy appearance without necrotic and chlorotic foci. ITs 1–2 necrotic to chlorotic foci without uredia. IT 3 = small chlorotic foci containing small amounts of urediospores. IT 4 = foci with abundant urediospores surrounded by bright green tissue islands. Isolates with IT 3 or 4 reactions on Mingxian 169 wheat were used for virulence tests.
Inoculation of barberry seedlings with teliospores from telial samples of grasses
Grass plants with stripe rust uredia were labelled at collection sites in the previous autumn, from which telial samples were collected after overwintering, and the germination of teliospores was evaluated during the following spring by inoculation of barberry seedlings. Grass leaf samples with telia were cut into 5-cm-long segments and soaked in sterile deionized water at room temperature for 24 h. The leaf segments were put onto a clean glass slide to abraded until telia were broken to expose teliospores, after which the segments were placed onto 2% (m/v) water agar plates and incubated at 16 °C in a condition-controlled growth chamber. After the teliospores began to germinate, the leaf segments were used to inoculate barberry seedlings as described by Zhao et al. (2013). After inoculation, the barberry plants were incubated for 3–4 d days at 16 °C and then were transferred to a condition-controlled growth chamber under the same conditions mentioned above until pycnial nectar appeared. Pycnial fertilization was conducted by transferring nectars from one pycnium to another with a clean plastic inoculation loop. Individual emerging aecia were excised, placed on a clean glass slide disinfected with 75% ethanol solution, and broken to expose aeciospores by gentle pressure with a clean scalpel. The aeciospores were then suspended in 50 μL of sterile deionized water and misted onto seedlings of wheat cultivar Mingxian 169.
Virulence tests on differential hosts
To characterize avirulence and virulence responses of Pst isolates recovered from the grass telial samples, uredia of ITs 3 and 4 were inoculated to Mingxian 169 seedlings and evaluated for avirulence and virulence patterns on a set of 19 Chinese differential host genotypes as described by Zhao et al. (2013). Mingxian 169 was used as a susceptible control in all tests. The scale of 0 to 4 described by Hungerford and Owens (1923) was used to score infection types on the differential varieties. ITs 0 to 2 were considered to be avirulent, and ITs 3 and 4 were designated as virulent.
Availability of data and materials
- Pst :
Puccinia striiformis f. sp. tritici
Abiev SA, Zhakhanov A, Kencsarina G, Esengulova BZ. Specialization of yellow rust of wheat in South-Eastern Kazakhstan. Botaniki Botanicheskie Materialy Gerbariya Instituta Botaniki Akademii Nauk Kzazkhstoi SSR. 1982;12:96–8 (in Russian).
Anikster Y. Teliospore germination in some rust fungi. Phytopathology. 1986;76:1026–30. https://doi.org/10.1094/Phyto-76-1026.
Becker H, Hart H. Das Auftreten und die Verbreitung von Gelbrost im Ostharz und den daran angrenzenden Weizenanbaugebieten (in German). Ztschrift für Pflanzenkrankheiten (Pflanzenpathologie) und Pflanzenschutz. 1939;49:449–81.
Berlin A, Kyaschenko J, Justesen AF, Yuen J. Rust fungi forming aecia on Berberis spp. in Sweden. Plant Dis. 2013;97:1281–7. https://doi.org/10.1094/PDIS-10-12-0989-RE.
Chen XM. Epidemiology and control of stripe rust [Puccinia striiformis f. sp. tritici] on wheat. Can J Plant Pathol. 2005;27(3):314–37. https://doi.org/10.1080/07060660509507230.
Chen SM, Zhou JP, Li RB, Wang KN, Ou YY, Hong XW, et al. Studies on the epidemiology of stripe rust on winter wheat in North China. Acta Phytopathol Sin. 1957;3(1):63–85 (in Chinese).
Chen W, Zhang ZD, Chen XM, Meng Y, Huang LL, Kang ZS, et al. Field production, germinability, and survival of Puccinia striiformis f. sp. tritici teliospores in China. Plant Dis. 2021;105(8):2122–8. https://doi.org/10.1094/PDIS-09-20-2018-RE.
Cheng P, Chen XM, See DR. Grass hosts harbor more diverse isolates of Puccinia striiformis than cereal crops. Phytopathology. 2016;106(4):362–71. https://doi.org/10.1094/PHYTO-07-15-0155-R.
Eriksson J, Henning E. “Die Getreideroste.” Norstedt & SÖner, Stockolm. 1896.
Hassebrauk K. Nomenklatur, geographische Verbreitung und Wirtsbereich des Gelbrostes, Puccinia striiformis West. Mitt. Biol. Bundesanst. Land-und Forstwirtsch., Berlin-Dahlem. 1965;116:1–75. https://doi.org/10.1002/jpln.19661120115.
Hendrix JW, Burleigh JR, Tu JC. Oversummering of stripe rust at high elevations in the Pacific Northwest-1963. Plant Dis Rep. 1965;49:275–8.
Hovmøller MS, Sørensen C, Walter S, Justesen AF. Diversity of Puccinia striiformis on cereals and grasses. Annu Rev Phytopathol. 2011;49:197–217. https://doi.org/10.1146/annurev-phyto-072910-095230.
Hungerford CW, Owens CE. Specialized varieties of Puccinia glumarum and hosts for variety tritici. J Agric Res. 1923;25(9):363–401.
Jia QZ, Cao SQ, Huang J, Zhang B, Sun ZY, Luo HS, et al. Monitoring the variation of physiological races of Puccinia striiformis f. sp. tritici in Gansu province, China during 2013–2016 (in Chinese). Plant Prot. 2018;44(6):162–7 (in Chinese).
Jia QZ, Cao SQ, Wang XM, Huang J, Sun ZY, Zhang B, et al. 2021) Monitoring the variation of physiological races of Puccinia striiformis f. sp. tritici in Gansu province during 2017–2018. Plant Prot. 2021;47(2):214–8 (in Chinese).
Jin Y, Szabo LJ, Carson M. Century-old mystery of Puccinia striiformis life history solved with the identification of Berberis as an alternate host. Phytopathology. 2010;100(5):432–5. https://doi.org/10.1094/PHYTO-100-5-0432.
Li ZQ, Zeng SM. Wheat rusts in China. Beijing: China Agriculture Press. 2002. p. 211–8 (in Chinese).
Li Q, Qin JF, Zhao YY, Zhao J, Huang LL, Kang ZS. Virulence analysis of sexual progeny of the wheat stripe rust pathogen recovered from wild barberry in Shaanxi and Gansu. Acta Phytopathol Sin. 2016;46(6):809–20. https://doi.org/10.13926/j.cnki.apps.000181.
Lin XM, Li ZQ. On the host range of stripe rust of wheat in China. Acta Phytopathol Sin. 1990;20(4):265–70 (in Chinese).
Line RF. Factors contributing to an epidemic of stripe rust on wheat in the Sacramento Valley of California in 1974. Plant Dis Rep. 1976;60:312–6.
Ling L. Epidemiology studies on stripe rust of wheat in Chengtu plain, China. Phytopathol. 1945;35:885–94.
Little R, Manners JG. Somatic recombination in yellow rust of wheat (Puccinia striiformis): I—the production and possible origin of two new physiologic races. Trans Br Mycol Soc. 1969;53(2):251–8.
Lu SY, Fan GF, Xie SM, Wu WZ, Kong XL, Yang ZM, et al. Studies on stripe rust of wheat I—physiologic specialization of Puccinia glumarum (Schmidt) Erikss. & Henn. Acta Phytopathol Sin. 1956; 2(2):152–66, 213–4. https://doi.org/10.13926/j.cnki.apps.1956.02.006 (in Chinese).
Niu YC, Li ZQ, Shang HS. Evaluation of 50 grass species for resistance to stripe rust. Pratac Sci. 1991;8(3):46–8 (in Chinese).
Peng YF, Chen SM. Comparative studies on pathogenicity of Puccinia striiformis on grasses and wheat in China. Plant Prot. 1987;13(6):19–20 (in Chinese).
Raeder JM, Bever WM. Spore germination of Puccinia glumarum with notes on related species. Phytopathology. 1931;21:767–89.
Shaner G, Powelson RL. The oversummering and dispersal of inoculum of Puccinia striiformis in Oregon. Phytopathology. 1973;63:13–7. https://doi.org/10.1094/Phyto-63-13.
Sharp EL, Hehn ER. Overwintering of stripe rust in winter wheat in Montana. Phytopathology. 1963;53:1239–40.
Stubbs W. Stripe rust. In: Roelfs AP, Bushnell WR, editors. The cereal rusts, vol. II. New York: Academic Press; 1985. p. 61–101.
Tollenaar H, Houston BR. A study on the epidemiology of stripe rust, Puccinia striiformis West, in California. Can J Bot. 1967;45:291–307. https://doi.org/10.1139/b67-028.
Wan AM, Zhao ZH, Chen XM, He ZH, Jin SL, Jia QZ, et al. Wheat stripe rust epidemic and virulence of Puccinia striiformis f. sp. tritici in China in 2002. Plant Dis. 2004;88(8):896–904. https://doi.org/10.1094/PDIS.2004.88.8.896.
Wang MN, Chen XM. Barberry does not function as an alternate host for Puccinia striiformis f. sp. tritici in the US Pacific Northwest due to teliospore degradation and barberry phenology. Plant Dis. 2015;99(11):1500–6. https://doi.org/10.1094/PDIS-12-14-1280-RE.
Wang ZY, Zhao J, Chen XM, Peng YL, Ji JJ, Zhao SL, et al. Virulence variations of Puccinia striiformis f. sp. tritici isolates collected from Berberis spp. in China. Plant Dis. 2016;100:131–8. https://doi.org/10.1094/PDIS-12-14-1296-RE.
Wellings CR. Global status of stripe rust : a review of historical and current threats. Euphytica. 2011;179:129–41. https://doi.org/10.1007/s10681-011-0360-y.
Yuan WH, Li GB, Wang BT. Aegilops squarrosa L.-a host of Puccinia striiformis West. J Hebei Agric Univ. 1994;17(3):75–7 (in Chinese).
Zadoks JC. Yellow rust on wheat studies in epidemiology and physiologic specialization. Tiidschr Plantenziekten. 1961;67:69–256. https://doi.org/10.1007/BF01984044.
Zhao J, Wang L, Wang ZY, Chen XM, Kang ZS. Identification of eighteen Berberis species as alternate hosts of Puccinia striiformis f. sp. tritici and virulence variation in the pathogen isolates from natural infection of barberry plants in China. Phytopathology. 2013;103(9):927–34. https://doi.org/10.1094/PHYTO-09-12-0249-R.
This work was supported by the National Key Research and Development Program of China (2021YFD1401000), the National Natural Science Foundation of China (32072358, 31871918, and 31071641), the Natural Science Basic Research Plan in Shaanxi Province of China (2020JZ-15), National “111 Plan” (BP0719026).
Ethics approval and consent to participate
Consent for publication
The authors declare that they have no competing interests.
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
About this article
Cite this article
Qin, J., Wang, Z., Lv, Y. et al. Grasses are able to harbor the oversummering of urediospores and the overwintering of teliospores of Puccinia striiformis f. sp. tritici in China. Phytopathol Res 4, 24 (2022). https://doi.org/10.1186/s42483-022-00129-x
- Wheat stripe rust
- Disease management